Role of Lipid Metabolism and Signaling in Mammalian Oocyte Maturation, Quality, and Acquisition of Competence by Ranjha Khan, Xiaohua Jiang, Uzma Hameed, Qinghua Shi

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Identification of Frameshift Variants in <i>POLH</i> Gene Causing Xeroderma Pigmentosum in Two Consanguineous Pakistani Families by Ghazala Y. Zamani, Ranjha Khan, Noreen Karim, Zubair M. Ahmed, Muhammad Naeem

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AAV-SPL 2.0, a Modified Adeno-Associated Virus Gene Therapy Agent for the Treatment of Sphingosine Phosphate Lyase Insufficiency Syndrome by Ranjha Khan, Babak Oskouian, Joanna Y. Lee, Jeffrey B. Hodgin, Yingbao Yang, Gizachew Tassew, Julie D. Saba

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A Homozygous Loss-of-Function Mutation in <i>MSH5 </i>Abolishes MutSγ Axial Loading and Causes Meiotic Arrest in NOA-Affected Individuals by Chenjia Gong, Tanveer Abbas, Zubair Muhammad, Jianteng Zhou, Ranjha Khan, Hui Ma, Huan Zhang, Qinghua Shi, Baolu Shi

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Nuclear translocation of MTL5 from cytoplasm requires its direct interaction with LIN9 and is essential for male meiosis and fertility. by Xingxia Zhang, Ming Li, Xiaohua Jiang, Hui Ma, Suixing Fan, Yang Li, Changping Yu, Jianze Xu, Ranjha Khan, Hanwei Jiang, Qinghua Shi

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Comparative study of microscale and macroscale technique for encapsulation of Calotropis gigantea extract in metal-conjugated nanomatrices for invasive ductal carcinoma by Ayesha Aftab, Bashir Ahmad, Shazia Bashir, Saima Rafique, Muhammad Bashir, Tayyaba Ghani, Asma Gul, Atta Ullah Shah, Ranjha Khan, Abdulrahim A. Sajini

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CFTR mutations causing congenital unilateral absence of the vas deferens (CUAVD) and congenital absence of the uterus (CAU) in a consanguineous family by Mahdieh Daliri Ghouchanatigh, Ranjha Khan, Majid Mojarrad, Uzma Hameed, Muhammad Zubair, Ahmed Waqas, Mohsen Jalali, Mahmoudreza Kalantari, Ali Shamsa, Huan Zhang, Qing-Hua Shi

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Biallelic Variants in CFAP61 Cause Multiple Morphological Abnormalities of the Flagella and Male Infertility by Ao Ma, Aurang Zeb, Imtiaz Ali, Daren Zhao, Asad Khan, Beibei Zhang, Jianteng Zhou, Ranjha Khan, Huan Zhang, Yuanwei Zhang, Ihsan Khan, Wasim Shah, Haider Ali, Abdul Rafay Javed, Hui Ma, Qinghua Shi

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Novel Loss-of-Function Mutations in DNAH1 Displayed Different Phenotypic Spectrum in Humans and Mice by Ranjha Khan, Qumar Zaman, Jing Chen, Manan Khan, Ao Ma, Jianteng Zhou, Beibei Zhang, Asim Ali, Muhammad Naeem, Muhammad Zubair, Daren Zhao, Wasim Shah, Mazhar Khan, Yuanwei Zhang, Bo Xu, Huan Zhang, Qinghua Shi

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ZFP541 maintains the repression of pre-pachytene transcriptional programs and promotes male meiosis progression by Jianze Xu, Jianing Gao, Junyan Liu, Xue Huang, Huan Zhang, Ao Ma, Jingwei Ye, Xingxia Zhang, Yang Li, Gang Yang, Hao Yin, Ranjha Khan, Tao Li, Suixing Fan, Xiaohua Jiang, Yuanwei Zhang, Hanwei Jiang, Hui Ma, Qinghua Shi

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A recurrent homozygous missense mutation in CCDC103 causes asthenoteratozoospermia due to disorganized dynein arms by Muhammad Zubair, Ranjha Khan, Ao Ma, Uzma Hameed, Mazhar Khan, Tanveer Abbas, Riaz Ahmad, Jian-Teng Zhou, Wasim Shah, Ansar Hussain, Nisar Ahmed, Ihsan Khan, Khalid Khan, Yuan-Wei Zhang, Huan Zhang, Li-Min Wu, Qing-Hua Shi

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A homozygous missense variant in DND1 causes non-obstructive azoospermia in humans by Xuefeng Xie, Mazhar Khan, Muhammad Zubair, Abbas Khan, Ranjha Khan, Jianteng Zhou, Yuanwei Zhang, Muzafar Said, Sher Ali Khan, Qamar Zaman, Ghulam Murtaza, Muzamil Ahmad Khan, Wei Liu, Xiaoning Hou, Huan Zhang, Bo Xu, Xiaohua Jiang, Shun Bai, Qinghua Shi

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