Spontaneous nonsense mutation in

Tuft1 (tuftelin 1) gene hepatic proteome lipid and glucose metabolism rat spontaneous nonsense mutation

Journal

Physiological genomics
ISSN: 1531-2267
Titre abrégé: Physiol Genomics
Pays: United States
ID NLM: 9815683

Informations de publication

Date de publication:
13 Nov 2023
Historique:
medline: 13 11 2023
pubmed: 13 11 2023
entrez: 13 11 2023
Statut: aheadofprint

Résumé

Recently, we identified a recessive mutation, an abnormal coat appearance in BXH6 strain, a member of the HXB/BXH set of recombinant inbred (RI) strains. The RI strains were derived from the SHR (spontaneously hypertensive rat) and BN-

Identifiants

pubmed: 37955133
doi: 10.1152/physiolgenomics.00084.2023
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : European Union/Ministry of Education of the Czech Republic
ID : LX22NPO5104
Organisme : Ministry of Education of the Czech Republic
ID : LM2023067
Organisme : Czech Science Foundation
ID : 21-18993S

Auteurs

Jan Silhavy (J)

Genetics of Model Diseases, Institute of Physiology, Czech Academy of Sciences, Prague, Czech Republic, 14220, Prague, Czech Republic.

Petr Mlejnek (P)

Genetics of Model Diseases, Institute of Physiology, Czech Academy of Sciences, Prague, Czech Republic, 14220, Prague, Czech Republic.

Miroslava Simakova (M)

Genetics of Model Diseases, Institute of Physiology, Czech Academy of Sciences, Prague, Czech Republic, 14220, Prague, Czech Republic.

Frantisek Liska (F)

Institute of Biology and Medical Genetics, First Faculty of Medicine and General University Hospital, Charles University, Prague, Czech Republic.

Denisa Miklankova (D)

Center for Experimental Medicine, Institute for Clinical and Experimental Medicine, Prague, Czech Republic, Prague, Czech Republic.

Dita Musalkova (D)

Research Unit for Rare Diseases, Institute for Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, 12000 Prague, Czech Republic, Prague, Czech Republic.

Viktor Stranecky (V)

Dpt. of Inherited Metabolic Disorders, Institute of interited metabolic disorders, Prague, Czech Republic.

Stanislav Kmoch (S)

Research Unit for Rare Diseases, Institute for Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, 12000 Prague, Czech Republic, Prague, Czech Republic.

Eva Sticova (E)

Center for Experimental Medicine, Institute for Clinical and Experimental Medicine, 14021 Prague, Czech Republic, Prague, Czech Republic.

Marek Vrbacky (M)

Bioenergetics, Institute of Physiology, Czech Academy of Sciences, 14220 Prague, Czech Republic, Prague, Czech Republic.

Tomas Mracek (T)

bioenergetics, Institute of Physiology, Czech Academy of Sciences, Prague, Czech Republic.

Michal Pravenec (M)

Genetics of Model Diseases, Institute of Physiology, Czech Academy of Sciences, Prague, Czech Republic, 14220, Prague, Czech Republic.

Classifications MeSH