Isolation from cochlea of a novel human intronless gene with predominant fetal expression
about
KCTD5, a putative substrate adaptor for cullin3 ubiquitin ligasesIon channel gene expression in the inner earPentameric Assembly of Potassium Channel Tetramerization Domain-Containing Protein 5Application of proteomics to soft tissue sarcomasResequencing of the auxiliary GABA(B) receptor subunit gene KCTD12 in chronic tinnitus.Expression studies of osteoglycin/mimecan (OGN) in the cochlea and auditory phenotype of Ogn-deficient miceCharacterization of an abundant COL9A1 transcript in the cochlea with a novel 3' UTR: Expression studies and detection of miRNA target sequence.Evolutionary history of Tibetans inferred from whole-genome sequencing.Pfetin as a risk factor of recurrence in gastrointestinal stromal tumors.Genome-wide association study of bipolar I disorder in the Han Chinese population.Mutation of a potassium channel-related gene in progressive myoclonic epilepsy.Developmental expression of Kcnq4 in vestibular neurons and neurosensory epitheliaKCTD12 Regulates Colorectal Cancer Cell Stemness through the ERK Pathway.Global protein-expression analysis of bone and soft tissue sarcomas.Proteomic analysis of soft tissue sarcoma.Proteomic approach toward personalized sarcoma treatment: lessons from prognostic biomarker discovery in gastrointestinal stromal tumor.Proteogenomics for the Study of Gastrointestinal Stromal Tumors.Microarray analyses of otospheres derived from the cochlea in the inner ear identify putative transcription factors that regulate the characteristics of otospheres.GABAB receptor constituents revealed by tandem affinity purification from transgenic miceKCTD12 promotes tumorigenesis by facilitating CDC25B/CDK1/Aurora A-dependent G2/M transition.Current status of proteomics of soft tissue sarcomas.Zebrafish enhancer trap line showing maternal and neural expression of kctd15a.Pure monosomy and pure trisomy of 13q21.2-31.1 consequent to a familial insertional translocation: exclusion of PCDH9 as the responsible gene for autosomal dominant auditory neuropathy (AUNA1).Contribution of KCTD12 to esophageal squamous cell carcinoma
P2860
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P2860
Isolation from cochlea of a novel human intronless gene with predominant fetal expression
description
2004 nî lūn-bûn
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2004 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
Isolation from cochlea of a novel human intronless gene with predominant fetal expression
@ast
Isolation from cochlea of a novel human intronless gene with predominant fetal expression
@en
Isolation from cochlea of a novel human intronless gene with predominant fetal expression
@nl
type
label
Isolation from cochlea of a novel human intronless gene with predominant fetal expression
@ast
Isolation from cochlea of a novel human intronless gene with predominant fetal expression
@en
Isolation from cochlea of a novel human intronless gene with predominant fetal expression
@nl
prefLabel
Isolation from cochlea of a novel human intronless gene with predominant fetal expression
@ast
Isolation from cochlea of a novel human intronless gene with predominant fetal expression
@en
Isolation from cochlea of a novel human intronless gene with predominant fetal expression
@nl
P2093
P2860
P1433
P1476
Isolation from cochlea of a novel human intronless gene with predominant fetal expression
@en
P2093
Anne B S Giersch
Barbara L Resendes
Cynthia C Morton
Dynio Honrubia
Joe C Adams
Nahid G Robertson
Sharon F Kuo
P2860
P2888
P304
P356
10.1007/S10162-003-4042-X
P407
P50
P577
2004-06-01T00:00:00Z
P5875
P6179
1038170463