"genetic mutation for drug resistance" trang 2 - tải miễn phí từ tailieuXANH
Genetic investigation confirmed the clinical phenotype of congenital chloride diarrhea in a Hungarian patient: A case report

Genetic investigation confirmed the clinical phenotype of congenital chloride diarrhea in a Hungarian patient: A case report
4    85    0
Báo cáo y học:

Báo cáo y học: "Deafblindness in French Canadians from Quebec: a predominant founder mutation in the USH1C gene provides the first genetic link with the Acadian population"
1    50    0
Induction of variability through mutagenesis in opium poppy (Papaver somniferum L.)

Induction of variability through mutagenesis in opium poppy (Papaver somniferum L.)
11    44    0
Induction of salt-tolerant potato (Solanum tuberosum L.) mutants with gamma irradiation and characterization of genetic variations via RAPD-PCR analysis

Induction of salt-tolerant potato (Solanum tuberosum L.) mutants with gamma irradiation and characterization of genetic variations via RAPD-PCR analysis
8    57    0
Study on application of multiplex ligation dependent probe amplification (MLPA) assay in molecular diagnosis of retinoblastoma

Study on application of multiplex ligation dependent probe amplification (MLPA) assay in molecular diagnosis of retinoblastoma
7    70    0
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
6    44    0
A two-headed calf – Case report

A two-headed calf – Case report
3    58    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
7    45    0
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    68    0
Uncommon clinical presentation of cystic fibrosis in a patient homozygous for a rare CFTR mutation: A case report

Uncommon clinical presentation of cystic fibrosis in a patient homozygous for a rare CFTR mutation: A case report
6    48    0
Improved CRISPR/Cas9 gene editing by fluorescence activated cell sorting of green fluorescence protein tagged protoplasts

Improved CRISPR/Cas9 gene editing by fluorescence activated cell sorting of green fluorescence protein tagged protoplasts
12    66    0
Molecular genetic characterization reveals linear tumor evolution in a pulmonary sarcomatoid carcinomas patient with a novel PHF20-NTRK1 fusion: A case report

Molecular genetic characterization reveals linear tumor evolution in a pulmonary sarcomatoid carcinomas patient with a novel PHF20-NTRK1 fusion: A case report
5    54    0
Expression of C-terminal ALK, RET, or ROS1 in lung cancer cells with or without fusion

Expression of C-terminal ALK, RET, or ROS1 in lung cancer cells with or without fusion
10    46    0
BRAF V600E mutation and 9p21: CDKN2A/B and MTAP co-deletions - Markers in the clinical stratification of pediatric gliomas

BRAF V600E mutation and 9p21: CDKN2A/B and MTAP co-deletions - Markers in the clinical stratification of pediatric gliomas
10    70    0
GENESIS: A French national resource to study the missing heritability of breast cancer

GENESIS: A French national resource to study the missing heritability of breast cancer
9    63    0
Germline mutation in the RAD51B gene confers predisposition to breast cancer

Germline mutation in the RAD51B gene confers predisposition to breast cancer
8    58    0
Isolation of high-yielding mutants through EMS-induced mutagenesis in linseed (Linum usitatissimum L.)

Isolation of high-yielding mutants through EMS-induced mutagenesis in linseed (Linum usitatissimum L.)
8    44    0
Age-dependent ferritin elevations and HFE C282Y mutation as risk factors for symptomatic knee osteoarthritis in males: A longitudinal cohort study

Age-dependent ferritin elevations and HFE C282Y mutation as risk factors for symptomatic knee osteoarthritis in males: A longitudinal cohort study
9    51    1
Homozygous truncating NEK10 mutation, associated with primary ciliary dyskinesia: A case report

Homozygous truncating NEK10 mutation, associated with primary ciliary dyskinesia: A case report
5    57    1
MicroRNA-124-3p suppresses mouse lip mesenchymal cell proliferation through the regulation of genes associated with cleft lip in the mouse

MicroRNA-124-3p suppresses mouse lip mesenchymal cell proliferation through the regulation of genes associated with cleft lip in the mouse
17    145    2
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