Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

207 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
A truncating variant of RAD51B associated with primary ovarian insufficiency provides insights into its meiotic and somatic functions.
Franca MM, Condezo YB, Elzaiat M, Felipe-Medina N, Sánchez-Sáez F, Muñoz S, Sainz-Urruela R, Martín-Hervás MR, García-Valiente R, Sánchez-Martín MA, Astudillo A, Mendez J, Llano E, Veitia RA, Mendonca BB, Pendás AM. Franca MM, et al. Among authors: veitia ra. Cell Death Differ. 2022 Dec;29(12):2347-2361. doi: 10.1038/s41418-022-01021-z. Epub 2022 May 27. Cell Death Differ. 2022. PMID: 35624308 Free PMC article.
Mutant cohesin in premature ovarian failure.
Caburet S, Arboleda VA, Llano E, Overbeek PA, Barbero JL, Oka K, Harrison W, Vaiman D, Ben-Neriah Z, García-Tuñón I, Fellous M, Pendás AM, Veitia RA, Vilain E. Caburet S, et al. Among authors: veitia ra. N Engl J Med. 2014 Mar 6;370(10):943-949. doi: 10.1056/NEJMoa1309635. N Engl J Med. 2014. PMID: 24597867 Free PMC article.
STAG3 is a strong candidate gene for male infertility.
Llano E, Gomez-H L, García-Tuñón I, Sánchez-Martín M, Caburet S, Barbero JL, Schimenti JC, Veitia RA, Pendas AM. Llano E, et al. Among authors: veitia ra. Hum Mol Genet. 2014 Jul 1;23(13):3421-31. doi: 10.1093/hmg/ddu051. Epub 2014 Mar 7. Hum Mol Genet. 2014. PMID: 24608227 Free article.
A missense in HSF2BP causing primary ovarian insufficiency affects meiotic recombination by its novel interactor C19ORF57/BRME1.
Felipe-Medina N, Caburet S, Sánchez-Sáez F, Condezo YB, de Rooij DG, Gómez-H L, Garcia-Valiente R, Todeschini AL, Duque P, Sánchez-Martin MA, Shalev SA, Llano E, Veitia RA, Pendás AM. Felipe-Medina N, et al. Among authors: veitia ra. Elife. 2020 Aug 26;9:e56996. doi: 10.7554/eLife.56996. Elife. 2020. PMID: 32845237 Free PMC article.
The Oncogenic FOXL2 C134W Mutation Is a Key Driver of Granulosa Cell Tumors.
Llano E, Todeschini AL, Felipe-Medina N, Corte-Torres MD, Condezo YB, Sanchez-Martin M, López-Tamargo S, Astudillo A, Puente XS, Pendas AM, Veitia RA. Llano E, et al. Among authors: veitia ra. Cancer Res. 2023 Jan 18;83(2):239-250. doi: 10.1158/0008-5472.CAN-22-1880. Cancer Res. 2023. PMID: 36409821
A truncating MEIOB mutation responsible for familial primary ovarian insufficiency abolishes its interaction with its partner SPATA22 and their recruitment to DNA double-strand breaks.
Caburet S, Todeschini AL, Petrillo C, Martini E, Farran ND, Legois B, Livera G, Younis JS, Shalev S, Veitia RA. Caburet S, et al. Among authors: veitia ra. EBioMedicine. 2019 Apr;42:524-531. doi: 10.1016/j.ebiom.2019.03.075. Epub 2019 Apr 15. EBioMedicine. 2019. PMID: 31000419 Free PMC article.
207 results