"gene mutation" trang 3 - tải miễn phí từ tailieunhanh
A germline mutation of CDKN2A and a novel RPLP1-C19MC fusion detected in a rare melanotic neuroectodermal tumor of infancy: A case report

A germline mutation of CDKN2A and a novel RPLP1-C19MC fusion detected in a rare melanotic neuroectodermal tumor of infancy: A case report
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Gene-guided Gefitinib switch maintenance therapy for patients with advanced EGFR mutation-positive Non-small cell lung cancer: An economic analysis

Gene-guided Gefitinib switch maintenance therapy for patients with advanced EGFR mutation-positive Non-small cell lung cancer: An economic analysis
11    56    1
Gene expression and immune infiltration in melanoma patients with different mutation burden

Gene expression and immune infiltration in melanoma patients with different mutation burden
12    25    1
Các loại đột biến đơn gene (single - gene mutation)

Các loại đột biến đơn gene (single - gene mutation)

6    137    1
Correlation of E-cadherin gene polymorphisms and epidermal growth factor receptor mutation in lung adenocarcinoma

Correlation of E-cadherin gene polymorphisms and epidermal growth factor receptor mutation in lung adenocarcinoma
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Functional analysis of a nonsyndromic hearing loss-associated mutation in the transmembrane II domain of the GJC3 gene

Functional analysis of a nonsyndromic hearing loss-associated mutation in the transmembrane II domain of the GJC3 gene
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Analysis of the relationship between the mutation site of the SLC39A4 gene and acrodermatitis enteropathica by reporting a rare Chinese twin: A case report and review of the literature

Analysis of the relationship between the mutation site of the SLC39A4 gene and acrodermatitis enteropathica by reporting a rare Chinese twin: A case report and review of the literature
7    77    0
Research characteristics of immunologic markers in pediatric acute lymphoblastic leukemia with genetic mutation in national institute of hematology and blood transfusion from 2016 to 2018

Research characteristics of immunologic markers in pediatric acute lymphoblastic leukemia with genetic mutation in national institute of hematology and blood transfusion from 2016 to 2018
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UMOD gene mutations in Chinese patients with autosomal dominant tubulointerstitial kidney disease: A pediatric case report and literature review

UMOD gene mutations in Chinese patients with autosomal dominant tubulointerstitial kidney disease: A pediatric case report and literature review
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A novel mutation of WFS1 gene in a Chinese patient with Wolfram syndrome: A case report

A novel mutation of WFS1 gene in a Chinese patient with Wolfram syndrome: A case report
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Clinical and molecular report of c.1331 + 1G > A mutation of the AAAS gene in a Moroccan family with Allgrove syndrome: A case report

Clinical and molecular report of c.1331 + 1G > A mutation of the AAAS gene in a Moroccan family with Allgrove syndrome: A case report
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A novel homozygous mutation in POLR3A gene causing 4H syndrome: A case report

A novel homozygous mutation in POLR3A gene causing 4H syndrome: A case report
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Mapping and identification of CsUp, a gene encoding an Auxilin-like protein, as a putative candidate gene for the upwardpedicel mutation (up) in cucumber

Mapping and identification of CsUp, a gene encoding an Auxilin-like protein, as a putative candidate gene for the upwardpedicel mutation (up) in cucumber
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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    43    1
Recurrent pneumothorax and intrapulmonary cavitary lesions in a male patient with vascular Ehlers-Danlos syndrome and a novel missense mutation in the COL3A1 gene: A case report

Recurrent pneumothorax and intrapulmonary cavitary lesions in a male patient with vascular Ehlers-Danlos syndrome and a novel missense mutation in the COL3A1 gene: A case report
7    28    1
A novel mutation of KCNQ2 gene in a patient with self-limited non-familial neonatal epilepsy: A case report

A novel mutation of KCNQ2 gene in a patient with self-limited non-familial neonatal epilepsy: A case report
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A new mechanism for a familiar mutation – bovine DGAT1 K232A modulates gene expression through multi-junction exon splice enhancement

A new mechanism for a familiar mutation – bovine DGAT1 K232A modulates gene expression through multi-junction exon splice enhancement
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Distinct esophageal adenocarcinoma molecular subtype has subtype-specific gene expression and mutation patterns

Distinct esophageal adenocarcinoma molecular subtype has subtype-specific gene expression and mutation patterns
12    29    1
Core promoter mutation contributes to abnormal gene expression in bladder cancer

Core promoter mutation contributes to abnormal gene expression in bladder cancer
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Predicting the most deleterious missense nsSNPs of the protein isoforms of the human HLA-G gene and in silico evaluation of their structural and functional consequences

Predicting the most deleterious missense nsSNPs of the protein isoforms of the human HLA-G gene and in silico evaluation of their structural and functional consequences
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