Mutations in LHX3 result in a new syndrome revealed by combined pituitary hormone deficiency-Reference-Cited by-同舟云学术

Mutations in LHX3 result in a new syndrome revealed by combined pituitary hormone deficiency

Published:2000-06 Issue:2 Volume:25 Page:182-186
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Netchine Irène,Sobrier Marie-Laure,Krude Heiko,Schnabel Dirk,Maghnie Mohamed,Marcos Elisabeth,Duriez Bénédicte,Cacheux Valère,Moers Arpard v.,Goossens Michel,Grüters Annette,Amselem Serge

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng0600_182.pdf

Reference20 articles.

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2. Sheng, H.Z. et al. Specification of pituitary cell lineages by the LIM homeobox gene Lhx3. Science 272, 1004–1007 (1996).

3. Dawid, I.B., Breen, J.J. & Toyama, R. LIM domains: multiple roles as adapters and functional modifiers in protein interactions. Trends Genet. 14, 156–162 (1998).

4. Couly, G. & Le Douarin, N.M. The fate map of the cephalic neural primordium at the presomitic to the 3-somite stage in the avian embryo. Development 103, 101–113 (1988).

5. Eagleson, G.W. & Harris, W.A. Mapping of the presumptive brain regions in the neural plate of Xenopus laevis. J. Neurobiol. 21, 427–440 (1990).

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