R-spondin2, a novel target of NOBOX: identification of variants in a cohort of women with primary ovarian insufficiency-Reference-Cited by-同舟云学术

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R-spondin2, a novel target of NOBOX: identification of variants in a cohort of women with primary ovarian insufficiency

Published:2017-07-25 Issue:1 Volume:10 Page:
ISSN:1757-2215
Container-title:Journal of Ovarian Research
language:en
Short-container-title:J Ovarian Res

Author:

Bouilly Justine,Beau Isabelle,Barraud Sara,Bernard Valérie,Delemer Brigitte,Young Jacques,Binart Nadine

Publisher

Springer Science and Business Media LLC

Subject

Obstetrics and Gynaecology,Oncology

Link

http://link.springer.com/content/pdf/10.1186/s13048-017-0345-0.pdf

Reference30 articles.

1. De Vos M, Devroey P, Fauser BC. Primary ovarian insufficiency. Lancet. 2010;376:911–21.

2. Nelson LM. Clinical practice. Primary ovarian insufficiency. N Engl J Med. 2009;360:606–14.

3. Skillern A, Rajkovic A. Recent developments in identifying genetic determinants of premature ovarian failure. Sex dev. 2008;2:228–43.

4. Persani L, Rossetti R, Cacciatore C. Genes involved in human premature ovarian failure. J Mol Endocrinol. 2010;45:257–79.

5. Bouilly J, Beau I, Barraud S, Bernard V, Azibi K, Fagart J, et al. Identification of multiple gene mutations accounts for a new genetic architecture of primary ovarian insufficiency. J Clin Endocrinol Metab. 2016;101:4541–50.

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2. Effects of N-Acetylcysteine on the Proliferation, Hormone Secretion Level, and Gene Expression Profiles of Goat Ovarian Granulosa Cells;Genes;2022-12-07

3. RSPO2 promotes progression of ovarian cancer through dual receptor-mediated FAK/Src signaling activation;iScience;2022-10

4. Loss of Nobox prevents ovarian differentiation from juvenile ovaries in zebrafish;Biology of Reproduction;2022-02-14

5. Compound heterozygous null mutations of NOBOX in sisters with delayed puberty and primary amenorrhea;Molecular Genetics & Genomic Medicine;2021-09-04

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