On the public citation graph
Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1
0 signed · 1289 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known work and none has been retracted — and get a dated CiteStamped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/10.1002/(sici)1096-8628(19970502)70:1<80::aid-ajmg15>3.0.co;2-topenalex-snapshot
Deletions of 20p12 in Alagille syndrome: Frequency and molecular characterization
inferredcites →https://doi.org/10.1002/hep.1840060514openalex-snapshot
Nonsyndromatic paucity of interlobular bile ducts: Light and electron microscopic evaluation of sequential liver biopsies in early childhood
inferredcites →https://doi.org/10.1006/dbio.1996.0310openalex-snapshot
Jagged2: A Serrate-like Gene Expressed during Rat Embryogenesis
inferredcites →https://doi.org/10.1006/geno.1994.1517openalex-snapshot
Three Genes in the Human MHC Class III Region near the Junction with the Class II: Gene for Receptor of Advanced Glycosylation End Products, PBX2 Homeobox Gene and a Notch Homolog, Human Counterpart of Mouse Mammary Tumor Gene int-3
inferredcites →https://doi.org/10.1006/geno.1995.1078openalex-snapshot
Construction of a 3.7-Mb Physical Map within Human Chromosome 20p12 Ordering 18 Markers in the Alagille Syndrome Locus
inferredcites →https://doi.org/10.1006/geno.1996.0268openalex-snapshot
Construction and Characterization of a Human Bacterial Artificial Chromosome Library
inferredcites →https://doi.org/10.1006/mcne.1996.0040openalex-snapshot
Expression Patterns ofJagged, Delta1, Notch1, Notch2,andNotch3Genes Identify Ligand–Receptor Pairs That May Function in Neural Development
inferredcites →https://doi.org/10.1007/bf00285164openalex-snapshot
Molecular and cytogenetic analysis of an interstitial 20p deletion associated with syndromic intrahepatic ductular hypoplasia (Alagille syndrome)
inferredcites →https://doi.org/10.1016/0012-1606(92)90076-sopenalex-snapshot
Expression analysis of a Notch homologue in the mouse embryo
inferredcites →https://doi.org/10.1016/0092-8674(91)90111-bopenalex-snapshot
TAN-1, the human homolog of the Drosophila Notch gene, is broken by chromosomal translocations in T lymphoblastic neoplasms
inferredcites →https://doi.org/10.1016/0092-8674(91)90263-xopenalex-snapshot
The choice of cell fate in the epidermis of Drosophila
inferredcites →https://doi.org/10.1016/0092-8674(92)90470-wopenalex-snapshot
Making a difference: The role of cell-cell interactions in establishing separate identities for equivalent cells
inferredcites →https://doi.org/10.1016/0092-8674(95)90294-5openalex-snapshot
Jagged: A mammalian ligand that activates notch1
inferredcites →https://doi.org/10.1016/0888-7543(95)80092-zopenalex-snapshot
A physical map of chromosome 20 established using fluorescence in situ hybridization and digital image analysis
inferredcites →https://doi.org/10.1016/0896-6273(92)90238-9openalex-snapshot
Single amino acid substitutions in EGF-like elements of notch and delta modify drosophila development and affect cell adhesion in vitro
inferredcites →https://doi.org/10.1016/0925-4773(94)90081-7openalex-snapshot
The novel Notch homologue mouse Notch 3 lacks specific epidermal growth factor-repeats and is expressed in proliferating neuroepithelium
inferredcites →https://doi.org/10.1016/s0022-3476(87)80153-1openalex-snapshot
Syndromic paucity of interlobular bile ducts (Alagille syndrome or arteriohepatic dysplasia): Review of 80 cases
inferredcites →https://doi.org/10.1016/s0070-2153(08)60091-5openalex-snapshot
10 Homologs of Vertebrate Growth Factors in Drosophila melanogaster and Other Invertebrates
inferredcites →https://doi.org/10.1016/s0092-8674(00)81368-9openalex-snapshot
An Activated Form of Notch Influences the Choice between CD4 and CD8 T Cell Lineages
inferredcites →https://doi.org/10.1016/s0092-8674(00)81929-7openalex-snapshot
Notch Activity Influences the αβ versus γδ T Cell Lineage Decision
inferredcites →https://doi.org/10.1038/365555a0openalex-snapshot
An activated Notch receptor blocks cell-fate commitment in the developing Drosophila eye
inferredcites →https://doi.org/10.1038/376348a0openalex-snapshot
Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP
inferredcites →https://doi.org/10.1038/383707a0openalex-snapshot
Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia
inferredcites →https://doi.org/10.1038/386717a0openalex-snapshot
Maintenance of somite borders in mice requires the Delta homologue Dll1
inferredcites →https://doi.org/10.1038/ng0797-235openalex-snapshot
Mutations in the human Jagged1 gene are responsible for Alagille syndrome
inferredcites →https://doi.org/10.1073/pnas.89.18.8794openalex-snapshot
Cloning and stable maintenance of 300-kilobase-pair fragments of human DNA in Escherichia coli using an F-factor-based vector.
inferredcites →https://doi.org/10.1073/pnas.91.7.2629openalex-snapshot
Preparation and screening of an arrayed human genomic library generated with the P1 cloning system.
inferredcites →https://doi.org/10.1074/jbc.271.51.32499openalex-snapshot
An Antisense Oligonucleotide to the Notch Ligand Jagged Enhances Fibroblast Growth Factor-induced Angiogenesis in Vitro
inferredcites →https://doi.org/10.1083/jcb.121.3.631openalex-snapshot
Mouse notch: expression in hair follicles correlates with cell fate determination.
inferredcites →https://doi.org/10.1101/gad.8.6.707openalex-snapshot
Notch1 is essential for postimplantation development in mice.
inferredcites →https://doi.org/10.1101/gr.6.11.1029openalex-snapshot
Complete genomic sequence and analysis of 117 kb of human DNA containing the gene BRCA1.
inferredcites →https://doi.org/10.1126/science.8235655openalex-snapshot
Genetic relationships determined by a DNA heteroduplex mobility assay: analysis of HIV-1 env genes
inferredcites →https://doi.org/10.1136/adc.48.6.459openalex-snapshot
Arteriohepatic dysplasia: Familial pulmonary arterial stenosis with neonatal liver disease
inferredcites →https://doi.org/10.1136/adc.52.5.360openalex-snapshot
Studies of the aetiology of neonatal hepatitis and biliary atresia.
inferredcites →https://doi.org/10.1136/jmg.31.2.89openalex-snapshot
The molecular basis of genetic dominance.
inferredcites →https://doi.org/10.1136/jmg.31.6.453openalex-snapshot
Segregation analysis of Alagille syndrome.
inferredcites →https://doi.org/10.1159/000472362openalex-snapshot
Mapping of Microsatellite Markers in the Alagille Region and Screening of Microdeletions by Genotyping 23 Patients
inferredcites →https://doi.org/10.1242/dev.113.1.199openalex-snapshot
A homolog of Drosophila Notch expressed during mammalian development
inferredcites →https://doi.org/10.1242/dev.115.3.737openalex-snapshot
Expression pattern of Motch , a mouse homolog of Drosophila Notch , suggests an important role in early postimplantation mouse development
inferredcites →https://doi.org/10.1242/dev.116.4.931openalex-snapshot
Notch2: a second mammalian Notch gene
inferredcites →https://doi.org/10.1242/dev.120.10.2913openalex-snapshot
lag-2 may encode a signaling ligand for the GLP-1 and LIN-12 receptors of C. elegans
inferredcites →https://doi.org/10.1242/dev.121.5.1533openalex-snapshot
Notch1 is required for the coordinate segmentation of somites
inferredcites →https://doi.org/10.1242/dev.122.7.2251openalex-snapshot
Notch4/int-3, a mammary proto-oncogene, is an endothelial cell-specific mammalian Notch gene
inferredcites →https://doi.org/10.1523/jneurosci.17-04-01425.1997openalex-snapshot
The Expression and Function of Notch Pathway Genes in the Developing Rat Eye
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.3756810openalex-extracted
Maralixibat Treatment Significantly Reduces Pruritus and Serum Bile Acids in Patients with Alagille Syndrome: Results from a Randomized Phase II Study with 4 Years of Follow-Up
inferred← citeshttps://doi.org/10.2139/ssrn.4771923openalex-extracted
Cellular Landscape of Adrenocortical Carcinoma at Single-Nuclei Resolution
inferred← citeshttps://doi.org/10.1001/archotol.126.10.1244openalex-snapshot
Notch Signaling and the Emergence of Auditory Hair Cells
inferred← citeshttps://doi.org/10.1002/(sici)1096-8628(19980707)78:3<267::aid-ajmg12>3.0.co;2-dopenalex-snapshot
Submicroscopic deletion of chromosome 16p13.3 in patients with Rubinstein-Taybi syndrome
inferred← citeshttps://doi.org/10.1002/(sici)1096-8628(19990507)84:1<56::aid-ajmg11>3.0.co;2-wopenalex-snapshot
Jagged1 mutations in patients ascertained with isolated congenital heart defects
inferred← citeshttps://doi.org/10.1002/(sici)1096-8628(19991229)89:4<224::aid-ajmg7>3.0.co;2-copenalex-snapshot
Genetics of the female reproductive ducts
inferred← citeshttps://doi.org/10.1002/(sici)1097-4547(19981015)54:2<125::aid-jnr1>3.0.co;2-gopenalex-snapshot
Notch and neurogenesis
inferred← citeshttps://doi.org/10.1002/(sici)1098-1004(199911)14:5<394::aid-humu5>3.0.co;2-1openalex-snapshot
Jagged-1 mutation analysis in Italian Alagille syndrome patients
inferred← citeshttps://doi.org/10.1002/1096-8628(20000731)93:3<250::aid-ajmg18>3.0.co;2-aopenalex-snapshot
Severe hypodontia and oral xanthomas in Alagille syndrome
inferred← citeshttps://doi.org/10.1002/1096-8628(200024)97:4<297::aid-ajmg1280>3.0.co;2-oopenalex-snapshot
Molecular determinants of left and right outflow tract obstruction
inferred← citeshttps://doi.org/10.1002/1097-0177(2000)9999:9999<::aid-dvdy1046>3.0.co;2-9openalex-snapshot
Mouse mutant “rib‐vertebrae” (rv): A defect in somite polarity
inferred← citeshttps://doi.org/10.1002/1098-1004(200007)16:1<92::aid-humu23>3.0.co;2-4openalex-snapshot
Identification of a larger than 3 Mb deletion including JAG1 in an Alagille syndrome patient with a translocation t(3;20)(q13.3;p12.2)
inferred← citeshttps://doi.org/10.1002/1098-1004(200007)16:1<92::aid-humu23>3.3.co;2-wopenalex-snapshot
Identification of a larger than 3 Mb deletion including JAG1 in an Alagille syndrome patient with a translocation t(3;20)(q13.3;p12.2) Communicated by: Mark H. Paalman Online Citation: Human Mutation, Mutation in Brief #344 (2000) Online http://journals.wiley.com/1059-7794/pdf/mutation/344.pdf
inferred← citeshttps://doi.org/10.1002/1098-1004(200011)16:5<408::aid-humu5>3.0.co;2-9openalex-snapshot
Jagged1 (JAG1) mutation detection in an Australian Alagille syndrome population
inferred← citeshttps://doi.org/10.1002/1098-1004(2001)17:1<18::aid-humu3>3.0.co;2-topenalex-snapshot
Jagged1 mutations in Alagille syndrome
inferred← citeshttps://doi.org/10.1002/1098-1004(200102)17:2<151::aid-humu8>3.0.co;2-topenalex-snapshot
Mutation analysis of Jagged1 (JAG1) in Alagille syndrome patients
inferred← citeshttps://doi.org/10.1002/1098-1004(200102)17:2<151::aid-humu8>3.3.co;2-kopenalex-snapshot
Mutation analysis of Jagged1 (JAG1) in Alagille syndrome patients Communicated by Ian McIntosh Online Citation: Human Mutation, Mutation in Brief #397 (2000) Online http://journals.wiley.com/1059-7794/pdf/mutation/397.pdf
inferred← citeshttps://doi.org/10.1002/3527600906.mcb.200500071openalex-snapshot
Vascular Development and Angiogenesis
inferred← citeshttps://doi.org/10.1002/9780470015902.a0021440openalex-snapshot
Pathogenetic Mechanisms in Alagille Syndrome
inferred← citeshttps://doi.org/10.1002/9780470015902.a0021440.pub2openalex-snapshot
Pathogenetic Mechanisms in A lagille Syndrome
inferred← citeshttps://doi.org/10.1002/9780470015902.a0026850openalex-snapshot
At the Heart of a Complex Disease ‘Molecular Genetics of Congenital Heart Disease’
inferred← citeshttps://doi.org/10.1002/9780470691861.ch21fopenalex-snapshot
The Effect of Liver Disease on the Skin
inferred← citeshttps://doi.org/10.1002/9780470986820.ch26openalex-snapshot
The Liver in Infancy and Childhood
inferred← citeshttps://doi.org/10.1002/9780470986981.ch23openalex-snapshot
Biliary Disease in Infants and Children
inferred← citeshttps://doi.org/10.1002/9781118321386.ch94openalex-snapshot
Genetic and metabolic liver diseases in childhood
inferred← citeshttps://doi.org/10.1002/9781118512074.ch1openalex-snapshot
Development and Differentiation of the Gastrointestinal System
inferred← citeshttps://doi.org/10.1002/9781118512074.ch26openalex-snapshot
Bile Secretion and Cholestasis
inferred← citeshttps://doi.org/10.1002/9781118663387.ch2openalex-snapshot
Signaling pathways in biliary epithelial cells
inferred← citeshttps://doi.org/10.1002/9781119237662.ch31openalex-snapshot
The Liver in the Neonate, in Infancy, and Childhood
inferred← citeshttps://doi.org/10.1002/9781444341294.ch29openalex-snapshot
The Liver in the Neonate, in Infancy and Childhood
inferred← citeshttps://doi.org/10.1002/ajmg.10579openalex-snapshot
Facial features in Alagille syndrome: Specific or cholestasis facies?
inferred← citeshttps://doi.org/10.1002/ajmg.10592openalex-snapshot
Characterization of Notch receptor expression in the developing mammalian heart and liver
inferred← citeshttps://doi.org/10.1002/ajmg.10609openalex-snapshot
Alagille syndrome: Chipping away at the tip of the iceberg
inferred← citeshttps://doi.org/10.1002/ajmg.10610openalex-snapshot
Monozygotic twins with a severe form of Alagille syndrome and phenotypic discordance
inferred← citeshttps://doi.org/10.1002/ajmg.10616openalex-snapshot
Alagille syndrome inherited from a phenotypically normal mother with a mosaic 20p microdeletion
inferred← citeshttps://doi.org/10.1002/ajmg.10628openalex-snapshot
Supernumerary digital flexion creases: An additional clinical manifestation of Alagille syndrome
inferred← citeshttps://doi.org/10.1002/ajmg.10652openalex-snapshot
Jagged1 gene mutation for abdominal coarctation of the aorta in Alagille syndrome
inferred← citeshttps://doi.org/10.1002/ajmg.1531openalex-snapshot
Alagille syndrome associated with a paracentric inversion 20p12.2p13 disrupting theJAG1 gene
inferred← citeshttps://doi.org/10.1002/ajmg.a.20123openalex-snapshot
Sequence‐Based, in situ detection of chromosomal abnormalities at high resolution
inferred← citeshttps://doi.org/10.1002/ajmg.a.20333openalex-snapshot
Re: Article by Kamath et al.—“Facial features in Alagille Syndrome”
inferred← citeshttps://doi.org/10.1002/ajmg.a.20387openalex-snapshot
Hepatic fibrosis in Kabuki syndrome
inferred← citeshttps://doi.org/10.1002/ajmg.a.20430openalex-snapshot
Mosaic paternal uniparental (iso)disomy for chromosome 20 associated with multiple anomalies
inferred← citeshttps://doi.org/10.1002/ajmg.a.30071openalex-snapshot
A female with complete lack of Müllerian fusion, postaxial polydactyly, and tetralogy of fallot: Genetic heterogeneity of McKusick–Kaufman syndrome or a unique syndrome?
inferred← citeshttps://doi.org/10.1002/ajmg.a.30136openalex-snapshot
Subtelomeric deletions of chromosome 9q: A novel microdeletion syndrome
inferred← citeshttps://doi.org/10.1002/ajmg.a.30461openalex-snapshot
Diagnostic FISH probes for del(17)(p11.2p11.2) associated with Smith–Magenis syndrome should contain the RAI1 gene
inferred← citeshttps://doi.org/10.1002/ajmg.a.31509openalex-snapshot
DLL3 as a candidate gene for vertebral malformations
inferred← citeshttps://doi.org/10.1002/ajmg.a.32356openalex-snapshot
Williams syndrome in a preterm infant with phenotype of Alagille syndrome
inferred← citeshttps://doi.org/10.1002/ajmg.a.32640openalex-snapshot
Molecular cytogenetic characterization of the first reported case of inv dup del 20p compatible with a U‐type exchange model
inferred← citeshttps://doi.org/10.1002/ajmg.a.33449openalex-snapshot
Segmental paternal uniparental disomy (patUPD) of 14q32 with abnormal methylation elicits the characteristic features of complete patUPD14
inferred← citeshttps://doi.org/10.1002/ajmg.a.34369openalex-snapshot
Renal anomalies in Alagille syndrome: A disease‐defining feature
inferred← citeshttps://doi.org/10.1002/ajmg.a.35255openalex-snapshot
Alagille syndrome in a Vietnamese cohort: Mutation analysis and assessment of facial features
inferred← citeshttps://doi.org/10.1002/ajmg.a.35594openalex-snapshot
Cleft palate in a multigenerational family with a microdeletion of 20p12.3 involving BMP2
inferred← citeshttps://doi.org/10.1002/ajmg.a.35638openalex-snapshot
Clinical geneticists' views of VACTERL/VATER association
inferred← citeshttps://doi.org/10.1002/ajmg.a.36148openalex-snapshot
JAG1 Mutation in a patient with deletion 22q11.2 syndrome and tetralogy of Fallot
inferred← citeshttps://doi.org/10.1002/ajmg.a.36921openalex-snapshot
Dissecting the phenotype of supernumerary marker chromosome 20 in a patient with syndromic pierre robin sequence: Combinatorial effect of gene dosage and uniparental disomy
inferred← citeshttps://doi.org/10.1002/ajmg.a.37429openalex-snapshot
Discordant clinical phenotype in monozygotic twins with Alagille syndrome: Possible influence of non‐genetic factors
inferred← citeshttps://doi.org/10.1002/ajmg.a.62028openalex-snapshot
Alagille syndrome and risk for hepatocellular carcinoma: Need for increased surveillance in adults with mild liver phenotypes
inferred← citeshttps://doi.org/10.1002/ajmg.a.64098openalex-snapshot
A Novel Heterozygous Likely Pathogenic JAG1 Germline Variant in an Adult With Unilateral Persistent Fetal Vasculature
inferred← citeshttps://doi.org/10.1002/ajmg.a.70266openalex-snapshot
Familial Isolated Tetralogy of Fallot Associated With JAG1 Variant: Justifying Phenotype‐Agnostic Genetic Workup for Critical Congenital Heart Disease
inferred← citeshttps://doi.org/10.1002/ajmg.c.31763openalex-snapshot
The genetics of isolated congenital heart disease
inferred← citeshttps://doi.org/10.1002/bdra.20815openalex-snapshot
Notch signaling in cardiac valve development and disease
inferred← citeshttps://doi.org/10.1002/bdrc.20090openalex-snapshot
The vertebrate segmentation clock and its role in skeletal birth defects
inferred← citeshttps://doi.org/10.1002/bdrc.20094openalex-snapshot
Molecular clocks underlying vertebrate embryo segmentation: A 10‐year‐old hairy‐go‐round
inferred← citeshttps://doi.org/10.1002/bies.20090openalex-snapshot
Bile ducts as a source of pancreatic β cells
inferred← citeshttps://doi.org/10.1002/bies.200900140openalex-snapshot
Notch: Implications of endogenous inhibitors for therapy
inferred← citeshttps://doi.org/10.1002/biof.70071openalex-snapshot
BACE1 : Biological Functions and Involvement in the Pathophysiology of Alzheimer's Disease and Other Neurological Disorders
inferred← citeshttps://doi.org/10.1002/cbin.70009openalex-snapshot
Alagille Syndrome: Unraveling the Complexities of Genotype–Phenotype Relationships and Exploring Avenues for Improved Diagnosis and Treatment
inferred← citeshttps://doi.org/10.1002/ccr3.8927openalex-snapshot
Subtelomeric microdeletion in chromosome 20p13 associated with short stature
inferred← citeshttps://doi.org/10.1002/cne.1059openalex-snapshot
Expression patterns of Notch1, Notch2, and Notch3 suggest multiple functional roles for the Notch‐DSL signaling system during brain development
inferred← citeshttps://doi.org/10.1002/cphy.c120021openalex-snapshot
Zebrafish Models of Human Liver Development and Disease
inferred← citeshttps://doi.org/10.1002/cphy.c120022openalex-snapshot
Cellular and Molecular Basis of Liver Development
inferred← citeshttps://doi.org/10.1002/dvdy.10146openalex-snapshot
Notch1 and Jagged1 expression by the developing pulmonary vasculature
inferred← citeshttps://doi.org/10.1002/dvdy.20098openalex-snapshot
Presenilin 1 is essential for cardiac morphogenesis
inferred← citeshttps://doi.org/10.1002/dvdy.21182openalex-snapshot
Abnormal vertebral segmentation and the notch signaling pathway in man
inferred← citeshttps://doi.org/10.1002/dvdy.21296openalex-snapshot
Dll3 and Notch1 genetic interactions model axial segmental and craniofacial malformations of human birth defects
inferred← citeshttps://doi.org/10.1002/dvdy.21502openalex-snapshot
Notch2 is required for the proliferation of cardiac neural crest‐derived smooth muscle cells
inferred← citeshttps://doi.org/10.1002/dvdy.21520openalex-snapshot
FGF signaling segregates biliary cell‐lineage from chick hepatoblasts cooperatively with BMP4 and ECM components in vitro
inferred← citeshttps://doi.org/10.1002/dvdy.22220openalex-snapshot
Reiterative use of the notch signal during zebrafish intrahepatic biliary development
inferred← citeshttps://doi.org/10.1002/dvdy.22345openalex-snapshot
Serum and glucocorticoid‐inducible kinase 1 (SGK1) is necessary for vascular remodeling during angiogenesis
inferred← citeshttps://doi.org/10.1002/dvdy.23739openalex-snapshot
Requirements for Jag1‐Rbpj mediated Notch signaling during early mouse lens development
inferred← citeshttps://doi.org/10.1002/dvdy.24127openalex-snapshot
A Notch‐dependent transcriptional hierarchy promotes mesenchymal transdifferentiation in the cardiac cushion
inferred← citeshttps://doi.org/10.1002/dvg.20727openalex-snapshot
A phenotype‐driven ENU mutagenesis screen identifies novel alleles with functional roles in early mouse craniofacial development
inferred← citeshttps://doi.org/10.1002/dvg.22904openalex-snapshot
Loss of Notch2 and Notch3 in vascular smooth muscle causes patent ductus arteriosus
inferred← citeshttps://doi.org/10.1002/gcc.20616openalex-snapshot
Integration of genomic and gene expression data of childhood ALL without known aberrations identifies subgroups with specific genetic hallmarks
inferred← citeshttps://doi.org/10.1002/glia.20978openalex-snapshot
TGFβ1 induces Jagged1 expression in astrocytes via ALK5 and Smad3 and regulates the balance between oligodendrocyte progenitor proliferation and differentiation
inferred← citeshttps://doi.org/10.1002/hep.20571openalex-snapshot
Inducible inactivation of Notch1 causes nodular regenerative hyperplasia in mice†‡
inferred← citeshttps://doi.org/10.1002/hep.20640openalex-snapshot
Another Notch to be added to the list of hepatocellular growth regulatory factors?†‡
inferred← citeshttps://doi.org/10.1002/hep.20691openalex-snapshot
Embryonic development of the liver†
inferred← citeshttps://doi.org/10.1002/hep.20729openalex-snapshot
Intrahepatic Cholestasis: Summary of an American Association for the Study of Liver Diseases Single-Topic Conference *
inferred← citeshttps://doi.org/10.1002/hep.21460openalex-snapshot
Bile duct proliferation in liver-specific Jag1 conditional knockout mice: Effects of gene dosage
inferred← citeshttps://doi.org/10.1002/hep.21501openalex-snapshot
SgIGSF is a novel biliary–epithelial cell adhesion molecule mediating duct/ductule development
inferred← citeshttps://doi.org/10.1002/hep.21860openalex-snapshot
Increasing the mutation rate for jagged1 mutations in patients with Alagille syndrome†
inferred← citeshttps://doi.org/10.1002/hep.22381openalex-snapshot
Liver‐specific inactivation of Notch2, but not Notch1, compromises intrahepatic bile duct development in mice†‡
inferred← citeshttps://doi.org/10.1002/hep.22480openalex-snapshot
Notch signaling in bile duct development
inferred← citeshttps://doi.org/10.1002/hep.22485openalex-snapshot
A mutation in the canalicular phospholipid transporter gene, ABCB4, is associated with cholestasis, ductopenia, and cirrhosis in adults†‡
inferred← citeshttps://doi.org/10.1002/hep.22538openalex-snapshot
Bile duct proliferation in Jag1 /fringe heterozygous mice identifies candidate modifiers of the alagille syndrome hepatic phenotype
inferred← citeshttps://doi.org/10.1002/hep.23048openalex-snapshot
Notch2 signaling promotes biliary epithelial cell fate specification and tubulogenesis during bile duct development in mice #
inferred← citeshttps://doi.org/10.1002/hep.23431openalex-snapshot
Notch signaling regulates formation of the three‐dimensional architecture of intrahepatic bile ducts in mice†
inferred← citeshttps://doi.org/10.1002/hep.24631openalex-snapshot
Genetic Interactions Between Hepatocyte Nuclear Factor–6 and Notch Signaling Regulate Mouse Intrahepatic Bile Duct Development in Vivo
inferred← citeshttps://doi.org/10.1002/hep.25911openalex-snapshot
The role of paracrine signals during liver regeneration
inferred← citeshttps://doi.org/10.1002/hep.26165openalex-snapshot
Constitutive Notch2 signaling induces hepatic tumors in mice
inferred← citeshttps://doi.org/10.1002/hep.26580openalex-snapshot
Growth and Development of a New Subspecialty: Pediatric Hepatology
inferred← citeshttps://doi.org/10.1002/hep.27191openalex-snapshot
Evaluation of the Pediatric Patient for Liver Transplantation: 2014 Practice Guideline by the American Association for the Study of Liver Diseases, American Society of Transplantation and the North American Society for Pediatric Gastroenterology, Hepatology and Nutrition
inferred← citeshttps://doi.org/10.1002/hep.27268openalex-snapshot
Emerging roles of Notch signaling in liver disease
inferred← citeshttps://doi.org/10.1002/hep.28024openalex-snapshot
Jagged1 heterozygosity in mice results in a congenital cholangiopathy which is reversed by concomitant deletion of one copy of Poglut1 (Rumi)
inferred← citeshttps://doi.org/10.1002/hep.29752openalex-snapshot
Wnt/β‐catenin signaling controls intrahepatic biliary network formation in zebrafish by regulating notch activity
inferred← citeshttps://doi.org/10.1002/hep.30912openalex-snapshot
Sox9 Is a Modifier of the Liver Disease Severity in a Mouse Model of Alagille Syndrome
inferred← citeshttps://doi.org/10.1002/hep.32173openalex-snapshot
Intrahepatic cholangiocyte regeneration from an Fgf‐dependent extrahepatic progenitor niche in a zebrafish model of Alagille Syndrome
inferred← citeshttps://doi.org/10.1002/hep.32437openalex-snapshot
Cholestatic liver diseases of genetic etiology: Advances and controversies
inferred← citeshttps://doi.org/10.1002/hep.510290331openalex-snapshot
Features of Alagille Syndrome in 92 Patients: Frequency and Relation to Prognosis
inferred← citeshttps://doi.org/10.1002/hep.510300512openalex-snapshot
Hepatic jagged1 expression studies
inferred← citeshttps://doi.org/10.1002/hep4.1468openalex-snapshot
Outcomes of Childhood Cholestasis in Alagille Syndrome: Results of a Multicenter Observational Study
inferred← citeshttps://doi.org/10.1002/humu.20310openalex-snapshot
Jagged1 (JAG1) mutations in Alagille syndrome: increasing the mutation detection rate
inferred← citeshttps://doi.org/10.1002/humu.20863openalex-snapshot
SNP array mapping of chromosome 20p deletions: Genotypes, phenotypes, and copy number variation
inferred← citeshttps://doi.org/10.1002/humu.21231openalex-snapshot
Jagged1 (JAG1) mutations in patients with tetralogy of fallot or pulmonic stenosis
inferred← citeshttps://doi.org/10.1002/humu.21563openalex-snapshot
Serpentine fibula-polycystic kidney syndrome caused by truncating mutations in NOTCH2
inferred← citeshttps://doi.org/10.1002/humu.23879openalex-snapshot
Alagille syndrome mutation update: Comprehensive overview ofJAG1andNOTCH2mutation frequencies and insight into missense variant classification
inferred← citeshttps://doi.org/10.1002/humu.9102openalex-snapshot
Identification of 36 novel Jagged1 (JAG1) mutations in patients with Alagille syndrome
inferred← citeshttps://doi.org/10.1002/humu.9313openalex-snapshot
Twelve novelJAG1gene mutations in polish Alagille syndrome patients
inferred← citeshttps://doi.org/10.1002/j.1536-4801.1998.tb00814.xopenalex-snapshot
The Biology of Inherited Disorders of the Gastrointestinal Tract Part II: Pancreatic and Hepatobiliary Disorders
inferred← citeshttps://doi.org/10.1002/j.1536-4801.1999.tb02023.xopenalex-snapshot
Genetic Cholestasis Syndromes
inferred← citeshttps://doi.org/10.1002/j.1536-4801.1999.tb02446.xopenalex-snapshot
Variable Morbidity in Alagille Syndrome: A Review of 43 Cases
inferred← citeshttps://doi.org/10.1002/j.1536-4801.2000.tb02695.xopenalex-snapshot
Long-term Outcome After Partial External Biliary Diversion for Intractable Pruritus in Patients With Intrahepatic Cholestasis
inferred← citeshttps://doi.org/10.1002/j.1536-4801.2002.tb07742.xopenalex-snapshot
Intrahepatic Cholestasis
inferred← citeshttps://doi.org/10.1002/j.1536-4801.2002.tb07874.xopenalex-snapshot
Rethinking Growth Failure in Alagille Syndrome: The Role of Dietary Intake and Steatorrhea
inferred← citeshttps://doi.org/10.1002/j.1536-4801.2004.tb12118.xopenalex-snapshot
Prenatal Diagnosis of Alagille Syndrome
inferred← citeshttps://doi.org/10.1002/j.1536-4801.2005.tb00930.xopenalex-snapshot
Deficits in Size‐Adjusted Bone Mass in Children with Alagille Syndrome
inferred← citeshttps://doi.org/10.1002/j.1536-4801.2006.tb00020.xopenalex-snapshot
Visual Loss and Idiopathic Intracranial Hypertension in Children With Alagille Syndrome
inferred← citeshttps://doi.org/10.1002/j.2040-4603.2013.tb00508.xopenalex-snapshot
Cellular and Molecular Basis of Liver Development
inferred← citeshttps://doi.org/10.1002/j.2040-4603.2013.tb00516.xopenalex-snapshot
Zebrafish Models of Human Liver Development and Disease
inferred← citeshttps://doi.org/10.1002/jbm.a.34825openalex-snapshot
Jagged1 immobilization to an osteoconductive polymer activates the Notch signaling pathway and induces osteogenesis
inferred← citeshttps://doi.org/10.1002/jcb.20125openalex-snapshot
Soluble form of Jagged1: Unique product of epithelial keratinocytes and a regulator of keratinocyte differentiation
inferred← citeshttps://doi.org/10.1002/jcb.21232openalex-snapshot
Jedi—a novel transmembrane protein expressed in early hematopoietic cells
inferred← citeshttps://doi.org/10.1002/jcb.22065openalex-snapshot
The autonomous notch signal pathway is activated by baicalin and baicalein but is suppressed by niclosamide in K562 cells
inferred← citeshttps://doi.org/10.1002/jcp.20542openalex-snapshot
Physiology and pathology of notch signalling system
inferred← citeshttps://doi.org/10.1002/jcp.26304openalex-snapshot
TGFβ signaling controls intrahepatic bile duct development may through regulating the Jagged1‐Notch‐Sox9 signaling axis
inferred← citeshttps://doi.org/10.1002/jgh3.12830openalex-snapshot
Different clinical and genetic features of Alagille patients with progressive disease versus a jaundice‐free course
inferred← citeshttps://doi.org/10.1002/jnr.23924openalex-snapshot
Studying the pathophysiologic connection between cardiovascular and nervous systems using stem cells
inferred← citeshttps://doi.org/10.1002/lt.23437openalex-snapshot
Outcomes of liver transplantation for patients with alagille syndrome: The studies of pediatric liver transplantation experience
inferred← citeshttps://doi.org/10.1002/lt.23472openalex-snapshot
Liver transplantation for alagille syndrome: The jagged edge
inferred← citeshttps://doi.org/10.1002/mus.22115openalex-snapshot
Association of common variants in the human eyes shut ortholog (EYS) with statin‐induced myopathy: Evidence for additional functions of EYS
inferred← citeshttps://doi.org/10.1002/mus.27684openalex-snapshot
The Notch signaling pathway in skeletal muscle health and disease
inferred← citeshttps://doi.org/10.1002/path.1615openalex-snapshot
The role of Notch receptor expression in bile duct development and disease
inferred← citeshttps://doi.org/10.1002/path.2789openalex-snapshot
Notch signalling in T‐cell lymphoblastic leukaemia/lymphoma and other haematological malignancies
inferred← citeshttps://doi.org/10.1002/path.2967openalex-snapshot
Notch in the kidney: development and disease
inferred← citeshttps://doi.org/10.1002/path.888openalex-snapshot
Gene profiling techniques and their application in angiogenesis and vascular development
inferred← citeshttps://doi.org/10.1002/pbc.21255openalex-snapshot
Alagille syndrome and nephroblastoma: Unusual coincidence of two rare disorders
inferred← citeshttps://doi.org/10.1002/pd.1668openalex-snapshot
Advantages of multiple markers and polar body analysis in preimplantation genetic diagnosis for Alagille disease
inferred← citeshttps://doi.org/10.1002/pd.214openalex-snapshot
Normal and abnormal development of the urogenital tract
inferred← citeshttps://doi.org/10.1002/stem.1353openalex-snapshot
PKCδ Is Required for Jagged-1 Induction of Human Mesenchymal Stem Cell Osteogenic Differentiation
inferred← citeshttps://doi.org/10.1002/wdev.340openalex-snapshot
Understanding the marvels behind liver regeneration
inferred← citeshttps://doi.org/10.1002/wdev.47openalex-snapshot
Molecular mechanisms of liver and bile duct development
inferred← citeshttps://doi.org/10.1002/wsbm.1537openalex-snapshot
The crucial role of model systems in understanding the complexity of cell signaling in human neurocristopathies
inferred← citeshttps://doi.org/10.1006/dbio.2001.0517openalex-snapshot
Intracellular Cell-Autonomous Association of Notch and Its Ligands: A Novel Mechanism of Notch Signal Modification
inferred← citeshttps://doi.org/10.1006/excr.1998.4285openalex-snapshot
Reactivation of Delta–Notch Signaling after Injury: Complementary Expression Patterns of Ligand and Receptor in Dental Pulp
inferred← citeshttps://doi.org/10.1006/excr.2000.5034openalex-snapshot
Isolation and Characterization of the Notch Ligand Delta4
inferred← citeshttps://doi.org/10.1006/geno.1999.6045openalex-snapshot
Characterization, Chromosomal Localization, and the Complete 30-kb DNA Sequence of the Human Jagged2 (JAG2) Gene
inferred← citeshttps://doi.org/10.1006/geno.2000.6146openalex-snapshot
Identification of a New EGF-Repeat-Containing Gene from Human Xp22: A Candidate for Developmental Disorders
inferred← citeshttps://doi.org/10.1006/geno.2000.6224openalex-snapshot
A Novel Conserved Cochlear Gene, OTOR: Identification, Expression Analysis, and Chromosomal Mapping
inferred← citeshttps://doi.org/10.1006/mpev.1998.0588openalex-snapshot
Phylogenetic Analysis of Vertebrate and Invertebrate Delta/Serrate/LAG-2 (DSL) Proteins
inferred← citeshttps://doi.org/10.1006/mthe.2001.0591openalex-snapshot
Rep/Cap Gene Amplification and High-Yield Production of AAV in an A549 Cell Line Expressing Rep/Cap
inferred← citeshttps://doi.org/10.1007/0-387-21853-x_5openalex-snapshot
Cytogenetics and Cochlear Expressed Sequence Tags (ESTs) for Identification of Genes Involved in Hearing and Deafness
inferred← citeshttps://doi.org/10.1007/0-387-30678-1_5openalex-snapshot
Notch Signaling and Cell Fate Determination in the Vertebrate Inner Ear
inferred← citeshttps://doi.org/10.1007/1-4020-8126-x_2openalex-snapshot
Embryonic Development of Collateral Arteries
inferred← citeshttps://doi.org/10.1007/1-4020-8126-x_9openalex-snapshot
Cell - Cell and Cell - Matrix Interactions
inferred← citeshttps://doi.org/10.1007/3-540-26524-4_16openalex-snapshot
Molekulare Ursachen von Störungen des hepatogastroenterologischen Systems bei Neugeborenen
inferred← citeshttps://doi.org/10.1007/3-540-27194-5_16openalex-snapshot
Notch Signaling in Liver Disease
inferred← citeshttps://doi.org/10.1007/978-0-387-09606-3_9openalex-snapshot
Defective Somitogenesis and Abnormal Vertebral Segmentation in Man
inferred← citeshttps://doi.org/10.1007/978-1-4419-0284-9_28openalex-snapshot
How the NOTCH Pathway Contributes to the Ability of Osteosarcoma Cells to Metastasize
inferred← citeshttps://doi.org/10.1007/978-1-4419-6041-2_2openalex-snapshot
Physiology and Development of the Term and Preterm Neonate
inferred← citeshttps://doi.org/10.1007/978-1-4419-6082-5_16openalex-snapshot
Heterogeneity of Liver Cancer Stem Cells
inferred← citeshttps://doi.org/10.1007/978-1-4419-7107-4_15openalex-snapshot
Bile Duct Development and Biliary Differentiation
inferred← citeshttps://doi.org/10.1007/978-1-4419-9034-1_7openalex-snapshot
Genetics, Mutations, and Polymorphisms
inferred← citeshttps://doi.org/10.1007/978-1-4419-9066-2_9openalex-snapshot
Diseases of the Biliary Tree in Infancy and Childhood
inferred← citeshttps://doi.org/10.1007/978-1-4419-9461-5_10openalex-snapshot
Signaling in Congenital Heart Disease
inferred← citeshttps://doi.org/10.1007/978-1-4471-4619-3_89openalex-snapshot
Genetics of Congenital and Acquired Cardiovascular Disease
inferred← citeshttps://doi.org/10.1007/978-1-4614-0899-4_8openalex-snapshot
The Role of Notch Signaling in Kidney Development and Disease
inferred← citeshttps://doi.org/10.1007/978-1-4614-0899-4_9openalex-snapshot
Notch Signaling and the Developing Skeleton
inferred← citeshttps://doi.org/10.1007/978-1-4614-5505-9_1openalex-snapshot
Short History of Stem Cells Transplantation with Emphasis on Hematological Disorders
inferred← citeshttps://doi.org/10.1007/978-1-4615-4517-0_19openalex-snapshot
Holt-Oram Syndrome and the TBX5 Transcription Factor in Cardiogenesis
inferred← citeshttps://doi.org/10.1007/978-1-4615-4517-0_22openalex-snapshot
The Molecular Genetics of Conotruncal Defects
inferred← citeshttps://doi.org/10.1007/978-1-4939-1013-7_6openalex-snapshot
Rare Causes of Cholestasis
inferred← citeshttps://doi.org/10.1007/978-1-4939-7795-6_13openalex-snapshot
Targeted Gene Knock Out Using Nuclease-Assisted Vector Integration: Hemi- and Homozygous Deletion of JAG1
inferred← citeshttps://doi.org/10.1007/978-1-4939-9420-5_14openalex-snapshot
Mouse Models for Diseases in the Cholangiocyte Lineage
showing the first 200 of 1243 · page through all 1243
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.