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9 results for uniprot:P61457 in Computationally mapped citations

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A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease.

Grupe A., Li Y., Rowland C., Nowotny P., Hinrichs A.L., Smemo S., Kauwe J.S., Maxwell T.J., Cherny S., Doil L. et al.

Am. J. Hum. Genet. 78:78-88(2006) GAD 594212 GeneRIF 5092 · Mapped (1,497)
Not Associated with NEUROLOGICAL: Alzheimer's disease ; GAD 594212 Observational study of gene-disease association. (HuGE Navigator) GeneRIF 5092

Studies of the variability of the hepatocyte nuclear factor-1beta (HNF-1beta / TCF2) and the dimerization cofactor of HNF-1 (DcoH / PCBD) genes in relation to type 2 diabetes mellitus and beta-cell function.

Ek J., Grarup N., Urhammer S.A., Gaede P.H., Drivsholm T., Borch-Johnsen K., Hansen T., Pedersen O.

Hum. Mutat. 18:356-357(2001) GeneRIF 5092 · Mapped (5)
Observational study of gene-disease association. (HuGE Navigator); variants of the hepatocyte nuclear factor-1beta (HNF-1beta / TCF2) and the dimerization cofactor of HNF-1 (DcoH/PCBD) genes in relation to type 2 diabetes mellitus and beta-cell function GeneRIF 5092

In situ and in vitro evidence for DCoH/HNF-1 alpha transcription of tyrosinase in human skin melanocytes.

Schallreuter K.U., Kothari S., Hasse S., Kauser S., Lindsey N.J., Gibbons N.C., Hibberts N., Wood J.M.

Biochem. Biophys. Res. Commun. 301:610-616(2003) GeneRIF 5092 · Mapped (8)
Data reveal DCoH/HNF-1 alpha expression and transcriptional activity in human epidermal melanocytes in vitro and in situ and identified tyrosinase the key enzyme for pigmentation as a new transcriptional target. GeneRIF 5092

In vivo and in vitro evidence for autocrine DCoH/HNF-1alpha transcription of albumin in the human epidermis.

Hasse S., Kothari S., Rokos H., Kauser S., Schurer N.Y., Schallreuter K.U.

Exp. Dermatol. 14:182-187(2005) GeneRIF 5092 · Mapped (35)
Albumin colocalized together with its transcription factor PCD/DCoH/HNF-1alpha in suprabasal keratinocytes in human full-thickness skin sections and in keratinocytes cultured in serum-free medium. GeneRIF 5092

Can the DCoHalpha isozyme compensate in patients with 4a-hydroxy-tetrahydrobiopterin dehydratase/DCoH deficiency?

Hevel J.M., Stewart J.A., Gross K.L., Ayling J.E.

Mol. Genet. Metab. 88:38-46(2006) GeneRIF 5092 · Mapped (5)
Properties of dehydratase/DCoHalpha are consistent with hypothesis that activity of this isozyme could account for relatively mild symptoms reported for patients with a defect in dehydratase/DCoH GeneRIF 5092

Exhaustive analysis of BH4 and dopamine biosynthesis genes in patients with Dopa-responsive dystonia.

Clot F., Grabli D., Cazeneuve C., Roze E., Castelnau P., Chabrol B., Landrieu P., Nguyen K., Ponsot G., Abada M. et al.

Brain 132:1753-1763(2009) GeneRIF 5092 · Mapped (53)
Observational study of gene-disease association gene-environment interaction and pharmacogenomic / toxicogenomic. (HuGE Navigator) GeneRIF 5092

Examination of tetrahydrobiopterin pathway genes in autism.

Schnetz-Boutaud N.C., Anderson B.M., Brown K.D., Wright H.H., Abramson R.K., Cuccaro M.L., Gilbert J.R., Pericak-Vance M.A., Haines J.L.

Genes Brain Behav. 8:753-757(2009) GeneRIF 5092 · Mapped (49)
Observational study of gene-disease association and gene-gene interaction. (HuGE Navigator) GeneRIF 5092

Use of genome-wide expression data to mine the "Gray Zone" of GWA studies leads to novel candidate obesity genes.

ENGAGE Consortium
Naukkarinen J., Surakka I., Pietilainen K.H., Rissanen A., Salomaa V., Ripatti S., Yki-Jarvinen H., van Duijn C.M., Wichmann H.E., Kaprio J. et al.

PLoS Genet. 6:e1000976-e1000976(2010) GeneRIF 5092 · Mapped (73)
Observational study and genome-wide association study of gene-disease association. (HuGE Navigator) GeneRIF 5092

Towards a proteome-scale map of the human protein-protein interaction network.

Rual J.F., Venkatesan K., Hao T., Hirozane-Kishikawa T., Dricot A., Li N., Berriz G.F., Gibbons F.D., Dreze M., Ayivi-Guedehoussou N. et al.

Nature 437:1173-1178(2005) MINT MINT-1436903 MINT MINT-1436903 MINT MINT-1436903 MINT MINT-1436903 MINT MINT-1436903 MINT MINT-1436903 MINT MINT-1436903 MINT MINT-1436903 · UniProtKB (1) · Mapped (1,321)
MINT-66084. PCBD1 (uniprotkb:P61457) physically interacts (MI:0915) with NUDT18 (uniprotkb:Q6ZVK8) by two hybrid (MI:0018). From mint MINT MINT-1436903 MINT-66113. DVL2 (uniprotkb:O14641) physically interacts (MI:0915) with PCBD1 (uniprotkb:P61457) by two hybrid (MI:0018). From mint MINT MINT-1436903 MINT-66136. PCBD1 (uniprotkb:P61457) physically interacts (MI:0915) with PCBD1 (uniprotkb:P61457) by two hybrid (MI:0018). From mint MINT MINT-1436903 MINT-66448. PCBD1 (uniprotkb:P61457) physically interacts (MI:0915) with FXR2 (uniprotkb:P51116) by two hybrid (MI:0018). From mint MINT MINT-1436903 MINT-67195. PCBD1 (uniprotkb:P61457) physically interacts (MI:0915) with LNX1 (uniprotkb:Q8TBB1) by two hybrid (MI:0018). From mint MINT MINT-1436903 MINT-67817. PCBD1 (uniprotkb:P61457) physically interacts (MI:0915) with GORASP2 (uniprotkb:Q53TE3) by two hybrid (MI:0018). From mint MINT MINT-1436903 MINT-68078. PCBD1 (uniprotkb:P61457) physically interacts (MI:0915) with NIF3L1 (uniprotkb:Q9GZT8) by two hybrid (MI:0018). From mint MINT MINT-1436903 MINT-68267. PCBD1 (uniprotkb:P61457) physically interacts (MI:0915) with WDYHV1 (uniprotkb:Q96HA8) by two hybrid (MI:0018). From mint MINT MINT-1436903

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