A leptin missense mutation associated with hypogonadism and morbid obesity - PubMed (original) (raw)
Case Reports
A leptin missense mutation associated with hypogonadism and morbid obesity
A Strobel et al. Nat Genet. 1998 Mar.
No abstract available
Similar articles
- Dominant and recessive inheritance of morbid obesity associated with melanocortin 4 receptor deficiency.
Farooqi IS, Yeo GS, Keogh JM, Aminian S, Jebb SA, Butler G, Cheetham T, O'Rahilly S. Farooqi IS, et al. J Clin Invest. 2000 Jul;106(2):271-9. doi: 10.1172/JCI9397. J Clin Invest. 2000. PMID: 10903343 Free PMC article. - [From gene to disease; leptin and obesity].
Pijl H, Meinders AE. Pijl H, et al. Ned Tijdschr Geneeskd. 2001 Mar 24;145(12):572-4. Ned Tijdschr Geneeskd. 2001. PMID: 11293996 Review. Dutch. - A novel non-synonymous mutation in the melanocortin-4 receptor gene (MC4R) in a 2-year-old Austrian girl with extreme obesity.
Rettenbacher E, Tarnow P, Brumm H, Prayer D, Wermter AK, Hebebrand J, Biebermann H, Hinney A, Widhalm K. Rettenbacher E, et al. Exp Clin Endocrinol Diabetes. 2007 Jan;115(1):7-12. doi: 10.1055/s-2007-949150. Exp Clin Endocrinol Diabetes. 2007. PMID: 17286227 Clinical Trial. - Reproductive biology. A powerful first KiSS-1.
Vogel G. Vogel G. Science. 2005 Jul 22;309(5734):551-2. doi: 10.1126/science.309.5734.551. Science. 2005. PMID: 16040685 No abstract available. - [The genetics of hypogonadotropic hypogonadism in the male].
Sievers C, Schneider HJ, Stalla GK. Sievers C, et al. MMW Fortschr Med. 2005 Nov 10;147(45):32-4, 36. MMW Fortschr Med. 2005. PMID: 16320650 Review. German.
Cited by
- Novel perspectives on leptin in osteoarthritis: Focus on aging.
Liu Z, Xie W, Li H, Liu X, Lu Y, Lu B, Deng Z, Li Y. Liu Z, et al. Genes Dis. 2023 Nov 4;11(6):101159. doi: 10.1016/j.gendis.2023.101159. eCollection 2024 Nov. Genes Dis. 2023. PMID: 39229323 Free PMC article. Review. - Novel compound heterozygous mutations in LEP responsible for obesity in a Chinese family.
Li H, Liu G, Lu B, Zhou X. Li H, et al. Mol Genet Metab Rep. 2024 Jun 29;40:101114. doi: 10.1016/j.ymgmr.2024.101114. eCollection 2024 Sep. Mol Genet Metab Rep. 2024. PMID: 39041042 Free PMC article. - A quantitative pipeline to assess secretion of human leptin coding variants reveals mechanisms underlying leptin deficiencies.
Baird HJM, Shun-Shion AS, Mendes de Oliveira E, Stalder D, Liang L, Eden J, Chambers JE, Farooqi IS, Gershlick DC, Fazakerley DJ. Baird HJM, et al. J Biol Chem. 2024 Aug;300(8):107562. doi: 10.1016/j.jbc.2024.107562. Epub 2024 Jul 19. J Biol Chem. 2024. PMID: 39002670 Free PMC article. - Signatures of metabolic diseases on spermatogenesis and testicular metabolism.
Carrageta DF, Pereira SC, Ferreira R, Monteiro MP, Oliveira PF, Alves MG. Carrageta DF, et al. Nat Rev Urol. 2024 Aug;21(8):477-494. doi: 10.1038/s41585-024-00866-y. Epub 2024 Mar 25. Nat Rev Urol. 2024. PMID: 38528255 Review. - Classification of Congenital Leptin Deficiency.
von Schnurbein J, Zorn S, Nunziata A, Brandt S, Moepps B, Funcke JB, Hussain K, Farooqi IS, Fischer-Posovszky P, Wabitsch M. von Schnurbein J, et al. J Clin Endocrinol Metab. 2024 Sep 16;109(10):2602-2616. doi: 10.1210/clinem/dgae149. J Clin Endocrinol Metab. 2024. PMID: 38470203 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases