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 *

207 related articles for article (PubMed ID: 8499898)

  • 1. Isolation of the human Xp21 glycerol kinase gene by positional cloning.
    Walker AP; Muscatelli F; Monaco AP
    Hum Mol Genet; 1993 Feb; 2(2):107-14. PubMed ID: 8499898
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genomic scanning for expressed sequences in Xp21 identifies the glycerol kinase gene.
    Guo W; Worley K; Adams V; Mason J; Sylvester-Jackson D; Zhang YH; Towbin JA; Fogt DD; Madu S; Wheeler DA
    Nat Genet; 1993 Aug; 4(4):367-72. PubMed ID: 8401584
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cloning of the X-linked glycerol kinase deficiency gene and its identification by sequence comparison to the Bacillus subtilis homologue.
    Sargent CA; Affara NA; Bentley E; Pelmear A; Bailey DM; Davey P; Dow D; Leversha M; Aplin H; Besley GT
    Hum Mol Genet; 1993 Feb; 2(2):97-106. PubMed ID: 8499912
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A YAC contig in Xp21 containing the adrenal hypoplasia congenita and glycerol kinase deficiency genes.
    Walker AP; Chelly J; Love DR; Brush YI; Récan D; Chaussain JL; Oley CA; Connor JM; Yates J; Price DA
    Hum Mol Genet; 1992 Nov; 1(8):579-85. PubMed ID: 1301166
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Yeast artificial chromosome cloning in the glycerol kinase and adrenal hypoplasia congenita region of Xp21.
    Worley KC; Ellison KA; Zhang YH; Wang DF; Mason J; Roth EJ; Adams V; Fogt DD; Zhu XM; Towbin JA
    Genomics; 1993 May; 16(2):407-16. PubMed ID: 8314578
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Cloning and characterization of a putative human glycerol 3-phosphate permease gene (SLC37A1 or G3PP) on 21q22.3: mutation analysis in two candidate phenotypes, DFNB10 and a glycerol kinase deficiency.
    Bartoloni L; Wattenhofer M; Kudoh J; Berry A; Shibuya K; Kawasaki K; Wang J; Asakawa S; Talior I; Bonne-Tamir B; Rossier C; Michaud J; McCabe ER; Minoshima S; Shimizu N; Scott HS; Antonarakis SE
    Genomics; 2000 Dec; 70(2):190-200. PubMed ID: 11112347
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The glycerol kinase gene family: structure of the Xp gene, and related intronless retroposons.
    Sargent CA; Young C; Marsh S; Ferguson-Smith MA; Affara NA
    Hum Mol Genet; 1994 Aug; 3(8):1317-24. PubMed ID: 7987308
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Identification of a ferritin light chain pseudogene near the glycerol kinase locus in Xp21 by cDNA amplification for identification of genomic expressed sequences.
    Guo W; Adams V; Mason J; McCabe ER
    Biochem Mol Med; 1997 Apr; 60(2):169-73. PubMed ID: 9169099
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Fine mapping of glycerol kinase deficiency and congenital adrenal hypoplasia within Xp21 on the short arm of the human X chromosome.
    Davies KE; Patterson MN; Kenwrick SJ; Bell MV; Sloan HR; Westman JA; Elsas LJ; Mahan J
    Am J Med Genet; 1988 Mar; 29(3):557-64. PubMed ID: 2837087
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A yeast artificial chromosome contig containing the complete Duchenne muscular dystrophy gene.
    Monaco AP; Walker AP; Millwood I; Larin Z; Lehrach H
    Genomics; 1992 Mar; 12(3):465-73. PubMed ID: 1559698
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Cloning of a novel, anonymous gene from a megabase-range YAC and cosmid contig in the neurofibromatosis type 2/meningioma region on human chromosome 22q12.
    Xie YG; Han FY; Peyrard M; Ruttledge MH; Fransson I; DeJong P; Collins J; Dunham I; Nordenskjöld M; Dumanski JP
    Hum Mol Genet; 1993 Sep; 2(9):1361-8. PubMed ID: 8242058
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Isolation and characterization of a MAGE gene family in the Xp21.3 region.
    Muscatelli F; Walker AP; De Plaen E; Stafford AN; Monaco AP
    Proc Natl Acad Sci U S A; 1995 May; 92(11):4987-91. PubMed ID: 7761436
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Construction of cosmid contigs and high-resolution restriction mapping of the Huntington disease region of human chromosome 4.
    Zuo J; Robbins C; Baharloo S; Cox DR; Myers RM
    Hum Mol Genet; 1993 Jul; 2(7):889-99. PubMed ID: 8364572
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A strategy for the selection of transcribed sequences in the Xq28 region.
    Korn B; Sedlacek Z; Manca A; Kioschis P; Konecki D; Lehrach H; Poustka A
    Hum Mol Genet; 1992 Jul; 1(4):235-42. PubMed ID: 1303192
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A cosmid and yeast artificial chromosome contig containing the complete ryanodine receptor (RYR1) gene.
    Rouquier S; Giorgi D; Trask B; Bergmann A; Phillips MS; MacLennan DH; de Jong P
    Genomics; 1993 Aug; 17(2):330-40. PubMed ID: 8406483
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Isolation of a human gene (HES1) with homology to an Escherichia coli and a zebrafish protein that maps to chromosome 21q22.3.
    Scott HS; Chen H; Rossier C; Lalioti MD; Antonarakis SE
    Hum Genet; 1997 May; 99(5):616-23. PubMed ID: 9150728
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mutations and phenotype in isolated glycerol kinase deficiency.
    Walker AP; Muscatelli F; Stafford AN; Chelly J; Dahl N; Blomquist HK; Delanghe J; Willems PJ; Steinmann B; Monaco AP
    Am J Hum Genet; 1996 Jun; 58(6):1205-11. PubMed ID: 8651297
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Physical mapping distal to the DMD locus.
    Love DR; Bloomfield JF; Kenwrick SJ; Yates JR; Davies KE
    Genomics; 1990 Sep; 8(1):106-12. PubMed ID: 2081587
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Isolation and characterization of GT335, a novel human gene conserved in Escherichia coli and mapping to 21q22.3.
    Lafrenière RG; Rochefort DL; Kibar Z; Fon EA; Han F; Cochius J; Kang X; Baird S; Korneluk RG; Andermann E; Rommens JM; Rouleau GA
    Genomics; 1996 Dec; 38(3):264-72. PubMed ID: 8975701
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Transcript mapping of the human chromosome 11q12-q13.1 gene-rich region identifies several newly described conserved genes.
    Cooper PR; Nowak NJ; Higgins MJ; Church DM; Shows TB
    Genomics; 1998 May; 49(3):419-29. PubMed ID: 9615227
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.