Association of the leptin gene with knee osteoarthritis susceptibility in a Han Chinese population : a case-control study
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概要
- 論文の詳細を見る
- Nature Publishing Groupの論文
- 2010-10-01
著者
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Shi Dongquan
中華人民共和国
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Shi Dongquan
Center Of Diagnosis And Treatment For Joint Disease Drum Tower Hospital Affiliated To Medical School
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Dai Jin
理化学研究所ゲノム医科学研究センター 骨関節疾患研究チーム
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Dai Jin
The Center Of Diagnosis And Treatment For Joint Disease Drum Tower Hospital Affiliated To Medical Sc
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Qin Jianghui
中華人民共和国
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QIN Jianghui
The Center of Diagnosis and Treatment for Joint Disease, Drum Tower Hospital Affiliated to Medical S
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Tsezou Aspasia
Department Of Biology University Of Thessalia Medical School
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Tsezou Aspasia
Department Of Biology Medical School University Of Thessaly
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Jiang Qing
The Center Of Diagnosis And Treatment For Joint Disease Department Of Orthopaedic Surgery Drum Tower Hospital Affiliated To Medical School Of Nanjing University
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Shi Dongquan
The Center Of Diagnosis And Treatment For Joint Disease Department Of Orthopaedic Surgery Drum Tower Hospital Affiliated To Medical School Of Nanjing University
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ZHU Lunqing
The Center of Diagnosis and Treatment for Joint Disease, Department of Orthopaedic Surgery, Drum Tower Hospital Affiliated to Medical School of Nanjing University
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Zhu Lunqing
The Center Of Diagnosis And Treatment For Joint Disease Department Of Orthopaedic Surgery Drum Tower Hospital Affiliated To Medical School Of Nanjing University
関連論文
- Association of the leptin gene with knee osteoarthritis susceptibility in a Han Chinese population: a case-control study
- Lack of association of single nucleotide polymorphism in LRCH1 with knee osteoarthritis susceptibility
- Association of the aspartic acid-repeat polymorphism in the asporin gene with age at onset of knee osteoarthritis in Han Chinese Population
- Replication of the association of the aspartic acid repeat polymorphism in the asporin gene with knee-osteoarthritis susceptibility in Han Chinese
- The canine copper toxicosis gene MURR1 is not implicated in the pathogenesis of Wilson disease
- A founder mutation of CANT1 common in Korean and Japanese Desbuquois dysplasia
- TRPV4-pathy, a novel channelopathy affecting diverse systems
- Association of the leptin gene with knee osteoarthritis susceptibility in a Han Chinese population : a case-control study