ANOS1 Gene

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1		Vicky Zhou	+ 568 word(s)	568	2020-12-15 07:44:31

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Zhou, V. ANOS1 Gene. Encyclopedia. Available online: https://encyclopedia.pub/entry/4701 (accessed on 28 September 2026).

Zhou V. ANOS1 Gene. Encyclopedia. Available at: https://encyclopedia.pub/entry/4701. Accessed September 28, 2026.

Zhou, Vicky. "ANOS1 Gene" Encyclopedia, https://encyclopedia.pub/entry/4701 (accessed September 28, 2026).

Zhou, V. (2020, December 24). ANOS1 Gene. In Encyclopedia. https://encyclopedia.pub/entry/4701

Zhou, Vicky. "ANOS1 Gene." Encyclopedia. Web. 24 December, 2020.

ANOS1 Gene

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This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/gene/anos1

anosmin 1

genes

References

Balasubramanian R, Crowley WF Jr. Isolated Gonadotropin-Releasing Hormone(GnRH) Deficiency. 2007 May 23 [updated 2017 Mar 2]. In: Adam MP, Ardinger HH,Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews®[Internet]. Seattle (WA): University of Washington, Seattle; 1993-2020. Availablefrom http://www.ncbi.nlm.nih.gov/books/NBK1334/
Cariboni A, Pimpinelli F, Colamarino S, Zaninetti R, Piccolella M, Rumio C,Piva F, Rugarli EI, Maggi R. The product of X-linked Kallmann's syndrome gene(KAL1) affects the migratory activity of gonadotropin-releasing hormone(GnRH)-producing neurons. Hum Mol Genet. 2004 Nov 15;13(22):2781-91.
Choy C, Kim SH. Biological actions and interactions of anosmin-1. Front HormRes. 2010;39:78-93. doi: 10.1159/000312695.
de Castro F, Esteban PF, Bribián A, Murcia-Belmonte V, García-González D,Clemente D. The adhesion molecule anosmin-1 in neurology: Kallmann syndrome andbeyond. Adv Neurobiol. 2014;8:273-92. Review.
Hardelin JP, Julliard AK, Moniot B, Soussi-Yanicostas N, Verney C,Schwanzel-Fukuda M, Ayer-Le Lievre C, Petit C. Anosmin-1 is a regionallyrestricted component of basement membranes and interstitial matrices duringorganogenesis: implications for the developmental anomalies of Xchromosome-linked Kallmann syndrome. Dev Dyn. 1999 May;215(1):26-44.
Hardelin JP, Levilliers J, del Castillo I, Cohen-Salmon M, Legouis R,Blanchard S, Compain S, Bouloux P, Kirk J, Moraine C, et al. X chromosome-linked Kallmann syndrome: stop mutations validate the candidate gene. Proc Natl Acad SciU S A. 1992 Sep 1;89(17):8190-4.
Legouis R, Hardelin JP, Levilliers J, Claverie JM, Compain S, Wunderle V,Millasseau P, Le Paslier D, Cohen D, Caterina D, et al. The candidate gene forthe X-linked Kallmann syndrome encodes a protein related to adhesion molecules.Cell. 1991 Oct 18;67(2):423-35.

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Subjects: Genetics & Heredity

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Update Date: 24 Dec 2020

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