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Publications by E A Pierce

Human Neutrophil Cytochrome B Light Chain (P22-Phox). Gene Structure, Chromosomal Location, and Mutations in Cytochrome-Negative Autosomal Recessive Chronic Granulomatous Disease.

Journal of Clinical Investigation

Medicine

1990

English

Oligonucleotide-Directed Single-Base DNA Alterations in Mouse Embryonic Stem Cells

English

Related publications

Chronic Granulomatous Disease With Neutrophil Membrane Cytochrome B Deficiency: Demonstration by Immunochemical Staining With Monoclonal Antibody.

Tohoku Journal of Experimental Medicine

English

Cloning the Gene for an Inherited Human Disorder—chronic Granulomatous Disease—on the Basis of Its Chromosomal Location

Nature

Multidisciplinary

1986

English

Successful Lung Transplant for Bronchiectasis in an Adult Male With Autosomal Recessive Chronic Granulomatous Disease With a Novel NF1 Gene Mutation

Journal of Allergy and Clinical Immunology

Allergy

Immunology

2016

English

332. ZFN-Mediated Minigene or Dinucleotide Gene Correction of P47phox Deficient Autosomal Recessive Chronic Granulomatous Disease iPSC to Generate Oxidase Functional Neutrophils

English

Aspergillus Osteomyelitis in a Child Who Has P67-Phox-Deficient Chronic Granulomatous Disease.

Kurume Medical Journal

Medicine

1999

English

Mutations in the Nebulin Gene Associated With Autosomal Recessive Nemaline Myopathy

Proceedings of the National Academy of Sciences of the United States of America

Multidisciplinary

1999

English

Possible Application of Cytochrome B Gene for Human Identification = التطبيقات المحتملة لاستخدام الموقع الوراثي سيتوكروم ب ( Cytochrome B ) لتحديد الهوية البشرية

Arab Journal of Forensic Sciences and Forensic Medicine

2015

English

Mutations in NSUN2 Cause Autosomal- Recessive Intellectual Disability

American Journal of Human Genetics

Genetics

2012

English

Mutations in FYCO1 Cause Autosomal-Recessive Congenital Cataracts

American Journal of Human Genetics

Genetics

2011

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by E A Pierce

Human Neutrophil Cytochrome B Light Chain (P22-Phox). Gene Structure, Chromosomal Location, and Mutations in Cytochrome-Negative Autosomal Recessive Chronic Granulomatous Disease.

Oligonucleotide-Directed Single-Base DNA Alterations in Mouse Embryonic Stem Cells

Related publications

Chronic Granulomatous Disease With Neutrophil Membrane Cytochrome B Deficiency: Demonstration by Immunochemical Staining With Monoclonal Antibody.

Cloning the Gene for an Inherited Human Disorder—chronic Granulomatous Disease—on the Basis of Its Chromosomal Location

Successful Lung Transplant for Bronchiectasis in an Adult Male With Autosomal Recessive Chronic Granulomatous Disease With a Novel NF1 Gene Mutation

332. ZFN-Mediated Minigene or Dinucleotide Gene Correction of P47phox Deficient Autosomal Recessive Chronic Granulomatous Disease iPSC to Generate Oxidase Functional Neutrophils

Aspergillus Osteomyelitis in a Child Who Has P67-Phox-Deficient Chronic Granulomatous Disease.

Mutations in the Nebulin Gene Associated With Autosomal Recessive Nemaline Myopathy

Possible Application of Cytochrome B Gene for Human Identification = التطبيقات المحتملة لاستخدام الموقع الوراثي سيتوكروم ب ( Cytochrome B ) لتحديد الهوية البشرية

Mutations in NSUN2 Cause Autosomal- Recessive Intellectual Disability

Mutations in FYCO1 Cause Autosomal-Recessive Congenital Cataracts