A unique point mutation in the human vitamin D receptor chromosomal gene confers hereditary resistance to 1,25-dihydroxyvitamin D3
about
A unique mutation in the vitamin D receptor gene in three Japanese patients with vitamin D-dependent rickets type II: utility of single-strand conformation polymorphism analysis for heterozygous carrier detectionReview article: vitamin D and inflammatory bowel disease--established concepts and future directionsA mutation in the DNA-binding domain of the androgen receptor gene causes complete testicular feminization in a patient with receptor-positive androgen resistance.Differential splicing of human androgen receptor pre-mRNA in X-linked Reifenstein syndrome, because of a deletion involving a putative branch siteVitamin d and its role in cancer and immunity: a prescription for sunlight.Androgen receptor gene mutations in human prostate cancer.Hereditary vitamin D resistant rickets caused by a novel mutation in the vitamin D receptor that results in decreased affinity for hormone and cellular hyporesponsiveness.Rapid accumulation of cyclic GMP near activated vitamin D receptors.Vitamin D receptor mutations in patients with hereditary 1,25-dihydroxyvitamin D-resistant rickets.Vitamin D and Crohn's disease in the adult patient: a review.Disruption of vitamin D receptor-retinoid X receptor heterodimer formation following ras transformation of human keratinocytes.Immunocytology with microwave-fixed fibroblasts shows 1 alpha,25-dihydroxyvitamin D3-dependent rapid and estrogen-dependent slow reorganization of vitamin D receptorsA unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia.Dimerization with retinoid X receptors promotes nuclear localization and subnuclear targeting of vitamin D receptors.Biology and Mechanisms of Action of the Vitamin D Hormone.
P2860
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P2860
A unique point mutation in the human vitamin D receptor chromosomal gene confers hereditary resistance to 1,25-dihydroxyvitamin D3
description
1990 nî lūn-bûn
@nan
1990 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1990 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1990年の論文
@ja
1990年論文
@yue
1990年論文
@zh-hant
1990年論文
@zh-hk
1990年論文
@zh-mo
1990年論文
@zh-tw
1990年论文
@wuu
name
A unique point mutation in the ...... ce to 1,25-dihydroxyvitamin D3
@ast
A unique point mutation in the ...... ce to 1,25-dihydroxyvitamin D3
@en
A unique point mutation in the ...... ce to 1,25-dihydroxyvitamin D3
@nl
type
label
A unique point mutation in the ...... ce to 1,25-dihydroxyvitamin D3
@ast
A unique point mutation in the ...... ce to 1,25-dihydroxyvitamin D3
@en
A unique point mutation in the ...... ce to 1,25-dihydroxyvitamin D3
@nl
prefLabel
A unique point mutation in the ...... ce to 1,25-dihydroxyvitamin D3
@ast
A unique point mutation in the ...... ce to 1,25-dihydroxyvitamin D3
@en
A unique point mutation in the ...... ce to 1,25-dihydroxyvitamin D3
@nl
P2093
P356
P1476
A unique point mutation in the ...... ce to 1,25-dihydroxyvitamin D3
@en
P2093
P304
P356
10.1210/MEND-4-4-623
P407
P577
1990-04-01T00:00:00Z