Detection of carrier Booroola (Fec B) allele in BMPR1B gene of MEGA (Merino × Garut) sheep and its association with growth traits

Autor: Endang Tri Margawati, Widya Pintaka Bayu Putra, Muhammad Rizki, Edi Soetrisno, Herman Willem Raadsma

Publikováno v: Journal of Genetic Engineering and Biotechnology, Vol 21, Iss 1, Pp 1-7 (2023)

Abstract Background Bone morphogenetic protein receptor 1B (BMPR1B) gene is one of candidate genes for reproductive and growth traits in sheep. The present study was aimed to detect the Booroola (Fec B) allele in BMPR1B gene and its association with

Externí odkaz: https://doaj.org/article/0527488f2d964006b9701646d33e1c99

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Survey of the relationship between polymorphisms within the BMPR1B gene and sheep reproductive traits

Autor: Haixia Li, Zhanerke Akhatayeva, Rajwali Khan, Jie Li, Chuanying Pan, Xianyong Lan, Yiwen He, Yi Bi

Publikováno v: Animal Biotechnology. 34:718-727

The BMPRIB gene is one of the main genes that can be used as a molecular genetic marker for the early selection of highly productive ewes. It is well-documented that the p.Q249R (g.746A > G) is the first mutation in the kinase domain of the BMPR1B ge

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92e09b599982e19b147a212e13dae5fd
https://doi.org/10.1080/10495398.2021.1979023

Association Study of Fecundity Gene BMPR1B with Prolificacy in Surti Goats under Farm and Field Condition

Autor: Y.D. Padheriya, N. S. Dangar, Umed V. Ramani, T. Sangma, S. S. Patel, S. Devkatte, Gaurav Pandya

Publikováno v: THE INDIAN JOURNAL OF VETERINARY SCIENCES AND BIOTECHNOLOGY. 14

The Surti is a dual purpose goat breed of Gujarat. The bone morphogenetic protein receptor type 1B (BMPR1B) gene of transforming growth factor beta (TGF-β) superfamily ligands is playing a role in ovulation as well as litter size. Mutation in Exon-6

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::c6216a6c34334b3a7aacf62ca58ffcc8
https://doi.org/10.21887/ijvsbt.14.4.5

New mutations in non-syndromic primary ovarian insufficiency patients identified via whole-exome sequencing

Autor: Manuel A. Patarroyo, Jacques Young, July Constanza Buitrago, Liliana C Patiño, Brigitte Delemer, Nadine Binart, Isabelle Beau, Carlos F. Suárez, Paul Laissue, Ronald Gonzalez, Carolina Carlosama

Publikováno v: Repositorio Institucional UDCA
Universidad de Ciencias Aplicadas y Ambientales U.D.C.A
instacron:Universidad de Ciencias Aplicadas y Ambientales U.D.C.A
Repositorio EdocUR-U. Rosario
Universidad del Rosario
instacron:Universidad del Rosario

STUDY QUESTION Is it possible to identify new mutations potentially associated with non-syndromic primary ovarian insufficiency (POI) via whole-exome sequencing (WES)? SUMMARY ANSWER WES is an efficient tool to study genetic causes of POI as we have

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c869e5368507c83a5e34bd9707c9935
https://academic.oup.com/humrep/article/32/7/1512/3823627