"Disease mutations" trang 1 - tải miễn phí từ tailieuXANH
New insights into the generation and role of de novo mutations in health and disease

New insights into the generation and role of de novo mutations in health and disease
19    201    2
UMOD gene mutations in Chinese patients with autosomal dominant tubulointerstitial kidney disease: A pediatric case report and literature review

UMOD gene mutations in Chinese patients with autosomal dominant tubulointerstitial kidney disease: A pediatric case report and literature review
5    82    0
iRegNet3D: Three-dimensional integrated regulatory network for the genomic analysis of coding and non-coding disease mutations

iRegNet3D: Three-dimensional integrated regulatory network for the genomic analysis of coding and non-coding disease mutations
16    150    2
Investigation of somatic NKX2-5 mutations in Chinese children with congenital heart disease

Investigation of somatic NKX2-5 mutations in Chinese children with congenital heart disease
6    50    0
Clinical and molecular report of novel GALC mutations in Moroccan patient with Krabbe disease: Case report

Clinical and molecular report of novel GALC mutations in Moroccan patient with Krabbe disease: Case report
4    53    0
Whole exome sequencing coupled with unbiased functional analysis reveals new Hirschsprung disease genes

Whole exome sequencing coupled with unbiased functional analysis reveals new Hirschsprung disease genes
13    29    2
Microsatellite instability and mutations in BRAF and KRAS are significant predictors of disseminated disease in colon cancer

Microsatellite instability and mutations in BRAF and KRAS are significant predictors of disseminated disease in colon cancer
11    62    0
Báo cáo sinh học:

Báo cáo sinh học: "Pitfalls in the phylogenomic evaluation of human disease-causing mutations"
5    48    0
Báo cáo y học:

Báo cáo y học: " A new category of autoinflammatory disease associated with NOD2 gene mutations"
21    38    0
Báo cáo y học:

Báo cáo y học: "‘CFTR-opathies’: disease phenotypes associated with cystic fibrosis transmembrane regulator gene mutations"
5    45    0
Báo cáo y học:

Báo cáo y học: "Three novel beta-galactosidase gene mutations in Han Chinese patients with GM1 gangliosidosis are correlated with disease severity"
8    40    0
Báo cáo y học:

Báo cáo y học: " All that glitters is not gold - founder effects complicate associations of flu mutations to disease severity"
7    29    0
DIAGNOSIS AND TREATMENT OF PARKINSON’S DISEASE

DIAGNOSIS AND TREATMENT OF PARKINSON’S DISEASE
274    61    0
Báo cáo khoa học: Functional analysis of disease-causing mutations in human UDP-galactose 4-epimerase

Báo cáo khoa học: Functional analysis of disease-causing mutations in human UDP-galactose 4-epimerase
8    39    0
Báo cáo khoa học: Functional analysis of disease-causing mutations in human galactokinase

Báo cáo khoa học: Functional analysis of disease-causing mutations in human galactokinase
8    38    0
Báo cáo khoa học: Disease-related mutations in cytochrome c oxidase studied in yeast and bacterial models

Báo cáo khoa học: Disease-related mutations in cytochrome c oxidase studied in yeast and bacterial models
9    27    0
Báo cáo Y học: Introducing Wilson disease mutations into the zinc-transporting P-type ATPase ofEscherichia coli The mutation P634L in theÔhingeÕ motif (GDGXNDXP) perturbs the formation of the E2P state

Báo cáo Y học: Introducing Wilson disease mutations into the zinc-transporting P-type ATPase ofEscherichia coli The mutation P634L in theÔhingeÕ motif (GDGXNDXP) perturbs the formation of the E2P state
8    28    0
Báo cáo Y học: Effect of the disease-causing mutations identified in human ribonuclease (RNase) H2 on the activities and stabilities of yeast RNase H2 and archaeal RNase HII

Báo cáo Y học: Effect of the disease-causing mutations identified in human ribonuclease (RNase) H2 on the activities and stabilities of yeast RNase H2 and archaeal RNase HII
14    188    0
Báo cáo Y học: Toxicity of novel C-terminal prion protein fragments and peptides harbouring disease-related C-terminal mutations

Báo cáo Y học: Toxicity of novel C-terminal prion protein fragments and peptides harbouring disease-related C-terminal mutations
10    37    0
Compound heterozygous POMGNT1 mutations leading to muscular dystrophydystroglycanopathy type A3: A case report

Compound heterozygous POMGNT1 mutations leading to muscular dystrophydystroglycanopathy type A3: A case report
8    83    0
Đã phát hiện trình chặn quảng cáo AdBlock
Trang web này phụ thuộc vào doanh thu từ số lần hiển thị quảng cáo để tồn tại. Vui lòng tắt trình chặn quảng cáo của bạn hoặc tạm dừng tính năng chặn quảng cáo cho trang web này.