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Articles (16)

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1-10 of 16 results for non-sense mutation

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Select article: Genotype-Phenotype Effects of Bmpr2 Mutations on Disease Severity in Mouse Models of Pulmonary Hypertension

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Research article

First published 2016-12

Genotype-Phenotype Effects of Bmpr2 Mutations on Disease Severity in Mouse Models of Pulmonary Hypertension

Andrea L. Frump, Arunima Datta, Sampa Ghose [...]

Pulmonary Circulation

Select article: Clinical presentations and molecular basis of complement C1r deficiency in a male African–American patient with systemic lupus erythematosus

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Research article

First published 2011-10

Clinical presentations and molecular basis of complement C1r deficiency in a male African–American patient with systemic lupus erythematosus

YL Wu, BP Brookshire, RR Verani [...]

Lupus

Select article: A Novel Mutation of the ARX Gene in a Male With Nonsyndromic Mental Retardation

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Other

First published 2007-06

A Novel Mutation of the ARX Gene in a Male With Nonsyndromic Mental Retardation

Matthew M. Troester, Tamara Trachtenberg, Vinodh Narayanan

Journal of Child Neurology

Select article: Antisense Oligonucleotides to p53 Tumor Suppressor Suppress the Induction of Apoptosis by Epidermal Growth Factor in NCI-H 596 Human Lung Cancer Cells

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Research article

First published 1997-04

Antisense Oligonucleotides to p53 Tumor Suppressor Suppress the Induction of Apoptosis by Epidermal Growth Factor in NCI-H 596 Human Lung Cancer Cells

Yoichi Murayama, Sankichi Horiuchi

Nucleic Acid Therapeutics

Select article: Characterization of Recessive Severe Type 1 and 3 von Willebrand Disease (VWD),Asymptomatic Heterozygous Carriers Versus Bloodgroup O-Related von Willebrand Factor Deficiency,and Dominant Type 1 VWD

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Research article

First published 2006-07

Characterization of Recessive Severe Type 1 and 3 von Willebrand Disease (VWD),Asymptomatic Heterozygous Carriers Versus Bloodgroup O-Related von Willebrand Factor Deficiency,and Dominant Type 1 VWD

Jan Jacques Michiels, Zwi Berneman, Alain Gadisseur [...]

Clinical and Applied Thrombosis/Hemostasis

Select article: Affective Pedagogies,Equine-assisted Experiments and Posthuman Leadership

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Research article

First published 2019-3

Affective Pedagogies,Equine-assisted Experiments and Posthuman Leadership

Dorthe Staunæs, Sverre Raffnsøe

Body & Society

Select article: A Novel Splice-Acceptor Site Mutation in GRN (c.709-2 A>T) Causes Frontotemporal Dementia Spectrum in a Large Family from Southern Italy

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Research article

First published 2016-7-13

A Novel Splice-Acceptor Site Mutation in GRN (c.709-2 A>T) Causes Frontotemporal Dementia Spectrum in a Large Family from Southern Italy

Celeste Sassi, Rosa Capozzo, Raphael Gibbs [...]

Journal of Alzheimer’s Disease

Select article: Labour outcomes in siblings with channelopathy associated insensitivity to pain due to bi-alleleic SCN9A mutations

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Case report

First published 2012-12

Labour outcomes in siblings with channelopathy associated insensitivity to pain due to bi-alleleic SCN9A mutations

A Haestier, S Hamilton, R J Chilvers

Obstetric Medicine

Select article: H-trees: a Model of Evolutionary Scenarios with Horizontal Gene Transfer

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Research article

First published 2010-9

H-trees: a Model of Evolutionary Scenarios with Horizontal Gene Transfer

Paweł Górecki

Fundamenta Informaticae

Select article: Indeterminate Subjects,Irreducible Worlds

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Research article

First published 2017-9

Indeterminate Subjects,Irreducible Worlds

Kathryn Yusoff

Body & Society

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