Search Results - "Mendelian inheritance"

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  1. 41
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    Prenatal diagnosis and molecular cytogenetic characterization of an interstitial deletion of 18q12.1-q12.3 encompassing DTNA, CELF4 and SETBP1 by Chih-Ping Chen, Chih-Heng Hsieh, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, Chien-Wen Yang, Chen-Chi Lee, Wayseen Wang

    Published 2017
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  2. 42
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    Prenatal diagnosis of a 1.651-Mb 19q13.42-q13.43 microdeletion in a fetus with micrognathia and bilateral pyelectasis on prenatal ultrasound by Chih-Ping Chen, Chin-Yuan Hsu, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Wayseen Wang

    Published 2020
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  3. 43
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    Network-Based Pharmacological Study on the Mechanism of Guishao-Liujun Decoction in the Treatment of Gastric Cancer by Xiaoqing Qian, Xiaoqing Qian, Lingle Zhang, Feng Xie, Yingsheng Cheng, Daxiang Cui

    Published 2022
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  4. 44
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    Global Text Mining and Development of Pharmacogenomic Knowledge Resource for Precision Medicine by Debleena Guin, Debleena Guin, Jyoti Rani, Jyoti Rani, Priyanka Singh, Priyanka Singh, Sandeep Grover, Shivangi Bora, Shivangi Bora, Puneet Talwar, Muthusamy Karthikeyan, K Satyamoorthy, C Adithan, S Ramachandran, S Ramachandran, Luciano Saso, Yasha Hasija, Ritushree Kukreti, Ritushree Kukreti

    Published 2019
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  5. 45
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    Dental anomalies in syndromes displaying hypertrichosis in the clinical spectrum by Vinícius Figueiredo CARNEIRO, Renato Assis MACHADO, Mauro Costa BARBOSA, Verônica Oliveira DIAS, Daniella Reis Barbosa MARTELLI, Hercílio MARTELLI-JÚNIOR

    Published 2023
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  6. 46
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    A 13-year-old girl with 18p deletion syndrome presenting Turner syndrome-like clinical features of short stature, short webbed neck, low posterior hair line, puffy eyelids and incr... by Chih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, Wen-Lin Chen, Wayseen Wang

    Published 2018
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  7. 47
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    Neonatal presentation of ventricular tachycardia and a Reye-like syndrome episode associated with disturbed mitochondrial energy metabolism by Armstrong Dawna L, Towbin Jeffrey A, Scheuerle Angela E, Scaglia Fernando, Sweetman Lawrence, Wong Lee-Jun C

    Published 2002
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  8. 48
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    Essential role of DNA-PKcs and plasminogen for the development of doxorubicin-induced glomerular injury in mice by Bernhard N. Bohnert, Irene Gonzalez-Menendez, Thomas Dörffel, Jonas C. Schneider, Mengyun Xiao, Andrea Janessa, M. Zaher Kalo, Birgit Fehrenbacher, Martin Schaller, Nicolas Casadei, Kerstin Amann, Christoph Daniel, Andreas L. Birkenfeld, Florian Grahammer, Lahoucine Izem, Edward F. Plow, Leticia Quintanilla-Martinez, Ferruh Artunc

    Published 2021
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  9. 49
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    Prenatal diagnosis and molecular cytogenetic characterization of de novo distal 5p deletion and distal 22q duplication by Chih-Ping Chen, Jian-Pei Huang, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Wen-Lin Chen, Meng-Shan Lee, Wayseen Wang

    Published 2020
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  10. 50
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    Pathway networks generated from human disease phenome by Ann G. Cirincione, Kaylyn L. Clark, Maricel G. Kann

    Published 2018
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  11. 51
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    Multi-factor regulatory network and different clusters in hypertrophic obstructive cardiomyopathy by Xianyu Qin, Lei Huang, Sicheng Chen, Shaoxian Chen, Pengju Wen, Yueheng Wu, Jian Zhuang

    Published 2021
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  12. 52
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    VNTR polymorphism in the breakpoint region of ABL1 and susceptibility to bladder cancer by Min-Hye Kim, Gi-Eun Yang, Mi-So Jeong, Jeong-Yeon Mun, Sang-Yeop Lee, Jong-Kil Nam, Yung Hyun Choi, Tae Nam Kim, Sun-Hee Leem

    Published 2021
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  13. 53
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    Prenatal diagnosis and molecular cytogenetic characterization of a pure ring chromosome 21 with a 4.657-Mb 21q22.3 deletion by Chih-Ping Chen, Liang-Kai Wang, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Yun-Yi Chen, Dai-Dyi Town, Wayseen Wang

    Published 2021
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  14. 54
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    Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 15 in a pregnancy associated with recurrent Down sy... by Chih-Ping Chen, Chia-Hao Chan, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Dai-Dyi Town, Meng-Shan Lee, Wayseen Wang

    Published 2021
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  15. 55
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    Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 3 by Chih-Ping Chen, Tsang-Ming Ko, Chen-Yu Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Chen-Wen Pan, Wayseen Wang

    Published 2019
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  16. 56
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    Molecular and Genetic Basis of Non-Syndromic Tooth Agenesis by L. Kramerová, P. Krejčí, E. Míšová, A. Ševecová

    Published 2015
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  17. 57
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    Detection of a familial 1q21.1 microdeletion and concomitant CHD1L mutation in a fetus with oligohydramnios and bilateral renal dysplasia on prenatal ultrasound by Chih-Ping Chen, Jian-Pei Huang, Yi-Yung Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Wayseen Wang, Chen-Chi Lee

    Published 2019
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  18. 58
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    Mechanism of Action of Shenerjiangzhi Formulation on Hyperlipidemia Induced by Consumption of a High-Fat Diet in Rats Using Network Pharmacology and Analyses of the Gut Microbiota by Shuang Zhang, Yu Wang, Fang Lu, Shadi A. D. Mohammed, Hanxing Liu, Song Ding, Shu-min Liu

    Published 2022
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  19. 59
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    Prenatal diagnosis of concomitant distal 5q duplication and terminal 10q deletion in a fetus with intrauterine growth restriction, congenital diaphragmatic hernia and congenital he... by Chih-Ping Chen, Jian-Pei Huang, Shin-Wen Chen, Schu-Rern Chern, Peih-Shan Wu, Fang-Tzu Wu, Wen-Lin Chen, Li-Feng Chen, Wayseen Wang

    Published 2020
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  20. 60
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    Study on the mechanism of action of colchicine in the treatment of coronary artery disease based on network pharmacology and molecular docking technology by Yunfeng Yu, Yunfeng Yu, Manli Zhou, Xi Long, Shuang Yin, Gang Hu, Xinyu Yang, Weixiong Jian, Weixiong Jian, Rong Yu

    Published 2023
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