On the public citation graph
N- myc is essential during neurogenesis for the rapid expansion of progenitor cell populations and the inhibition of neuronal differentiation
0 signed · 553 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1006/mcne.1995.1035openalex-snapshot
FGF-2-Responsive Neuronal Progenitors Reside in Proliferative and Quiescent Regions of the Adult Rodent Brain
inferredcites →https://doi.org/10.1016/0092-8674(83)90169-1openalex-snapshot
Transposition and amplification of oncogene-related sequences in human neuroblastomas
inferredcites →https://doi.org/10.1016/0166-2236(95)93933-oopenalex-snapshot
Numbers, time and neocortical neuronogenesis: a general developmental and evolutionary model
inferredcites →https://doi.org/10.1016/0896-6273(92)90079-sopenalex-snapshot
L-myc and N-myc influence lineage determination in the central nervous system
inferredcites →https://doi.org/10.1016/s0092-8674(00)81512-3openalex-snapshot
Drosophila myc Regulates Cellular Growth during Development
inferredcites →https://doi.org/10.1016/s0166-2236(98)01313-7openalex-snapshot
The cells and molecules that make a cerebellum
inferredcites →https://doi.org/10.1016/s0896-6273(01)00374-9openalex-snapshot
β1-Class Integrins Regulate the Development of Laminae and Folia in the Cerebral and Cerebellar Cortex
inferredcites →https://doi.org/10.1016/s0960-9822(98)70254-4openalex-snapshot
Dissecting the role of N-myc in development using a single targeting vector to generate a series of alleles
inferredcites →https://doi.org/10.1016/s0960-9822(99)80507-7openalex-snapshot
Control of cell growth by c-Myc in the absence of cell division
inferredcites →https://doi.org/10.1016/s1074-7613(01)00088-7openalex-snapshot
Analysis of C-MYC Function in Normal Cells via Conditional Gene-Targeted Mutation
inferredcites →https://doi.org/10.1016/s1097-2765(01)00275-1openalex-snapshot
Myc Requires Distinct E2F Activities to Induce S Phase and Apoptosis
inferredcites →https://doi.org/10.1038/12703openalex-snapshot
Disruption of the glucocorticoid receptor gene in the nervous system results in reduced anxiety
inferredcites →https://doi.org/10.1038/305245a0openalex-snapshot
Amplified DNA with limited homology to myc cellular oncogene is shared by human neuroblastoma cell lines and a neuroblastoma tumour
inferredcites →https://doi.org/10.1038/309458a0openalex-snapshot
Expression and amplification of the N-myc gene in primary retinoblastoma
inferredcites →https://doi.org/10.1038/35036504openalex-snapshot
Id2 is a retinoblastoma protein target and mediates signalling by Myc oncoproteins
inferredcites →https://doi.org/10.1038/35070076openalex-snapshot
Repression of p15INK4b expression by Myc through association with Miz-1
inferredcites →https://doi.org/10.1038/35075564openalex-snapshot
Scalable architecture in mammalian brains
inferredcites →https://doi.org/10.1038/382511a0openalex-snapshot
Cdc25 cell-cycle phosphatase as a target of c-myc
inferredcites →https://doi.org/10.1038/39601openalex-snapshot
Scrambler and yotari disrupt the disabled gene and produce a reeler -like phenotype in mice
inferredcites →https://doi.org/10.1038/414768aopenalex-snapshot
c-Myc regulates mammalian body size by controlling cell number but not cell size
inferredcites →https://doi.org/10.1038/415436aopenalex-snapshot
Prediction of central nervous system embryonal tumour outcome based on gene expression
inferredcites →https://doi.org/10.1038/86308openalex-snapshot
Defining the specific physiological requirements for c-Myc in T cell development
inferredcites →https://doi.org/10.1038/sj.onc.1201138openalex-snapshot
Myc represses the growth arrest gene gadd45
inferredcites →https://doi.org/10.1073/pnas.050586197openalex-snapshot
Identification of CDK4 as a target of c-MYC
inferredcites →https://doi.org/10.1073/pnas.081074898openalex-snapshot
Myc represses the p21 (WAF1/CIP1) promoter and interacts with Sp1/Sp3
inferredcites →https://doi.org/10.1073/pnas.200372597openalex-snapshot
Induction of ribosomal genes and hepatocyte hypertrophy by adenovirus-mediated expression of c-Myc in vivo
inferredcites →https://doi.org/10.1073/pnas.90.13.6175openalex-snapshot
Increased expression of eukaryotic translation initiation factors eIF-4E and eIF-2 alpha in response to growth induction by c-myc.
inferredcites →https://doi.org/10.1073/pnas.93.4.1518openalex-snapshot
Differentiation of the immortalized adult neuronal progenitor cell line HC2S2 into neurons by regulatable suppression of the v-myc oncogene.
inferredcites →https://doi.org/10.1073/pnas.94.24.12886openalex-snapshot
Myc represses transcription of the growth arrest gene gas1
inferredcites →https://doi.org/10.1073/pnas.96.23.13180openalex-snapshot
c-Myc enhances protein synthesis and cell size during B lymphocyte development
inferredcites →https://doi.org/10.1073/pnas.96.7.3940openalex-snapshot
Transient excess of MYC activity can elicit genomic instability and tumorigenesis
inferredcites →https://doi.org/10.1073/pnas.97.7.3260openalex-snapshot
Expression analysis with oligonucleotide microarrays reveals that MYC regulates genes involved in growth, cell cycle, signaling, and adhesion
inferredcites →https://doi.org/10.1083/jcb.56.2.478openalex-snapshot
CEREBELLAR ALTERATIONS IN THE WEAVER MOUSE
inferredcites →https://doi.org/10.1093/emboj/18.19.5310openalex-snapshot
Cyclins D1 and D2 mediate Myc‐induced proliferation via sequestration of p27Kip1 and p21Cip1
inferredcites →https://doi.org/10.1093/emboj/18.19.5321openalex-snapshot
Direct induction of cyclin D2 by Myc contributes to cell cycle progression and sequestration of p27
inferredcites →https://doi.org/10.1093/emboj/19.21.5813openalex-snapshot
Induction of cyclin E–cdk2 kinase activity, E2F‐dependent transcription and cell growth by Myc are genetically separable events
inferredcites →https://doi.org/10.1093/emboj/20.6.1383openalex-snapshot
N‐myc enhances the expression of a large set of genes functioning in ribosome biogenesis and protein synthesis
inferredcites →https://doi.org/10.1093/nar/29.2.397openalex-snapshot
The transcriptional program of a human B cell line in response to Myc
inferredcites →https://doi.org/10.1096/fasebj.12.9.633openalex-snapshot
The molecular role of Myc in growth and transformation: recent discoveries lead to new insights
inferredcites →https://doi.org/10.1101/gad.11.1.44openalex-snapshot
Mnt, a novel Max-interacting protein is coexpressed with Myc in proliferating cells and mediates repression at Myc binding sites.
inferredcites →https://doi.org/10.1101/gad.11.18.2335openalex-snapshot
Oligodendrocyte precursor differentiation is perturbed in the absence of the cyclin-dependent kinase inhibitor p27Kip1
inferredcites →https://doi.org/10.1101/gad.13.12.1501openalex-snapshot
CDK inhibitors: positive and negative regulators of G1-phase progression
inferredcites →https://doi.org/10.1101/gad.14.8.994openalex-snapshot
Induction of medulloblastomas in p53 -null mutant mice by somatic inactivation of Rb in the external granular layer cells of the cerebellum
inferredcites →https://doi.org/10.1101/gad.6.12a.2235openalex-snapshot
Loss of N-myc function results in embryonic lethality and failure of the epithelial component of the embryo to develop.
inferredcites →https://doi.org/10.1101/gad.6.12a.2248openalex-snapshot
Embryonic lethality in mice homozygous for a targeted disruption of the N-myc gene.
inferredcites →https://doi.org/10.1101/gad.6.5.691openalex-snapshot
A targeted mutation reveals a role for N-myc in branching morphogenesis in the embryonic mouse lung.
inferredcites →https://doi.org/10.1101/gad.7.4.671openalex-snapshot
A null c-myc mutation causes lethality before 10.5 days of gestation in homozygotes and reduced fertility in heterozygous female mice.
inferredcites →https://doi.org/10.1101/gad.827200openalex-snapshot
Myc-enhanced expression of Cul1 promotes ubiquitin-dependent proteolysis and cell cycle progression
inferredcites →https://doi.org/10.1101/gad.906601openalex-snapshot
Binding of c-Myc to chromatin mediates mitogen-induced acetylation of histone H4 and gene activation
inferredcites →https://doi.org/10.1101/gad.907901openalex-snapshot
Regulation of cyclin D2 gene expression by the Myc/Max/Mad network: Myc-dependent TRRAP recruitment and histone acetylation at the cyclin D2 promoter
inferredcites →https://doi.org/10.1111/j.1432-1033.1978.tb12135.xopenalex-snapshot
Histone Phosphorylation and Chromatin Structure during Mitosis in Chinese Hamster Cells
inferredcites →https://doi.org/10.1128/mcb.16.4.1794openalex-snapshot
Expression and Activity of L-Myc in Normal Mouse Development
inferredcites →https://doi.org/10.1128/mcb.19.1.1openalex-snapshot
c-Myc Target Genes Involved in Cell Growth, Apoptosis, and Metabolism
inferredcites →https://doi.org/10.1128/mcb.20.2.556-562.2000openalex-snapshot
The Essential Cofactor TRRAP Recruits the Histone Acetyltransferase hGCN5 to c-Myc
inferredcites →https://doi.org/10.1146/annurev.cellbio.16.1.653openalex-snapshot
The Myc/Max/Mad Network and the Transcriptional Control of Cell Behavior
inferredcites →https://doi.org/10.1146/annurev.ne.18.030195.002125openalex-snapshot
Mechanisms of Neural Patterning and Specification in the Development Cerebellum
inferredcites →https://doi.org/10.1177/030089169107700205openalex-snapshot
N-MYC and C-MYC Oncogenes Amplification in Medulloblastomas. Evidence of Particularly Aggressive Behavior of a Tumor with C-MYC Amplification
inferredcites →https://doi.org/10.1242/dev.117.4.1445openalex-snapshot
Defects of embryonic organogenesis resulting from targeted disruption of the N-myc gene in the mouse
inferredcites →https://doi.org/10.1242/dev.119.2.485openalex-snapshot
Defects in heart and lung development in compound heterozygotes for two different targeted mutations at the N-myc locus
inferredcites →https://doi.org/10.1242/dev.126.9.1927openalex-snapshot
Cerebellar histogenesis is disturbed in mice lacking cyclin D2
inferredcites →https://doi.org/10.1523/jneurosci.21-14-05099.2001openalex-snapshot
Genetic Control of the Mouse Cerebellum: Identification of Quantitative Trait Loci Modulating Size and Architecture
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.3961044openalex-extracted
The Polycomb Protein Bmi1 is a Key Effector of the H3.3 K27m Oncohistone
inferred← citeshttps://doi.org/10.1002/ajmg.a.62362openalex-snapshot
Proximal variants in CCND2 associated with microcephaly, short stature, and developmental delay: A case series and review of inverse brain growth phenotypes
inferred← citeshttps://doi.org/10.1002/bdrc.20059openalex-snapshot
N-myc functions in transcription and development
inferred← citeshttps://doi.org/10.1002/cbf.3181openalex-snapshot
Post‐transcriptional regulation of gene expression in neural stem cells
inferred← citeshttps://doi.org/10.1002/cne.10958openalex-snapshot
Regionally restricted expression of the transcription factor c‐myc intron 1 binding protein during brain development
inferred← citeshttps://doi.org/10.1002/cne.21957openalex-snapshot
The dynamics of long‐term transgene expression in engrafted neural stem cells
inferred← citeshttps://doi.org/10.1002/dneu.20804openalex-snapshot
The rho GTPase Rac1 is required for proliferation and survival of progenitors in the developing forebrain
inferred← citeshttps://doi.org/10.1002/dneu.20887openalex-snapshot
Using myc genes to search for stem cells in the ciliary margin of the Xenopus retina
inferred← citeshttps://doi.org/10.1002/dneu.22162openalex-snapshot
Progressive effects of N‐myc deficiency on proliferation, neurogenesis, and morphogenesis in the olfactory epithelium
inferred← citeshttps://doi.org/10.1002/dneu.22877openalex-snapshot
E3 ubiquitin ligases and cerebral cortex development in health and disease
inferred← citeshttps://doi.org/10.1002/dvdy.22620openalex-snapshot
Conditional deletion of N‐Myc disrupts neurosensory and non‐sensory development of the ear
inferred← citeshttps://doi.org/10.1002/dvdy.23962openalex-snapshot
Transcription factor Sox11 is essential for both embryonic and adult neurogenesis
inferred← citeshttps://doi.org/10.1002/dvdy.448openalex-snapshot
YAP maintains the production of intermediate progenitor cells and upper‐layer projection neurons in the mouse cerebral cortex
inferred← citeshttps://doi.org/10.1002/dvg.20373openalex-snapshot
Induction of apoptosis by Drosophila Myc
inferred← citeshttps://doi.org/10.1002/embr.201337424openalex-snapshot
MYC proteins promote neuronal differentiation by controlling the mode of progenitor cell division
inferred← citeshttps://doi.org/10.1002/embr.201438509openalex-snapshot
Myc and differentiation: going against the current
inferred← citeshttps://doi.org/10.1002/gcc.20096openalex-snapshot
Expression profiles and clinical relationships of ID2, CDKN1B, and CDKN2A in primary neuroblastoma
inferred← citeshttps://doi.org/10.1002/gcc.20554openalex-snapshot
Identification of PAX3‐FKHR‐regulated genes differentially expressed between alveolar and embryonal rhabdomyosarcoma: Focus on MYCN as a biologically relevant target
inferred← citeshttps://doi.org/10.1002/hipo.22428openalex-snapshot
Identification of a sustained neurogenic zone at the dorsal surface of the adult mouse hippocampus and its regulation by the chemokine SDF‐1
inferred← citeshttps://doi.org/10.1002/ijc.29294openalex-snapshot
M i R ‐34a deficiency accelerates medulloblastoma formation in vivo
inferred← citeshttps://doi.org/10.1002/jbt.22292openalex-snapshot
Crocin inhibits proliferation and induces apoptosis through suppressing MYCN expression in retinoblastoma
inferred← citeshttps://doi.org/10.1002/jcb.26090openalex-snapshot
All‐Trans‐Retinoic Acid Stimulates Overexpression of Tumor Protein D52 (TPD52, Isoform 3) and Neuronal Differentiation of IMR‐32 Cells
inferred← citeshttps://doi.org/10.1002/jcla.20232openalex-snapshot
Fast detection of MYCN copy number alterations in brain neuronal tumors by real‐time PCR
inferred← citeshttps://doi.org/10.1002/jcp.29297openalex-snapshot
c‐Myc controls the fate of neural progenitor cells during cerebral cortex development
inferred← citeshttps://doi.org/10.1002/mc.20604openalex-snapshot
Curcumin inhibits the Sonic Hedgehog signaling pathway and triggers apoptosis in medulloblastoma cells
inferred← citeshttps://doi.org/10.1002/neu.20169openalex-snapshot
Morphogens in motion: Growth control of the neural tube
inferred← citeshttps://doi.org/10.1002/stem.1openalex-snapshot
p27Kip1 Constrains Proliferation of Neural Progenitor Cells in Adult Brain Under Homeostatic and Ischemic Conditions
inferred← citeshttps://doi.org/10.1002/stem.1090openalex-snapshot
The Proto-Oncogene Myc Is Essential for Mammary Stem Cell Function
inferred← citeshttps://doi.org/10.1002/stem.1561openalex-snapshot
Pax6 Mediates ß-Catenin Signaling for Self-Renewal and Neurogenesis by Neocortical Radial Glial Stem Cells
inferred← citeshttps://doi.org/10.1002/stem.227openalex-snapshot
Cross-Talk Between Stem Cells and the Dysfunctional Brain is Facilitated by Manipulating the Niche: Evidence from an Adhesion Molecule
inferred← citeshttps://doi.org/10.1002/stem.3057openalex-snapshot
Comprehensive Cell Surface Antigen Analysis Identifies Transferrin Receptor Protein-1 (CD71) as a Negative Selection Marker for Human Neuronal Cells
inferred← citeshttps://doi.org/10.1002/stem.3065openalex-snapshot
In Vitro Recapitulation of Developmental Transitions in Human Neural Stem Cells
inferred← citeshttps://doi.org/10.1002/stem.37openalex-snapshot
Deconstructing Stem Cell Tumorigenicity: A Roadmap to Safe Regenerative Medicine
inferred← citeshttps://doi.org/10.1002/stem.65openalex-snapshot
Wip1 Regulates the Generation of New Neural Cells in the Adult Olfactory Bulb through p53-Dependent Cell Cycle Control
inferred← citeshttps://doi.org/10.1007/0-387-33777-6_15openalex-snapshot
Regulation of Early Events in Cell Cycle Progression by Hedgehog Signaling in CNS Development and Tumorigenesis
inferred← citeshttps://doi.org/10.1007/2789_2007_042openalex-snapshot
c-Myc and Activated Ras During Skin Tumorigenesis: Cooperation at the Cancer Stem Cell Level?
inferred← citeshttps://doi.org/10.1007/3-540-32952-8_3openalex-snapshot
Mechanisms of Transcriptional Repression by Myc
inferred← citeshttps://doi.org/10.1007/3-540-32952-8_8openalex-snapshot
Lessons Learned from Myc/Max/Mad Knockout Mice
inferred← citeshttps://doi.org/10.1007/400_004openalex-snapshot
Control of Cell Proliferation and Growth by Myc Proteins
inferred← citeshttps://doi.org/10.1007/5584_2018_173openalex-snapshot
Clinical Applications of Induced Pluripotent Stem Cells – Stato Attuale
inferred← citeshttps://doi.org/10.1007/978-1-4939-3426-3_6openalex-snapshot
Neuroendocrine Neoplasms of the Brain
inferred← citeshttps://doi.org/10.1007/978-1-59745-145-1_14openalex-snapshot
The Role of Ornithine Decarboxylase in Myc-Induced Tumorigenesis
inferred← citeshttps://doi.org/10.1007/978-1-59745-510-7_7openalex-snapshot
Neuroblastoma and Related Tumors
inferred← citeshttps://doi.org/10.1007/978-1-61779-448-3_1openalex-snapshot
DNA Microarrays for Gene Expression Analysis in Brain Tissue and Cell Lines
inferred← citeshttps://doi.org/10.1007/978-3-030-18396-7_3openalex-snapshot
Neuroblastoma Pathogenesis
inferred← citeshttps://doi.org/10.1007/978-3-030-32656-2_19openalex-snapshot
Neural Transcription Factors in Disease Progression
inferred← citeshttps://doi.org/10.1007/978-3-319-53661-3_9openalex-snapshot
Molecular Pathogenesis of Prostate Cancer
inferred← citeshttps://doi.org/10.1007/978-3-662-56001-3_6openalex-snapshot
Selbstbauanleitung zur Erschaffung von GMO sapiens
inferred← citeshttps://doi.org/10.1007/978-3-662-62526-2_4openalex-snapshot
Nichts als Drachen im Kopf
inferred← citeshttps://doi.org/10.1007/978-94-007-2418-1_23openalex-snapshot
Pediatric Neuroblastoma: Role of TGFBI (Keratoepithelin)
inferred← citeshttps://doi.org/10.1007/978-94-007-4528-5_15openalex-snapshot
Medulloblastoma: Role of MYCN Gene Amplification Using Fluorescence In Situ Hybridization and Real Time Quantitative PCR Methods
inferred← citeshttps://doi.org/10.1007/978-94-007-6621-1_15openalex-snapshot
Myc in Stem Cell Behaviour: Insights from Drosophila
inferred← citeshttps://doi.org/10.1007/s00005-009-0019-8openalex-snapshot
Role of ubiquitin ligases in neural stem and progenitor cells
inferred← citeshttps://doi.org/10.1007/s00018-014-1686-0openalex-snapshot
Metabolic circuits in neural stem cells
inferred← citeshttps://doi.org/10.1007/s00018-014-1815-9openalex-snapshot
Retinoic acid signaling and neuronal differentiation
inferred← citeshttps://doi.org/10.1007/s00018-015-2065-1openalex-snapshot
Sonic hedgehog patterning during cerebellar development
inferred← citeshttps://doi.org/10.1007/s00383-012-3239-7openalex-snapshot
The role of genetic and epigenetic alterations in neuroblastoma disease pathogenesis
inferred← citeshttps://doi.org/10.1007/s00401-006-0168-3openalex-snapshot
Recurrent cytogenetic aberrations in central neurocytomas and their biological relevance
inferred← citeshttps://doi.org/10.1007/s00401-019-02056-2openalex-snapshot
MYCN amplification drives an aggressive form of spinal ependymoma
inferred← citeshttps://doi.org/10.1007/s00441-005-0011-5openalex-snapshot
Increased progenitor proliferation and apoptotic cell death in the sensory lineage of mice overexpressing N-myc
inferred← citeshttps://doi.org/10.1007/s00441-014-2046-yopenalex-snapshot
Deregulated proliferation and differentiation in brain tumors
inferred← citeshttps://doi.org/10.1007/s00467-007-0602-3openalex-snapshot
End-stage renal failure, reflux nephropathy and Feingold’s syndrome
inferred← citeshttps://doi.org/10.1007/s10555-017-9700-2openalex-snapshot
The ubiquitin-proteasome pathway in adult and pediatric brain tumors: biological insights and therapeutic opportunities
inferred← citeshttps://doi.org/10.1007/s11060-004-2746-3openalex-snapshot
Developmental neurobiology and the origin of brain tumors
inferred← citeshttps://doi.org/10.1007/s11064-013-1200-3openalex-snapshot
Differential Regulation of GLT-1/EAAT2 Gene Expression by NF-κB and N-myc in Male Mouse Brain During Postnatal Development
inferred← citeshttps://doi.org/10.1007/s11864-021-00898-1openalex-snapshot
Biomarkers in Neuroblastoma: An Insight into Their Potential Diagnostic and Prognostic Utilities
inferred← citeshttps://doi.org/10.1007/s12015-012-9381-8openalex-snapshot
Lessons from the Embryonic Neural Stem Cell Niche for Neural Lineage Differentiation of Pluripotent Stem Cells
inferred← citeshttps://doi.org/10.1007/s12029-011-9258-0openalex-snapshot
Pancreatic Ductal Adenocarcinoma and Transcription Factors: Role of c-Myc
inferred← citeshttps://doi.org/10.1007/s12035-013-8587-3openalex-snapshot
Developmental Hypothyroxinemia and Hypothyroidism Reduce Proliferation of Cerebellar Granule Neuron Precursors in Rat Offspring by Downregulation of the Sonic Hedgehog Signaling Pathway
inferred← citeshttps://doi.org/10.1007/s12035-015-9287-yopenalex-snapshot
Age-Dependent Alterations in the Interactions of NF-κB and N-myc with GLT-1/EAAT2 Promoter in the Pericontusional Cortex of Mice Subjected to Traumatic Brain Injury
inferred← citeshttps://doi.org/10.1007/s12035-021-02584-7openalex-snapshot
Function of Oncogene Mycn in Adult Neurogenesis and Oligodendrogenesis
inferred← citeshttps://doi.org/10.1007/s12311-009-0094-8openalex-snapshot
SHH Pathway and Cerebellar Development
inferred← citeshttps://doi.org/10.1007/s12311-010-0190-9openalex-snapshot
c- and N-myc Regulate Neural Precursor Cell Fate, Cell Cycle, and Metabolism to Direct Cerebellar Development
inferred← citeshttps://doi.org/10.1007/s12311-010-0234-1openalex-snapshot
Role of Nitric Oxide in Cerebellar Development and Function: Focus on Granule Neurons
inferred← citeshttps://doi.org/10.1007/s12311-015-0724-2openalex-snapshot
Consensus Paper: Cerebellar Development
inferred← citeshttps://doi.org/10.1007/s12311-020-01138-2openalex-snapshot
Shh-Mediated Increase in β-Catenin Levels Maintains Cerebellar Granule Neuron Progenitors in Proliferation
inferred← citeshttps://doi.org/10.1007/s12311-020-01219-2openalex-snapshot
Simultaneous Brg1 Knockout and MYCN Overexpression in Cerebellar Granule Neuron Precursors Is Insufficient to Drive Tumor Formation but Temporarily Enhances their Proliferation and Delays their Migration
inferred← citeshttps://doi.org/10.1007/s12311-022-01431-2openalex-snapshot
The Transcription Factor, α1ACT, Acts Through a MicroRNA Network to Regulate Neurogenesis and Cell Death During Neonatal Cerebellar Development
inferred← citeshttps://doi.org/10.1007/s13577-024-01037-2openalex-snapshot
MYCN immunohistochemistry as surrogate marker for MYCN-amplified spinal ependymomas
inferred← citeshttps://doi.org/10.1016/b978-0-12-380916-2.00004-8openalex-snapshot
The Connections Between Neural Crest Development and Neuroblastoma
inferred← citeshttps://doi.org/10.1016/b978-0-12-397265-1.00067-8openalex-snapshot
Neurogenesis in the Cerebellum
inferred← citeshttps://doi.org/10.1016/b978-0-12-800781-5.00010-4openalex-snapshot
Comprehensive Overview of CD133 Biology in Neural Tissues across Species
inferred← citeshttps://doi.org/10.1016/b978-0-12-812005-7.00002-3openalex-snapshot
Role of Genetic and Epigenetic Alterations in Pathogenesis of Neuroblastoma
inferred← citeshttps://doi.org/10.1016/b978-0-323-85766-6.00002-4openalex-snapshot
Current reprogramming methods to generate high-quality iPSCs
inferred← citeshttps://doi.org/10.1016/b978-0-443-13212-4.00006-4openalex-snapshot
An overview of the potent role of proto-oncogenes in tissue-specific stem cells
inferred← citeshttps://doi.org/10.1016/b978-1-4557-5414-4.00054-1openalex-snapshot
10.1016/b978-1-4557-5414-4.00054-1
inferred← citeshttps://doi.org/10.1016/bs.acr.2014.10.005openalex-snapshot
ABC Transporters and Neuroblastoma
inferred← citeshttps://doi.org/10.1016/j.ajpath.2020.10.015openalex-snapshot
RAD6B Loss Disrupts Expression of Melanoma Phenotype in Part by Inhibiting WNT/β-Catenin Signaling
inferred← citeshttps://doi.org/10.1016/j.bbaexp.2005.06.001openalex-snapshot
Cloning and characterization of the human and rabbit NUDEL-oligopeptidase promoters and their negative regulation
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2012.08.001openalex-snapshot
CDKL5, a novel MYCN-repressed gene, blocks cell cycle and promotes differentiation of neuronal cells
inferred← citeshttps://doi.org/10.1016/j.bbcan.2023.188992openalex-snapshot
Current and future directions of USP7 interactome in cancer study
inferred← citeshttps://doi.org/10.1016/j.bbrc.2007.08.064openalex-snapshot
c-Myc interacts with TRF1/PIN2 and regulates telomere length
inferred← citeshttps://doi.org/10.1016/j.bcp.2019.08.002openalex-snapshot
Parkin is transcriptionally regulated by the aryl hydrocarbon receptor: Impact on α-synuclein protein levels
inferred← citeshttps://doi.org/10.1016/j.bea.2025.100172openalex-snapshot
Stem cells in regenerative medicine: Unlocking therapeutic potential through stem cell therapy, 3D bioprinting, gene editing, and drug discovery
inferred← citeshttps://doi.org/10.1016/j.biocel.2008.06.017openalex-snapshot
Cerebellar granule cells: Insights into proliferation, differentiation, and role in medulloblastoma pathogenesis
inferred← citeshttps://doi.org/10.1016/j.brainres.2012.09.027openalex-snapshot
N-Myc and L-Myc are essential for hair cell formation but not maintenance
inferred← citeshttps://doi.org/10.1016/j.canlet.2014.02.017openalex-snapshot
Adaptations of energy metabolism during cerebellar neurogenesis are co-opted in medulloblastoma
inferred← citeshttps://doi.org/10.1016/j.cbi.2024.111187openalex-snapshot
Developmental exposure to nonylphenol leads to depletion of the neural precursor cell pool in the hippocampal dentate gyrus
inferred← citeshttps://doi.org/10.1016/j.ccr.2008.12.005openalex-snapshot
Stabilization of N-Myc Is a Critical Function of Aurora A in Human Neuroblastoma
inferred← citeshttps://doi.org/10.1016/j.ccr.2011.12.023openalex-snapshot
A Mouse Model of the Most Aggressive Subgroup of Human Medulloblastoma
inferred← citeshttps://doi.org/10.1016/j.ccr.2012.04.012openalex-snapshot
Distinct Neural Stem Cell Populations Give Rise to Disparate Brain Tumors in Response to N-MYC
inferred← citeshttps://doi.org/10.1016/j.ceb.2009.09.006openalex-snapshot
Myc's other life: stem cells and beyond
inferred← citeshttps://doi.org/10.1016/j.cell.2008.12.024openalex-snapshot
The TRIM-NHL Protein TRIM32 Activates MicroRNAs and Prevents Self-Renewal in Mouse Neural Progenitors
inferred← citeshttps://doi.org/10.1016/j.cell.2015.12.033openalex-snapshot
Myc Depletion Induces a Pluripotent Dormant State Mimicking Diapause
inferred← citeshttps://doi.org/10.1016/j.celrep.2016.06.052openalex-snapshot
Regulation of Nuclear Hormone Receptors by MYCN-Driven miRNAs Impacts Neural Differentiation and Survival in Neuroblastoma Patients
inferred← citeshttps://doi.org/10.1016/j.celrep.2026.117522openalex-snapshot
MYCN drives pediatric glioma transformation from neural progenitors and creates distinct therapeutic vulnerabilities
inferred← citeshttps://doi.org/10.1016/j.celrep.2026.118024openalex-snapshot
Mycn facilitates hematopoietic stem and progenitor cell generation from endothelial cells by inhibiting adhesion signaling
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2018.10.040openalex-snapshot
Maternal di-(2-ethylhexyl) phthalate exposure inhibits cerebellar granule precursor cell proliferation via down-regulating the Shh signaling pathway in male offspring
inferred← citeshttps://doi.org/10.1016/j.copbio.2007.09.007openalex-snapshot
Reprogramming somatic cells towards pluripotency by defined factors
inferred← citeshttps://doi.org/10.1016/j.devcel.2005.05.009openalex-snapshot
Shh Controls Epithelial Proliferation via Independent Pathways that Converge on N-Myc
inferred← citeshttps://doi.org/10.1016/j.devcel.2005.07.014openalex-snapshot
The Cdk1 Complex Plays a Prime Role in Regulating N-Myc Phosphorylation and Turnover in Neural Precursors
inferred← citeshttps://doi.org/10.1016/j.devcel.2009.01.005openalex-snapshot
AMP-Activated Protein Kinase Phosphorylates Retinoblastoma Protein to Control Mammalian Brain Development
inferred← citeshttps://doi.org/10.1016/j.devcel.2009.07.009openalex-snapshot
The N-Myc-DLL3 Cascade Is Suppressed by the Ubiquitin Ligase Huwe1 to Inhibit Proliferation and Promote Neurogenesis in the Developing Brain
inferred← citeshttps://doi.org/10.1016/j.devcel.2014.05.014openalex-snapshot
Shh Signaling Protects Atoh1 from Degradation Mediated by the E3 Ubiquitin Ligase Huwe1 in Neural Precursors
inferred← citeshttps://doi.org/10.1016/j.diff.2010.04.003openalex-snapshot
CIP2A increases self-renewal and is linked to Myc in neural progenitor cells
inferred← citeshttps://doi.org/10.1016/j.diff.2010.05.001openalex-snapshot
myc maintains embryonic stem cell pluripotency and self-renewal
inferred← citeshttps://doi.org/10.1016/j.ejmech.2021.113821openalex-snapshot
Synthesis and biological evaluation of selective histone deacetylase 6 inhibitors as multifunctional agents against Alzheimer's disease
inferred← citeshttps://doi.org/10.1016/j.expneurol.2005.04.018openalex-snapshot
Expression profile of an operationally-defined neural stem cell clone
inferred← citeshttps://doi.org/10.1016/j.expneurol.2006.03.008openalex-snapshot
“Is there any need to argue…” about the nature and genetic signature of in vitro neural stem cells?
inferred← citeshttps://doi.org/10.1016/j.expneurol.2006.03.016openalex-snapshot
Neural stem cells may be uniquely suited for combined gene therapy and cell replacement: Evidence from engraftment of Neurotrophin-3-expressing stem cells in hypoxic–ischemic brain injury
inferred← citeshttps://doi.org/10.1016/j.expneurol.2006.04.002openalex-snapshot
Acute injury directs the migration, proliferation, and differentiation of solid organ stem cells: Evidence from the effect of hypoxia–ischemia in the CNS on clonal “reporter” neural stem cells
inferred← citeshttps://doi.org/10.1016/j.expneurol.2013.01.027openalex-snapshot
Signals that regulate the oncogenic fate of neural stem cells and progenitors
inferred← citeshttps://doi.org/10.1016/j.expneurol.2013.11.010openalex-snapshot
The effect of hemorrhage on the development of the postnatal mouse cerebellum
inferred← citeshttps://doi.org/10.1016/j.gendis.2023.101156openalex-snapshot
Targeting the MYCN-MDM2 pathways for cancer therapy: Are they druggable?
inferred← citeshttps://doi.org/10.1016/j.gene.2024.148447openalex-snapshot
Exploring Myc puzzle: Insights into cancer, stem cell biology, and PPI networks
inferred← citeshttps://doi.org/10.1016/j.isci.2024.109386openalex-snapshot
Modeling gene expression cascades during cell state transitions
inferred← citeshttps://doi.org/10.1016/j.jaci.2026.03.017openalex-snapshot
Context-specific genetic effects inform endotypes and treatment in asthma
inferred← citeshttps://doi.org/10.1016/j.jbc.2023.102928openalex-snapshot
Inositol pyrophosphate profiling reveals regulatory roles of IP6K2-dependent enhanced IP7 metabolism in the enteric nervous system
inferred← citeshttps://doi.org/10.1016/j.jbc.2023.102993openalex-snapshot
RhoA rescues cardiac senescence by regulating Parkin-mediated mitophagy
inferred← citeshttps://doi.org/10.1016/j.jnutbio.2015.12.019openalex-snapshot
Gamma-tocotrienol acts as a BH3 mimetic to induce apoptosis in neuroblastoma SH-SY5Y cells
inferred← citeshttps://doi.org/10.1016/j.jocn.2010.06.004openalex-snapshot
The molecular pathology of central neurocytomas
inferred← citeshttps://doi.org/10.1016/j.jocn.2013.01.001openalex-snapshot
Update on the diagnosis, pathogenesis, and treatment strategies for central neurocytoma
inferred← citeshttps://doi.org/10.1016/j.mcn.2005.06.003openalex-snapshot
Transcriptional changes during neuronal death and replacement in the olfactory epithelium
inferred← citeshttps://doi.org/10.1016/j.mcn.2009.02.011openalex-snapshot
NOV/CCN3 promotes maturation of cerebellar granule neuron precursors
inferred← citeshttps://doi.org/10.1016/j.molmed.2004.11.008openalex-snapshot
Medulloblastoma: developmental mechanisms out of control
inferred← citeshttps://doi.org/10.1016/j.molonc.2010.10.004openalex-snapshot
N‐Myc is a downstream target of RET signaling and is required for transcriptional regulation of p18Ink4c by the transforming mutant RETC634R
inferred← citeshttps://doi.org/10.1016/j.nbd.2006.08.022openalex-snapshot
Cancer stem cells and “stemness” genes in neuro-oncology
inferred← citeshttps://doi.org/10.1016/j.nec.2014.09.001openalex-snapshot
Histology and Molecular Aspects of Central Neurocytoma
inferred← citeshttps://doi.org/10.1016/j.neuint.2004.03.021openalex-snapshot
Role of nitric oxide in the regulation of neuronal proliferation, survival and differentiation
inferred← citeshttps://doi.org/10.1016/j.neuron.2004.06.005openalex-snapshot
The AP-1 Transcription Factor c-Jun Is Required for Efficient Axonal Regeneration
inferred← citeshttps://doi.org/10.1016/j.neuropharm.2012.07.028openalex-snapshot
Prenatal exposure to valproic acid increases the neural progenitor cell pool and induces macrocephaly in rat brain via a mechanism involving the GSK-3β/β-catenin pathway
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2008.06.039openalex-snapshot
Identification of genes that restrict astrocyte differentiation of midgestational neural precursor cells
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2014.01.051openalex-snapshot
c-Myc-dependent transcriptional regulation of cell cycle and nucleosomal histones during oligodendrocyte differentiation
inferred← citeshttps://doi.org/10.1016/j.omtn.2022.03.014openalex-snapshot
SAP30, an oncogenic driver of progression, poor survival, and drug resistance in neuroblastoma
inferred← citeshttps://doi.org/10.1016/j.pneurobio.2008.01.002openalex-snapshot
Regulation of transcription factors by nitric oxide in neurons and in neural-derived tumor cells
inferred← citeshttps://doi.org/10.1016/j.pneurobio.2008.10.002openalex-snapshot
Epigenetic background of neuronal fate determination
inferred← citeshttps://doi.org/10.1016/j.pneurobio.2021.102000openalex-snapshot
3D promoter architecture re-organization during iPSC-derived neuronal cell differentiation implicates target genes for neurodevelopmental disorders
inferred← citeshttps://doi.org/10.1016/j.pnpbp.2017.10.003openalex-snapshot
Integrating genome-wide association study and expression quantitative trait locus study identifies multiple genes and gene sets associated with schizophrenia
inferred← citeshttps://doi.org/10.1016/j.prp.2019.03.025openalex-snapshot
Central neurocytoma: SNP array analyses, subtel FISH, and review of the literature
inferred← citeshttps://doi.org/10.1016/j.scr.2016.07.006openalex-snapshot
BET bromodomain inhibition promotes neurogenesis while inhibiting gliogenesis in neural progenitor cells
inferred← citeshttps://doi.org/10.1016/j.semcancer.2006.07.009openalex-snapshot
The MAX-interacting transcription factor network
inferred← citeshttps://doi.org/10.1016/j.semcancer.2011.08.001openalex-snapshot
The MYCN oncogene and differentiation in neuroblastoma
inferred← citeshttps://doi.org/10.1016/j.semcancer.2011.09.011openalex-snapshot
Genetically engineered murine models – Contribution to our understanding of the genetics, molecular pathology and therapeutic targeting of neuroblastoma
inferred← citeshttps://doi.org/10.1016/j.semcancer.2017.11.009openalex-snapshot
PD-L1, inflammation, non-coding RNAs, and neuroblastoma: Immuno-oncology perspective
inferred← citeshttps://doi.org/10.1016/j.semcdb.2012.03.010openalex-snapshot
What is bad in cancer is good in the embryo: Importance of EMT in neural crest development
inferred← citeshttps://doi.org/10.1016/j.stem.2007.05.016openalex-snapshot
Stem Cell Epigenetics: Is It All Downhill from Here?
inferred← citeshttps://doi.org/10.1016/j.stem.2007.12.004openalex-snapshot
Why Myc? An Unexpected Ingredient in the Stem Cell Cocktail
inferred← citeshttps://doi.org/10.1016/j.stem.2008.09.005openalex-snapshot
Hematopoietic Stem Cell Function and Survival Depend on c-Myc and N-Myc Activity
inferred← citeshttps://doi.org/10.1016/j.stem.2009.07.003openalex-snapshot
The Cell Cycle and Myc Intersect with Mechanisms that Regulate Pluripotency and Reprogramming
inferred← citeshttps://doi.org/10.1016/j.stem.2010.06.023openalex-snapshot
Myc Represses Primitive Endoderm Differentiation in Pluripotent Stem Cells
inferred← citeshttps://doi.org/10.1016/j.stemcr.2022.05.002openalex-snapshot
Arp2/3 complex activity is necessary for mouse ESC differentiation, times formative pluripotency, and enables lineage specification
inferred← citeshttps://doi.org/10.1016/j.tcb.2005.01.008openalex-snapshot
More than just proliferation: Myc function in stem cells
inferred← citeshttps://doi.org/10.1016/j.tins.2011.01.002openalex-snapshot
Development and cancer of the cerebellum
inferred← citeshttps://doi.org/10.1016/j.tox.2012.04.011openalex-snapshot
Mono-(2-ethylhexyl)-phthalate (MEHP) affects ERK-dependent GDNF signalling in mouse stem-progenitor spermatogonia
inferred← citeshttps://doi.org/10.1016/j.urolonc.2011.11.031openalex-snapshot
Polymorphisms of TP53 are markers of bladder cancer vulnerability and prognosis
inferred← citeshttps://doi.org/10.1016/j.xinn.2022.100364openalex-snapshot
Dynamic network biomarker factors orchestrate cell-fate determination at tipping points during hESC differentiation
inferred← citeshttps://doi.org/10.1016/j.ydbio.2004.03.009openalex-snapshot
Sonic hedgehog signaling regulates Gli3 processing, mesenchymal proliferation, and differentiation during mouse lung organogenesis
inferred← citeshttps://doi.org/10.1016/j.ydbio.2008.02.026openalex-snapshot
Primary cilia are required for cerebellar development and Shh-dependent expansion of progenitor pool
inferred← citeshttps://doi.org/10.1016/j.ydbio.2008.04.044openalex-snapshot
Mechanisms of TGFβ inhibition of LUNG endodermal morphogenesis: The role of TβRII, Smads, Nkx2.1 and Pten
inferred← citeshttps://doi.org/10.1016/j.ydbio.2011.07.030openalex-snapshot
The F-box protein Fbw7 is required for cerebellar development
inferred← citeshttps://doi.org/10.1016/j.ydbio.2012.10.005openalex-snapshot
Myocardial Mycn is essential for mouse ventricular wall morphogenesis
inferred← citeshttps://doi.org/10.1016/j.ydbio.2013.10.019openalex-snapshot
Cerebellar cortical lamination and foliation require cyclin A2
inferred← citeshttps://doi.org/10.1016/j.ydbio.2017.07.002openalex-snapshot
N-myc regulates growth and fiber cell differentiation in lens development
inferred← citeshttps://doi.org/10.1016/j.yexcr.2006.11.001openalex-snapshot
Generation of human cortical neurons from a new immortal fetal neural stem cell line
inferred← citeshttps://doi.org/10.1016/j.yexcr.2010.03.025openalex-snapshot
The Yin and Yang functions of the Myc oncoprotein in cancer development and as targets for therapy
inferred← citeshttps://doi.org/10.1016/j.ymgme.2003.08.019openalex-snapshot
Development and malformations of the cerebellum in mice
inferred← citeshttps://doi.org/10.1016/s0065-230x(06)97003-1openalex-snapshot
Mnt Takes Control as Key Regulator of the Myc/Max/Mxd Network
inferred← citeshttps://doi.org/10.1016/s0065-230x(10)07001-6openalex-snapshot
Breaking Tolerance in a Mouse Model of Multiple Myeloma by Chemoimmunotherapy
inferred← citeshttps://doi.org/10.1016/s0065-230x(10)07006-5openalex-snapshot
MYC in Oncogenesis and as a Target for Cancer Therapies
inferred← citeshttps://doi.org/10.1016/s0074-7696(04)38004-6openalex-snapshot
Functions of Myc:Max in the Control of Cell Proliferation and Tumorigenesis
inferred← citeshttps://doi.org/10.1016/s0074-7696(07)65002-5openalex-snapshot
Neural Stem Cells in the Mammalian Brain
inferred← citeshttps://doi.org/10.1016/s0304-3835(03)00451-8openalex-snapshot
Hedgehog–Gli signaling in brain tumors: stem cells and paradevelopmental programs in cancer
inferred← citeshttps://doi.org/10.1016/s1357-2725(03)00254-1openalex-snapshot
N-myc transcription molecule and oncoprotein
inferred← citeshttps://doi.org/10.1016/s1877-1173(10)93007-xopenalex-snapshot
Roles of Heparan Sulfate in Mammalian Brain Development
inferred← citeshttps://doi.org/10.1038/cdd.2015.81openalex-snapshot
The MRN complex is transcriptionally regulated by MYCN during neural cell proliferation to control replication stress
inferred← citeshttps://doi.org/10.1038/cddis.2014.42openalex-snapshot
MYCN gene expression is required for the onset of the differentiation programme in neuroblastoma cells
inferred← citeshttps://doi.org/10.1038/cgt.2008.73openalex-snapshot
Transcription factors: their potential as targets for an individualized therapeutic approach to cancer
inferred← citeshttps://doi.org/10.1038/emboj.2009.254openalex-snapshot
Myc‐regulated microRNAs attenuate embryonic stem cell differentiation
inferred← citeshttps://doi.org/10.1038/labinvest.3700061openalex-snapshot
Neuroblastoma cells with overexpressed MYCN retain their capacity to undergo neuronal differentiation
inferred← citeshttps://doi.org/10.1038/nature02385openalex-snapshot
Bmi1 is essential for cerebellar development and is overexpressed in human medulloblastomas
inferred← citeshttps://doi.org/10.1038/nature08544openalex-snapshot
Division and apoptosis of E2f-deficient retinal progenitors
inferred← citeshttps://doi.org/10.1038/ncb1224openalex-snapshot
c-Myc binds to human ribosomal DNA and stimulates transcription of rRNA genes by RNA polymerase I
inferred← citeshttps://doi.org/10.1038/ncb1727openalex-snapshot
The HECT-domain ubiquitin ligase Huwe1 controls neural differentiation and proliferation by destabilizing the N-Myc oncoprotein
inferred← citeshttps://doi.org/10.1038/ng.336openalex-snapshot
Multiple recurrent genetic events converge on control of histone lysine methylation in medulloblastoma
inferred← citeshttps://doi.org/10.1038/ng.86openalex-snapshot
Mutations in the cyclin family member FAM58A cause an X-linked dominant disorder characterized by syndactyly, telecanthus and anogenital and renal malformations
inferred← citeshttps://doi.org/10.1038/ng1546openalex-snapshot
MYCN haploinsufficiency is associated with reduced brain size and intestinal atresias in Feingold syndrome
showing the first 200 of 491 · page through all 491
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.