"Function mutation" trang 1 - tải miễn phí từ tailieuXANH
The secondary KIT mutation p.Ala510Val in a cutaneous mast cell tumour carrying the activating mutation p.Asn508Ile confers resistance to masitinib in dogs

The secondary KIT mutation p.Ala510Val in a cutaneous mast cell tumour carrying the activating mutation p.Asn508Ile confers resistance to masitinib in dogs
9    18    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    72    1
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
Genome analysis and pleiotropy assessment using causal networks with loss of function mutation and metabolomics

Genome analysis and pleiotropy assessment using causal networks with loss of function mutation and metabolomics
16    59    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    45    0
Báo cáo y học:

Báo cáo y học: " Loss of function mutation in toll-like receptor-4 does not offer protection against obesity and insulin resistance induced by a diet high in trans fat in miceg"
7    34    0
Báo cáo y học:

Báo cáo y học: "Loss of function mutation in toll-like receptor-4 does not offer protection against obesity and insulin resistance induced by a diet high in trans fat in mice"
7    36    0
Báo cáo Y học: A novel gain-of-function mutation of the integrin a2 VWFA domain

Báo cáo Y học: A novel gain-of-function mutation of the integrin a2 VWFA domain
9    34    0
A SHOX2 loss-of-function mutation underlying familial atrial fibrillation

A SHOX2 loss-of-function mutation underlying familial atrial fibrillation
9    56    0
MEF2C loss-of-function mutation contributes to congenital heart defects

MEF2C loss-of-function mutation contributes to congenital heart defects
11    252    0
The loss-of-function GLABROUS 3 mutation in cucumber is due to LTR-retrotransposon insertion in a class IV HD-ZIP transcription factor gene CsGL3 that is epistatic over CsGL1

The loss-of-function GLABROUS 3 mutation in cucumber is due to LTR-retrotransposon insertion in a class IV HD-ZIP transcription factor gene CsGL3 that is epistatic over CsGL1
15    44    0
The curious case of Gαs gain-of-function in neoplasia

The curious case of Gαs gain-of-function in neoplasia
15    50    0
SomInaClust: Detection of cancer genes based on somatic mutation patterns of inactivation and clustering

SomInaClust: Detection of cancer genes based on somatic mutation patterns of inactivation and clustering
12    58    0
Challenging the diagnosis of Cystic Fibrosis in a patient carrying the 186-8T/C allelic variant in the CF Transmembrane Conductance Regulator gene

Challenging the diagnosis of Cystic Fibrosis in a patient carrying the 186-8T/C allelic variant in the CF Transmembrane Conductance Regulator gene
7    36    1
MAESTRO - multi agent stability prediction upon point mutations

MAESTRO - multi agent stability prediction upon point mutations
13    56    0
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