期刊信息
| Human Molecular Genetics | |
| 印刷版ISSN： | 0964-6906 |
| 电子版ISSN： | 1460-2083 |
| 出版者： | Oxford University Press |
| 国家： | United Kingdom |
| 状态： | Active |
| 创刊年： | 1992 |
| 周期： | 26 times a year |
| 类型： | Journal; Academic/Scholarly |
| 语种： | Text in English |
| 学科： | BIOLOGY - GENETICS; MEDICAL SCIENCES |
| 期刊URL： | 链接地址 |
| 来源： | oxford |
| 中图分类号： | 医学、卫生 |
| 收录机构： | SCI SCI SCI |
《Human Molecular Genetics》
| 刊内检索 |
| 1. Mapping eQTLs with RNA-seq reveals novel susceptibility genes, non-coding RNAs and alternative-splicing events in systemic lupus erythematosus |
| [外文期刊] 刊名:《Human Molecular Genetics》 2017 , Volume 26 , Number 5 作者:Odhams, Christopher A. | |
| Studies attempting to functionally interpret complex-disease susceptibility loci by GWAS and eQTL in |
| 2. Comparison of the in vivo induction and transmission of alpha-synuclein pathology by mutant alpha-synuclein fibril seeds in transgenic mice |
| [外文期刊] 刊名:《Human Molecular Genetics》 2017 , Volume 26 , Number 24 作者:Rutherford, Nicola J. | |
| Parkinson's disease (PD) is one of many neurodegenerative diseases termed synucleinopathies, neuropa |
| 3. Gclc deficiency in mouse CNS causes mitochondrial damage and neurodegeneration |
| [外文期刊] 刊名:《Human Molecular Genetics》 2017 , Volume 26 , Number 7 作者:Feng, Weiyi | |
| Gamma glutamyl cysteine ligase (GCL) is the rate-limiting enzyme for intracellular glutathione (GSH) |
| 4. Brain ventriculomegaly in Down syndrome mice is caused by Pcp4 dose-dependent cilia dysfunction |
| [外文期刊] 刊名:《Human Molecular Genetics》 2017 , Volume 26 , Number 5 作者:Raveau, Matthieu | |
| Down syndrome is a leading cause of congenital intellectual disability caused by an additional copy |
| 5. MED12-related XLID disorders are dose-dependent of immediate early genes (IEGs) expression |
| [外文期刊] 刊名:《Human Molecular Genetics》 2017 , Volume 26 , Number 11 作者:Donnio, Lise-Marie | |
| Mediator occupies a key role in protein coding genes expression in mediating the contacts between ge |
| 6. GLI1 inactivation is associated with developmental phenotypes overlapping with Ellis-van Creveld syndrome |
| [外文期刊] 刊名:《Human Molecular Genetics》 2017 , Volume 26 , Number 23 作者:Palencia-Campos, Adrian | |
| GLI1, GLI2 and GLI3 form a family of transcription factors which regulate development by mediating t |
| 7. BDNF overexpression prevents cognitive deficit elicited by adolescent cannabis exposure and host susceptibility interaction |
| [外文期刊] 刊名:《Human Molecular Genetics》 2017 , Volume 26 , Number 13 作者:Segal-Gavish, Hadar | |
| Cannabis abuse in adolescence is associated with increased risk of psychotic disorders. Delta-9-tetr |
| 8. High resolution time-course mapping of early transcriptomic, molecular and cellular phenotypes in Huntington's disease CAG knock-in mice across multiple genetic backgrounds |
| [外文期刊] 刊名:《Human Molecular Genetics》 2017 , Volume 26 , Number 5 作者:Ament, Seth A. | |
| Huntington's disease is a dominantly inherited neurodegenerative disease caused by the expansion of |
| 9. Annexin A2 links poor myofiber repair with inflammation and adipogenic replacement of the injured muscle |
| [外文期刊] 刊名:《Human Molecular Genetics》 2017 , Volume 26 , Number 11 作者:Defour, Aurelia | |
| Repair of skeletal muscle after sarcolemmal damage involves dysferlin and dysferlin-interacting prot |
| 10. Genome-wide association of white blood cell counts in Hispanic/Latino Americans: the Hispanic Community Health Study/Study of Latinos |
| [外文期刊] 刊名:《Human Molecular Genetics》 2017 , Volume 26 , Number 6 作者:Jain, Deepti | |
| Circulating white blood cell (WBC) counts (neutrophils, monocytes, lymphocytes, eosinophils, basophi |