Prediction of the coding sequences of unidentified human genes. XX. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro
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The evolution of extracellular fibrillins and their functional domainsEndoplasmic reticulum stress and Parkinson's disease: the role of HRD1 in averting apoptosis in neurodegenerative diseaseMutations in MEGF10, a regulator of satellite cell myogenesis, cause early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD)The von Hippel-Lindau tumor suppressor stabilizes novel plant homeodomain protein Jade-1Characterization of the second type of human beta-galactoside alpha 2,6-sialyltransferase (ST6Gal II), which sialylates Galbeta 1,4GlcNAc structures on oligosaccharides preferentially. Genomic analysis of human sialyltransferase genesA ubiquitin ligase HRD1 promotes the degradation of Pael receptor, a substrate of ParkinCysteine mutations cause defective tyrosine phosphorylation in MEGF10 myopathyHUGE: a database for human large proteins identified in the Kazusa cDNA sequencing projectVCIP135, a novel essential factor for p97/p47-mediated membrane fusion, is required for Golgi and ER assembly in vivoMolecular phylogeny of the kelch-repeat superfamily reveals an expansion of BTB/kelch proteins in animalsCell adhesion to fibrillin-1 molecules and microfibrils is mediated by alpha 5 beta 1 and alpha v beta 3 integrinsIdentification of new human mastermind proteins defines a family that consists of positive regulators for notch signalingMegf10 regulates the progression of the satellite cell myogenic programIdentification and characterization of Mlr1,2: two mouse homologues of Mblk-1, a transcription factor from the honeybee brain(1)Identification of recurrent regions of chromosome loss and gain in vestibular schwannomas using comparative genomic hybridisation.Alterations in CDH15 and KIRREL3 in patients with mild to severe intellectual disability.Identification of four candidate cGMP targets in DictyosteliumMEGF10 functions as a receptor for the uptake of amyloid-β.Novel SPG11 mutations in Asian kindreds and disruption of spatacsin function in the zebrafishRetinoic Acid Induced 1, RAI1: A Dosage Sensitive Gene Related to Neurobehavioral Alterations Including Autistic BehaviorRAI1 transcription factor activity is impaired in mutants associated with Smith-Magenis Syndrome.AF6 negatively regulates Rap1-induced cell adhesion.Fibrillin-1 interactions with fibulins depend on the first hybrid domain and provide an adaptor function to tropoelastin.RNA-Seq analysis of yak ovary: improving yak gene structure information and mining reproduction-related genes.FIE2: A program for the extraction of genomic DNA sequences around the start and translation initiation site of human genesBiological functions of melanoma-associated antigensCloning and Initial Functional Characterization of Mlk4α and Mlk4βMutations in the satellite cell gene MEGF10 cause a recessive congenital myopathy with minicoresColorectal cancer linkage on chromosomes 4q21, 8q13, 12q24, and 15q22.Insulin clearance: confirmation as a highly heritable trait, and genome-wide linkage analysis.Fibrillin-containing microfibrils are key signal relay stations for cell function.De novo pathogenic variants in CHAMP1 are associated with global developmental delay, intellectual disability, and dysmorphic facial featuresFibrillin assembly requires fibronectin.Fibrillin-3 expression in human development.Novel SNP array analysis and exome sequencing detect a homozygous exon 7 deletion of MEGF10 causing early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD).A Novel Deletion Mutation in ASPM Gene in an Iranian Family with Autosomal Recessive Primary Microcephaly.Homo- and heterotypic fibrillin-1 and -2 interactions constitute the basis for the assembly of microfibrils.Conserved DNA methylation combined with differential frontal cortex and cerebellar expression distinguishes C9orf72-associated and sporadic ALS, and implicates SERPINA1 in disease.Structure, function and regulation of jade family PHD finger 1 (JADE1).HCMV-encoded glycoprotein M (UL100) interacts with Rab11 effector protein FIP4.
P2860
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P2860
Prediction of the coding sequences of unidentified human genes. XX. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro
description
2001 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2001
@ast
im April 2001 veröffentlichter wissenschaftlicher Artikel
@de
scientific article (publication date: 27 April 2001)
@en
vedecký článok (publikovaný 2001/04/27)
@sk
vědecký článek publikovaný v roce 2001
@cs
wetenschappelijk artikel (gepubliceerd op 2001/04/27)
@nl
наукова стаття, опублікована у квітні 2001
@uk
مقالة علمية نشرت في 27-4-2001 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
P356
10.1093/DNARES/8.2.85
P407
P50
P577
2001-04-27T00:00:00Z