Prediction of the coding sequences of unidentified human genes. XIII. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro
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Syne-1, a dystrophin- and Klarsicht-related protein associated with synaptic nuclei at the neuromuscular junctionAndrogen-induced proliferative quiescence in prostate cancer cells: the role of AS3 as its mediatorIdentification of pleckstrin-homology-domain-containing proteins with novel phosphoinositide-binding specificitiesMolecular cloning and characterization of DEFCAP-L and -S, two isoforms of a novel member of the mammalian Ced-4 family of apoptosis proteinsCharacterization of vertebrate cohesin complexes and their regulation in prophaseIdentification of a novel neuroligin in humans which binds to PSD-95 and has a widespread expressionMolecular cloning and characterization of a dermatan-specific N-acetylgalactosamine 4-O-sulfotransferaseCharacterization of human palladin, a microfilament-associated proteinIdentification of dynein heavy chain 7 as an inner arm component of human cilia that is synthesized but not assembled in a case of primary ciliary dyskinesiaHuman Na(+)/H(+) exchanger isoform 6 is found in recycling endosomes of cells, not in mitochondriaThe cancer-related protein SSX2 interacts with the human homologue of a Ras-like GTPase interactor, RAB3IP, and a novel nuclear protein, SSX2IPArylsulfatase G, a novel lysosomal sulfataseHuman BAHD1 promotes heterochromatic gene silencing.The PD-(D/E)XK superfamily revisited: identification of new members among proteins involved in DNA metabolism and functional predictions for domains of (hitherto) unknown function.Mammalian P4-ATPases and ABC transporters and their role in phospholipid transportIdentification and characterization of a family of Rab11-interacting proteinsExpression, cellular distribution and protein binding of the glioma amplified sequence (GAS41), a highly conserved putative transcription factorThe PDZ and band 4.1 containing protein Frmpd1 regulates the subcellular location of activator of G-protein signaling 3 and its interaction with G-proteinsDifferential localization of septins in the mouse brainMolecular Analysis of Alternative Transcripts of the Equine Cordon-Bleu WH2 Repeat Protein-Like 1 (COBLL1) Gene.Noninvasive in vivo monitoring of tissue-specific global gene expression in humans.Genes associated with prognosis after surgery for malignant pleural mesothelioma promote tumor cell survival in vitro.A novel class of gene controlling virulence in plant pathogenic ascomycete fungi.Hypertension, chronic kidney disease, and renal pathology in a child with hermansky-pudlak syndrome.CPEB proteins control two key steps in spermatogenesis in C. elegans.STAMP, a novel predicted factor assisting TIF2 actions in glucocorticoid receptor-mediated induction and repression.Differential expression and function of members of the zfh-1 family of zinc finger/homeodomain repressors.Gene expression profiles of hepatocytes treated with La(NO3)3 of rare earth in rats.Two-marker association tests yield new disease associations for coronary artery disease and hypertensionSingle-nucleotide Polymorphism rs2275294 in ZNF512B is not Associated with Susceptibility to Amyotrophic Lateral Sclerosis in a Large Chinese CohortGlycan gene expression signatures in normal and malignant breast tissue; possible role in diagnosis and progressionDynamin-2 in nervous system disorders.Cobll1 is linked to drug resistance and blastic transformation in chronic myeloid leukemia.Genomewide differential expression profiling of long non-coding RNAs in androgenetic alopecia in a Chinese male population.Clinical, cytogenetic and molecular study of a case of ring chromosome 10.Molecular and clinical characterization of new patient with 1,08 Mb deletion in 10p15.3 region.QN1/KIAA1009: a new essential protein for chromosome segregation and mitotic spindle assembly.Mosaic deletion of EXOC6B: further evidence for an important role of the exocyst complex in the pathogenesis of intellectual disability.Microduplication of 4p16.3 due to an unbalanced translocation resulting in a mild phenotype.Severe clinical presentation in monozygotic twins with 10p15.3 microdeletion syndrome.
P2860
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P2860
Prediction of the coding sequences of unidentified human genes. XIII. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro
description
1999 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 1999
@ast
im Februar 1999 veröffentlichter wissenschaftlicher Artikel
@de
scientific article (publication date: 26 February 1999)
@en
vedecký článok (publikovaný 1999/02/26)
@sk
vědecký článek publikovaný v roce 1999
@cs
wetenschappelijk artikel (gepubliceerd op 1999/02/26)
@nl
наукова стаття, опублікована в лютому 1999
@uk
مقالة علمية نشرت في 26-2-1999 حول موضوع: دماغ
@ar
name
Prediction of the coding seque ...... de for large proteins in vitro
@ast
Prediction of the coding seque ...... de for large proteins in vitro
@en
Prediction of the coding seque ...... de for large proteins in vitro
@nl
type
label
Prediction of the coding seque ...... de for large proteins in vitro
@ast
Prediction of the coding seque ...... de for large proteins in vitro
@en
Prediction of the coding seque ...... de for large proteins in vitro
@nl
prefLabel
Prediction of the coding seque ...... de for large proteins in vitro
@ast
Prediction of the coding seque ...... de for large proteins in vitro
@en
Prediction of the coding seque ...... de for large proteins in vitro
@nl
P2093
P356
P1433
P1476
Prediction of the coding seque ...... de for large proteins in vitro
@en
P2093
K Ishikawa
M Hirosawa
N Miyajima
P356
10.1093/DNARES/6.1.63
P407
P577
1999-02-26T00:00:00Z