Gene mutation trang 1 tải miễn phí từ TAILIEUCHUNG

"Gene mutation" trang 1 - tải miễn phí từ Tailieuchung

MUFFINN: Cancer gene discovery via network analysis of somatic mutation data

MUFFINN: Cancer gene discovery via network analysis of somatic mutation data

16 52 1

Case report: Maple syrup urine disease with a novel DBT gene mutation

Case report: Maple syrup urine disease with a novel DBT gene mutation

5 51 0

Epidermal growth factor receptor gene mutation status in pure squamous-cell lung cancer in Chinese patients

Epidermal growth factor receptor gene mutation status in pure squamous-cell lung cancer in Chinese patients

6 41 1

Correlation between EGFR gene mutation, cytologic tumor markers, 18F-FDG uptake in non-small cell lung cancer

Correlation between EGFR gene mutation, cytologic tumor markers, 18F-FDG uptake in non-small cell lung cancer

8 43 1

Lecture Genetics: From genes to genomes - Chapter 7: Anatomy and function of a gene: dissection through mutation

Lecture Genetics: From genes to genomes - Chapter 7: Anatomy and function of a gene: dissection through mutation

72 94 0

PHD thesis abstrac: Isolation, point mutation of P5CS gene conferring drought tolerance and transformion into soybean varieties of Vietnam

PHD thesis abstrac: Isolation, point mutation of P5CS gene conferring drought tolerance and transformion into soybean varieties of Vietnam

21 50 0

Research on clinical characteristics, immunohistochemistry and mutation of BRAF gene in patients with thyroid carcinoma

Research on clinical characteristics, immunohistochemistry and mutation of BRAF gene in patients with thyroid carcinoma

9 62 0

Identification of a novel splicing mutation in the SLC25A13 gene from a patient with NICCD: A case report

Identification of a novel splicing mutation in the SLC25A13 gene from a patient with NICCD: A case report

5 76 0

Recurrent exercise-induced acute kidney injury by idiopathic renal hypouricemia with a novel mutation in the SLC2A9 gene and literature review

Recurrent exercise-induced acute kidney injury by idiopathic renal hypouricemia with a novel mutation in the SLC2A9 gene and literature review

7 51 0

Single point mutation in adeno-associated viral vectors -DJ capsid leads to improvement for gene delivery in vivo

Single point mutation in adeno-associated viral vectors -DJ capsid leads to improvement for gene delivery in vivo

8 38 0

Identification of p.HIS119LEU mutation in the G6PC gene of a Vietnamese patient with glycogen storage disease type Ia

Identification of p.HIS119LEU mutation in the G6PC gene of a Vietnamese patient with glycogen storage disease type Ia

8 38 1

Clinicopathological features and EGFR gene mutation status in elderly patients with resected non–small-cell lung cancer

Clinicopathological features and EGFR gene mutation status in elderly patients with resected non–small-cell lung cancer

7 28 1

Multi gene mutation signatures in colorectal cancer patients: Predict for the diagnosis, pathological classification, staging and prognosis

Multi gene mutation signatures in colorectal cancer patients: Predict for the diagnosis, pathological classification, staging and prognosis

16 21 1

Identification of a de novo mutation in KRT5 gene underlying epidermolysis bullosa simplex by whole exome sequencing in a Vietnamese patient

Identification of a de novo mutation in KRT5 gene underlying epidermolysis bullosa simplex by whole exome sequencing in a Vietnamese patient

6 22 1

The mutation of BCOR is highly recurrent and oncogenic in mature T-cell lymphoma

The mutation of BCOR is highly recurrent and oncogenic in mature T-cell lymphoma

11 29 1

TBX20 loss-of-function mutation responsible for familial tetralogy of Fallot or sporadic persistent truncus arteriosus

TBX20 loss-of-function mutation responsible for familial tetralogy of Fallot or sporadic persistent truncus arteriosus

10 68 0

Revalence and spectrum of TBX5 mutation in patients with lone atrial fibrillation

Revalence and spectrum of TBX5 mutation in patients with lone atrial fibrillation

8 80 0

Study on rate and some risk factors for egfr mutation in 152 patients with lung adenocarcinoma at Bachmai hospital

Study on rate and some risk factors for egfr mutation in 152 patients with lung adenocarcinoma at Bachmai hospital

5 64 0

Lethal perinatal hypophosphatasia caused by a novel compound heterozygous mutation: A case report

Lethal perinatal hypophosphatasia caused by a novel compound heterozygous mutation: A case report

5 33 0

TRMA syndrome with a severe phenotype, cerebral infarction, and novel compound heterozygous SLC19A2 mutation: A case report

TRMA syndrome with a severe phenotype, cerebral infarction, and novel compound heterozygous SLC19A2 mutation: A case report

6 45 0

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