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.
4. Coding sequence mutations in the alpha subunit of propionyl-CoA carboxylase in patients with propionic acidemia. Campeau E; Dupuis L; León-Del-Rio A; Gravel R Mol Genet Metab; 1999 May; 67(1):11-22. PubMed ID: 10329019 [TBL] [Abstract][Full Text] [Related]
5. Effect of PCCB gene mutations on the heteromeric and homomeric assembly of propionyl-CoA carboxylase. Muro S; Pérez B; Desviat LR; Rodríguez-Pombo P; Pérez-Cerdá C; Clavero S; Ugarte M Mol Genet Metab; 2001 Dec; 74(4):476-83. PubMed ID: 11749052 [TBL] [Abstract][Full Text] [Related]
6. Three novel splice mutations in the PCCA gene causing identical exon skipping in propionic acidemia patients. Richard E; Desviat LR; Pérez B; Pérez-Cerdá C; Ugarte M Hum Genet; 1997 Nov; 101(1):93-6. PubMed ID: 9385377 [TBL] [Abstract][Full Text] [Related]
7. Identification of novel mutations in the PCCB gene in European propionic acidemia patients. Mutation in brief no. 253. Online. Muro S; Rodríguez-Pombo P; Pérez B; Pérez-Cerdá C; Desviat LR; Sperl W; Skladal D; Sass JO; Ugarte M Hum Mutat; 1999; 14(1):89-90. PubMed ID: 10447268 [TBL] [Abstract][Full Text] [Related]
8. Propionic acidemia: mutation update and functional and structural effects of the variant alleles. Desviat LR; Pérez B; Pérez-Cerdá C; Rodríguez-Pombo P; Clavero S; Ugarte M Mol Genet Metab; 2004; 83(1-2):28-37. PubMed ID: 15464417 [TBL] [Abstract][Full Text] [Related]
9. Feasibility of DNA based methods for prenatal diagnosis and carrier detection of propionic acidaemia. Muro S; Perez-Cerdá C; Roddríguez-Pombo P; Pérez B; Briones P; Ribes A; Ugarte M J Med Genet; 1999 May; 36(5):412-4. PubMed ID: 10353789 [TBL] [Abstract][Full Text] [Related]
10. Human propionyl-CoA carboxylase beta subunit gene: exon-intron definition and mutation spectrum in Spanish and Latin American propionic acidemia patients. Rodríguez-Pombo P; Hoenicka J; Muro S; Pérez B; Pérez-Cerdá C; Richard E; Desviat LR; Ugarte M Am J Hum Genet; 1998 Aug; 63(2):360-9. PubMed ID: 9683601 [TBL] [Abstract][Full Text] [Related]
11. Mutations participating in interallelic complementation in propionic acidemia. Gravel RA; Akerman BR; Lamhonwah AM; Loyer M; Léon-del-Rio A; Italiano I Am J Hum Genet; 1994 Jul; 55(1):51-8. PubMed ID: 8023851 [TBL] [Abstract][Full Text] [Related]
12. [Gene mutation analysis in patients with propionic acidemia]. Hu YH; Han LS; Ye J; Qiu WJ; Zhang YF; Yang YL; Liu L; Ma HW; Gao XL; Gu XF Zhonghua Er Ke Za Zhi; 2008 Jun; 46(6):416-20. PubMed ID: 19099776 [TBL] [Abstract][Full Text] [Related]
13. Promoter cloning and characterization of the rabbit BK channel beta1 subunit gene. Zhang XY; Wang S; Yan Z; Zhang YQ; Wan Y; Zhang B; Wang LF; Chai YB; Wei JG Gene; 2009 Jun; 438(1-2):33-9. PubMed ID: 19303925 [TBL] [Abstract][Full Text] [Related]
14. The gonadotropin-regulated long-chain acyl CoA synthetase gene: a novel downstream Sp1/Sp3 binding element critical for transcriptional promoter activity. Sheng Y; Li J; Dufau ML; Tsai-Morris CH Gene; 2005 Oct; 360(1):20-6. PubMed ID: 16125341 [TBL] [Abstract][Full Text] [Related]
15. [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]
16. Changes in the carboxyl terminus of the beta subunit of human propionyl-CoA carboxylase affect the oligomer assembly and catalysis: expression and characterization of seven patient-derived mutant forms of PCC in Escherichia coli. Chloupková M; Ravn K; Schwartz M; Kraus JP Mol Genet Metab; 2000 Dec; 71(4):623-32. PubMed ID: 11136555 [TBL] [Abstract][Full Text] [Related]
17. Fine structure of the human translocation protein 1 (HTP1/TLOC1) gene. Daimon M; Susa S; Kato T IUBMB Life; 1999 Dec; 48(6):619-24. PubMed ID: 10683767 [TBL] [Abstract][Full Text] [Related]
18. High incidence of propionic acidemia in greenland is due to a prevalent mutation, 1540insCCC, in the gene for the beta-subunit of propionyl CoA carboxylase. Ravn K; Chloupkova M; Christensen E; Brandt NJ; Simonsen H; Kraus JP; Nielsen IM; Skovby F; Schwartz M Am J Hum Genet; 2000 Jul; 67(1):203-6. PubMed ID: 10820128 [TBL] [Abstract][Full Text] [Related]
19. Propionic acidemia: identification of twenty-four novel mutations in Europe and North America. Pérez B; Desviat LR; Rodríguez-Pombo P; Clavero S; Navarrete R; Perez-Cerdá C; Ugarte M Mol Genet Metab; 2003 Jan; 78(1):59-67. PubMed ID: 12559849 [TBL] [Abstract][Full Text] [Related]
20. Structural organization of the human isovaleryl-CoA dehydrogenase gene. Parimoo B; Tanaka K Genomics; 1993 Mar; 15(3):582-90. PubMed ID: 8468053 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]