Hasil Pencarian - Xiaoping Xing

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  1. 1
    Identification and Quality Assessment of Chrysanthemum Buds by CE Fingerprinting

    Identification and Quality Assessment of Chrysanthemum Buds by CE Fingerprinting oleh Xiaoping Xing, Dan Li

    Diterbitkan 2015-01-01
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  2. 2
    V876E mutation in CACNA1S gene associated with severe hypokalemic periodic paralysis in a Chinese woman

    V876E mutation in CACNA1S gene associated with severe hypokalemic periodic paralysis in a Chinese woman oleh Hongbo Yang, Huabing Zhang, Xiaoping Xing

    Diterbitkan 2015-04-01
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  3. 3
    Whole‐genome sequencing revealed a novel long‐range deletion mutation spanning GNAS in familial pseudohypoparathyroidism

    Whole‐genome sequencing revealed a novel long‐range deletion mutation spanning GNAS in familial pseudohypoparathyroidism oleh Yangfan Fei, Lv Liu, Lixia Wu, Ou Wang, Xiaoping Xing, Aiping Li, Lingyi Huang

    Diterbitkan 2023-05-01
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  4. 4
    The first case report of Kyphoscoliotic Ehlers-Danlos syndrome of chinese origin with a novel PLOD1 gene mutation

    The first case report of Kyphoscoliotic Ehlers-Danlos syndrome of chinese origin with a novel PLOD1 gene mutation oleh Xiaolin Ni, Chenxi Jin, Yan Jiang, Ou Wang, Mei Li, Xiaoping Xing, Weibo Xia

    Diterbitkan 2020-10-01
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  5. 5
    The preliminary study on cardiac structure and function in Chinese patients with primary hyperparathyroidism

    The preliminary study on cardiac structure and function in Chinese patients with primary hyperparathyroidism oleh Rong Chen, An Song, Ou Wang, Yan Jiang, Mei Li, Weibo Xia, Xue Lin, Xiaoping Xing

    Diterbitkan 2023-02-01
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  6. 6
    Clinical and genetic analysis of atypical parathyroid adenoma compared with parathyroid carcinoma and benign lesions in a Chinese cohort

    Clinical and genetic analysis of atypical parathyroid adenoma compared with parathyroid carcinoma and benign lesions in a Chinese cohort oleh Yingyu Chen, An Song, Min Nie, Yan Jiang, Mei Li, Weibo Xia, Ou Wang, Xiaoping Xing

    Diterbitkan 2023-01-01
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  7. 7
    Autosomal recessive hypophosphatemic rickets Type 1 caused by different DMP1 mutations in three Chinese families

    Autosomal recessive hypophosphatemic rickets Type 1 caused by different DMP1 mutations in three Chinese families oleh Xiaolin Ni, Xiang Li, Qi Zhang, Mei Li, Xiaoping Xing, Ou Wang, Yan Jiang, Weibo Xia

    Diterbitkan 2020-10-01
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  8. 8
    Cushing’s Syndrome With Nocardiosis: A Case Report and a Systematic Review of the Literature

    Cushing’s Syndrome With Nocardiosis: A Case Report and a Systematic Review of the Literature oleh Da Zhang, Da Zhang, Yan Jiang, Lin Lu, Zhaolin Lu, Weibo Xia, Xiaoping Xing, Hongwei Fan

    Diterbitkan 2021-03-01
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  9. 9
    The First Mutation Identified in a Chinese Acrodysostosis Patient Confirms a p.G289E Variation of PRKAR1A Causes Acrodysostosis

    The First Mutation Identified in a Chinese Acrodysostosis Patient Confirms a p.G289E Variation of PRKAR1A Causes Acrodysostosis oleh Nan Li, Min Nie, Mei Li, Yan Jiang, Xiaoping Xing, Ou Wang, Chunlin Li, Weibo Xia

    Diterbitkan 2014-07-01
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  10. 10
    Explorative research on glucolipid metabolism and levels of adipokines in pseudohypoparathyroidism type 1 patients

    Explorative research on glucolipid metabolism and levels of adipokines in pseudohypoparathyroidism type 1 patients oleh Yi Yang, An Song, Fengying Gong, Yan Jiang, Mei Li, Weibo Xia, Xiaoping Xing, Ou Wang, Hui Pan

    Diterbitkan 2023-11-01
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  11. 11
    Low HbA1c With Normal Hemoglobin in a Diabetes Patient Caused by PIEZO1 Gene Variant: A Case Report

    Low HbA1c With Normal Hemoglobin in a Diabetes Patient Caused by PIEZO1 Gene Variant: A Case Report oleh An Song, Lin Lu, Yuxiu Li, Mei Lin, Xingxing Yuan, Xinqi Cheng, Weibo Xia, Ou Wang, Xiaoping Xing

    Diterbitkan 2020-06-01
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  12. 12
    Prevalence of Parathyroid Carcinoma and Atypical Parathyroid Neoplasms in 153 Patients With Multiple Endocrine Neoplasia Type 1: Case Series and Literature Review

    Prevalence of Parathyroid Carcinoma and Atypical Parathyroid Neoplasms in 153 Patients With Multiple Endocrine Neoplasia Type 1: Case Series and Literature Review oleh An Song, Yi Yang, Shuzhong Liu, Min Nie, Yan Jiang, Mei Li, Weibo Xia, Ou Wang, Xiaoping Xing

    Diterbitkan 2020-09-01
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  13. 13
    Effects of bisphosphonates on osteoporosis induced by Duchenne muscular dystrophy: A prospective study

    Effects of bisphosphonates on osteoporosis induced by Duchenne muscular dystrophy: A prospective study oleh Wenbin Zheng, Yi Dai, Jing Hu, Dichen Zhao, Ou Wang, Yan Jiang, Weibo Xia, Xiaoping Xing, Mei Li

    Diterbitkan 2020-10-01
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  14. 14
    Manifestations of left ventricular dysfunction and arrhythmia in patients with chronic hypoparathyroidism and pseudohypoparathyroidism: a preliminary study

    Manifestations of left ventricular dysfunction and arrhythmia in patients with chronic hypoparathyroidism and pseudohypoparathyroidism: a preliminary study oleh Yabing Wang, Kun He, Ou Wang, Xue Lin, Sixing Chen, Yan Jiang, Mei Li, Weibo Xia, Xiaoping Xing

    Diterbitkan 2020-05-01
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  15. 15
    Glucose tolerance and insulin responsiveness in Gitelman syndrome patients

    Glucose tolerance and insulin responsiveness in Gitelman syndrome patients oleh Tao Yuan, Lanping Jiang, Chen Chen, Xiaoyan Peng, Min Nie, Xuemei Li, Xiaoping Xing, Xuewang Li, Limeng Chen

    Diterbitkan 2017-05-01
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  16. 16
    The first case of primary hypertrophic osteoarthropathy with soft tissue giant tumors caused by HPGD loss-of-function mutation

    The first case of primary hypertrophic osteoarthropathy with soft tissue giant tumors caused by HPGD loss-of-function mutation oleh Qianqian Pang, Yuping Xu, Xuan Qi, Yan Jiang, Ou Wang, Mei Li, Xiaoping Xing, Ling Qin, Weibo Xia

    Diterbitkan 2019-06-01
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  17. 17
    Novel mutations in FKBP10 and PLOD2 cause rare Bruck syndrome in Chinese patients.

    Novel mutations in FKBP10 and PLOD2 cause rare Bruck syndrome in Chinese patients. oleh Peiran Zhou, Yi Liu, Fang Lv, Min Nie, Yan Jiang, Ou Wang, Weibo Xia, Xiaoping Xing, Mei Li

    Diterbitkan 2014-01-01
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  18. 18
    Novel HRPT2/CDC73 gene mutations and loss of expression of parafibromin in Chinese patients with clinically sporadic parathyroid carcinomas.

    Novel HRPT2/CDC73 gene mutations and loss of expression of parafibromin in Chinese patients with clinically sporadic parathyroid carcinomas. oleh Ou Wang, Chunyan Wang, Min Nie, Quancai Cui, Heng Guan, Yan Jiang, Mei Li, Weibo Xia, Xunwu Meng, Xiaoping Xing

    Diterbitkan 2012-01-01
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  19. 19
    Clinical and Genetic Analysis of Multiple Endocrine Neoplasia Type 1-Related Primary Hyperparathyroidism in Chinese.

    Clinical and Genetic Analysis of Multiple Endocrine Neoplasia Type 1-Related Primary Hyperparathyroidism in Chinese. oleh Jing Kong, Ou Wang, Min Nie, Jie Shi, Yingying Hu, Yan Jiang, Mei Li, Weibo Xia, Xunwu Meng, Xiaoping Xing

    Diterbitkan 2016-01-01
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  20. 20
    FpCzf14 is a putative C2H2 transcription factor regulating conidiation in Fusarium pseudograminearum

    FpCzf14 is a putative C2H2 transcription factor regulating conidiation in Fusarium pseudograminearum oleh Linlin Chen, Jingya Zhao, Huiqing Xia, Yuming Ma, Yankun Liu, Mengya Peng, Xiaoping Xing, Bingjian Sun, Yan Shi, Honglian Li

    Diterbitkan 2020-11-01
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