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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

168 related articles for article (PubMed ID: 11401427)

  • 1. Human biotin-containing subunit of 3-methylcrotonyl-CoA carboxylase gene (MCCA): cDNA sequence, genomic organization, localization to chromosomal band 3q27, and expression.
    Obata K; Fukuda T; Morishita R; Abe S; Asakawa S; Yamaguchi S; Yoshino M; Ihara K; Murayama K; Shigemoto K; Shimizu N; Kondo I
    Genomics; 2001 Mar; 72(2):145-52. PubMed ID: 11401427
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Cloning of the human MCCA and MCCB genes and mutations therein reveal the molecular cause of 3-methylcrotonyl-CoA: carboxylase deficiency.
    Holzinger A; Röschinger W; Lagler F; Mayerhofer PU; Lichtner P; Kattenfeld T; Thuy LP; Nyhan WL; Koch HG; Muntau AC; Roscher AA
    Hum Mol Genet; 2001 Jun; 10(12):1299-306. PubMed ID: 11406611
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Functional analysis of MCCA and MCCB mutations causing methylcrotonylglycinuria.
    Desviat LR; Pérez-Cerdá C; Pérez B; Esparza-Gordillo J; Rodríguez-Pombo P; Peñalva MA; Rodríguez De Córdoba S; Ugarte M
    Mol Genet Metab; 2003 Nov; 80(3):315-20. PubMed ID: 14680978
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [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]  

  • 5. Genetic dissection of methylcrotonyl CoA carboxylase indicates a complex role for mitochondrial leucine catabolism during seed development and germination.
    Ding G; Che P; Ilarslan H; Wurtele ES; Nikolau BJ
    Plant J; 2012 May; 70(4):562-77. PubMed ID: 22211474
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 3-Methylcrotonyl-CoA carboxylase deficiency: mutation analysis in 28 probands, 9 symptomatic and 19 detected by newborn screening.
    Dantas MF; Suormala T; Randolph A; Coelho D; Fowler B; Valle D; Baumgartner MR
    Hum Mutat; 2005 Aug; 26(2):164. PubMed ID: 16010683
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular characterization of the non-biotin-containing subunit of 3-methylcrotonyl-CoA carboxylase.
    McKean AL; Ke J; Song J; Che P; Achenbach S; Nikolau BJ; Wurtele ES
    J Biol Chem; 2000 Feb; 275(8):5582-90. PubMed ID: 10681539
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The molecular basis of 3-methylcrotonylglycinuria, a disorder of leucine catabolism.
    Gallardo ME; Desviat LR; Rodríguez JM; Esparza-Gordillo J; Pérez-Cerdá C; Pérez B; Rodríguez-Pombo P; Criado O; Sanz R; Morton DH; Gibson KM; Le TP; Ribes A; de Córdoba SR; Ugarte M; Peñalva MA
    Am J Hum Genet; 2001 Feb; 68(2):334-46. PubMed ID: 11170888
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Metabolic and environmental regulation of 3-methylcrotonyl-coenzyme A carboxylase expression in Arabidopsis.
    Che P; Wurtele ES; Nikolau BJ
    Plant Physiol; 2002 Jun; 129(2):625-37. PubMed ID: 12068107
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The molecular basis of human 3-methylcrotonyl-CoA carboxylase deficiency.
    Baumgartner MR; Almashanu S; Suormala T; Obie C; Cole RN; Packman S; Baumgartner ER; Valle D
    J Clin Invest; 2001 Feb; 107(4):495-504. PubMed ID: 11181649
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Isolated 3-methylcrotonyl-CoA carboxylase deficiency: evidence for an allele-specific dominant negative effect and responsiveness to biotin therapy.
    Baumgartner MR; Dantas MF; Suormala T; Almashanu S; Giunta C; Friebel D; Gebhardt B; Fowler B; Hoffmann GF; Baumgartner ER; Valle D
    Am J Hum Genet; 2004 Nov; 75(5):790-800. PubMed ID: 15359379
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Isolation and characterization of mutations in the human holocarboxylase synthetase cDNA.
    Suzuki Y; Aoki Y; Ishida Y; Chiba Y; Iwamatsu A; Kishino T; Niikawa N; Matsubara Y; Narisawa K
    Nat Genet; 1994 Oct; 8(2):122-8. PubMed ID: 7842009
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Isolation and characterization of a novel gene from the DiGeorge chromosomal region that encodes for a mediator subunit.
    Berti L; Mittler G; Przemeck GK; Stelzer G; Günzler B; Amati F; Conti E; Dallapiccola B; Hrabé de Angelis M; Novelli G; Meisterernst M
    Genomics; 2001 Jun; 74(3):320-32. PubMed ID: 11414760
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Structure of the PCCA gene and distribution of mutations causing propionic acidemia.
    Campeau E; Desviat LR; Leclerc D; Wu X; Pérez B; Ugarte M; Gravel RA
    Mol Genet Metab; 2001; 74(1-2):238-47. PubMed ID: 11592820
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular cloning, genomic organization, and mapping of PRKAG2, a heart abundant gamma2 subunit of 5'-AMP-activated protein kinase, to human chromosome 7q36.
    Lang T; Yu L; Tu Q; Jiang J; Chen Z; Xin Y; Liu G; Zhao S
    Genomics; 2000 Dec; 70(2):258-63. PubMed ID: 11112354
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Human gamma-aminobutyraldehyde dehydrogenase (ALDH9): cDNA sequence, genomic organization, polymorphism, chromosomal localization, and tissue expression.
    Lin SW; Chen JC; Hsu LC; Hsieh CL; Yoshida A
    Genomics; 1996 Jun; 34(3):376-80. PubMed ID: 8786138
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cryptic exon activation by disruption of exon splice enhancer: novel mechanism causing 3-methylcrotonyl-CoA carboxylase deficiency.
    Stucki M; Suormala T; Fowler B; Valle D; Baumgartner MR
    J Biol Chem; 2009 Oct; 284(42):28953-7. PubMed ID: 19706617
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Geranoyl-CoA carboxylase: a novel biotin-containing enzyme in plants.
    Guan X; Diez T; Prasad TK; Nikolau BJ; Wurtele ES
    Arch Biochem Biophys; 1999 Feb; 362(1):12-21. PubMed ID: 9917324
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The human glycine receptor beta subunit gene (GLRB): structure, refined chromosomal localization, and population polymorphism.
    Milani N; Mülhardt C; Weber RG; Lichter P; Kioschis P; Poustka A; Becker CM
    Genomics; 1998 Jun; 50(3):341-5. PubMed ID: 9676428
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genomic organization and sequence variation of the human integrin subunit alpha8 gene (ITGA8).
    Ekwa-Ekoka C; Diaz GA; Carlson C; Hasegawa T; Samudrala R; Lim KC; Yabu JM; Levy B; Schnapp LM
    Matrix Biol; 2004 Nov; 23(7):487-96. PubMed ID: 15579315
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.