(Q36835581)

English

Murine fumarylacetoacetate hydrolase (Fah) gene is disrupted by a neonatally lethal albino deletion that defines the hepatocyte-specific developmental regulation 1 (hsdr-1) locus

scientific article published on February 1992

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Murine fumarylacetoacetate hydrolase (Fah) gene is disrupted by a neonatally lethal albino deletion that defines the hepatocyte-specific developmental regulation 1 (hsdr-1) locus (English)

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

1 reference

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author name string

Klebig ML

1

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Russell LB

2

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Rinchik EM

3

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

language of work or name

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publication date

1 February 1992

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

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

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Europe PubMed Central

PMC publication ID

16 August 2017

89

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

4

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

1363-1367

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Analysis of the albino-locus region of the mouse: IV. Characterization of 34 deficiencies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48450

29 September 2017

Mice homozygous for chromosomal deletions at the albino locus region lack specific polypeptides in two-dimensional gels

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48450

29 September 2017

Double cos site vectors: simplified cosmid cloning.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48450

29 September 2017

Ultrastructural basis of biochemical effects in a series of lethal alleles in the mouse. Neonatal and developmental studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48450

29 September 2017

Glucose-6-phosphatase deficiency caused by radiation-induced alleles at the albino locus in the mouse

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48450

29 September 2017

Metallothionein mRNA expression in mice homozygous for chromosomal deletions around the albino locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48450

29 September 2017

Hereditary tyrosinemia type I--an overview

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48450

29 September 2017

Developmental regulation of constitutive and inducible expression of hepatocyte-specific genes in the mouse

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48450

29 September 2017

Multiple transcripts of the mouse tyrosinase gene are generated by alternative splicing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48450

29 September 2017

Is CCAAT/enhancer-binding protein a central regulator of energy metabolism?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48450

29 September 2017

Marked increases in hepatic NAD(P)H:oxidoreductase gene transcription and mRNA levels correlated with a mouse chromosome 7 deletion

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48450

29 September 2017

Different molecular basis for fumarylacetoacetate hydrolase deficiency in the two clinical forms of hereditary tyrosinemia (type I)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48450

29 September 2017

Nucleotide sequence of cDNA encoding human fumarylacetoacetase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48450

29 September 2017

Cloning and expression of the cDNA encoding human fumarylacetoacetate hydrolase, the enzyme deficient in hereditary tyrosinemia: assignment of the gene to chromosome 15

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48450

29 September 2017

The albino-deletion complex of the mouse: molecular mapping of deletion breakpoints that define regions necessary for development of the embryonic and extraembryonic ectoderm.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48450

29 September 2017

A simple method for DNA restriction site mapping

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48450

29 September 2017

DNA sequencing with chain-terminating inhibitors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48450

29 September 2017

On the enzymic defects in hereditary tyrosinemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48450

29 September 2017

Genetic control of morphogenetic and biochemical differentiation: Lethal albino deletions in the mouse

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48450

29 September 2017

Hereditary tyrosinemia. Formation of succinylacetone-amino acid adducts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48450

27 June 2018

Physical analysis of murine albino deletions that disrupt liver-specific gene regulation or mesoderm development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48450

27 June 2018

Effects of deletions in mouse chromosome 7 on expression of genes encoding the urea-cycle enzymes and phosphoenolpyruvate carboxykinase (GTP) in liver, kidney, and intestine

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48450

5 September 2018

Premature development of ligandin (GSH transferase B) in mice with an inherited defect in endoplasmic reticulum-Golgi structure and function

1 reference

https://pubmed.ncbi.nlm.nih.gov/1741389

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetically determined abnormalities of microsomal enzymes in liver of mutant newborn mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/1741389

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A large inverted duplication allows homologous recombination between chromosomes heterozygous for the proximal t complex inversion

1 reference

https://pubmed.ncbi.nlm.nih.gov/1741389

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neurologic crises in hereditary tyrosinemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/1741389

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two genetically defined trans-acting loci coordinately regulate overlapping sets of liver-specific genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/1741389

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1073/PNAS.89.4.1363

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

1992PNAS...89.1363K

0 references

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

ResearchGate publication ID

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