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1.
J Endocrinol Invest ; 29(7): 657-64, 2006.
Artículo en Inglés | MEDLINE | ID: mdl-16957417

RESUMEN

Insulin-like factor 3 (INSL3) is expressed in Leydig cells of the testis and theca cells of the ovary. This peptide affects testicular descent by acting on gubernaculum via its specific receptor leucine-rich repeat-containing G protein-coupled receptor 8 (LGR8). From initial animal data showing the cryptorchid phenotype of Insl3/Lgr8 mutants, an extensive search for mutations in INSL3 and LGR8 genes was undertaken in human patients with cryptorchidism, and a frequency of mutation of 4-5% has been detected. However, definitive proofs of a causative role for some of these mutations are still lacking. More recent data suggest additional paracrine (in the testis and ovary) and endocrine actions of INSL3 in adults. INSL3 circulates at high concentrations in serum of adult males and its production is dependent on the differentiation effect of LH. Therefore, INSL3 is increasingly used as a specific marker of Leydig cell differentiation and function.


Asunto(s)
Sistema Endocrino/fisiología , Insulina/fisiología , Comunicación Paracrina/fisiología , Proteínas/fisiología , Animales , Criptorquidismo/etiología , Criptorquidismo/genética , Femenino , Humanos , Insulina/genética , Masculino , Proteínas/genética , Testículo/fisiología
2.
Am J Hum Genet ; 65(3): 829-46, 1999 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-10441590

RESUMEN

To define Y-chromosome haplotypes, we studied seven biallelic polymorphic sites. We combined data with those from four dinucleotide-repeat polymorphisms, to establish Y-chromosome compound superhaplotypes. Eight biallelic haplotypes that matched the dendrogram proposed by other investigators were identified in 762 Y chromosomes from 25 African populations. For each biallelic site, coalescence time of lineages carrying the derived allele was estimated and compared with previous estimates. The "ancestral" haplotype (haplotype 1A) was observed among Ethiopians, "Khoisan" (!Kung and Khwe), and populations from northern Cameroon. Microsatellite distributions within this haplotype showed that the Khoisan haplotypes 1A are widely divergent from those of the other two groups. Populations from northern Africa and northern Cameroon share a haplotype (i.e., 1C), which is not observed in other African populations but represents a major Eurasian cluster. Haplotypes 1C of northern Cameroon are clearly distinct from those of Europe, whereas haplotypes 1C of northern African are well intermingled with those of the other two groups. Apportionment of diversity for the Y-chromosomal biallelic haplotypes was calculated after populations were clustered into different configurations. Despite some correspondence between language affiliation and genetic similarity, geographic proximity seems to be a better predictor of genetic affinity.


Asunto(s)
Población Negra/genética , Haplotipos/genética , Repeticiones de Microsatélite/genética , Polimorfismo Genético/genética , Cromosoma Y/genética , África , Alelos , Europa (Continente) , Frecuencia de los Genes , Variación Genética/genética , Geografía , Humanos , Lenguaje , Masculino , Modelos Genéticos , Filogenia
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