On the public citation graph
Recruitment and activation of caspase-8 by the Huntingtin-interacting protein Hip-1 and a novel partner Hippi
0 signed · 326 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known work and none has been retracted — and get a dated CiteStamped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/ana.410310111openalex-snapshot
Neurofilament and neural cell adhesion molecule immunocytochemistry of Huntington's disease striatum
inferredcites →https://doi.org/10.1006/exnr.1995.1029openalex-snapshot
DNA End Labeling (TUNEL) in Huntington's Disease and Other Neuropathological Conditions
inferredcites →https://doi.org/10.1007/s003350010195openalex-snapshot
HIP12 is a non-proapoptotic member of a gene family including HIP1, an interacting protein with huntingtin
inferredcites →https://doi.org/10.1007/s100380050087openalex-snapshot
Cloning, expression analysis, and chromosomal localization of HIP1R, an isolog of huntingtin interacting protein (HIP1)
inferredcites →https://doi.org/10.1016/0092-8674(93)90585-eopenalex-snapshot
A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes
inferredcites →https://doi.org/10.1016/0166-2236(90)90111-mopenalex-snapshot
Excitotoxic injury of the neostriatum: a model for Huntington's disease
inferredcites →https://doi.org/10.1016/s0021-9258(18)43211-5openalex-snapshot
Affinity purification of antibodies from diazotized paper blots of heterogeneous protein samples.
inferredcites →https://doi.org/10.1016/s0021-9258(18)82075-0openalex-snapshot
A novel protein domain required for apoptosis. Mutational analysis of human Fas antigen
inferredcites →https://doi.org/10.1016/s0092-8674(00)81266-0openalex-snapshot
FLICE, A Novel FADD-Homologous ICE/CED-3–like Protease, Is Recruited to the CD95 (Fas/APO-1) Death-Inducing Signaling Complex
inferredcites →https://doi.org/10.1016/s0896-6273(00)80716-3openalex-snapshot
Caspase-8 Is Required for Cell Death Induced by Expanded Polyglutamine Repeats
inferredcites →https://doi.org/10.1016/s0955-0674(97)80154-8openalex-snapshot
ERM (ezrin/radixin/moesin) family: from cytoskeleton to signal transduction
inferredcites →https://doi.org/10.1016/s0968-0004(96)10071-2openalex-snapshot
ERM proteins: head-to-tail regulation of actin-plasma membrane interaction
inferredcites →https://doi.org/10.1016/s0968-0004(97)01043-8openalex-snapshot
The CARD domain: a new apoptotic signalling motif
inferredcites →https://doi.org/10.1016/s0968-0004(97)01085-2openalex-snapshot
Caspases: killer proteases
inferredcites →https://doi.org/10.1016/s0968-0004(98)01341-3openalex-snapshot
The domains of death: evolution of the apoptosis machinery
inferredcites →https://doi.org/10.1038/31972openalex-snapshot
NMR structure and mutagenesis of the FADD (Mort1) death-effector domain
inferredcites →https://doi.org/10.1038/347685a0openalex-snapshot
Sequence and domain structure of talin
inferredcites →https://doi.org/10.1038/81593openalex-snapshot
Inactivation of Hdh in the brain and testis results in progressive neurodegeneration and sterility in mice
inferredcites →https://doi.org/10.1038/ng0597-44openalex-snapshot
HIP1, a human homologue of S. cerevisiae Sla2p, interacts with membrane-associated huntingtin in the brain
inferredcites →https://doi.org/10.1038/ng0896-442openalex-snapshot
Cleavage of huntingtin by apopain, a proapoptotic cysteine protease, is modulated by the polyglutamine tract
inferredcites →https://doi.org/10.1038/sj.cdd.4400497openalex-snapshot
Purification and catalytic properties of human caspase family members
inferredcites →https://doi.org/10.1056/nejm199405193302001openalex-snapshot
A Worldwide Study of the Huntington's Disease Mutation: The Sensitivity and Specificity of Measuring CAG Repeats
inferredcites →https://doi.org/10.1074/jbc.273.15.9158openalex-snapshot
Caspase Cleavage of Gene Products Associated with Triplet Expansion Disorders Generates Truncated Fragments Containing the Polyglutamine Tract
inferredcites →https://doi.org/10.1074/jbc.c100401200openalex-snapshot
HIP1 Functions in Clathrin-mediated Endocytosis through Binding to Clathrin and Adaptor Protein 2
inferredcites →https://doi.org/10.1074/jbc.m008408200openalex-snapshot
Huntingtin Interacting Protein 1 Induces Apoptosis via a Novel Caspase-dependent Death Effector Domain
inferredcites →https://doi.org/10.1083/jcb.109.5.2067openalex-snapshot
Molecular trapping of a fluorescent ceramide analogue at the Golgi apparatus of fixed cells: interaction with endogenous lipids provides a trans-Golgi marker for both light and electron microscopy.
inferredcites →https://doi.org/10.1083/jcb.113.6.1267openalex-snapshot
A novel fluorescent ceramide analogue for studying membrane traffic in animal cells: accumulation at the Golgi apparatus results in altered spectral properties of the sphingolipid precursor.
inferredcites →https://doi.org/10.1083/jcb.120.1.55openalex-snapshot
end3 and end4: two mutants defective in receptor-mediated and fluid-phase endocytosis in Saccharomyces cerevisiae.
inferredcites →https://doi.org/10.1083/jcb.122.3.635openalex-snapshot
Synthetic-lethal interactions identify two novel genes, SLA1 and SLA2, that control membrane cytoskeleton assembly in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1084/jem.192.8.f21openalex-snapshot
Cross-Talk in Cell Death Signaling
inferredcites →https://doi.org/10.1086/318207openalex-snapshot
Wild-Type Huntingtin Reduces the Cellular Toxicity of Mutant Huntingtin In Vivo
inferredcites →https://doi.org/10.1091/mbc.8.11.2291openalex-snapshot
End4p/Sla2p Interacts with Actin-associated Proteins for Endocytosis inSaccharomyces cerevisiae
inferredcites →https://doi.org/10.1091/mbc.8.8.1481openalex-snapshot
Yeast actin cytoskeleton mutants accumulate a new class of Golgi-derived secretary vesicle.
inferredcites →https://doi.org/10.1093/oxfordjournals.jbchem.a124803openalex-snapshot
Organization of the Functional Domains in Membrane Cytoskeletal Protein Talin1
inferredcites →https://doi.org/10.1097/00001756-199505090-00026openalex-snapshot
In situ evidence for DNA fragmentation in Huntingtonʼs disease striatum and Alzheimerʼs disease temporal lobes
inferredcites →https://doi.org/10.1097/00005072-199902000-00006openalex-snapshot
Axonal Transport of N-terminal Huntingtin Suggests Early Pathology of Corticostriatal Projections in Huntington Disease
inferredcites →https://doi.org/10.1126/science.1056784openalex-snapshot
Interference by Huntingtin and Atrophin-1 with CBP-Mediated Transcription Leading to Cellular Toxicity
inferredcites →https://doi.org/10.1126/science.277.5334.1990openalex-snapshot
Aggregation of Huntingtin in Neuronal Intranuclear Inclusions and Dystrophic Neurites in Brain
inferredcites →https://doi.org/10.1242/jcs.103.1.131openalex-snapshot
A gene family consisting of ezrin, radixin and moesin Its specific localization at actin filament/plasma membrane association sites
inferredcites →https://doi.org/10.1242/jcs.109.11.2715openalex-snapshot
Talin contains three actin-binding sites each of which is adjacent to a vinculin-binding site
inferredcites →https://doi.org/10.1523/jneurosci.15-05-03775.1995openalex-snapshot
Evidence for apoptotic cell death in Huntington disease and excitotoxic animal models
inferredcites →https://doi.org/10.1523/jneurosci.18-19-07674.1998openalex-snapshot
The Cellular and Subcellular Localization of Huntingtin-Associated Protein 1 (HAP1): Comparison with Huntingtin in Rat and Human
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/9781444346183.ch10openalex-snapshot
Huntington Disease and Other Genetic Choreas
inferred← citeshttps://doi.org/10.1002/ana.24694openalex-snapshot
Globus pallidus degeneration and clinicopathological features of Huntington disease
inferred← citeshttps://doi.org/10.1002/biot.201300560openalex-snapshot
Stem cell therapy and cellular engineering for treatment of neuronal dysfunction in Huntington's disease
inferred← citeshttps://doi.org/10.1002/cyto.a.20422openalex-snapshot
Two optimized combination assays to examine apoptosis pathways in clinical samples
inferred← citeshttps://doi.org/10.1002/jnr.10746openalex-snapshot
Role of proteolysis in polyglutamine disorders
inferred← citeshttps://doi.org/10.1002/jnr.20534openalex-snapshot
Regulation of the proapoptotic activity of huntingtin interacting protein 1 by Dyrk1 and caspase-3 in hippocampal neuroprogenitor cells
inferred← citeshttps://doi.org/10.1002/prot.21856openalex-snapshot
Huntingtin interacting protein HYPK is intrinsically unstructured
inferred← citeshttps://doi.org/10.1007/0-387-34573-6_6openalex-snapshot
Fas—More Than an Apoptosis Inducer
inferred← citeshttps://doi.org/10.1007/1-4020-2898-9_27openalex-snapshot
Treatment Options in Huntington’s Disease
inferred← citeshttps://doi.org/10.1007/1-4020-5466-1_12openalex-snapshot
Chromatin Acetylation Status in the Manifestation of Neurodegenerative Diseases
inferred← citeshttps://doi.org/10.1007/978-1-60327-120-2_2openalex-snapshot
Huntington Disease and Other Choreas
inferred← citeshttps://doi.org/10.1007/978-3-319-57193-5_4openalex-snapshot
Huntington’s Disease: Pathogenic Mechanisms and Therapeutic Targets
inferred← citeshttps://doi.org/10.1007/978-3-540-87941-1_9openalex-snapshot
Huntington's Disease: Function and Dysfunction of Huntingtin in Axonal Transport
inferred← citeshttps://doi.org/10.1007/978-90-481-3415-1_1openalex-snapshot
Physiological and Pathological Role of Apoptosis
inferred← citeshttps://doi.org/10.1007/978-981-13-2218-1_7openalex-snapshot
Notch Signaling: From Neurogenesis to Neurodegeneration
inferred← citeshttps://doi.org/10.1007/978-981-97-7905-5_2openalex-snapshot
Apoptosis: A Controlled Cell’s Fate
inferred← citeshttps://doi.org/10.1007/bf03036448openalex-snapshot
Role of activated astrocytes in neuronal damage: Potential links to HIV-1-associated dementia
inferred← citeshttps://doi.org/10.1007/s00018-006-6242-0openalex-snapshot
Huntington’s disease: from huntingtin function and dysfunction to therapeutic strategies
inferred← citeshttps://doi.org/10.1007/s00018-008-8489-0openalex-snapshot
Death Effector Domain-Containing Proteins
inferred← citeshttps://doi.org/10.1007/s00439-006-0221-2openalex-snapshot
Genetic analysis of candidate genes modifying the age-at-onset in Huntington’s disease
inferred← citeshttps://doi.org/10.1007/s00441-010-0995-3openalex-snapshot
Brain region-specific vulnerability of astrocytes in response to 3-nitropropionic acid is mediated by cytochrome c oxidase isoform expression
inferred← citeshttps://doi.org/10.1007/s10495-005-0930-3openalex-snapshot
Apoptin: Specific killer of tumor cells?
inferred← citeshttps://doi.org/10.1007/s10495-006-0018-8openalex-snapshot
Caspase-3 antisense oligodeoxynucleotides inhibit apoptosis in γ-irradiated human leukemia HL-60 cells
inferred← citeshttps://doi.org/10.1007/s10495-006-4065-yopenalex-snapshot
Prolonged activation of ERK1,2 induces FADD-independent caspase 8 activation and cell death
inferred← citeshttps://doi.org/10.1007/s10495-007-0131-3openalex-snapshot
Rybp interacts with Hippi and enhances Hippi-mediated apoptosis
inferred← citeshttps://doi.org/10.1007/s10495-007-0176-3openalex-snapshot
BLOC1S2 interacts with the HIPPI protein and sensitizes NCH89 glioblastoma cells to apoptosis
inferred← citeshttps://doi.org/10.1007/s10522-023-10034-1openalex-snapshot
The role of Smo-Shh/Gli signaling activation in the prevention of neurological and ageing disorders
inferred← citeshttps://doi.org/10.1007/s10571-007-9220-7openalex-snapshot
Increased Caspase-2, Calpain Activations and Decreased Mitochondrial Complex II Activity in Cells Expressing Exogenous Huntingtin Exon 1 Containing CAG Repeat in the Pathogenic Range
inferred← citeshttps://doi.org/10.1007/s11910-003-0003-3openalex-snapshot
Huntington’s disease: A decade beyond gene discovery
inferred← citeshttps://doi.org/10.1007/s12031-015-0498-5openalex-snapshot
Caspase-8 Mediates Amyloid-β-induced Apoptosis in Differentiated PC12 Cells
inferred← citeshttps://doi.org/10.1007/s12035-012-8316-3openalex-snapshot
Mouse Models of Polyglutamine Diseases in Therapeutic Approaches: Review and Data Table. Part II
inferred← citeshttps://doi.org/10.1007/s12253-020-00837-9openalex-snapshot
Gene Expression Signature of BRAF Inhibitor Resistant Melanoma Spheroids
inferred← citeshttps://doi.org/10.1007/s12311-008-0026-zopenalex-snapshot
Spinocerebellar ataxias caused by polyglutamine expansions: A review of therapeutic strategies
inferred← citeshttps://doi.org/10.1007/s12640-018-9989-9openalex-snapshot
Protective Effects of Antioxidants in Huntington’s Disease: an Extensive Review
inferred← citeshttps://doi.org/10.1016/b978-0-12-381328-2.00014-6openalex-snapshot
Genetics and Neuropathology of Huntington's Disease
inferred← citeshttps://doi.org/10.1016/b978-0-12-385883-2.00010-2openalex-snapshot
Huntington Disease and the Huntingtin Protein
inferred← citeshttps://doi.org/10.1016/b978-0-323-31071-0.00013-5openalex-snapshot
Huntington disease
inferred← citeshttps://doi.org/10.1016/b978-0-443-07941-2.50018-8openalex-snapshot
Huntington Disease
inferred← citeshttps://doi.org/10.1016/b978-0-443-40467-2.00011-7openalex-snapshot
Gene therapy in Huntington’s disease (HD)
inferred← citeshttps://doi.org/10.1016/b978-0-444-52002-9.00030-9openalex-snapshot
Huntington's disease
inferred← citeshttps://doi.org/10.1016/b978-012369509-3.50019-6openalex-snapshot
Polyglutamine Disorders Including Huntington's Disease
inferred← citeshttps://doi.org/10.1016/b978-012566652-7/50035-6openalex-snapshot
Molecular Biology of Huntington's Disease (HD) and HD-Like Disorders
inferred← citeshttps://doi.org/10.1016/b978-1-4377-2369-4.00014-7openalex-snapshot
Huntington disease
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2005.03.002openalex-snapshot
Golgi structure in stress sensing and apoptosis
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2008.01.020openalex-snapshot
Protein folding diseases and neurodegeneration: Lessons learned from yeast
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2024.119720openalex-snapshot
Network analysis of S-nitrosylated synaptic proteins demonstrates unique roles in health and disease
inferred← citeshttps://doi.org/10.1016/j.bbapap.2021.140670openalex-snapshot
The nuclear localization sequence of the epigenetic factor RYBP binds to human importin α3
inferred← citeshttps://doi.org/10.1016/j.bbrc.2006.10.167openalex-snapshot
Homer1c interacts with Hippi and protects striatal neurons from apoptosis
inferred← citeshttps://doi.org/10.1016/j.biopha.2017.05.105openalex-snapshot
RETRACTED: Overexpression of FADD and Caspase-8 inhibits proliferation and promotes apoptosis of human glioblastoma cells
inferred← citeshttps://doi.org/10.1016/j.brainres.2009.06.049openalex-snapshot
ATF3 plays a protective role against toxicity by N-terminal fragment of mutant huntingtin in stable PC12 cell line
inferred← citeshttps://doi.org/10.1016/j.cell.2009.03.023openalex-snapshot
The Vertebrate Primary Cilium in Development, Homeostasis, and Disease
inferred← citeshttps://doi.org/10.1016/j.coph.2003.09.008openalex-snapshot
Mechanisms of cell death in polyglutamine expansion diseases
inferred← citeshttps://doi.org/10.1016/j.dci.2017.09.002openalex-snapshot
The self-activation and LPS binding activity of executioner caspase-1 in oyster Crassostrea gigas
inferred← citeshttps://doi.org/10.1016/j.diff.2011.11.001openalex-snapshot
Architecture and function of IFT complex proteins in ciliogenesis
inferred← citeshttps://doi.org/10.1016/j.febslet.2006.08.076openalex-snapshot
Huntingtin‐interacting protein 1‐mediated neuronal cell death occurs through intrinsic apoptotic pathways and mitochondrial alterations
inferred← citeshttps://doi.org/10.1016/j.febslet.2012.07.011openalex-snapshot
Replacement of charged and polar residues in the coiled‐coiled interface of huntingtin‐interacting protein 1 (HIP1) causes aggregation and cell death
inferred← citeshttps://doi.org/10.1016/j.febslet.2013.05.022openalex-snapshot
Pharmacological protein targets in polyglutamine diseases: Mutant polypeptides and their interactors
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2011.01.011openalex-snapshot
The role of the Golgi apparatus in oxidative stress: is this organelle less significant than mitochondria?
inferred← citeshttps://doi.org/10.1016/j.gene.2014.08.041openalex-snapshot
MicroRNA and mRNA cargo of extracellular vesicles from porcine adipose tissue-derived mesenchymal stem cells
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2023.125632openalex-snapshot
The intrinsically disordered, epigenetic factor RYBP binds to the citrullinating enzyme PADI4 in cancer cells
inferred← citeshttps://doi.org/10.1016/j.jchemneu.2004.02.005openalex-snapshot
Differential loss of striatal projection systems in Huntington’s disease: a quantitative immunohistochemical study
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2024.133819openalex-snapshot
Exposure to virgin and marine incubated microparticles of biodegradable and conventional polymers modulates the hepatopancreas transcriptome of Mytilus galloprovincialis
inferred← citeshttps://doi.org/10.1016/j.jmb.2006.12.052openalex-snapshot
Crystal Structure at 2.8 Å of the DLLRKN-containing Coiled-coil Domain of Huntingtin-interacting Protein 1 (HIP1) Reveals a Surface Suitable for Clathrin Light Chain Binding
inferred← citeshttps://doi.org/10.1016/j.jmb.2007.11.036openalex-snapshot
Crystal Structure at 2.8 Å of Huntingtin-Interacting Protein 1 (HIP1) Coiled-Coil Domain Reveals a Charged Surface Suitable for HIP1 Protein Interactor (HIPPI)
inferred← citeshttps://doi.org/10.1016/j.jns.2004.11.024openalex-snapshot
Neuroacanthocytosis: new developments in a neglected group of dementing disorders
inferred← citeshttps://doi.org/10.1016/j.molmed.2003.08.006openalex-snapshot
Huntington's disease: a synaptopathy?
inferred← citeshttps://doi.org/10.1016/j.molmed.2004.02.003openalex-snapshot
HIP1: trafficking roles and regulation of tumorigenesis
inferred← citeshttps://doi.org/10.1016/j.nbd.2003.09.013openalex-snapshot
Death of cortical and striatal neurons induced by mitochondrial defect involves differential molecular mechanisms
inferred← citeshttps://doi.org/10.1016/j.nbd.2005.11.003openalex-snapshot
Induction of apoptosis in cells expressing exogenous Hippi, a molecular partner of huntingtin-interacting protein Hip1
inferred← citeshttps://doi.org/10.1016/j.nbd.2015.05.008openalex-snapshot
A novel function of Huntingtin in the cilium and retinal ciliopathy in Huntington's disease mice
inferred← citeshttps://doi.org/10.1016/j.nbd.2017.12.015openalex-snapshot
Effect of early embryonic deletion of huntingtin from pyramidal neurons on the development and long-term survival of neurons in cerebral cortex and striatum
inferred← citeshttps://doi.org/10.1016/j.nbd.2019.02.002openalex-snapshot
Olfactory bulb atrophy and caspase activation observed in the BACHD rat models of Huntington disease
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2017.01.008openalex-snapshot
Targeting sonic hedgehog signaling in neurological disorders
inferred← citeshttps://doi.org/10.1016/j.neurobiolaging.2004.09.018openalex-snapshot
Endosome function and dysfunction in Alzheimer's disease and other neurodegenerative diseases
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2021.06.023openalex-snapshot
Apoptosis, Autophagy, Necrosis and Their Multi Galore Crosstalk in Neurodegeneration
inferred← citeshttps://doi.org/10.1016/j.patbio.2003.06.004openalex-snapshot
Huntington’s disease: how does huntingtin, an anti-apoptotic protein, become toxic?
inferred← citeshttps://doi.org/10.1016/j.pharmr.2025.100053openalex-snapshot
Activating autophagy to eliminate toxic protein aggregates with small molecules in neurodegenerative diseases
inferred← citeshttps://doi.org/10.1016/j.pharmthera.2018.09.010openalex-snapshot
DYRK1A and cognition: A lifelong relationship
inferred← citeshttps://doi.org/10.1016/j.pneurobio.2012.08.004openalex-snapshot
Therapeutic approaches to preventing cell death in Huntington disease
inferred← citeshttps://doi.org/10.1016/j.pneurobio.2013.10.004openalex-snapshot
Autophagy and apoptosis dysfunction in neurodegenerative disorders
inferred← citeshttps://doi.org/10.1016/j.pneurobio.2016.01.006openalex-snapshot
The therapeutic potential of cell identity reprogramming for the treatment of aging-related neurodegenerative disorders
inferred← citeshttps://doi.org/10.1016/j.str.2021.10.011openalex-snapshot
An engineered construct of cFLIP provides insight into DED1 structure and interactions
inferred← citeshttps://doi.org/10.1016/j.tig.2004.01.008openalex-snapshot
Huntingtin–protein interactions and the pathogenesis of Huntington's disease
inferred← citeshttps://doi.org/10.1016/j.tins.2011.06.005openalex-snapshot
Emerging roles for cholesterol in Huntington's disease
inferred← citeshttps://doi.org/10.1016/j.ydbio.2006.09.001openalex-snapshot
Hippi is essential for node cilia assembly and Sonic hedgehog signaling
inferred← citeshttps://doi.org/10.1016/s0006-291x(03)00764-2openalex-snapshot
The viral death protein Apoptin interacts with Hippi, the protein interactor of Huntingtin-interacting protein 1
inferred← citeshttps://doi.org/10.1016/s0014-4827(02)00089-7openalex-snapshot
Identification of CHE-13, a novel intraflagellar transport protein required for cilia formation
inferred← citeshttps://doi.org/10.1016/s0014-5793(03)01294-8openalex-snapshot
Caspase 8 mediated apoptotic cell death induced by β‐sheet forming polyalanine peptides
inferred← citeshttps://doi.org/10.1016/s0072-9752(07)01257-2openalex-snapshot
The biology of Huntington's disease
inferred← citeshttps://doi.org/10.1016/s0074-7742(04)61010-5openalex-snapshot
Influence of Huntington's Disease on the Human and Mouse Proteome
inferred← citeshttps://doi.org/10.1016/s0079-6123(03)46014-7openalex-snapshot
Neurotrophic factors in Huntington's disease
inferred← citeshttps://doi.org/10.1016/s0165-6147(02)02032-1openalex-snapshot
HIPPI–HIP1 – a deadly duo
inferred← citeshttps://doi.org/10.1016/s0896-6273(02)00872-3openalex-snapshot
Polyglutamine Pathogenesis
inferred← citeshttps://doi.org/10.1016/s0962-8924(02)02410-8openalex-snapshot
Intraflagellar transport and cilia-dependent diseases
inferred← citeshttps://doi.org/10.1016/s0968-0004(03)00168-3openalex-snapshot
The hunt for huntingtin function: interaction partners tell many different stories
inferred← citeshttps://doi.org/10.1016/s1474-4422(03)00411-3openalex-snapshot
Adenosine receptors and Huntington's disease: implications for pathogenesis and therapeutics
inferred← citeshttps://doi.org/10.1016/s1534-5807(02)00121-1openalex-snapshot
Hip1 and Hippi Participate in a Novel Cell Death-Signaling Pathway
inferred← citeshttps://doi.org/10.1016/s1534-5807(03)00091-1openalex-snapshot
BAK Alters Neuronal Excitability and Can Switch from Anti- to Pro-Death Function during Postnatal Development
inferred← citeshttps://doi.org/10.1016/s1566-2772(03)00055-0openalex-snapshot
Huntingtin proteolysis in Huntington disease
inferred← citeshttps://doi.org/10.1016/s1566-2772(03)00057-4openalex-snapshot
Huntingtin phosphorylation and signaling pathways that regulate toxicity in Huntington's disease
inferred← citeshttps://doi.org/10.1016/s1566-2772(03)00062-8openalex-snapshot
Plans for HDBase—a research community website for Huntington's Disease
inferred← citeshttps://doi.org/10.1017/cbo9780511544873.008openalex-snapshot
Apoptosis in neurodegenerative diseases
inferred← citeshttps://doi.org/10.1017/cbo9780511544873.010openalex-snapshot
Protein misfolding and cellular defense mechanisms in neurodegenerative diseases
inferred← citeshttps://doi.org/10.1017/cbo9780511663543.005openalex-snapshot
Neuronal cell death in human neurodegenerative diseases and their animal/cell models
inferred← citeshttps://doi.org/10.1017/s1462399403006549openalex-snapshot
Huntington's disease: molecular basis of neurodegeneration
inferred← citeshttps://doi.org/10.1021/bi801933copenalex-snapshot
The Transcriptional Repressor RYBP Is a Natively Unfolded Protein Which Folds upon Binding to DNA
inferred← citeshttps://doi.org/10.1023/b:appt.0000012118.95548.88openalex-snapshot
Induction of apoptosis by tumor cell-targeted toxins
inferred← citeshttps://doi.org/10.1023/b:appt.0000025808.48885.9copenalex-snapshot
The viral death effector Apoptin reveals tumor-specific processes
inferred← citeshttps://doi.org/10.1034/j.1399-0004.2002.620503_3.xopenalex-snapshot
Enteroviruses prefer the dystrophin‐deficient heart
inferred← citeshttps://doi.org/10.1034/j.1399-0004.2002.620503_4.xopenalex-snapshot
HIP1 as a marker of aggressive prostate cancer
inferred← citeshttps://doi.org/10.1034/j.1600-065x.2003.00045.xopenalex-snapshot
Overview: apoptotic signaling pathways in the immune system
inferred← citeshttps://doi.org/10.1034/j.1600-0854.2003.t01-1-00103.xopenalex-snapshot
The Intraflagellar Transport Machinery of Chlamydomonas reinhardtii
inferred← citeshttps://doi.org/10.1038/cdd.2008.53openalex-snapshot
Direct activation of caspase 8 by the proapoptotic E2 protein of HPV18 independent of adaptor proteins
inferred← citeshttps://doi.org/10.1038/cddis.2013.300openalex-snapshot
Defining the role of the Bcl-2 family proteins in Huntington’s disease
inferred← citeshttps://doi.org/10.1038/emboj.2010.346openalex-snapshot
Fis1 and Bap31 bridge the mitochondria–ER interface to establish a platform for apoptosis induction
inferred← citeshttps://doi.org/10.1038/ng1418openalex-snapshot
Loss of BBS proteins causes anosmia in humans and defects in olfactory cilia structure and function in the mouse
inferred← citeshttps://doi.org/10.1038/ni0503-404openalex-snapshot
The death effector domain protein family: regulators of cellular homeostasis
inferred← citeshttps://doi.org/10.1038/nrd2755openalex-snapshot
Cell death and endoplasmic reticulum stress: disease relevance and therapeutic opportunities
inferred← citeshttps://doi.org/10.1038/nrg1557openalex-snapshot
The centrosome in human genetic disease
inferred← citeshttps://doi.org/10.1038/nrn1100openalex-snapshot
Targeting programmed cell death in neurodegenerative diseases
inferred← citeshttps://doi.org/10.1038/nrn1477openalex-snapshot
Adult neuron survival strategies — slamming on the brakes
inferred← citeshttps://doi.org/10.1038/nrn1806openalex-snapshot
Normal huntingtin function: an alternative approach to Huntington's disease
inferred← citeshttps://doi.org/10.1038/nsmb1043openalex-snapshot
Structural definition of the F-actin–binding THATCH domain from HIP1R
inferred← citeshttps://doi.org/10.1038/s41598-020-74042-8openalex-snapshot
Wild-type huntingtin regulates human macrophage function
inferred← citeshttps://doi.org/10.1038/sj.cdd.4401014openalex-snapshot
‘Centennial’ Nobel Conference on apoptosis and human disease
inferred← citeshttps://doi.org/10.1038/sj.cdd.4401287openalex-snapshot
Bifunctional apoptosis inhibitor (BAR) protects neurons from diverse cell death pathways
inferred← citeshttps://doi.org/10.1038/sj.cdd.4401967openalex-snapshot
Increased apoptosis, huntingtin inclusions and altered differentiation in muscle cell cultures from Huntington's disease subjects
inferred← citeshttps://doi.org/10.1038/sj.onc.1207103openalex-snapshot
The death effector domain protein family
inferred← citeshttps://doi.org/10.1038/srep21408openalex-snapshot
Insights into the mechanism of human papillomavirus E2-induced procaspase-8 activation and cell death
inferred← citeshttps://doi.org/10.1042/bj20071619openalex-snapshot
Huntington's disease: from pathology and genetics to potential therapies
inferred← citeshttps://doi.org/10.1042/bst0380187openalex-snapshot
The Sla2p/HIP1/HIP1R family: similar structure, similar function in endocytosis?
inferred← citeshttps://doi.org/10.1046/j.1537-2995.2003.t01-1-00434.xopenalex-snapshot
McLeod phenotype associated with a XK missense mutation without hematologic, neuromuscular, or cerebral involvement
inferred← citeshttps://doi.org/10.1051/medsci/20021889861openalex-snapshot
Implications physiopathologiques des altérations des gènes impliqués dans la régulation de la mort cellulaire
inferred← citeshttps://doi.org/10.1073/pnas.1616119114openalex-snapshot
Formation of neurodegenerative aggresome and death-inducing signaling complex in maternal diabetes-induced neural tube defects
inferred← citeshttps://doi.org/10.1073/pnas.1619932114openalex-snapshot
Intrinsically disordered chromatin protein NUPR1 binds to the C-terminal region of Polycomb RING1B
inferred← citeshttps://doi.org/10.1073/pnas.1621279114openalex-snapshot
TCTE1 is a conserved component of the dynein regulatory complex and is required for motility and metabolism in mouse spermatozoa
inferred← citeshttps://doi.org/10.1073/pnas.162362299openalex-snapshot
Tauroursodeoxycholic acid, a bile acid, is neuroprotective in a transgenic animal model of Huntington's disease
inferred← citeshttps://doi.org/10.1073/pnas.1719861115openalex-snapshot
FGFR1-mediated protocadherin-15 loading mediates cargo specificity during intraflagellar transport in inner ear hair-cell kinocilia
inferred← citeshttps://doi.org/10.1074/jbc.c200353200openalex-snapshot
Calcium-dependent Cleavage of Endogenous Wild-type Huntingtin in Primary Cortical Neurons
inferred← citeshttps://doi.org/10.1074/jbc.m111.265173openalex-snapshot
Regulation of RE1 Protein Silencing Transcription Factor (REST) Expression by HIP1 Protein Interactor (HIPPI)
inferred← citeshttps://doi.org/10.1074/jbc.m209208200openalex-snapshot
Post-translational Modification of Bid Has Differential Effects on Its Susceptibility to Cleavage by Caspase 8 or Caspase 3
inferred← citeshttps://doi.org/10.1074/jbc.m209610200openalex-snapshot
Epoxycyclohexenone Inhibits Fas-mediated Apoptosis by Blocking Activation of Pro-caspase-8 in the Death-inducing Signaling Complex
inferred← citeshttps://doi.org/10.1074/jbc.m300156200openalex-snapshot
IFT20 Links Kinesin II with a Mammalian Intraflagellar Transport Complex That Is Conserved in Motile Flagella and Sensory Cilia
inferred← citeshttps://doi.org/10.1074/jbc.m312645200openalex-snapshot
HIP1 and HIP1r Stabilize Receptor Tyrosine Kinases and Bind 3-Phosphoinositides via Epsin N-terminal Homology Domains
inferred← citeshttps://doi.org/10.1074/jbc.m506600200openalex-snapshot
Disease-related Prion Protein Forms Aggresomes in Neuronal Cells Leading to Caspase Activation and Apoptosis
inferred← citeshttps://doi.org/10.1074/jbc.m705265200openalex-snapshot
Proteolytic Cleavage of Ataxin-7 by Caspase-7 Modulates Cellular Toxicity and Transcriptional Dysregulation
inferred← citeshttps://doi.org/10.1074/jbc.m802863200openalex-snapshot
Actin Binding by Hip1 (Huntingtin-interacting Protein 1) and Hip1R (Hip1-related Protein) Is Regulated by Clathrin Light Chain
inferred← citeshttps://doi.org/10.1074/mcp.m800277-mcp200openalex-snapshot
A Large Number of Protein Expression Changes Occur Early in Life and Precede Phenotype Onset in a Mouse Model for Huntington Disease
inferred← citeshttps://doi.org/10.1080/1521654031000153012openalex-snapshot
The Differential Susceptibility of Specific Neuronal Populations: Insights from Huntington's Disease
inferred← citeshttps://doi.org/10.1083/jcb.200312074openalex-snapshot
Switch from αvβ5 to αvβ6 integrin expression protects squamous cell carcinomas from anoikis
inferred← citeshttps://doi.org/10.1089/ars.2007.1511openalex-snapshot
Neuronal Apoptosis in Neurodegeneration
inferred← citeshttps://doi.org/10.1093/brain/awg077openalex-snapshot
Homozygosity for CAG mutation in Huntington disease is associated with a more severe clinical course
inferred← citeshttps://doi.org/10.1093/brain/awm044openalex-snapshot
Microglial activation in presymptomatic Huntington's disease gene carriers
inferred← citeshttps://doi.org/10.1093/emboj/cdg334openalex-snapshot
Disruption of the endocytic protein HIP1 results in neurological deficits and decreased AMPA receptor trafficking
inferred← citeshttps://doi.org/10.1093/emboj/cdg414openalex-snapshot
Interdimer processing mechanism of procaspase‐8 activation
inferred← citeshttps://doi.org/10.1093/hmg/11.23.2815openalex-snapshot
HIP14, a novel ankyrin domain-containing protein, links huntingtin to intracellular trafficking and endocytosis
inferred← citeshttps://doi.org/10.1093/hmg/ddaa099openalex-snapshot
Early deficits in olfaction are associated with structural and molecular alterations in the olfactory system of a Huntington disease mouse model
inferred← citeshttps://doi.org/10.1093/hmg/ddaf058openalex-snapshot
Defective IFT57 underlies a novel cause of Bardet-Biedl syndrome
inferred← citeshttps://doi.org/10.1093/hmg/ddg295openalex-snapshot
Pathogenesis of polyglutamine disorders: aggregation revisited
inferred← citeshttps://doi.org/10.1093/hmg/ddh102openalex-snapshot
Huntingtin Interacting Protein 1 mutations lead to abnormal hematopoiesis, spinal defects and cataracts
inferred← citeshttps://doi.org/10.1093/hmg/ddi053openalex-snapshot
The R6/2 transgenic mouse model of Huntington's disease develops diabetes due to deficient β-cell mass and exocytosis
inferred← citeshttps://doi.org/10.1093/hmg/ddm076openalex-snapshot
Degenerative phenotypes caused by the combined deficiency of murine HIP1 and HIP1r are rescued by human HIP1
inferred← citeshttps://doi.org/10.1093/hmg/ddn033openalex-snapshot
Dopamine determines the vulnerability of striatal neurons to the N-terminal fragment of mutant huntingtin through the regulation of mitochondrial complex II
inferred← citeshttps://doi.org/10.1093/hmg/ddr242openalex-snapshot
Wild-type HTT modulates the enzymatic activity of the neuronal palmitoyl transferase HIP14
inferred← citeshttps://doi.org/10.1093/nar/gkp1011openalex-snapshot
Transcription regulation of caspase-1 by R393 of HIPPI and its molecular partner HIP-1
inferred← citeshttps://doi.org/10.1093/pcp/pcz036openalex-snapshot
Plant AP180 N-Terminal Homolog Proteins Are Involved in Clathrin-Dependent Endocytosis during Pollen Tube Growth in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1093/toxsci/kfi162openalex-snapshot
Temporal and Dose-Dependent Hepatic Gene Expression Patterns in Mice Provide New Insights into TCDD-Mediated Hepatotoxicity
inferred← citeshttps://doi.org/10.1093/toxsci/kfm289openalex-snapshot
Comparative Toxicogenomic Examination of the Hepatic Effects of PCB126 and TCDD in Immature, Ovariectomized C57BL/6 Mice
inferred← citeshttps://doi.org/10.1097/01.wco.0000084229.82329.03openalex-snapshot
Huntington's disease
inferred← citeshttps://doi.org/10.1101/168187openalex-snapshot
A large kinome in a large cell: Stentor coeruleus possesses highly expanded kinase families and novel domain architectures
inferred← citeshttps://doi.org/10.1101/2022.03.21.485080openalex-snapshot
Deletion of CEP164 in mouse photoreceptors post-ciliogenesis interrupts ciliary intraflagellar transport (IFT)
inferred← citeshttps://doi.org/10.1101/cshperspect.a008839openalex-snapshot
Autophagy and Neuronal Cell Death in Neurological Disorders
inferred← citeshttps://doi.org/10.1101/cshperspect.a017004openalex-snapshot
Unconventional Functions for Clathrin, ESCRTs, and Other Endocytic Regulators in the Cytoskeleton, Cell Cycle, Nucleus, and Beyond: Links to Human Disease
inferred← citeshttps://doi.org/10.1107/s0907444909054535openalex-snapshot
Accommodation of structural rearrangements in the huntingtin-interacting protein 1 coiled-coil domain
inferred← citeshttps://doi.org/10.1107/s1744309106046628openalex-snapshot
Cloning, expression, purification, crystallization and preliminary crystallographic analysis of pseudo death-effector domain of HIPPI, a molecular partner of Huntingtin-interacting protein HIP-1
inferred← citeshttps://doi.org/10.1111/cga.12023openalex-snapshot
Spatiotemporal patterns of the H untingtin‐interacting protein 1‐related gene in the mouse head
inferred← citeshttps://doi.org/10.1111/cge.12785openalex-snapshot
Autosomal recessive IFT57 hypomorphic mutation cause ciliary transport defect in unclassified oral–facial–digital syndrome with short stature and brachymesophalangia
inferred← citeshttps://doi.org/10.1111/cns.12844openalex-snapshot
Disrupted striatal neuron inputs and outputs in Huntington's disease
inferred← citeshttps://doi.org/10.1111/j.0953-816x.2003.03131.xopenalex-snapshot
The serum‐ and glucocorticoid‐induced kinase SGK inhibits mutant huntingtin‐induced toxicity by phosphorylating serine 421 of huntingtin
inferred← citeshttps://doi.org/10.1111/j.1365-2796.2005.01570.xopenalex-snapshot
Apoptosis: a basic biological phenomenon with wide‐ranging implications in human disease
inferred← citeshttps://doi.org/10.1111/j.1460-9568.2005.03985.xopenalex-snapshot
Akt is altered in an animal model of Huntington's disease and in patients
inferred← citeshttps://doi.org/10.1111/j.1460-9568.2008.06310.xopenalex-snapshot
Mechanisms of neurodegeneration in Huntington’s disease
inferred← citeshttps://doi.org/10.1111/j.1460-9568.2008.06359.xopenalex-snapshot
Huntingtin interacting protein 1 can regulate neurogenesis in Drosophila
inferred← citeshttps://doi.org/10.1111/j.1471-4159.2009.06302.xopenalex-snapshot
The pathogenic mechanisms of polyglutamine diseases and current therapeutic strategies
inferred← citeshttps://doi.org/10.1111/j.1582-4934.2003.tb00199.xopenalex-snapshot
Physiological and pathological roles of Apaf1 and the apoptosome
inferred← citeshttps://doi.org/10.1111/j.1582-4934.2008.00292.xopenalex-snapshot
Caspases as therapeutic targets
inferred← citeshttps://doi.org/10.1111/j.1742-4658.2007.05922.xopenalex-snapshot
Interactions of HIPPI, a molecular partner of Huntingtin interacting protein HIP1, with the specific motif present at the putative promoter sequence of the caspase‐1, caspase‐8 and caspase‐10 genes
inferred← citeshttps://doi.org/10.1111/j.1742-4658.2008.06563.xopenalex-snapshot
Huntington’s disease: roles of huntingtin‐interacting protein 1 (HIP‐1) and its molecular partner HIPPI in the regulation of apoptosis and transcription
inferred← citeshttps://doi.org/10.1111/jeu.12423openalex-snapshot
The Ciliary Protein IFT 57 in the Macronucleus ofParamecium
inferred← citeshttps://doi.org/10.1126/sageke.2003.37.pe26openalex-snapshot
How Does the Huntington's Disease Mutation Damage Cells?
showing the first 200 of 284 · page through all 284
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.