scholarly article | Q13442814 |
P2093 | author name string | Hitoshi Okazawa | |
Ichiro Kanazawa | |||
Mei-Ling Qi | |||
Masaya Nakagawa | |||
Shigeki Marubuchi | |||
Tomohiro Okuda | |||
Yukiko Hara | |||
Masataka Hoshino | |||
Yo-Ichi Wada | |||
P2860 | cites work | Association of two nuclear proteins, Npw38 and NpwBP, via the interaction between the WW domain and a novel proline-rich motif containing glycine and arginine | Q22010920 |
The Huntington's disease protein interacts with p53 and CREB-binding protein and represses transcription | Q22254119 | ||
Bcl-xL regulates the membrane potential and volume homeostasis of mitochondria | Q24311858 | ||
The mammalian immediate-early TIS21 protein and the leukemia-associated BTG1 protein interact with a protein-arginine N-methyltransferase | Q24320461 | ||
Novel truncating mutations in the polyglutamine tract binding protein 1 gene (PQBP1) cause Renpenning syndrome and X-linked mental retardation in another family with microcephaly | Q24533381 | ||
PQBP-1/Npw38, a nuclear protein binding to the polyglutamine tract, interacts with U5-15kD/dim1p via the carboxyl-terminal domain | Q28139548 | ||
Evidence that dim1 associates with proteins involved in pre-mRNA splicing, and delineation of residues essential for dim1 interactions with hnRNP F and Npw38/PQBP-1 | Q28142421 | ||
PQBP-1, a novel polyglutamine tract-binding protein, inhibits transcription activation by Brn-2 and affects cell survival | Q28144288 | ||
Mutations in the polyglutamine binding protein 1 gene cause X-linked mental retardation | Q28186625 | ||
Interaction between mutant ataxin-1 and PQBP-1 affects transcription and cell death | Q28204152 | ||
Genotype-phenotype studies in three families with mutations in the polyglutamine-binding protein 1 gene (PQBP1) | Q28280938 | ||
Critical function of endogenous XIAP in regulating caspase activation during sympathetic neuronal apoptosis | Q28510508 | ||
Ribin, a protein encoded by a message complementary to rRNA, modulates ribosomal transcription and cell proliferation | Q28578720 | ||
Mitochondrial control of cell death | Q29617739 | ||
Molecular Pathways of Neurodegeneration in Parkinson's Disease | Q29619903 | ||
Insoluble detergent-resistant aggregates form between pathological and nonpathological lengths of polyglutamine in mammalian cells | Q30779186 | ||
T Cell Activation-Induced Mitochondrial Hyperpolarization Is Mediated by Ca2+- and Redox-Dependent Production of Nitric Oxide | Q33834238 | ||
Different responses of astrocytes and neurons to nitric oxide: the role of glycolytically generated ATP in astrocyte protection. | Q33953141 | ||
Apoptosis and caspases in neurodegenerative diseases | Q35097801 | ||
Antagonizing XIAP-mediated caspase-3 inhibition. Achilles' heel of cancers? | Q35641603 | ||
Minocycline inhibits caspase-independent and -dependent mitochondrial cell death pathways in models of Huntington's disease | Q35918549 | ||
Caspase inhibition extends the commitment to neuronal death beyond cytochrome c release to the point of mitochondrial depolarization | Q36342515 | ||
Biochemical and genetic analysis of the mitochondrial response of yeast to BAX and BCL-X(L) | Q39452632 | ||
Mutant huntingtin directly increases susceptibility of mitochondria to the calcium-induced permeability transition and cytochrome c release | Q40551652 | ||
Striatal cells from mutant huntingtin knock-in mice are selectively vulnerable to mitochondrial complex II inhibitor-induced cell death through a non-apoptotic pathway | Q40590116 | ||
Mitochondrial dysfunction in a cell culture model of familial amyotrophic lateral sclerosis | Q40723426 | ||
Dominant-negative suppression of HNF-1 alpha results in mitochondrial dysfunction, INS-1 cell apoptosis, and increased sensitivity to ceramide-, but not to high glucose-induced cell death. | Q40766274 | ||
CREB-binding protein sequestration by expanded polyglutamine | Q40859094 | ||
PQBP-1 increases vulnerability to low potassium stress and represses transcription in primary cerebellar neurons | Q42522108 | ||
Partial purification and characterization of human hepatoma-derived growth factor | Q42796084 | ||
Apoptosis-resistant mitochondria in T cells selected for resistance to Fas signaling | Q43509302 | ||
Release of cytochrome c into the extracellular space contributes to neuronal apoptosis induced by staurosporine | Q43960599 | ||
Minocycline inhibits cytochrome c release and delays progression of amyotrophic lateral sclerosis in mice | Q43977943 | ||
High glucose-induced oxidative stress and mitochondrial dysfunction in neurons. | Q44200273 | ||
Additive neuroprotective effects of minocycline with creatine in a mouse model of ALS. | Q44296123 | ||
Mutant huntingtin promotes the fibrillogenesis of wild-type huntingtin: a potential mechanism for loss of huntingtin function in Huntington's disease | Q44530908 | ||
AMPA-induced dark cell degeneration of cerebellar Purkinje neurons involves activation of caspases and apparent mitochondrial dysfunction | Q44671811 | ||
Mitochondrial hyperpolarization after transient oxygen-glucose deprivation and subsequent apoptosis in cultured rat hippocampal neurons | Q44672002 | ||
To learn better, keep the HAT on. | Q46135047 | ||
PQBP-1 transgenic mice show a late-onset motor neuron disease-like phenotype | Q48019311 | ||
P433 | issue | 3 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | cell death | Q2383867 |
P304 | page(s) | 858-70 | |
P577 | publication date | 2005-11-01 | |
P1433 | published in | Journal of Neurochemistry | Q6295643 |
P1476 | title | Polyglutamine tract-binding protein-1 dysfunction induces cell death of neurons through mitochondrial stress | |
P478 | volume | 95 |
Q38309416 | Hepatoma-derived growth factor, a new trophic factor for motor neurons, is up-regulated in the spinal cord of PQBP-1 transgenic mice before onset of degeneration |
Q30480195 | New insights into mitochondrial structure during cell death |
Q35854630 | PQBP1 Is a Proximal Sensor of the cGAS-Dependent Innate Response to HIV-1. |
Q28247678 | The splicing factor PQBP1 regulates mesodermal and neural development through FGF signaling |
Q47070332 | X chromosome-linked intellectual disability protein PQBP1 associates with and regulates the translation of specific mRNAs |
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