84 related articles for article (PubMed ID: 8575787)
1. Chromosomal localization of the mitochondrial phosphate carrier gene PHC to 12q23.
Marsh S; Carter NP; Dolce V; Iacobazzi V; Palmieri F
Genomics; 1995 Oct; 29(3):814-5. PubMed ID: 8575787
[No Abstract] [Full Text] [Related]
2. Localization of the gene encoding human BiP/GRP78, the endoplasmic reticulum cognate of the HSP70 family, to chromosome 9q34.
Hendershot LM; Valentine VA; Lee AS; Morris SW; Shapiro DN
Genomics; 1994 Mar; 20(2):281-4. PubMed ID: 8020977
[TBL] [Abstract][Full Text] [Related]
3. The human family of Deafness/Dystonia peptide (DDP) related mitochondrial import proteins.
Jin H; Kendall E; Freeman TC; Roberts RG; Vetrie DL
Genomics; 1999 Nov; 61(3):259-67. PubMed ID: 10552927
[TBL] [Abstract][Full Text] [Related]
4. Assignment of human ADP ribosylation factor (ARF) genes ARF1 and ARF3 to chromosomes 1q42 and 12q13, respectively.
Hirai M; Kusuda J; Hashimoto K
Genomics; 1996 Jun; 34(2):263-5. PubMed ID: 8661066
[No Abstract] [Full Text] [Related]
5. Chromosome localization of human genes for clathrin adaptor polypeptides AP2 beta and AP50 and the clathrin-binding protein, VCP.
Druck T; Gu Y; Prabhala G; Cannizzaro LA; Park SH; Huebner K; Keen JH
Genomics; 1995 Nov; 30(1):94-7. PubMed ID: 8595912
[TBL] [Abstract][Full Text] [Related]
6. NUP98-NSD1 fusion by insertion in acute myeloblastic leukemia.
Petit A; Radford I; Waill MC; Romana S; Berger R
Cancer Genet Cytogenet; 2008 Jan; 180(1):43-6. PubMed ID: 18068532
[TBL] [Abstract][Full Text] [Related]
7. Localization of human elav-like neuronal protein 1 (Hel-N1) on chromosome 9p21 by chromosome microdissection polymerase chain reaction and fluorescence in situ hybridization.
Han J; Knops JF; Longshore JW; King PH
Genomics; 1996 Aug; 36(1):189-91. PubMed ID: 8812435
[TBL] [Abstract][Full Text] [Related]
8. Inactivation of the P16INK4/MTS1 gene by a chromosome translocation t(9;14)(p21-22;q11) in an acute lymphoblastic leukemia of B-cell type.
Duro D; Bernard O; Della Valle V; Leblanc T; Berger R; Larsen CJ
Cancer Res; 1996 Feb; 56(4):848-54. PubMed ID: 8631023
[TBL] [Abstract][Full Text] [Related]
9. Mapping of the human PAWR (par-4) gene to chromosome 12q21.
Johnstone RW; Tommerup N; Hansen C; Vissing H; Shi Y
Genomics; 1998 Oct; 53(2):241-3. PubMed ID: 9790775
[No Abstract] [Full Text] [Related]
10. A dimorphic microsatellite in the porcine H-FABP gene at chromosome 6.
Gerbens F; Harders FL; Groenen MA; Veerkamp JH; te Pas MF
Anim Genet; 1998 Oct; 29(5):408. PubMed ID: 9800342
[No Abstract] [Full Text] [Related]
11. Localization of the human poly(A)-binding protein gene (PAB1) to chromosomal regions 3q22-q25, 12q13-q14, and 13q12-q13 by in situ hybridization.
Morris CM; Bodger MP
Genomics; 1993 Jan; 15(1):209-11. PubMed ID: 8432538
[TBL] [Abstract][Full Text] [Related]
12. Isolation, tissue distribution, and chromosomal localization of a novel testis-specific human four-transmembrane gene related to CD20 and FcepsilonRI-beta.
Hulett MD; Pagler E; Hornby JR; Hogarth PM; Eyre HJ; Baker E; Crawford J; Sutherland GR; Ohms SJ; Parish CR
Biochem Biophys Res Commun; 2001 Jan; 280(1):374-9. PubMed ID: 11162526
[TBL] [Abstract][Full Text] [Related]
13. Midkine gene (MDK), a gene for prenatal differentiation and neuroregulation, maps to band 11p11.2 by fluorescence in situ hybridization.
Kaname T; Kuwano A; Murano I; Uehara K; Muramatsu T; Kajii T
Genomics; 1993 Aug; 17(2):514-5. PubMed ID: 8406506
[TBL] [Abstract][Full Text] [Related]
14. Two highly polymorphic microsatellites within the porcine secretory carrier membrane protein 1 (SCAMP1) gene.
Wen G; Pfeiffer I; Leeb T; Baumgartner BG; Hui D; Brenig B
Anim Genet; 1998 Dec; 29(6):462. PubMed ID: 9883513
[No Abstract] [Full Text] [Related]
15. Import of carrier proteins into the mitochondrial inner membrane mediated by Tim22.
Sirrenberg C; Bauer MF; Guiard B; Neupert W; Brunner M
Nature; 1996 Dec; 384(6609):582-5. PubMed ID: 8955274
[TBL] [Abstract][Full Text] [Related]
16. Localization of the 70-kDa peroxisomal membrane protein to human 1p21-p22 and mouse 3.
Gärtner J; Kearns W; Rosenberg C; Pearson P; Copeland NG; Gilbert DJ; Jenkins NA; Valle D
Genomics; 1993 Feb; 15(2):412-4. PubMed ID: 8449508
[TBL] [Abstract][Full Text] [Related]
17. Isolation of a novel human voltage-dependent anion channel gene.
Rahmani Z; Maunoury C; Siddiqui A
Eur J Hum Genet; 1998; 6(4):337-40. PubMed ID: 9781040
[TBL] [Abstract][Full Text] [Related]
18. A reciprocal translocation 46,XY,t(8;9)(p11.2;q13) in a bladder exstrophy patient disrupts CNTNAP3 and presents evidence of a pericentromeric duplication on chromosome 9.
Boyadjiev SA; South ST; Radford CL; Patel A; Zhang G; Hur DJ; Thomas GH; Gearhart JP; Stetten G
Genomics; 2005 May; 85(5):622-9. PubMed ID: 15820314
[TBL] [Abstract][Full Text] [Related]
19. The Bin1 gene localizes to human chromosome 2q14 by PCR analysis of somatic cell hybrids and fluorescence in situ hybridization.
Negorev D; Riethman H; Wechsler-Reya R; Sakamuro D; Prendergast GC; Simon D
Genomics; 1996 Apr; 33(2):329-31. PubMed ID: 8725406
[No Abstract] [Full Text] [Related]
20. Haploinsufficiency of NSD1 causes Sotos syndrome.
Kurotaki N; Imaizumi K; Harada N; Masuno M; Kondoh T; Nagai T; Ohashi H; Naritomi K; Tsukahara M; Makita Y; Sugimoto T; Sonoda T; Hasegawa T; Chinen Y; Tomita Ha HA; Kinoshita A; Mizuguchi T; Yoshiura Ki K; Ohta T; Kishino T; Fukushima Y; Niikawa N; Matsumoto N
Nat Genet; 2002 Apr; 30(4):365-6. PubMed ID: 11896389
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
