位置：成果数据库 > 期刊 > 期刊详情页
The case for the continuing use of the revised Cambridge Reference Sequence (rCRS) and the standardi
  • ISSN号：1434-5161
  • 期刊名称：Journal of Human Genetics
  • 时间：0
  • 页码：-
  • 相关项目：线粒体突变和人类疾病
作者： Bandelt, Hans-Jürgen|Kloss-Brandst?tter, Anita|Richards, Martin B|Yao, Yong-Gang|Logan, Ian|
同期刊论文项目
线粒体突变和人类疾病
期刊论文 36
同项目期刊论文
Complete mitochondrial DNA genome sequence variation of Chinese families with mutation m.3635G >
Mitochondrial DNA Copy Number, but Not Haplogroup, Confers a Genetic Susceptibility to Leprosy in Ha
Is Mitochondrial tRNA(phe) Variant m.593T > C a Synergistically Pathogenic Mutation in Chinese LH
The MT-ND1 and MT-ND5 genes are mutational hotspots for Chinese families with clinical features of L
Presence of mutation m.14484T>C in a Chinese family with maternally inherited essential hypertens
Common promoter variants of the NDUFV2 gene do not confer susceptibility to schizophrenia in Han Chi
Screening for mutation R882 in the DNMT3A gene in Chinese patients with hematological disease
Deciphering the Signature of Selective Constraints on Cancerous Mitochondrial Genome
Genetic variants of complement genes Ficolin-2, Mannose-binding lectin and Complement factor H are a
An update to MitoTool: Using a new scoring system for faster mtDNA haplogroup determination
Leber's hereditary optic neuropathy
No association of the LRRK2 genetic variants with Alzheimer’s disease in Han Chinese individua
Apparent mtDNA sequence heterogeneity in single human blood CD34+ cells is markedly affected by stor
Large-Scale mtDNA Screening Reveals a Surprising Matrilineal Complexity in East Asia and Its Implica
IDH1 and IDH2 mutations are frequent in Chinese patients with acute myeloid leukemia but rare in oth
Screening the three LHON primary mutations in the general Chinese population by using an optimized m
No association between the SNPs (rs3749446 and rs1402000) in the PARL gene and LHON in Chinese patie
Molecular characterization of six Chinese families with m.3460G > A and Leber hereditary optic ne
mtDNA Data Mining in GenBank Needs Surveying
Mitochondrial DNA mutation m.10680G > A is associated with Leber hereditary optic neuropathy in C
Trends in new leprosy case detection over 57 years (1952-2008) in Yuxi, Yunnan Province of Southwest
Mitochondrial DNA Haplogroup Background Affects LHON, but Not Suspected LHON, in Chinese Patients
Identification of mutation c. 632G > A (p.G211D) in the ATP2A2 gene and genotype-phenotype correl
Polymorphisms in the promoter region of the CASP8 gene are not associated with non-Hodgkin';s ly
Rapid identification of mtDNA somatic mutations in gastric cancer tissues based on the mtDNA phyloge
MitoTool: A web server for the analysis and retrieval of human mitochondrial DNA sequence variations
Genetic variants of the MRC1 gene and the IFNG gene are associated with leprosy in Han Chinese from
Evaluating risk loci for schizophrenia distilled from genome-wide association studies in Han Chinese
Mitochondrial DNA Sequence Variation and Haplogroup Distribution in Chinese Patients with LHON and m
Accumulation of mtDNA variations in human single CD34+ cells from maternally related individuals: ef
The Acquisition of an Inheritable 50-bp Deletion in the Human mtDNA Control Region Does Not Affect t
Genetic Polymorphisms of the CASP8 Gene Promoter May Not Be Associated with Colorectal Cancer in Han
Leber遗传性视神经病变研究进展和挑战