About: Complementation studies of lethal alleles in the mouse causing deficiencies of glucose-6-phosphatase, tyrosine aminotransferase, and serine dehydratase

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About: Complementation studies of lethal alleles in the mouse causing deficiencies of glucose-6-phosphatase, tyrosine aminotransferase, and serine dehydratase Goto Sponge NotDistinct Permalink

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scientific article published on March 1974

Attributes	Values
rdf:type	Item
description	videnskabelig artikel (da) article científic (ca) articolo scientifico (it) artigo científico (pt) bilimsel makale (tr) vedecký článok (sk) vetenskaplig artikel (sv) vědecký článek (cs) wetenschappelijk artikel (nl) wissenschaftlicher Artikel (de) научни чланак (sr) article scientifique (fr) artículu científicu espublizáu en 1974 (ast) 1974年學術文章 (zh) наукова стаття, опублікована в березні 1974 (uk) مقالة علمية نشرت في مارس 1974 (ar) scientific article published on March 1974 (en)
publication date	wds:Q37434565-704F8E35-3642-4E18-A9CB-6D918908C01E
publication date	1974-03-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q37434565-70BDBDA9-56B5-43E1-B53D-7866C16791B6
language of work or name	English
cites work	wds:Q37434565-0B7C1146-ECED-4502-8539-E3E52C4FA9A8 wds:Q37434565-2C3A207F-7082-4556-80FE-1CDC95599A69 wds:Q37434565-6A5AB853-1CE0-4040-B930-9D78D7C3D360 wds:Q37434565-7B8CE6D8-4F82-4918-B171-DCCE4A24F910 wds:Q37434565-84D6F4D8-5B40-499F-B8CA-5D52E68BD04F wds:Q37434565-A69DF3C3-D63A-449A-B12A-917D3BBD9124 wds:Q37434565-B94D3444-BDC5-4126-882F-6ADC4BBADFD1
cites work	The developmental formation of liver glucose 6-phosphatase and reduced nicotinamide adenine dinucleotide phosphate dehydrogenase in fetal rats treated with thyroxine. The assay of aromatic amino acid transaminations and keto acid oxidation by the enol borate-tautomerase method Multiple biochemical effects of a series of x-ray induced mutations at the albino locus in the mouse Glucose 6-phosphatase deficiency: Mechanisms of genetic control and biochemistry The quinacrine fluorescence karyotype of Mus musculus and demonstration of strain differences in secondary constrictions Glucose-6-phosphatase deficiency caused by radiation-induced alleles at the albino locus in the mouse Ultrastructural basis of biochemical effects in a series of lethal alleles in the mouse. Neonatal and developmental studies
author name string	wds:Q37434565-0BD6BBC5-7754-4718-AF0D-81690555408B wds:Q37434565-5DAFD89F-C189-4A5A-83E3-906654083747 wds:Q37434565-ECF41F8D-949D-4938-B321-06B5A59A899C wds:Q37434565-EF8D5473-B444-4ED1-9C22-A13C143A169F
author name string	Gluecksohn-Waelsch S Schiffman MB Cori CF Thorndike J
rdfs:label	Complementation studies of lethal alleles in the mouse causing deficiencies of glucose-6-phosphatase, tyrosine aminotransferase, and serine dehydratase (en) Complementation studies of lethal alleles in the mouse causing deficiencies of glucose-6-phosphatase, tyrosine aminotransferase, and serine dehydratase (nl) Complementation studies of lethal alleles in the mouse causing deficiencies of glucose-6-phosphatase, tyrosine aminotransferase, and serine dehydratase (ast)
skos:prefLabel	Complementation studies of lethal alleles in the mouse causing deficiencies of glucose-6-phosphatase, tyrosine aminotransferase, and serine dehydratase (en) Complementation studies of lethal alleles in the mouse causing deficiencies of glucose-6-phosphatase, tyrosine aminotransferase, and serine dehydratase (nl) Complementation studies of lethal alleles in the mouse causing deficiencies of glucose-6-phosphatase, tyrosine aminotransferase, and serine dehydratase (ast)
name	Complementation studies of lethal alleles in the mouse causing deficiencies of glucose-6-phosphatase, tyrosine aminotransferase, and serine dehydratase (en) Complementation studies of lethal alleles in the mouse causing deficiencies of glucose-6-phosphatase, tyrosine aminotransferase, and serine dehydratase (nl) Complementation studies of lethal alleles in the mouse causing deficiencies of glucose-6-phosphatase, tyrosine aminotransferase, and serine dehydratase (ast)
title	wds:Q37434565-50A99B60-0B0A-4D87-8290-53EFAE12407E
title	Complementation studies of lethal alleles in the mouse causing deficiencies of glucose-6-phosphatase, tyrosine aminotransferase, and serine dehydratase (en)
page(s)	wds:Q37434565-8D159825-0CBF-4439-9002-067BBB58F8B2
page(s)	825-829
instance of	wds:Q37434565-C761FAAD-8093-4F32-8658-A398854456D3
instance of	scholarly article
main subject	wds:Q37434565-b9fbce0e-a149-48d8-9c47-adee02c4638e
main subject	glucose
PubMed ID	wds:Q37434565-0FA9380E-09C1-4F36-9B40-75FF55D94373
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/4150768
PubMed ID	4150768
published in	wds:Q37434565-C54F89D1-04F6-4833-895A-00965EE03B6E
published in	Proceedings of the National Academy of Sciences of the United States of America
issue	wds:Q37434565-E2F9FBAA-DCBD-42DC-8710-AEED9D7E75F0
volume	wds:Q37434565-70C43B75-EF38-4BF7-81B8-84618748378B
issue	3
volume	71
DOI	wds:Q37434565-D151BF87-77AE-48D7-B550-724A23B61A70
DOI	http://dx.doi.org/10.1073/PNAS.71.3.825
DOI	10.1073/PNAS.71.3.825
ResearchGate publication ID	wds:Q37434565-B54537EA-E67E-40F9-8750-DFAC67081015
ResearchGate publication ID	19014533
ADS bibcode	wds:Q37434565-6D8F5431-8E97-41C0-A3FA-3307D248C0F6
ADS bibcode	1974PNAS...71..825G
PMCID	wds:Q37434565-F53E1DA4-3AB4-43EA-9370-26803ADA2B7B
PMCID	388107
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q37434565
is cites work of	Pharmacological correction of neonatal lethal hepatic dysfunction in a murine model of hereditary tyrosinaemia type I. Murine albino-deletion complex: high-resolution microsatellite map and genetically anchored YAC framework map. Glycogen storage diseases in animals and their potential value as models of human disease Decreased lysyl oxidase activity in the aneurysm-prone, mottled mouse X-ray-induced mutations in mouse embryonic stem cells Complementation of gene deletions by cell hybridization Nonhomologous pairing in mice heterozygous for a t haplotype can produce recombinant chromosomes with duplications and deletions Cytological detection of the c-25H deletion involving the albino (c) locus on chromosome 7 in the mouse Chemical and immunological studies of liver microsomes from mouse mutants with ultrastructurally abnormal hepatic endoplasmic reticulum The albino-deletion complex of the mouse: molecular mapping of deletion breakpoints that define regions necessary for development of the embryonic and extraembryonic ectoderm. Deficiency in plasma protein synthesis caused by x-ray-incuded lethal albino alleles in mouse Glutamine synthetase in newborn mice homozygous for lethal albino alleles Regulatory genes linked to the albino locus in the mouse confer competence for inducible expression on the structural gene encoding serine dehydratase Monoclonal Antibodies and Cell Surface Antigens Analysis of the albino-locus region of the mouse. I. Origin and viability Analysis of the albino-locus region of the mouse. III. Time of death of prenatal lethals Inherited metabolic disease in laboratory animals: a review Protein synthesis with membrane-bound polysomes and albumin messenger RNA from livers of mutant mice Effect of gene dosage on expression of mitochondrial malic enzyme activity in the mouse Cytological observations of deletions in pachytene stages of oogenesis and spermatogenesis in the mouse

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