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113 related items for PubMed ID: 8703125
1. Acads gene deletion in BALB/cByJ mouse strain occurred after 1981 and is not present in BALB/cByJ-fld mutant mice. Reue K, Cohen RD. Mamm Genome; 1996 Sep; 7(9):694-5. PubMed ID: 8703125 [No Abstract] [Full Text] [Related]
4. The fld mutation maps near to but distinct from the Apob locus on mouse chromosome 12. Rowe LB, Sweet HO, Gordon JI, Birkenmeier EH. Mamm Genome; 1996 Jul; 7(7):555-7. PubMed ID: 8672142 [No Abstract] [Full Text] [Related]
7. Deficiency in short-chain fatty acid beta-oxidation affects theta oscillations during sleep. Tafti M, Petit B, Chollet D, Neidhart E, de Bilbao F, Kiss JZ, Wood PA, Franken P. Nat Genet; 2003 Jul; 34(3):320-5. PubMed ID: 12796782 [Abstract] [Full Text] [Related]
8. Mice bearing Acads mutation display altered postingestive but not 5-s orosensory response to dietary fat. Smith Richards BK, Belton BN, York B, Volaufova J. Am J Physiol Regul Integr Comp Physiol; 2004 Feb; 286(2):R311-9. PubMed ID: 14592933 [Abstract] [Full Text] [Related]
9. Pathologic characterization of short-chain acyl-CoA dehydrogenase deficiency in BALB/cByJ mice. Armstrong DL, Masiowski ML, Wood PA. Am J Med Genet; 1993 Nov 01; 47(6):884-92. PubMed ID: 8279487 [Abstract] [Full Text] [Related]
10. Differential induction of genes in liver and brown adipose tissue regulated by peroxisome proliferator-activated receptor-alpha during fasting and cold exposure in acyl-CoA dehydrogenase-deficient mice. Goetzman ES, Tian L, Wood PA. Mol Genet Metab; 2005 Jan 01; 84(1):39-47. PubMed ID: 15639194 [Abstract] [Full Text] [Related]
12. Analysis of polymerase chain reaction-product by capillary electrophoresis with laser-induced fluorescence detection and its application to the diagnosis of medium-chain acyl-coenzyme A dehydrogenase deficiency. Arakawa H, Uetanaka K, Maeda M, Tsuji A, Matsubara Y, Narisawa K. J Chromatogr A; 1994 Oct 07; 680(2):517-23. PubMed ID: 7981832 [Abstract] [Full Text] [Related]
13. Short-chain acyl-coenzyme A dehydrogenase activity, antigen, and biosynthesis are absent in the BALB/cByJ mouse. Amendt BA, Freneaux E, Reece C, Wood PA, Rhead WJ. Pediatr Res; 1992 Jun 07; 31(6):552-6. PubMed ID: 1635815 [Abstract] [Full Text] [Related]
14. Phenotype assessment: are you missing something? Wood PA. Comp Med; 2000 Feb 07; 50(1):12-5. PubMed ID: 10987661 [Abstract] [Full Text] [Related]
15. Abnormal nonshivering thermogenesis in mice with inherited defects of fatty acid oxidation. Guerra C, Koza RA, Walsh K, Kurtz DM, Wood PA, Kozak LP. J Clin Invest; 1998 Nov 01; 102(9):1724-31. PubMed ID: 9802886 [Abstract] [Full Text] [Related]
16. Frequency of the G985 MCAD mutation in the general population. Blakemore AI, Singleton H, Pollitt RJ, Engel PC, Kolvraa S, Gregersen N, Curtis D. Lancet; 1991 Feb 02; 337(8736):298-9. PubMed ID: 1671131 [No Abstract] [Full Text] [Related]
17. Hepatic triglyceride contents are genetically determined in mice: results of a strain survey. Lin X, Yue P, Chen Z, Schonfeld G. Am J Physiol Gastrointest Liver Physiol; 2005 Jun 02; 288(6):G1179-89. PubMed ID: 15591160 [Abstract] [Full Text] [Related]
18. Frequency of G-985 mutation in medium chain acyl-coenzyme A dehydrogenase (MCAD) deficiency in sudden infant death syndrome (SIDS). Miller M, Brooks J, Forbes N, Insel R. Prog Clin Biol Res; 1992 Jun 02; 375():495-8. PubMed ID: 1438393 [No Abstract] [Full Text] [Related]
19. The heavy chain genes of a lupus anti-DNA autoantibody are encoded in the germ line of a nonautoimmune strain of mouse and conserved in strains of mice polymorphic for this gene locus. Trepicchio W, Maruya A, Barrett KJ. J Immunol; 1987 Nov 01; 139(9):3139-45. PubMed ID: 3117887 [Abstract] [Full Text] [Related]
20. Cloning and characterization of the mouse short-chain acyl-CoA dehydrogenase gene. Kelly CL, Wood PA. Mamm Genome; 1996 Apr 01; 7(4):262-4. PubMed ID: 8661694 [Abstract] [Full Text] [Related] Page: [Next] [New Search]