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Livres
Articles (149)
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Mediating Role of Employee Emotions in the Relationship Between Authentic Leadership and Employee Innovation

Zhou, Juanmei, Ma, Yueru, Cheng, Weibo, Xia, Bing

Journal:

Social Behavior and Personality An International Journal

Année:

2014

Langue:

english

Fichier:

PDF, 104 KB

english, 2014

[IEEE 2018 19th International Conference on Electronic Packaging Technology (ICEPT) - Shanghai (2018.8.8-2018.8.11)] 2018 19th International Conference on Electronic Packaging Technology (ICEPT) - A Modified MEMS-Casting Based TSV Filling Method with Universal Nozzle Piece That Uses Surface Trenches as Nozzles

Gu, Jiebin, Xia, Xiaoyuan, Zhang, Weibo, Li, Xinxin

Année:

2018

Langue:

english

Fichier:

PDF, 4.56 MB

english, 2018

Concept of a high-resolution miniature spectrometer using an integrated filter array

Wang, Shao-Wei, Xia, Changsheng, Chen, Xiaoshuang, Lu, Wei, Li, Ming, Wang, Haiqian, Zheng, Weibo, Zhang, Tao

Journal:

Optics Letters

Année:

2007

Langue:

english

Fichier:

PDF, 328 KB

english, 2007

A haplotype of MATN3 is associated with vertebral fracture in Chinese postmenopausal women: Peking Vertebral Fracture (PK-VF) study

Jing Zhao, Weibo Xia, Min Nie, Xin Zheng, Qiuping Wang, Xiran Wang, Wenbo Wang, Zhiwei Ning, Wei Huang, Yan Jiang, Mei Li, Ou Wang, Xiaoping Xing, Yue Sun, Lianmei Luo, Shuli He, Wei Yu, Qiang Lin, Yu

Journal:

Bone

Année:

2012

Langue:

english

Fichier:

PDF, 332 KB

english, 2012

Bone turnover and bone mineral density in HIV-1 infected Chinese taking highly active antiretroviral therapy –a prospective observational study

Zhang, Lixia, Su, Yuanbo, Hsieh, Evelyn, Xia, Weibo, Xie, Jing, Han, Yang, Cao, Ying, Li, Yanling, Song, Xiaojing, Zhu, Ting, Li, Taisheng, Yu, Wei

Journal:

BMC Musculoskeletal Disorders

Année:

2013

Langue:

english

Fichier:

PDF, 231 KB

english, 2013

Novel COL2A1 mutations causing spondyloepiphyseal dysplasia congenita in three unrelated Chinese families

Liu, Limin, Pang, QianQian, Jiang, Yan, Li, Mei, Wang, Ou, Xia, Weibo

Journal:

European Spine Journal

Année:

2016

Langue:

english

Fichier:

PDF, 5.90 MB

english, 2016

Primary hyperparathyroidism in Chinese children and adolescents: A single-center experience at Peking Union Medical College Hospital

Wang, Wenbo, Kong, Jing, Nie, Min, Jiang, Yan, Li, Mei, Xia, Weibo, Meng, Xunwu, Xing, Xiaoping, Wang, Ou

Journal:

Clinical Endocrinology

Année:

2017

Langue:

english

Fichier:

PDF, 373 KB

english, 2017

Draft Genome Sequence of Phoma arachidicola Wb2 Causing Peanut Web Blotch in China

Zhang, Xia, Xu, Manlin, Wu, Juxiang, Dong, Weibo, Chen, Dianxu, Wang, Lei, Chi, Yucheng

Journal:

Current Microbiology

Année:

2018

Langue:

english

Fichier:

PDF, 1.27 MB

english, 2018

Surfactant-Stripped Pheophytin Micelles for Multimodal Tumor Imaging and Photodynamic Therapy

Moukheiber, Dana, Chitgupi, Upendra, Carter, Kevin A., Luo, Dandan, Sun, Boyang, Goel, Shreya, Ferreira, Carolina, Engle, Jonathan W., Wang, Depeng, Geng, Jumin, Zhang, Yumiao, Xia, Jun, Cai, Weibo, L

Journal:

ACS Applied Bio Materials

Année:

2018

Langue:

english

Fichier:

PDF, 900 KB

english, 2018

The epidemiology of osteoporosis, associated fragility fractures, and management gap in China

Yu, Fan, Xia, Weibo

Journal:

Archives of Osteoporosis

Année:

2019

Langue:

english

Fichier:

PDF, 1.67 MB

english, 2019

A Review of Perovskite Photovoltaic Materials’ Synthesis and Applications via Chemical Vapor Deposition Method

Liu, Xia, Cao, Lianzhen, Guo, Zhen, Li, Yingde, Gao, Weibo, Zhou, Lianqun

Journal:

Materials

Année:

2019

Fichier:

PDF, 2.21 MB

2019

A novel long-range deletion spanning STX16 and NPEPL1 causing imprinting defects of the GNAS locus discovered in a patient with autosomal-dominant pseudohypoparathyroidism type 1B

Yang, Yi, Chu, Xueying, Nie, Min, Song, An, Jiang, Yan, Li, Mei, Xia, Weibo, Xing, Xiaoping, Wang, Ou

Journal:

Endocrine (Springer)

Année:

2020

Fichier:

PDF, 1.02 MB

2020

Manifestations of left ventricular dysfunction and arrhythmia in patients with chronic hypoparathyroidism and pseudohypoparathyroidism: a preliminary study

Wang, Yabing, He, Kun, Wang, Ou, Lin, Xue, Chen, Sixing, Jiang, Yan, Li, Mei, Xia, Weibo, Xing, Xiaoping

Journal:

BMC Endocrine Disorders

Année:

2020

Fichier:

PDF, 580 KB

2020

The first case report of Kyphoscoliotic Ehlers-Danlos syndrome of chinese origin with a novel PLOD1 gene mutation

Ni, Xiaolin, Jin, Chenxi, Jiang, Yan, Wang, Ou, Li, Mei, Xing, Xiaoping, Xia, Weibo

Journal:

BMC Medical Genetics

Année:

2020

Fichier:

PDF, 1.44 MB

2020

Germinal mosaicism of GATA3 in a family with HDR syndrome

Yue Sun, Weibo Xia, Xiaoping Xing, Mei Li, Ou Wang, Yan Jiang, Yu Pei, Ping Ye, Huaicheng Liu, Yingying Hu, Xunwu Meng, Xueying Zhou

Journal:

American Journal of Medical Genetics Part A

Année:

2009

Langue:

english

Fichier:

PDF, 285 KB

english, 2009

Three Novel Mutations of thePHEXGene in Three Chinese Families with X-linked Dominant Hypophosphatemic Rickets

Weibo Xia, Xunwu Meng, Yan Jiang, Mei Li, Xiaoping Xing, Li Pang, Ou Wang, Yu Pei, Li-Yun Yu, Yue Sun, Yingying Hu, Xueying Zhou

Journal:

Calcified Tissue International

Année:

2007

Langue:

english

Fichier:

PDF, 247 KB

english, 2007

A Recurrent Mutation c.617G>A in theACVR1Gene Causes Fibrodysplasia Ossificans Progressiva in Two Chinese Patients

Yue Sun, Weibo Xia, Yan Jiang, Xiaoping Xing, Mei Li, Ou Wang, Huabing Zhang, Yingying Hu, Huaicheng Liu, Xunwu Meng, Xueying Zhou

Journal:

Calcified Tissue International

Année:

2009

Langue:

english

Fichier:

PDF, 282 KB

english, 2009

FGF23 analysis of a Chinese family with autosomal dominant hypophosphatemic rickets

Yue Sun, Ou Wang, Weibo Xia, Yan Jiang, Mei Li, Xiaoping Xing, Yingying Hu, Huaicheng Liu, Xunwu Meng, Xueying Zhou

Journal:

Journal of Bone and Mineral Metabolism

Année:

2012

Langue:

english

Fichier:

PDF, 331 KB

english, 2012

Simple diffusion delivery via brain interstitial route for the treatment of cerebral ischemia

HongBin Han, ZuoLi Xia, He Chen, Chao Hou, WeiBo Li

Journal:

SCIENCE CHINA Life Sciences

Année:

2011

Langue:

english

Fichier:

PDF, 1.61 MB

english, 2011

Exome Sequencing Identifies SLCO2A1 Mutations as a Cause of Primary Hypertrophic Osteoarthropathy

Zhenlin Zhang, Weibo Xia, Jinwei He, Zeng Zhang, Yaohua Ke, Hua Yue, Chun Wang, Hao Zhang, Jiemei Gu, Weiwei Hu, Wenzhen Fu, Yunqiu Hu, Miao Li, Yujuan Liu

Journal:

The American Journal of Human Genetics

Année:

2012

Langue:

english

Fichier:

PDF, 959 KB

english, 2012

Asiatic acid protects primary neurons against C2-ceramide-induced apoptosis

Xiangnan Zhang, Jiaying Wu, Yuan Dou, Binbin Xia, Weibo Rong, Gerald Rimbach, Yijia Lou

Journal:

European Journal of Pharmacology

Année:

2012

Langue:

english

Fichier:

PDF, 1.77 MB

english, 2012

All-solid-state cw frequency-doubling Nd:YLiF_4/LBO blue laser with 433 W output power at 454 nm under in-band diode pumping at 880 nm

Lü, Yanfei, Zhang, Xihe, Cheng, Weibo, Xia, Jing

Journal:

Applied Optics

Année:

2010

Langue:

english

Fichier:

PDF, 322 KB

english, 2010

All-solid-state cw sodium D_2 resonance radiation based on intracavity frequency-doubled self-Raman laser operation in double-end diffusion-bonded Nd^3+:LuVO_4 crystal

Lü, Yanfei, Zhang, Xihe, Li, Shutao, Xia, Jing, Cheng, Weibo, Xiong, Zheng

Journal:

Optics Letters

Année:

2010

Langue:

english

Fichier:

PDF, 193 KB

english, 2010

Diode-pumped cw Nd:YAG three-level laser at 869 nm

Lü, Yanfei, Xia, Jing, Cheng, Weibo, Chen, Jifeng, Ning, Guobin, Liang, Zuoliang

Journal:

Optics Letters

Année:

2010

Langue:

english

Fichier:

PDF, 358 KB

english, 2010

Myostatin regulates glucose metabolism via the AMP-activated protein kinase pathway in skeletal muscle cells

Yuewen Chen, Jianwei Ye, Lingzhi Cao, Yong Zhang, Weibo Xia, Dahai Zhu

Journal:

The International Journal of Biochemistry & Cell Biology

Année:

2010

Langue:

english

Fichier:

PDF, 964 KB

english, 2010

Epidemiological study of hip fracture in Beijing, China

Weibo Xia, Shuqin He, Aimin Liu, Ling Xu

Journal:

Bone

Année:

2008

Langue:

english

Fichier:

PDF, 108 KB

english, 2008

A Chinese family with primary osteoporosis probably due to a heterozygote mutation in the LRP5 gene

Yue Sun, Weibo Xia, Mei Li, Yan Jiang, Ou Wang, Xiaoping Xing, Zhenlin Zhang, Xunwu Meng

Journal:

Bone

Année:

2008

Langue:

english

Fichier:

PDF, 99 KB

english, 2008

Detection and therapy of tumor induced osteomalacia

Jiang Yan, Meng Xunwu, Xia Weibo, Xing Xiaoping, Li Mei, Wang Ou, Zhang Huabing, Li Fang, Zhong Dingrong

Journal:

Bone

Année:

2008

Langue:

english

Fichier:

PDF, 51 KB

english, 2008

Severe bilateral cataracts and intracranial calcifications in chronic hypoparathyroidism

Hongbo Yang, Naishi Li, Hanyi Min, Lue Li, Fei Gao, Weibo Xia

Journal:

Bone

Année:

2008

Langue:

english

Fichier:

PDF, 52 KB

english, 2008

Gorham's disease — One case with extensive massive osteolysis

Xiaodong He, Yan Jiang, Weibo Xia, Feng Gu, Ou Wang, Mei Li, Xunwu Meng, Xiaoping Xing, Wei Yu

Journal:

Bone

Année:

2008

Langue:

english

Fichier:

PDF, 68 KB

english, 2008

The role of fibroblast growth factor 23, matrix extracellular phosphoglycoprotein and secreted frizzled related protein 4 in pathogenesis of tumor induced osteomalacia

Yan Jiang, Xunwu Meng, Weibo Xia, Xiaoping Xing, Mei Li, Ou Wang, Yingying Hu, Huaicheng Liu, Xueying Zhou

Journal:

Bone

Année:

2008

Langue:

english

Fichier:

PDF, 49 KB

english, 2008

A recurrent mutation 617G>A in the ACVR1 gene causes fibrodysplasia ossificans progressiva in a Chinese patient

Yue Sun, Weibo Xia, Yan Jiang, Mei Li, Ou Wang, Xiaoping Xing, Yingying Hu, Xunwu Meng, HuaiCheng Liu, Xueying Zhou

Journal:

Bone

Année:

2008

Langue:

english

Fichier:

PDF, 54 KB

english, 2008

Clinical features of pregnancy and lactation-associated osteoporosis: Analysis of 4 cases Chinese patients

Weibo Xia, Xiaodong He, Lingling Xu, Yan Jiang, Mei Li, Ou Wang, Xiaoping Xia, Xueying Meng, Yingying Hu, HuaiCheng Liu

Journal:

Bone

Année:

2008

Langue:

english

Fichier:

PDF, 53 KB

english, 2008

Association between abdominal aortic calcification and osteoporosis in postmenopausal women in Beijing

Ningyi Cui, Weibo Xia, Yan Jiang, Qiang Lin, Wei Yu, Mei Li, Ou Wang, Min Nie, Yue Sun, Shuli He, Jing Sun, Xiaoping Xing, Xunwu Meng, Yingying Hu, Huaicheng Liu, Xueying Zhou

Journal:

Bone

Année:

2010

Langue:

english

Fichier:

PDF, 67 KB

english, 2010

Presence of two novel mutations of the ALPL gene in a Chinese patient with hypophosphatasia

Haijuan Liu, Mei Li, Xiaoping Xing, Weibo Xia, Wei Yu, Min Nie, Ou Wang, Yan Jiang, Xunwu Meng, Xueying Zhou, Yingying Hu, Huaicheng Liu

Journal:

Bone

Année:

2010

Langue:

english

Fichier:

PDF, 59 KB

english, 2010

Genetic analysis of 128 Chinese patients with hypophosphatemic rickets

Yue Sun, Weibo Xia, Mei Li, Yan Jiang, Ou Wang, Min Nie, Xunwu Meng, Xiaoping Xing, Yingying Hu, Huaicheng Liu

Journal:

Bone

Année:

2010

Langue:

english

Fichier:

PDF, 66 KB

english, 2010

Novel mutations of CYP27B1 gene lead to reduced activity of 1α-hydroxylase in Chinese patients

Ningyi Cui, Weibo Xia, Hua Su, Li Pang, Yan Jiang, Yue Sun, Min Nie, Xiaoping Xing, Mei Li, Ou Wang, Tao Yuan, Yue Chi, Yingying Hu, Huaicheng Liu, Xunwu Meng, Xueying Zhou

Journal:

Bone

Année:

2012

Langue:

english

Fichier:

PDF, 644 KB

english, 2012

Expression patterns of Nurr1 in rat retina development

Li, Yingmin, Qi, Qian, Cong, Bin, Shi, Weibo, Liu, Xia, Zhang, Guozhong, Ma, Chunling

Journal:

Journal of Molecular Histology

Année:

2012

Langue:

english

Fichier:

PDF, 821 KB

english, 2012

Validation of the Oxford classification of IgA nephropathy for pediatric patients from China

Le, Weibo, Zeng, Cai-Hong, Liu, Zhangsuo, Liu, Dong, Yang, Qing, Lin, Rui-Xia, Xia, Zheng-Kun, Fan, Zhong-Min, Zhu, Guanghua, Wu, Ying, Xu, Hong, Zhai, Yihui, Ding, Ying, Yang, Xiaoqing, Liang, Shaosh

Journal:

BMC Nephrology

Année:

2012

Langue:

english

Fichier:

PDF, 224 KB

english, 2012

Association ofESR1andC6orf97gene polymorphism with osteoporosis in postmenopausal women

Luo, Lianmei, Xia, Weibo, Nie, Min, Sun, Yue, Jiang, Yan, Zhao, Jing, He, Shuli, Xu, Ling

Journal:

Molecular Biology Reports

Année:

2014

Langue:

english

Fichier:

PDF, 421 KB

english, 2014

A compound heterozygous mutation in SLC34A3 causes hereditary hypophosphatemic rickets with hypercalciuria in a Chinese patient

Chi, Yue, Zhao, Zhen, He, Xiaodong, Sun, Yue, Jiang, Yan, Li, Mei, Wang, Ou, Xing, Xiaoping, Sun, Andrew Y., Zhou, Xueying, Meng, Xunwu, Xia, Weibo

Journal:

Bone

Année:

2014

Langue:

english

Fichier:

PDF, 1.28 MB

english, 2014

Major Complications After Lung Microwave Ablation: A Single-Center Experience on 204 Sessions

Zheng, Aimin, Wang, Xiuwen, Yang, Xia, Wang, Weibo, Huang, Guanghui, Gai, Yonghao, Ye, Xin

Journal:

The Annals of Thoracic Surgery

Année:

2014

Langue:

english

Fichier:

PDF, 168 KB

english, 2014

Aromatase deficiency in a Chinese adult man caused by novel compound heterozygous CYP19A1 mutations: Effects of estrogen replacement therapy on the bone, lipid, liver and glucose metabolism

Chen, Zhike, Wang, Ou, Nie, Min, Elison, Kathleen, Zhou, Dujin, Li, Mei, Jiang, Yan, Xia, Weibo, Meng, Xunwu, Chen, Shiuan, Xing, Xiaoping

Journal:

Molecular and Cellular Endocrinology

Année:

2015

Langue:

english

Fichier:

PDF, 2.41 MB

english, 2015

Hyperthyroidism Caused by an Ectopic Thyrotropin-Secreting Tumor of the Nasopharynx: A Case Report and Review of the Literature

Tong, Anli, Xia, Weibo, Qi, Fang, Jin, Zimeng, Yang, Di, Zhang, Zhuhua, Li, Fang, Xing, Xiaoping, Lian, Xiaolan

Journal:

Thyroid

Année:

2013

Langue:

english

Fichier:

PDF, 388 KB

english, 2013

Osteoporosis knowledge, self-efficacy, and health beliefs among Chinese individuals with HIV

Hsieh, Evelyn, Fraenkel, Liana, Bradley, Elizabeth H., Xia, Weibo, Insogna, Karl L., Cui, Qu, Li, Kunli, Li, Taisheng

Journal:

Archives of Osteoporosis

Année:

2014

Langue:

english

Fichier:

PDF, 224 KB

english, 2014

Familial isolated primary hyperparathyroidism/hyperparathyroidism-jaw tumour syndrome caused by germline gross deletion or point mutations of CDC73 gene in Chinese

Kong, Jing, Wang, Ou, Nie, Min, Shi, Jie, Hu, Yingying, Jiang, Yan, Li, Mei, Xia, Weibo, Meng, Xunwu, Xing, Xiaoping

Journal:

Clinical Endocrinology

Année:

2014

Langue:

english

Fichier:

PDF, 582 KB

english, 2014

Long-Term Outcome of IgA Nephropathy Patients with Recurrent Macroscopic Hematuria

Le, WeiBo, Liang, ShaoShan, Chen, Hao, Wang, ShaoFan, Zhang, WenZhen, Wang, Xia, Wang, JinQuan, Zeng, Cai-Hong, Liu, Zhi-Hong

Journal:

American Journal of Nephrology

Année:

2014

Langue:

english

Fichier:

PDF, 189 KB

english, 2014

First Report of a Novel MissenseCLDN19Mutations Causing Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis in a Chinese Family

Yuan, Tao, Pang, Qianqian, Xing, Xiaoping, Wang, Xi, Li, Yuhui, Li, Jingjun, Wu, Xueyan, Li, Mei, Wang, Ou, Jiang, Yan, Dong, Jin, Xia, Weibo

Journal:

Calcified Tissue International

Année:

2015

Langue:

english

Fichier:

PDF, 1.05 MB

english, 2015

A Mutation inCTSKGene in an Autosomal Recessive Pycnodysostosis Family of Chinese Origin

Huang, Xianglan, Qi, Xuan, Li, Mei, Wang, Ou, Jiang, Yan, Xing, Xiaoping, Hu, Ying Ying, Xia, Weibo

Journal:

Calcified Tissue International

Année:

2015

Langue:

english

Fichier:

PDF, 383 KB

english, 2015

Two novelCAIImutations causing carbonic anhydrase II deficiency syndrome in two unrelated Chinese families

Pang, Qianqian, Qi, Xuan, Jiang, Yan, Wang, Ou, Li, Mei, Xing, Xiaoping, Dong, Jin, Xia, Weibo

Journal:

Metabolic Brain Disease

Année:

2015

Langue:

english

Fichier:

PDF, 1.17 MB

english, 2015