(PDF) An Exon 10 Deletion in the Mouse Ferrochelatase Gene

An Exon 10 Deletion in the Mouse Ferrochelatase Gene Has a Dominant-Negative Effect and Causes Mild Protoporphyria

Blood - United States

doi 10.1182/blood-2001-12-0283

Full Text

Abstract

Available in full text

Categories

Date

August 15, 2002

Authors

Scott T. Magness

David A. Brenner

Publisher

American Society of Hematology

Related search

Erythropoietic Protoporphyria in the House Mouse. A Recessive Inherited Ferrochelatase Deficiency With Anemia, Photosensitivity, and Liver Disease.

Journal of Clinical Investigation

English

Deletion of Exon 8 From the EXT1 Gene Causes Multiple Osteochondromas (MO) in a Family With Three Affected Members

Multidisciplinary

English

Deletion of the Parkin Coregulated Gene Causes Male Sterility in the Quakingviable Mouse Mutant

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

Multidisciplinary

English

Uncoupling of P97 ATPase Activity Has a Dominant Negative Effect on Protein Extraction

Scientific Reports

Multidisciplinary

English

Deletion of a Branch-Point Consensus Sequence in the LMX1B Gene Causes Exon Skipping in a Family With Nail Patella Syndrome

European Journal of Human Genetics

English

Expression of an Amino-Terminal BRCA1 Deletion Mutant Causes a Dominant Growth Inhibition in McF10a Cells

Cancer Research

Molecular Biology

English

First Report of a Deletion Encompassing an Entire Exon in the Homogentisate 1,2-Dioxygenase Gene Causing Alkaptonuria

Multidisciplinary

English

CRISPR/Cas9-mediated Editing of GABRR2 Gene in RGC-5 Cells Induces Random Exon Deletion, Exon Splicing and New Exon Recruitment

Biochemical Engineering Journal

Environmental Engineering

Biomedical Engineering

English

Transgenic Mouse Model of the Mild Dominant Form of Osteogenesis Imperfecta.

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

Multidisciplinary

English