Specific mutations trang 1 tải miễn phí từ TAILIEUCHUNG

"Specific mutations" trang 1 - tải miễn phí từ Tailieuchung

Detection of EGFR mutations in liquid biopsy samples using allele-specific quantitative PCR: A comparative real-world evaluation of two popular diagnostic systems

Detection of EGFR mutations in liquid biopsy samples using allele-specific quantitative PCR: A comparative real-world evaluation of two popular diagnostic systems

7 41 2

Whole exome sequencing of microdissected splenic marginal zone lymphoma: A study to discover novel tumor-specific mutations

Whole exome sequencing of microdissected splenic marginal zone lymphoma: A study to discover novel tumor-specific mutations

10 28 1

A site specific model and analysis of the neutral somatic mutation rate in whole-genome cancer data

A site specific model and analysis of the neutral somatic mutation rate in whole-genome cancer data

15 42 1

Báo cáo hóa học:

Báo cáo hóa học: " Incidence of the V600K mutation among melanoma patients with BRAF mutations, and potential therapeutic response to the specific BRAF inhibitor PLX4032"

3 41 0

Báo cáo hóa học:

Báo cáo hóa học: " Detection of EGFR mutations with mutation-specific antibodies in stage IV non-small-cell lung cancer"

8 39 0

Báo cáo y học: "Selected amino acid mutations in HIV-1 B subtype gp41 are Associated with Specific gp120V3 signatures in the regulation of CoReceptor usag"

11 26 0

báo cáo khoa học:

báo cáo khoa học: "Loss-of-function mutations affecting a specific Glycine max R2R3 MYB transcription factor result in brown hilum and brown seed coats"

12 50 0

Two novel mutations in the ALPL gene of unrelated Chinese children with Hypophosphatasia: Case reports and literature review

Two novel mutations in the ALPL gene of unrelated Chinese children with Hypophosphatasia: Case reports and literature review

8 49 0

Direct stacking of sequence-specific nuclease-induced mutations to produce high oleic and low linolenic soybean oil

Direct stacking of sequence-specific nuclease-induced mutations to produce high oleic and low linolenic soybean oil

8 49 0

Tissue-specific impact of stem-loops and quadruplexes on cancer breakpoints formation

Tissue-specific impact of stem-loops and quadruplexes on cancer breakpoints formation

17 98 0

Promoter hypermethylation of HS3ST2, SEPTIN9 and SLIT2 combined with FGFR3 mutations as a sensitive/specific urinary assay for diagnosis and surveillance in patients with low or high-risk non-muscleinvasive bladder cancer

Promoter hypermethylation of HS3ST2, SEPTIN9 and SLIT2 combined with FGFR3 mutations as a sensitive/specific urinary assay for diagnosis and surveillance in patients with low or high-risk non-muscleinvasive bladder cancer

9 71 1

Genomics driven-oncology: Challenges and perspectives

Genomics driven-oncology: Challenges and perspectives

3 39 1

Screening of exon 11 of BRCA1 gene using the high resolution melting approach for diagnosis in Moroccan breast cancer patients

Screening of exon 11 of BRCA1 gene using the high resolution melting approach for diagnosis in Moroccan breast cancer patients

5 29 1

TarPan: An easily adaptable targeted sequencing panel viewer for research and clinical use

TarPan: An easily adaptable targeted sequencing panel viewer for research and clinical use

12 27 1

Fagin: Synteny-based phylostratigraphy and finer classification of young genes

Fagin: Synteny-based phylostratigraphy and finer classification of young genes

14 42 1

Cancerouspdomains: Comprehensive analysis of cancer type-specific recurrent somatic mutations in proteins and domains

Cancerouspdomains: Comprehensive analysis of cancer type-specific recurrent somatic mutations in proteins and domains

18 35 1

Discovery and characterization of the evolution, variation and functions of diversity-generating retroelements using thousands of genomes and metagenomes

Discovery and characterization of the evolution, variation and functions of diversity-generating retroelements using thousands of genomes and metagenomes

11 38 1

Targeting the autosomal Ceratitis capitata transformer gene using Cas9 or dCas9 to masculinize XX individuals without inducing mutations

Targeting the autosomal Ceratitis capitata transformer gene using Cas9 or dCas9 to masculinize XX individuals without inducing mutations

11 2 1

Computational inference of cancer-specific vulnerabilities in clinical samples

Computational inference of cancer-specific vulnerabilities in clinical samples

24 38 1

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 33 0

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