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Novel mutations in EPO-R and oxygen-dependent degradation (ODD) domain of EPAS1 genes-a causative reason for Congenital Erythrocytosis

Autor: Samundeshwari Echambadi Loganathan, Surekha Kattaru, Chodimella Chandrasekhar, B. Vengamma, Potukuchi Venkata Gurunadha Krishna Sarma

Publikováno v: European Journal of Medical Genetics. 65:104493

Congenital Erythrocytosis (CE) can be primary or secondary due to the mutations in genes involved in the erythropoietin receptor and oxygen sensing pathway. In this study, 42 patients with 38 unrelated patients and one family (4 patients) who were JA

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3002025063525d71a0eb648cc64f8e74
https://doi.org/10.1016/j.ejmg.2022.104493

Differentiation ability of hematopoietic stem cells and mesenchymal stem cells isolated from human peripheral blood.

Autor: Samundeshwari EL; Department of Biotechnology, Sri Venkateswara Institute of Medical Sciences, Tirupati, Andhra Pradesh, India., Kattaru S; Department of Biotechnology, Sri Venkateswara Institute of Medical Sciences, Tirupati, Andhra Pradesh, India., Kodavala S; Department of Biotechnology, Sri Venkateswara Institute of Medical Sciences, Tirupati, Andhra Pradesh, India., Chandrasekhar C; Department of Hematology, Sri Venkateswara Institute of Medical Sciences, Tirupati, Andhra Pradesh, India., Sarma PVGK; Department of Biotechnology, Sri Venkateswara Institute of Medical Sciences, Tirupati, Andhra Pradesh, India.

Publikováno v: Frontiers in cell and developmental biology [Front Cell Dev Biol] 2024 Dec 18; Vol. 12, pp. 1450543. Date of Electronic Publication: 2024 Dec 18 (Print Publication: 2024).