排序方式: 共有77条查询结果,搜索用时 125 毫秒
61.
62.
63.
64.
65.
L Ferland C Auclair F Labrie G Azadian-Boulanger J P Raynaud 《Comptes rendus des séances de l'Académie des sciences. Série D, Sciences naturelles》1978,286(14):1113-1116
The administration of LHRH or of its analog [D-Ala6, des-Gly-NH10(2)] LHRH ethylamide to the female rat on day 10 of gestation resulted in termination of pregnancy and in a marked decrease in ovarian LH receptors and plasma progesterone level. Asingle injection of either compound during diestrus I also led to a decrease in LH receptors. These data demonstrate the high sensitivity of the control of ovarian LH receptors by circulating gonadotrophins and suggest that the contraceptive action of pre- and postcoitally administered LHRH is mediated by negative control of LH receptors. 相似文献
66.
E. Bottini P. Lucarelli R. Palmarino C. Bongarzoni M. Midulla G. Raynaud L. Tucciarone E. Carapella de Luca 《Cellular and molecular life sciences : CMLS》1968,24(6):614-615
Riassunto Sono state studiate le frequenze degli alleli al locusPl per la fosfatasi alcalina della placenta umana in 175 parti singoli verificatisi nella popolazione di Roma. Sono stati identificati tutti e 6 i fenotipi più comuni descritti in precedenza; la loro frequenza corrisponde a quella attesa secondo la legge diHardy-Weinberg. Le frequenze geniche sono risultate sovrapponibili a quelle riportate per le popolazioni Inglese e Svedese. 相似文献
67.
68.
69.
FACL4, encoding fatty acid-CoA ligase 4, is mutated in nonspecific X-linked mental retardation 总被引:1,自引:0,他引:1
Meloni I Muscettola M Raynaud M Longo I Bruttini M Moizard MP Gomot M Chelly J des Portes V Fryns JP Ropers HH Magi B Bellan C Volpi N Yntema HG Lewis SE Schaffer JE Renieri A 《Nature genetics》2002,30(4):436-440
X-linked mental retardation (XLMR) is an inherited condition that causes failure to develop cognitive abilities, owing to mutations in a gene on the X chromosome. The latest XLMR update lists up to 136 conditions leading to 'syndromic', or 'specific', mental retardation (MRXS) and 66 entries leading to 'nonspecific' mental retardation (MRX). For 9 of the 66 MRX entries, the causative gene has been identified. Our recent discovery of the contiguous gene deletion syndrome ATS-MR (previously known as Alport syndrome, mental retardation, midface hypoplasia, elliptocytosis, OMIM #300194), characterized by Alport syndrome (ATS) and mental retardation (MR), indicated Xq22.3 as a region containing one mental retardation gene. Comparing the extent of deletion between individuals with ATS-MR and individuals with ATS alone allowed us to define a critical region for mental retardation of approximately 380 kb, containing four genes. Here we report the identification of two point mutations, one missense and one splice-site change, in the gene FACL4 in two families with nonspecific mental retardation. Analysis of enzymatic activity in lymphoblastoid cell lines from affected individuals of both families revealed low levels compared with normal cells, indicating that both mutations are null mutations. All carrier females with either point mutations or genomic deletions in FACL4 showed a completely skewed X-inactivation, suggesting that the gene influences survival advantage. FACL4 is the first gene shown to be involved in nonspecific mental retardation and fatty-acid metabolism. 相似文献
70.