The Molecular Basis of the Sparse Fur Mouse Mutation-Reference-Cited by-同舟云学术

The Molecular Basis of the Sparse Fur Mouse Mutation

Published:1987-07-24 Issue:4813 Volume:237 Page:415-417
ISSN:0036-8075
Container-title:Science
language:en
Short-container-title:Science

Author:

Veres Gabor¹,Gibbs Richard A.¹,Scherer Steven E.¹,Caskey C. Thomas¹

Affiliation:

1. Institute for Molecular Genetics, Howard Hughes Medical Institute, Baylor College of Medicine, Houston, TX 77030.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference24 articles.

1. Buffer gradient gels and 35S label as an aid to rapid DNA sequence determination.

2. BRIAND, P, ORNITHINE TRANSCARBAMYLASE DEFICIENCIES IN HUMAN MALES KINETIC AND IMMUNOCHEMICAL CLASSIFICATION, BIOCHIMICA ET BIOPHYSICA ACTA 704: 100 (1982).

3. CHEHAB, F.F., SPONTANEOUS MUTATION IN BETA-THALASSEMIA PRODUCING THE SAME NUCLEOTIDE SUBSTITUTION AS THAT IN A COMMON HEREDITARY FORM, LANCET 1: 3 (1986).

4. DEMARS, R, ABNORMAL ORNITHINE CARBAMOYLTRANSFERASE IN MICE HAVING SPARSE-FUR MUTATION, PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 73: 1693 (1976).

5. DOOLITTLE, D.P., NEW ALLELE OF SPARSE FUR GENE IN MOUSE, JOURNAL OF HEREDITY 65: 194 (1974).

Cited by 232 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Proteogenomics in Aid of Host–Pathogen Interaction Studies: A Bacterial Perspective;Proteomes;2017-10-11

2. Impaired novelty acquisition and synaptic plasticity in congenital hyperammonemia caused by hepatic glutamine synthetase deficiency;Scientific Reports;2017-01-09

3. RT-PCR;RNA Methodologies;2017

4. Functional Characterization of the spf/ash Splicing Variation in OTC Deficiency of Mice and Man;PLOS ONE;2015-04-08

5. Experimental nonalcoholic steatohepatitis compromises ureagenesis, an essential hepatic metabolic function;American Journal of Physiology-Gastrointestinal and Liver Physiology;2014-08-01