Hasil Pencarian - Ranjha Khan

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  1. 1
    Role of Lipid Metabolism and Signaling in Mammalian Oocyte Maturation, Quality, and Acquisition of Competence

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

    Diterbitkan 2021-03-01
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  2. 2
    The Molecular Mechanism of Sex Hormones on Sertoli Cell Development and Proliferation

    The Molecular Mechanism of Sex Hormones on Sertoli Cell Development and Proliferation oleh Wasim Shah, Ranjha Khan, Basit Shah, Asad Khan, Sobia Dil, Wei Liu, Jie Wen, Xiaohua Jiang

    Diterbitkan 2021-07-01
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  3. 3
    The Dispensable Roles of X-Linked Ubl4a and Its Autosomal Counterpart Ubl4b in Spermatogenesis Represent a New Evolutionary Type of X-Derived Retrogenes

    The Dispensable Roles of X-Linked Ubl4a and Its Autosomal Counterpart Ubl4b in Spermatogenesis Represent a New Evolutionary Type of X-Derived Retrogenes oleh Changping Yu, Runjie Diao, Ranjha Khan, Cheng Deng, Hui Ma, Zhijie Chang, Xiaohua Jiang, Qinghua Shi

    Diterbitkan 2021-06-01
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  4. 4
    AAV-SPL 2.0, a Modified Adeno-Associated Virus Gene Therapy Agent for the Treatment of Sphingosine Phosphate Lyase Insufficiency Syndrome

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

    Diterbitkan 2023-10-01
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  5. 5
    A Homozygous Loss-of-Function Mutation in <i>MSH5 </i>Abolishes MutSγ Axial Loading and Causes Meiotic Arrest in NOA-Affected Individuals

    A Homozygous Loss-of-Function Mutation in <i>MSH5 </i>Abolishes MutSĪ³ Axial Loading and Causes Meiotic Arrest in NOA-Affected Individuals oleh Chenjia Gong, Tanveer Abbas, Zubair Muhammad, Jianteng Zhou, Ranjha Khan, Hui Ma, Huan Zhang, Qinghua Shi, Baolu Shi

    Diterbitkan 2022-06-01
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  6. 6
    Nuclear translocation of MTL5 from cytoplasm requires its direct interaction with LIN9 and is essential for male meiosis and fertility.

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

    Diterbitkan 2021-08-01
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  7. 7
    Comparative study of microscale and macroscale technique for encapsulation of Calotropis gigantea extract in metal-conjugated nanomatrices for invasive ductal carcinoma

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

    Diterbitkan 2023-08-01
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  8. 8
    CFTR mutations causing congenital unilateral absence of the vas deferens (CUAVD) and congenital absence of the uterus (CAU) in a consanguineous family

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

    Diterbitkan 2022-01-01
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  9. 9
    Biallelic Variants in CFAP61 Cause Multiple Morphological Abnormalities of the Flagella and Male Infertility

    Biallelic Variants in CFAP61 Cause Multiple Morphological Abnormalities of the Flagella and Male Infertility oleh 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

    Diterbitkan 2022-01-01
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  10. 10
    Novel Loss-of-Function Mutations in DNAH1 Displayed Different Phenotypic Spectrum in Humans and Mice

    Novel Loss-of-Function Mutations in DNAH1 Displayed Different Phenotypic Spectrum in Humans and Mice oleh 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

    Diterbitkan 2021-11-01
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  11. 11
    ZFP541 maintains the repression of pre-pachytene transcriptional programs and promotes male meiosis progression

    ZFP541 maintains the repression of pre-pachytene transcriptional programs and promotes male meiosis progression oleh 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

    Diterbitkan 2022-03-01
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  12. 12
    A recurrent homozygous missense mutation in CCDC103 causes asthenoteratozoospermia due to disorganized dynein arms

    A recurrent homozygous missense mutation in CCDC103 causes asthenoteratozoospermia due to disorganized dynein arms oleh 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

    Diterbitkan 2022-01-01
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  13. 13
    A homozygous missense variant in DND1 causes non-obstructive azoospermia in humans

    A homozygous missense variant in DND1 causes non-obstructive azoospermia in humans oleh 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

    Diterbitkan 2022-09-01
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