Ranjha Khan
6PUBLICATIONS
7CO-AUTHORS
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Publications (6)
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|Jun 24, 2022
A Homozygous Loss-of-Function Mutation in MSH5 Abolishes MutSĪ³ Axial Loading and Causes Meiotic Arrest in NOA-Affected Individuals.Chenjia Gong, Tanveer Abbas, Zubair Muhammad
|Mar 25, 2022
Identification of Frameshift Variants in POLH Gene Causing Xeroderma Pigmentosum in Two Consanguineous Pakistani Families.Ghazala Y Zamani, Ranjha Khan, Noreen Karim
|Oct 21, 2021
Identification and Functional Investigation of Novel Heterozygous HELQ Mutations in Patients with Sertoli Cell-only Syndrome.Ghulam Murtaza, Li Yang, Ihsan Khan
|Aug 13, 2021
Nuclear translocation of MTL5 from cytoplasm requires its direct interaction with LIN9 and is essential for male meiosis and fertility.Xingxia Zhang, Ming Li, Xiaohua Jiang
|Jun 02, 2021
Inactivation of testis-specific gene C4orf46 is dispensable for spermatogenesis and fertility in mouse.Basit Shah, Ranjha Khan, Wasim Shah
|Mar 12, 2020
The testis-specific LINC component SUN3 is essential for sperm head shaping during mouse spermiogenesis.Qian Gao, Ranjha Khan, Changping Yu
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