"gene mutation" trang 4 - tải miễn phí từ tailieunhanh
Epidermal growth factor receptor gene mutations in patients with lung adenocarcinoma differ by frequency and type between Uighur and Han ethnic groups in Xinjiang Autonomous Region

Epidermal growth factor receptor gene mutations in patients with lung adenocarcinoma differ by frequency and type between Uighur and Han ethnic groups in Xinjiang Autonomous Region
5    10    1
Epidermal nevus syndrome with the mutation of PTCH1 gene and cerebral infarction: A case report and review of the literature

Epidermal nevus syndrome with the mutation of PTCH1 gene and cerebral infarction: A case report and review of the literature
5    1    1
Identification of the causative mutation in the ITGB2 gene in a LAD1 patient by whole exome sequencing

Identification of the causative mutation in the ITGB2 gene in a LAD1 patient by whole exome sequencing
7    1    1
Investigation of exon20 PIK3CA gene mutation in plasma of hormone receptor positive breast cancer patients

Investigation of exon20 PIK3CA gene mutation in plasma of hormone receptor positive breast cancer patients
9    1    1
Moderate phenotype of a congenital myasthenic syndrome type 19 caused by mutation of the COL13A1 gene: A case report

Moderate phenotype of a congenital myasthenic syndrome type 19 caused by mutation of the COL13A1 gene: A case report
3    15    1
Next generation sequencing identifies a pathogenic mutation of WFS1 gene in a Moroccan family with Wolfram syndrome: A case report

Next generation sequencing identifies a pathogenic mutation of WFS1 gene in a Moroccan family with Wolfram syndrome: A case report
5    19    1
Novel technique for rapid detection of a-globin gene mutations and deletions

Novel technique for rapid detection of a-globin gene mutations and deletions
8    67    0
Mutation analysis of EGFR and FGFR gene in glioblastoma patients in Vietnam

Mutation analysis of EGFR and FGFR gene in glioblastoma patients in Vietnam
6    74    0
Genetic investigation confirmed the clinical phenotype of congenital chloride diarrhea in a Hungarian patient: A case report

Genetic investigation confirmed the clinical phenotype of congenital chloride diarrhea in a Hungarian patient: A case report
4    92    0
Mutation allele frequency threshold does not affect prognostic analysis using nextgeneration sequencing in oral squamous cell carcinoma

Mutation allele frequency threshold does not affect prognostic analysis using nextgeneration sequencing in oral squamous cell carcinoma
10    77    1
IMAGENE trial: Multicenter, proof-of-concept, phase II study evaluating the efcacy and safety of combination therapy of niraparib with PD-1 inhibitor in solid cancer patients with homologous recombination repair genes mutation

IMAGENE trial: Multicenter, proof-of-concept, phase II study evaluating the efcacy and safety of combination therapy of niraparib with PD-1 inhibitor in solid cancer patients with homologous recombination repair genes mutation
6    1    1
A SHOX2 loss-of-function mutation underlying familial atrial fibrillation

A SHOX2 loss-of-function mutation underlying familial atrial fibrillation
9    90    0
Gillespie syndrome in a South Asian child: A case report with confirmation of a heterozygous mutation of the ITPR1 gene and review of the clinical and molecular features

Gillespie syndrome in a South Asian child: A case report with confirmation of a heterozygous mutation of the ITPR1 gene and review of the clinical and molecular features
5    36    0
The effect of a germline mutation in the APC gene on β-catenin in human embryonic stem cells

The effect of a germline mutation in the APC gene on β-catenin in human embryonic stem cells
13    46    1
Direct sequencing of β-globin gene reveals a rare combination of two exonic and two intronic variants in a β-thalassemia major patient: A case report

Direct sequencing of β-globin gene reveals a rare combination of two exonic and two intronic variants in a β-thalassemia major patient: A case report
5    1    1
Mutation of the RDR1 gene caused genome-wide changes in gene expression, regional variation in small RNA clusters and localized alteration in DNA methylation in rice

Mutation of the RDR1 gene caused genome-wide changes in gene expression, regional variation in small RNA clusters and localized alteration in DNA methylation in rice
12    70    0
Báo cáo y học:

Báo cáo y học: "A novel mutation in the ADA gene causing severe combined immunodeficiency in an Arab patient: a case report"
5    70    0
Báo cáo khoa học: K182G substitution in DevR or C8G mutation in the Dev box impairs protein–DNA interaction and abrogates DevR-mediated gene induction in Mycobacterium tuberculosis

Báo cáo khoa học: K182G substitution in DevR or C8G mutation in the Dev box impairs protein–DNA interaction and abrogates DevR-mediated gene induction in Mycobacterium tuberculosis
9    62    0
Báo cáo sinh học:

Báo cáo sinh học: " A mutation in the MATP gene causes the cream coat colour in the horse"
15    28    0
Báo cáo sinh học:

Báo cáo sinh học: "A mutation in the LAMC2 gene causes the Herlitz junctional epidermolysis bullosa (H-JEB) in two French draft horse breeds"
8    34    0