1.
Mutation Analysis of the GNE Gene in 12 Chinese Patients with Hereditary Inclusion Body Myopathy;
中国人遗传性包涵体肌病GNE基因突变分析
2.
The Endoplasmic Reticulum Stress and Apoptosis in Hereditary Inclusion Body Myopathy;
内质网应激和凋亡在遗传性包涵体肌病病理机制中的作用
3.
Unfolded Protein Response and Endoplasmic Reticulum Stress in Hereditary Inclusion Body Myopathy;
遗传性包涵体肌病非折叠蛋白反应及内质网应激蛋白表达分析
4.
The Pathomechanism and Genotype-Phenotype Relationship in Hereditary Inclusion Body Myopathy;
遗传包涵体肌病的病理机制研究及基因突变型-表现型分析
5.
Clinical, Pathological and Molecular Biological Study on Autosomal Dominant Inherited Centronuclear Myopathy;
常染色体显性遗传性中央核肌病一家系临床、病理和基因研究
6.
Association of the tumor necrosis factor receptor gene polymorphisms with the genetic susceptibility to dilated cardiomyopathy
肿瘤坏死因子受体基因多态性与扩张型心肌病遗传易感性的关系
7.
monkey-intranuclear-inclusion agent (MINIA)
猴核内包涵体病原体
8.
These pieces of DNA were found to contain genetic information that might play a role in the survival and infectiousness of this pathogen.
这些DNA片段包含的遗传信息可能与该病原体的存活和感染性有关。
9.
inclusion body of rhinitis
猪萎缩性鼻炎包涵体
10.
Here is a congenital cytomegalovirus infection in a fetus. Note the large CMV inclusions in the renal tubular epithelium.
胎儿先天性巨细胞病毒感染。肾小管上皮内可见巨细胞病毒包涵体。
11.
Cytomegalic inclusion disease (CMD)
巨细胞包涵体病——附173例病例分析
12.
"Causes include infection, allergy or autoimmune disease, Blockage in the urinary system, and hereditary diseases. Treatment addresses the cause where possible. "
引起肾炎的原因包括感染、过敏或自体免疫疾病;膀胱阻塞和遗传性疾
13.
Application of chromosomal technology in the etiological diagnosis of hereditary diseases
染色体技术诊断遗传性疾病病因的应用
14.
genetic and congenital disorder
遗传性与先天性疾病
15.
Laparoscopic Management of Autosomal Dominant Polycystic Kidney;
常染色体显性遗传性多囊肾病的腹腔镜治疗
16.
Study on Diversity of Population Genetics and Resistance of Magnaporthe Grisea in Guizhou Province;
贵州省稻瘟病菌群体遗传多样性及抗药性研究
17.
Studies on the Identification of Chicken Inclusion Hepatitis Virus CELOV Strain
鸡包涵体肝炎病毒CELOV株的鉴定研究
18.
Clinicopathologic and Molecular Cytogenetic Reserch on Inflammatory Myofibroblastic Tumor and Low-grade Myofibrosarcoma;
炎症性肌纤维母细胞瘤和低度恶性肌纤维母细胞肉瘤的临床病理与分子遗传学研究