"mutation estimators" trang 3 - tải miễn phí từ tailieuXANH
Targeting TKI resistance in non - small cell lung cancer patients caused by secondary EGFR T790m mutation

Targeting TKI resistance in non - small cell lung cancer patients caused by secondary EGFR T790m mutation
9    85    0
Inhibition of N822K T>A mutation-induced constitutive c-KIT activation in AML cells triggers apoptotic and autophagic pathways leading to death

Inhibition of N822K T>A mutation-induced constitutive c-KIT activation in AML cells triggers apoptotic and autophagic pathways leading to death
9    44    0
Transgenic expression of a venous malformation related mutation, TIE2-R849W, significantly induces multiple malformations of Zebrafish

Transgenic expression of a venous malformation related mutation, TIE2-R849W, significantly induces multiple malformations of Zebrafish
10    41    0
An alternative differential evolution algorithm for global optimization

An alternative differential evolution algorithm for global optimization
17    82    0
Evaluating the prognostic value of ERCC1 and thymidylate synthase expression and the epidermal growth factor receptor mutation status in adenocarcinoma non-small-cell lung cancer

Evaluating the prognostic value of ERCC1 and thymidylate synthase expression and the epidermal growth factor receptor mutation status in adenocarcinoma non-small-cell lung cancer
8    44    0
Impact of JAK2V617F mutation burden on disease phenotype in Chinese patients with JAK2V617F-positive Polycythemia vera (PV) and Essential thrombocythemia (ET)

Impact of JAK2V617F mutation burden on disease phenotype in Chinese patients with JAK2V617F-positive Polycythemia vera (PV) and Essential thrombocythemia (ET)
7    42    0
In vitro inductions of gamma ray mutation for fusarium wilt resistance and characterization of mutants in regionally grown banana cultiva

In vitro inductions of gamma ray mutation for fusarium wilt resistance and characterization of mutants in regionally grown banana cultiva
13    46    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    53    1
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    70    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    75    0
A de novo ANK1 mutation associated to hereditary spherocytosis: A case report

A de novo ANK1 mutation associated to hereditary spherocytosis: A case report
5    64    0
A case report of reversible generalized seizures in a patient with Waardenburg syndrome associated with a novel nonsense mutation in the penultimate exon of SOX10

A case report of reversible generalized seizures in a patient with Waardenburg syndrome associated with a novel nonsense mutation in the penultimate exon of SOX10
4    48    0
A novel compound heterozygous mutation of the SMARCAL1 gene leading to mild Schimke immune-osseous dysplasia: A case report

A novel compound heterozygous mutation of the SMARCAL1 gene leading to mild Schimke immune-osseous dysplasia: A case report
6    68    0
A novel fibrillin-1 gene missense mutation associated with neonatal Marfan syndrome: A case report and review of the mutation spectrum

A novel fibrillin-1 gene missense mutation associated with neonatal Marfan syndrome: A case report and review of the mutation spectrum
6    55    0
Mitochondrial mutation m.1555A>G as a risk factor for failed newborn hearing screening in a large cohort of preterm infants

Mitochondrial mutation m.1555A>G as a risk factor for failed newborn hearing screening in a large cohort of preterm infants
5    61    0
A novel Bruton’s tyrosine kinase gene (BTK) missense mutation in a Chinese family with X-linked agammaglobulinemia

A novel Bruton’s tyrosine kinase gene (BTK) missense mutation in a Chinese family with X-linked agammaglobulinemia
5    50    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    84    0
M1 Biological Injuries: Indicators for M2 macro - and micro-mutation in mungbean [Vigna radiata (L.) Wilczek]

M1 Biological Injuries: Indicators for M2 macro - and micro-mutation in mungbean [Vigna radiata (L.) Wilczek]
12    63    0
Selection of genotype and mutagens in M1 generation for establishment of mutation breeding programme in mungbean [Vigna radiata (L.) Wilczek]

Selection of genotype and mutagens in M1 generation for establishment of mutation breeding programme in mungbean [Vigna radiata (L.) Wilczek]
16    50    0
Mutation-induced polygenic variability and early prediction of high yielding mutants in greengram [Vigna radiata (L.) wilczek]

Mutation-induced polygenic variability and early prediction of high yielding mutants in greengram [Vigna radiata (L.) wilczek]
9    55    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.