gene mutation trang 5 tải miễn phí từ TAILIEUCHUNG

"gene mutation" trang 5 - tải miễn phí từ Tailieuchung

Modification by compositional antimutagens of the key stages of a mutation process

Modification by compositional antimutagens of the key stages of a mutation process

7 56 0

Characteristics of the pathological, immunohistochemical findings and EGFR gene mutation on biopsies in 193 lung cancer patients

Characteristics of the pathological, immunohistochemical findings and EGFR gene mutation on biopsies in 193 lung cancer patients

8 78 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 45 0

Plasmodium falciparum treated with artemisinin-based combined therapy exhibits enhanced mutation, heightened cortisol and TNF-α induction

Plasmodium falciparum treated with artemisinin-based combined therapy exhibits enhanced mutation, heightened cortisol and TNF-α induction

9 65 0

MEF2C loss-of-function mutation contributes to congenital heart defects

MEF2C loss-of-function mutation contributes to congenital heart defects

11 62 0

A two-headed calf – Case report

A two-headed calf – Case report

3 73 0

Congenital emphysematous lung disease associated with a novel Filamin A mutation: Case report and literature review

Congenital emphysematous lung disease associated with a novel Filamin A mutation: Case report and literature review

10 81 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 60 0

EIF2AK3 novel mutation in a child with early-onset diabetes mellitus, a case report

EIF2AK3 novel mutation in a child with early-onset diabetes mellitus, a case report

4 46 0

Intermittent low platelet counts hampering diagnosis of X-linked thrombocytopenia in children: Report of two unrelated cases and a novel mutation in the gene coding for the Wiskott-Aldrich syndrome protein

Intermittent low platelet counts hampering diagnosis of X-linked thrombocytopenia in children: Report of two unrelated cases and a novel mutation in the gene coding for the Wiskott-Aldrich syndrome protein

6 37 0

Recurrent c.G1636A (p.G546S) mutation of COL2A1 in a Chinese family with skeletal dysplasia and different metaphyseal changes: A case report

Recurrent c.G1636A (p.G546S) mutation of COL2A1 in a Chinese family with skeletal dysplasia and different metaphyseal changes: A case report

7 60 0

GM2 gangliosidosis AB variant: Novel mutation from India – a case report with a review

GM2 gangliosidosis AB variant: Novel mutation from India – a case report with a review

5 34 0

Mandibuloacral dysplasia type A-associated progeria caused by homozygous LMNA mutation in a family from Southern China

Mandibuloacral dysplasia type A-associated progeria caused by homozygous LMNA mutation in a family from Southern China

8 80 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 68 0

Cyclic neutropenia with a novel gene mutation presenting with a necrotizing soft tissue infection and severe sepsis: Case report

Cyclic neutropenia with a novel gene mutation presenting with a necrotizing soft tissue infection and severe sepsis: Case report

4 76 0

Lethal course of meconium ileus in preterm twins revealing a novel cystic fibrosis mutation (p.Cys524Tyr)

Lethal course of meconium ileus in preterm twins revealing a novel cystic fibrosis mutation (p.Cys524Tyr)

5 89 0

Sequential and counter-selectable cassettes for fission yeast

Sequential and counter-selectable cassettes for fission yeast

15 51 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 60 0

Eosinophilic colitis in a boy with a novel XIAP mutation: A case report

Eosinophilic colitis in a boy with a novel XIAP mutation: A case report

7 77 0

A case report of one vasovagal syncope patient with third-degree atrioventricular block caused by SCN5A gene mutation and literature review

A case report of one vasovagal syncope patient with third-degree atrioventricular block caused by SCN5A gene mutation and literature review

5 26 0

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