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Krüppel-like factor 3 inhibition by mutated lncRNA Reg1cp results in human high bone mass syndrome.
Yang, Mi; Guo, Qi; Peng, Hui; Xiao, Yu-Zhong; Xiao, Ye; Huang, Yan; Li, Chang-Jun; Su, Tian; Zhang, Yun-Lin; Lei, Min-Xiang; Chen, Hui-Ling; Jiang, Tie-Jian; Luo, Xiang-Hang.
Afiliación
  • Yang M; Department of Endocrinology, Endocrinology Research Center, Xiangya Hospital of Central South University, Changsha, China.
  • Guo Q; Department of Endocrinology, Endocrinology Research Center, Xiangya Hospital of Central South University, Changsha, China.
  • Peng H; Key Laboratory of Organ Injury, Aging and Regenerative Medicine of Hunan Province, Changsha, China.
  • Xiao YZ; Department of Endocrinology, Endocrinology Research Center, Xiangya Hospital of Central South University, Changsha, China.
  • Xiao Y; Department of Endocrinology, Endocrinology Research Center, Xiangya Hospital of Central South University, Changsha, China.
  • Huang Y; Key Laboratory of Organ Injury, Aging and Regenerative Medicine of Hunan Province, Changsha, China.
  • Li CJ; Department of Endocrinology, Endocrinology Research Center, Xiangya Hospital of Central South University, Changsha, China.
  • Su T; Department of Endocrinology, Endocrinology Research Center, Xiangya Hospital of Central South University, Changsha, China.
  • Zhang YL; Department of Endocrinology, Endocrinology Research Center, Xiangya Hospital of Central South University, Changsha, China.
  • Lei MX; Department of Endocrinology, Endocrinology Research Center, Xiangya Hospital of Central South University, Changsha, China.
  • Chen HL; Department of Metabolic Endocrinology, The Second People's Hospital of Xiangxiang, Xiangxiang, China.
  • Jiang TJ; Department of Endocrinology, Endocrinology Research Center, Xiangya Hospital of Central South University, Changsha, China.
  • Luo XH; Department of Endocrinology, Endocrinology Research Center, Xiangya Hospital of Central South University, Changsha, China.
J Exp Med ; 216(8): 1944-1964, 2019 08 05.
Article en En | MEDLINE | ID: mdl-31196982
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Osteopetrosis / Hiperostosis Cortical Congénita / Factores de Transcripción de Tipo Kruppel / ARN Largo no Codificante / Mutación Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Aged80 País/Región como asunto: Asia Idioma: En Revista: J Exp Med Año: 2019 Tipo del documento: Article País de afiliación: China Pais de publicación: Estados Unidos
Texto completo
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XML
PubMed Links
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Osteopetrosis / Hiperostosis Cortical Congénita / Factores de Transcripción de Tipo Kruppel / ARN Largo no Codificante / Mutación Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Aged80 País/Región como asunto: Asia Idioma: En Revista: J Exp Med Año: 2019 Tipo del documento: Article País de afiliación: China Pais de publicación: Estados Unidos