These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
129 related articles for article (PubMed ID: 7851882)
1. Human mitochondrial HMG CoA synthase: liver cDNA and partial genomic cloning, chromosome mapping to 1p12-p13, and possible role in vertebrate evolution. Boukaftane Y; Duncan A; Wang S; Labuda D; Robert MF; Sarrazin J; Schappert K; Mitchell GA Genomics; 1994 Oct; 23(3):552-9. PubMed ID: 7851882 [TBL] [Abstract][Full Text] [Related]
2. Isolation, characterization, and mapping of the mouse and human Fgd2 genes, faciogenital dysplasia (FGD1; Aarskog syndrome) gene homologues. Pasteris NG; Gorski JL Genomics; 1999 Aug; 60(1):57-66. PubMed ID: 10458911 [TBL] [Abstract][Full Text] [Related]
3. Cloning and characterization of human and mouse mitochondrial elongation factor G, GFM and Gfm, and mapping of GFM to human chromosome 3q25.1-q26.2. Gao J; Yu L; Zhang P; Jiang J; Chen J; Peng J; Wei Y; Zhao S Genomics; 2001 May; 74(1):109-14. PubMed ID: 11374907 [TBL] [Abstract][Full Text] [Related]
4. Immunolocalization of mitochondrial 3-hydroxy-3-methylglutaryl CoA synthase in rat liver. Royo T; Pedragosa MJ; Ayté J; Gil-Gómez G; Vilaró S; Hegardt FG J Cell Physiol; 1995 Jan; 162(1):103-9. PubMed ID: 7814442 [TBL] [Abstract][Full Text] [Related]
5. Rat mitochondrial and cytosolic 3-hydroxy-3-methylglutaryl-CoA synthases are encoded by two different genes. Ayté J; Gil-Gómez G; Haro D; Marrero PF; Hegardt FG Proc Natl Acad Sci U S A; 1990 May; 87(10):3874-8. PubMed ID: 1971108 [TBL] [Abstract][Full Text] [Related]
6. Mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase: a control enzyme in ketogenesis. Hegardt FG Biochem J; 1999 Mar; 338 ( Pt 3)(Pt 3):569-82. PubMed ID: 10051425 [TBL] [Abstract][Full Text] [Related]
7. Cloning and mapping of the cDNA for human sarcosine dehydrogenase, a flavoenzyme defective in patients with sarcosinemia. Eschenbrenner M; Jorns MS Genomics; 1999 Aug; 59(3):300-8. PubMed ID: 10444331 [TBL] [Abstract][Full Text] [Related]
8. Cloning of a portion of the chromosomal gene and cDNA for human beta-fodrin, the nonerythroid form of beta-spectrin. Chang JG; Scarpa A; Eddy RL; Byers MG; Harris AS; Morrow JS; Watkins P; Shows TB; Forget BG Genomics; 1993 Aug; 17(2):287-93. PubMed ID: 8406479 [TBL] [Abstract][Full Text] [Related]
9. [Analysis, identification and correction of some errors of model refseqs appeared in NCBI Human Gene Database by in silico cloning and experimental verification of novel human genes]. Zhang DL; Ji L; Li YD Yi Chuan Xue Bao; 2004 May; 31(5):431-43. PubMed ID: 15478601 [TBL] [Abstract][Full Text] [Related]
10. A genome-wide screen identifies a single beta-defensin gene cluster in the chicken: implications for the origin and evolution of mammalian defensins. Xiao Y; Hughes AL; Ando J; Matsuda Y; Cheng JF; Skinner-Noble D; Zhang G BMC Genomics; 2004 Aug; 5(1):56. PubMed ID: 15310403 [TBL] [Abstract][Full Text] [Related]
11. cDNA cloning and chromosomal mapping of the mouse type VII collagen gene (Col7a1): evidence for rapid evolutionary divergence of the gene. Li K; Christiano AM; Copeland NG; Gilbert DJ; Chu ML; Jenkins NA; Uitto J Genomics; 1993 Jun; 16(3):733-9. PubMed ID: 8325648 [TBL] [Abstract][Full Text] [Related]
12. Human cytoplasmic 3-hydroxy-3-methylglutaryl coenzyme A synthase: expression, purification, and characterization of recombinant wild-type and Cys129 mutant enzymes. Rokosz LL; Boulton DA; Butkiewicz EA; Sanyal G; Cueto MA; Lachance PA; Hermes JD Arch Biochem Biophys; 1994 Jul; 312(1):1-13. PubMed ID: 7913309 [TBL] [Abstract][Full Text] [Related]
13. Orthologues of the Caenorhabditis elegans longevity gene clk-1 in mouse and human. Asaumi S; Kuroyanagi H; Seki N; Shirasawa T Genomics; 1999 Jun; 58(3):293-301. PubMed ID: 10373327 [TBL] [Abstract][Full Text] [Related]
15. Divergent evolution of the thiolase superfamily and chalcone synthase family. Jiang C; Kim SY; Suh DY Mol Phylogenet Evol; 2008 Dec; 49(3):691-701. PubMed ID: 18824113 [TBL] [Abstract][Full Text] [Related]
16. A novel regucalcin gene promoter region-related protein: comparison of nucleotide and amino acid sequences in vertebrate species. Sawada N; Yamaguchi M Int J Mol Med; 2005 Jan; 15(1):97-104. PubMed ID: 15583834 [TBL] [Abstract][Full Text] [Related]
17. Human stearoyl-CoA desaturase: alternative transcripts generated from a single gene by usage of tandem polyadenylation sites. Zhang L; Ge L; Parimoo S; Stenn K; Prouty SM Biochem J; 1999 May; 340 ( Pt 1)(Pt 1):255-64. PubMed ID: 10229681 [TBL] [Abstract][Full Text] [Related]
18. Identification and characterization of two novel human mitochondrial elongation factor genes, hEFG2 and hEFG1, phylogenetically conserved through evolution. Hammarsund M; Wilson W; Corcoran M; Merup M; Einhorn S; Grandér D; Sangfelt O Hum Genet; 2001 Nov; 109(5):542-50. PubMed ID: 11735030 [TBL] [Abstract][Full Text] [Related]
19. Mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency: clinical course and description of causal mutations in two patients. Bouchard L; Robert MF; Vinarov D; Stanley CA; Thompson GN; Morris A; Leonard JV; Quant P; Hsu BY; Boneh A; Boukaftane Y; Ashmarina L; Wang S; Miziorko H; Mitchell GA Pediatr Res; 2001 Mar; 49(3):326-31. PubMed ID: 11228257 [TBL] [Abstract][Full Text] [Related]
20. Molecular cloning of human hippocalcin cDNA and chromosomal mapping of its gene. Takamatsu K; Kobayashi M; Saitoh S; Fujishiro M; Noguchi T Biochem Biophys Res Commun; 1994 Apr; 200(1):606-11. PubMed ID: 8166736 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]