"genetic mutations" trang 2 - tải miễn phí từ tailieunhanh
Screening of BRCA1/2 genes mutations and copy number variations in patients with high risk for hereditary breast and ovarian cancer syndrome (HBOC)

Screening of BRCA1/2 genes mutations and copy number variations in patients with high risk for hereditary breast and ovarian cancer syndrome (HBOC)
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Personalized prostate cancer screening among men with high risk genetic predisposition- study protocol for a prospective cohort study

Personalized prostate cancer screening among men with high risk genetic predisposition- study protocol for a prospective cohort study
9    40    1
Summary of Biology Doctoral Thesis: Study on polymorphisms mutations of CYP2C9, CYP2C19, CYP3A5 and CYP2D6 cytochrome P450 in Kinh Vietnamese

Summary of Biology Doctoral Thesis: Study on polymorphisms mutations of CYP2C9, CYP2C19, CYP3A5 and CYP2D6 cytochrome P450 in Kinh Vietnamese
27    39    1
Induction of targeted, heritable mutations in barley and Brassica oleracea using RNA-guided Cas9 nuclease

Induction of targeted, heritable mutations in barley and Brassica oleracea using RNA-guided Cas9 nuclease
13    51    1
Selection plays the hand it was dealt: Evidence that human adaptation commonly targets standing genetic variation

Selection plays the hand it was dealt: Evidence that human adaptation commonly targets standing genetic variation
4    44    1
CRISPR/Cas9-mediated targeted chromosome elimination

CRISPR/Cas9-mediated targeted chromosome elimination
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A simple method to estimate the in-house limit of detection for genetic mutations with low allele frequencies in whole-exome sequencing analysis by next-generation sequencing

A simple method to estimate the in-house limit of detection for genetic mutations with low allele frequencies in whole-exome sequencing analysis by next-generation sequencing
10    20    1
Successful use of emapalumab in refractory hemophagocytic lymphohistiocytosis in a child with Chédiak–Higashi syndrome: A case report

Successful use of emapalumab in refractory hemophagocytic lymphohistiocytosis in a child with Chédiak–Higashi syndrome: A case report
7    1    1
Anesthetic care of a child harboring the KCNH2 gene

Anesthetic care of a child harboring the KCNH2 gene
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Small extrachromosomal circular DNA harboring targeted tumor suppressor gene mutations supports intratumor heterogeneity in mouse liver cancer induced by multiplexed CRISPR/Cas9

Small extrachromosomal circular DNA harboring targeted tumor suppressor gene mutations supports intratumor heterogeneity in mouse liver cancer induced by multiplexed CRISPR/Cas9
24    7    1
Genetic differentiation and intrinsic genomic features explain variation in recombination hotspots among cocoa tree populations

Genetic differentiation and intrinsic genomic features explain variation in recombination hotspots among cocoa tree populations
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Genetic and treatment profiles of patients with concurrent Epidermal Growth Factor Receptor (EGFR) and Anaplastic Lymphoma Kinase (ALK) mutations

Genetic and treatment profiles of patients with concurrent Epidermal Growth Factor Receptor (EGFR) and Anaplastic Lymphoma Kinase (ALK) mutations
8    23    1
Genetic etiologies of the electrical status epilepticus during

Genetic etiologies of the electrical status epilepticus during
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MUTATIONS IN HUMAN GENETIC DISEASE

MUTATIONS IN HUMAN GENETIC DISEASE
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Phenotypic and genetic characterization of a cohort of pediatric wilson disease patients

Phenotypic and genetic characterization of a cohort of pediatric wilson disease patients
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A novel UGT1A1 gene mutation causing severe unconjugated hyperbilirubinemia: A case report

A novel UGT1A1 gene mutation causing severe unconjugated hyperbilirubinemia: A case report
3    66    0
Association of rs2282679 A>C polymorphism in vitamin D binding protein gene with colorectal cancer risk and survival: Effect modification by dietary vitamin D intake

Association of rs2282679 A>C polymorphism in vitamin D binding protein gene with colorectal cancer risk and survival: Effect modification by dietary vitamin D intake
12    77    1
Common variants in the hERG (KCNH2) voltage-gated potassium channel are associated with altered fasting and glucose-stimulated plasma incretin and glucagon responses

Common variants in the hERG (KCNH2) voltage-gated potassium channel are associated with altered fasting and glucose-stimulated plasma incretin and glucagon responses
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