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

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Storage Stability of Kinnow Fruit (Citrus reticulata) as Affected by CMC and Guar Gum-Based Silver Nanoparticle Coatings von Shah, Syed Wasim Ahmad, Jahangir, Muhammad, Qaisar, Muhammad, Khan, Sher Aslam, Mahmood, Talat, Saeed, Muhammad, Farid, Abid, Liaquat, Muhammad

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A novel missense mutation of CCDC34 causes male infertility with oligoasthenoteratozoospermia in a consanguineous Pakistani family von Ahmad, Nisar, Yang, Meng-Lei, Zeb, Aurang, Zhou, Jian-Teng, Zubair, Muhammad, Abbas, Tanveer, Jiang, Xiao-Hua, Zhang, Yuan-Wei, Zhang, Huan, Shah, Wasim, Shi, Qing-Hua

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

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

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Computational analyses of RPIA gene mutation causing Ribose-5-phosphate isomerase deficiency: a rarest known metabolic disorder in humans von Muzammal, Muhammad, Fatima, Sana, Gul, Aisha, Qayum, Junaid, Farid, Arshad, Ahmad, Safeer, Shah, Wasim, Khan, Muzammil Ahmad

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

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A novel homozygous TSGA10 missense variant causes acephalic spermatozoa syndrome in a Pakistani family von Khan, Khalid, Zhang, Xiangjun, Dil, Sobia, Khan, Ihsan, Unar, Ahsanullah, Ye, Jingwei, Zeb, Aurang, Zubair, Muhammad, Shah, Wasim, Zhang, Huan, Khan, Muzammil Ahmad, Wu, Limin, Xu, Bo, Ma, Hui, Wen, Zina, Shi, Qinghua

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Loss-of-function mutations in CFAP57 cause multiple morphological abnormalities of the flagella in humans and mice von Ma, Ao, Zhou, Jianteng, Ali, Haider, Abbas, Tanveer, Ali, Imtiaz, Muhammad, Zubair, Dil, Sobia, Chen, Jing, Huang, Xiongheng, Ma, Hui, Zhao, Daren, Zhang, Beibei, Zhang, Yuanwei, Shah, Wasim, Shah, Basit, Murtaza, Ghulam, Iqbal, Furhan, Khan, Muzammil Ahmad, Khan, Asad, Li, Qing, Xu, Bo, Wu, Limin, Zhang, Huan, Shi, Qinghua

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Loss-of-function variants in KCTD19 cause non-obstructive azoospermia in humans von Liu, Junyan, Rahim, Fazal, Zhou, Jianteng, Fan, Suixing, Jiang, Hanwei, Yu, Changping, Chen, Jing, Xu, Jianze, Yang, Gang, Shah, Wasim, Zubair, Muhammad, Khan, Asad, Li, Yang, Shah, Basit, Zhao, Daren, Iqbal, Furhan, Jiang, Xiaohua, Guo, Tonghang, Xu, Peng, Xu, Bo, Wu, Limin, Ma, Hui, Zhang, Yuanwei, Zhang, Huan, Shi, Qinghua

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A novel recombination protein C12ORF40/REDIC1 is required for meiotic crossover formation von Fan, Suixing, Wang, Yuewen, Jiang, Hanwei, Jiang, Xiaohua, Zhou, Jianteng, Jiao, Yuying, Ye, Jingwei, Xu, Zishuo, Wang, Yue, Xie, Xuefeng, Zhang, Huan, Li, Yang, Liu, Wei, Zhang, Xiangjun, Ma, Hui, Shi, Baolu, Zhang, Yuanwei, Zubair, Muhammad, Shah, Wasim, Xu, Zhipeng, Xu, Bo, Shi, Qinghua

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A homozygous KASH5 frameshift mutation causes diminished ovarian reserve, recurrent miscarriage, and non-obstructive azoospermia in humans von Hou, Xiaoning, Zeb, Aurang, Dil, Sobia, Zhou, Jianteng, Zhang, Huan, Shi, Baolu, Muhammad, Zubair, Khan, Ihsan, Zaman, Qamar, Shah, Wasim Akbar, Jiang, Xiaohua, Wu, Limin, Ma, Hui, Shi, Qinghua

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Clinical Characteristics and Variation in Musculoskeletal Complexity of Different Ethnic Populations Accessing Sandwell and West Birmingham Hospital's MSK Service: A Service Evalua... von Shah, Wasim, Newham, Roger, Casey, Carolyn, Burgess, Roanna

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Knockout of the family with sequence similarity 181, member A (Fam181a) gene does not impair spermatogenesis or male fertility in the mouse von Shah, Wasim, Khan, Ranjha, Shah, Basit, Dil, Sobia, Shi, Qinghua

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Knockout of the family with sequence similarity 181, member A von Shah, Wasim, Khan, Ranjha, Shah, Basit, Dil, Sobia, Shi, Qinghua

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Homozygous mutations in C14orf39/SIX6OS1 cause non-obstructive azoospermia and premature ovarian insufficiency in humans von Fan, Suixing, Jiao, Yuying, Khan, Ranjha, Jiang, Xiaohua, Javed, Abdul Rafay, Ali, Asim, Zhang, Huan, Zhou, Jianteng, Naeem, Muhammad, Murtaza, Ghulam, Li, Yang, Yang, Gang, Zaman, Qumar, Zubair, Muhammad, Guan, Haiyang, Zhang, Xingxia, Ma, Hui, Jiang, Hanwei, Ali, Haider, Dil, Sobia, Shah, Wasim, Ahmad, Niaz, Zhang, Yuanwei, Shi, Qinghua

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Shell side direct expansion evaporation of ammonia on a 3-D structured surface tube bundle with exit superheat effect von Shah, Wasim, Abbas, Ahmad, Ayub, Zahid H., Ayub, Adnan H., Moreira, Tiago Augusto, Ribatski, Gherhardt, Li, Wei

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Inactivation of testis-specific gene C4orf46 is dispensable for spermatogenesis and fertility in mouse von Shah, Basit, Khan, Ranjha, Shah, Wasim, Aftab, Ayesha, Khan, Manan, Dil, Sobia, Shi, Qinghua

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Novel biallelic ADCY10 variants cause asthenozoospermia with excessive residual cytoplasm and hydronephrosis in humans von Zeb, Aurang, Yang, Menglei, Ahmad, Nisar, Zhang, Huan, Shah, Wasim, Khan, Khalid, Uddin, Meftah, Mansoor, Abu, Rahim, Fazal, Hussain, Ansar, Ali, Imtiaz, Abbas, Tanveer, Zubair, Muhammad, Khan, Ihsan, Shi, Qinghua

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A novel homozygous missense TTC12 variant identified in an infertile Pakistani man with severe oligoasthenoteratozoospermia and primary ciliary dyskinesia von Ali, Imtiaz, Ali, Haider, Unar, Ahsanullah, Rahim, Fazal, Khan, Khalid, Dil, Sobia, Abbas, Tanveer, Hussain, Ansar, Zeb, Aurang, Zubair, Muhammad, Zhang, Huan, Ma, Hui, Jiang, Xiaohua, Khan, Muzammil Ahmad, Xu, Bo, Shah, Wasim, Shi, Qinghua

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