Zobrazeno 1 - 5
of 5
pro vyhledávání: '"G. S. MacColl"'
Publikováno v:
Journal of Endocrinology. 176:293-304
GnRH and sex steroids play an important role in immune system modulation and development. GnRH and the GnRH receptor are produced locally by immune cells, suggesting an autocrine role for GnRH. Experimental studies show a stimulatory action of exogen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::062d398f12050570e8daae58efb38502
https://doi.org/10.1677/joe.0.1760293
https://doi.org/10.1677/joe.0.1760293
Publikováno v:
Journal of Endocrinology. 162:1-9
Gene transfer into muscle tissue is currently being developed as a method for the production, secretion and delivery of therapeutic proteins. This methodology has been used to produce a variety of physiologically active proteins and may ultimately be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af27c2ff6c30a8b1b5c0f41e7688b0ec
https://doi.org/10.1677/joe.0.1620001
https://doi.org/10.1677/joe.0.1620001
Autor:
P.-M. G. Bouloux, Leticia Ferreira Gontijo Silveira, Paul M. Stewart, M. Thomas, G. S. MacColl, Duncan A. Clark
Publikováno v:
The Journal of clinical endocrinology and metabolism. 87(6)
Mutations in the GnRH receptor (GnRHR) have been shown to be responsible for a significant number of autosomic recessive and, less commonly, sporadic cases of idiopathic hypogonadotropic hypogonadism. We describe a woman with complete GnRH resistance
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95c86e8d8fe98aa75843f0ae49901fa7
https://pubmed.ncbi.nlm.nih.gov/12050282
https://pubmed.ncbi.nlm.nih.gov/12050282
Idiopathic gonadotrophin deficiency: genetic questions addressed through phenotypic characterization
Autor:
R, Quinton, V M, Duke, A, Robertson, J M, Kirk, G, Matfin, P A, de Zoysa, C, Azcona, G S, MacColl, H S, Jacobs, G S, Conway, M, Besser, R G, Stanhope, P M, Bouloux
Publikováno v:
Clinical endocrinology. 55(2)
The association of idiopathic hypogonadotrophic hypogonadism (IHH) with congenital olfactory deficit defines Kallmann's syndrome (KS). Although a small proportion of IHH patients have been found to harbour defined genetic lesions, the genetic basis o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6ca443622fa0d42af61a9855fee79059
https://pubmed.ncbi.nlm.nih.gov/11531920
https://pubmed.ncbi.nlm.nih.gov/11531920
Autor:
G. S. Maccoll, Francisco J. Novo, Geoffrey Goldspink, P. M. G. Bouloux, N. J. Marshall, Michael J. Waters
Publikováno v:
The Journal of endocrinology. 165(2)
The production of peptide hormones by skeletal muscle tissue is a promising area of gene therapy. Skeletal muscle myogenesis can be induced in vitro, resulting in the fusion of mononucleate myoblasts to form multinucleate myotubes, and delivery vecto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c80e0799ef8d9c1de1dd728782683dd
https://pubmed.ncbi.nlm.nih.gov/10810297
https://pubmed.ncbi.nlm.nih.gov/10810297