-
1
-
-
0028915206
-
Localization of short/branched chain acyl-CoA dehydrogenase (ACADSB) to human chromosome 10
-
Arden K, Rozen R, Viars C: Localization of short/branched chain acyl-CoA dehydrogenase (ACADSB) to human chromosome 10. Genomics 25:743-745 (1995).
-
(1995)
Genomics
, vol.25
, pp. 743-745
-
-
Arden, K.1
Rozen, R.2
Viars, C.3
-
2
-
-
0023255426
-
Chromosomal localization of human ornithine aminotransferase gene sequences to 10q26 and Xp11.2
-
Barrett DJ, Bateman JB, Sparkes RS, Mohandas T, Klisak I, Inana G: Chromosomal localization of human ornithine aminotransferase gene sequences to 10q26 and Xp11.2. Inv Ophthalm Vis Sci 28:1037-42 (1987).
-
(1987)
Inv Ophthalm Vis Sci
, vol.28
, pp. 1037-1042
-
-
Barrett, D.J.1
Bateman, J.B.2
Sparkes, R.S.3
Mohandas, T.4
Klisak, I.5
Inana, G.6
-
3
-
-
0029058473
-
Chromosomal mapping of the genes GPRK5 and GPRK6 encoding G protein-coupled receptor kinases GRK5 and GRK6
-
Bullrich F, Druck T, Kunapuli P, Gomez J, Gripp KW, Schlegelberger B, Lasota J, Aronson M, Cannizzaro LA, Huebner K: Chromosomal mapping of the genes GPRK5 and GPRK6 encoding G protein-coupled receptor kinases GRK5 and GRK6. Cytogenet Cell Genet 70:250-254 (1995).
-
(1995)
Cytogenet Cell Genet
, Issue.70
, pp. 250-254
-
-
Bullrich, F.1
Druck, T.2
Kunapuli, P.3
Gomez, J.4
Gripp, K.W.5
Schlegelberger, B.6
Lasota, J.7
Aronson, M.8
Cannizzaro, L.A.9
Huebner, K.10
-
4
-
-
0027246041
-
Expression of a cDNA cloning of a serine kinase transforming gene
-
Chan AM, Chedid M, McGowm ES, Popescu NC, Miki T, Aaronson SA: Expression of a cDNA cloning of a serine kinase transforming gene. Oncogene 8:1329-33 (1993).
-
(1993)
Oncogene
, vol.8
, pp. 1329-1333
-
-
Chan, A.M.1
Chedid, M.2
McGowm, E.S.3
Popescu, N.C.4
Miki, T.5
Aaronson, S.A.6
-
5
-
-
0027933734
-
A genome-wide search for human type 1 diabetes susceptibility genes
-
Davies JL, Kawaguchi Y, Bennett ST, Copeman JB, Cordell HJ, Pritchard LE, Reed PW, Gough SCL, Jenkins SC, Palmer SM, Balfour KM, Rowe BR, Farrall M, Barnett AH, Bain SC, Todd JA: A genome-wide search for human type 1 diabetes susceptibility genes. Nature 371:130-136 (1994).
-
(1994)
Nature
, vol.371
, pp. 130-136
-
-
Davies, J.L.1
Kawaguchi, Y.2
Bennett, S.T.3
Copeman, J.B.4
Cordell, H.J.5
Pritchard, L.E.6
Reed, P.W.7
Gough, S.C.L.8
Jenkins, S.C.9
Palmer, S.M.10
Balfour, K.M.11
Rowe, B.R.12
Farrall, M.13
Barnett, A.H.14
Bain, S.C.15
Todd, J.A.16
-
6
-
-
0028960579
-
Mapping of the human protein kinase C-theta (PRKCQ) gene locus to the short arm of chromosome 10 (10p15) by FISH
-
Erdel M, Baier-Bitterlich G, Duba C: Mapping of the human protein kinase C-theta (PRKCQ) gene locus to the short arm of chromosome 10 (10p15) by FISH. Genomics 25:595-597 (1995).
-
(1995)
Genomics
, vol.25
, pp. 595-597
-
-
Erdel, M.1
Baier-Bitterlich, G.2
Duba, C.3
-
7
-
-
0028048214
-
Functional identification of a vesicular acetylcholine transporter and its expression from a "cholinergic" gene locus
-
Erickson JD, Varoqui H, Schäfer MKH, Modi W, Diebler MF, Weihe E, Rand J, Eiden LE, Bonner TI, Usdin TB: Functional identification of a vesicular acetylcholine transporter and its expression from a "cholinergic" gene locus. J biol Chem 269:21929-32 (1994).
-
(1994)
J Biol Chem
, vol.269
, pp. 21929-21932
-
-
Erickson, J.D.1
Varoqui, H.2
Schäfer, M.K.H.3
Modi, W.4
Diebler, M.F.5
Weihe, E.6
Rand, J.7
Eiden, L.E.8
Bonner, T.I.9
Usdin, T.B.10
-
8
-
-
0029145950
-
Linkage disequilibrium mapping of the gene for Hermansky-Pudlak syndrome to chromosome 10q23.1-q23.3
-
Fukai K, Oh J, Frenk E, Amodovar C, Spritz RA: Linkage disequilibrium mapping of the gene for Hermansky-Pudlak syndrome to chromosome 10q23.1-q23.3. Hum mol Genet 4:1165-39 (1995).
-
(1995)
Hum Mol Genet
, vol.4
, pp. 1165-1239
-
-
Fukai, K.1
Oh, J.2
Frenk, E.3
Amodovar, C.4
Spritz, R.A.5
-
9
-
-
0028902430
-
Assignment of the 5HT7 receptor gene (HTR7) to chromosome 10q and exclusion of genetic linkage with Tourette syndrome
-
Gelernter J, Rao PA, Pauls DL, Hamblin MW, Simbley DR, Kidd KK: Assignment of the 5HT7 receptor gene (HTR7) to chromosome 10q and exclusion of genetic linkage with Tourette syndrome. Genomics 26:207-209 (1995).
-
(1995)
Genomics
, vol.26
, pp. 207-209
-
-
Gelernter, J.1
Rao, P.A.2
Pauls, D.L.3
Hamblin, M.W.4
Simbley, D.R.5
Kidd, K.K.6
-
10
-
-
0025894715
-
Deregulation of a homeobox gene, HOX11, by the t(10;14) in T Cell Leukemia
-
Hatano M, Roberts CWM, Minden M, Crist WM, Korsmeyer SJ: Deregulation of a homeobox gene, HOX11, by the t(10;14) in T Cell Leukemia, Science 253:79-82 (1991).
-
(1991)
Science
, vol.253
, pp. 79-82
-
-
Hatano, M.1
Roberts, C.W.M.2
Minden, M.3
Crist, W.M.4
Korsmeyer, S.J.5
-
11
-
-
84865666206
-
Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2
-
Jabs EW, Li X, Scott AF, Meyers G, Chen W, Eccles M, Mao J, Chamas LR, Jackson CE, Jaye M: Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2. Nature
-
Nature
-
-
Jabs, E.W.1
Li, X.2
Scott, A.F.3
Meyers, G.4
Chen, W.5
Eccles, M.6
Mao, J.7
Chamas, L.R.8
Jackson, C.E.9
Jaye, M.10
-
12
-
-
0028978034
-
Chromosomal localization of the ankyrin G gene (ANK3/Ank3) to human 10q21 and mouse 10
-
Kapfhamer D, Miller DE, Lambert S: Chromosomal localization of the ankyrin G gene (ANK3/Ank3) to human 10q21 and mouse 10. Genomics 27:189-191 (1995).
-
(1995)
Genomics
, vol.27
, pp. 189-191
-
-
Kapfhamer, D.1
Miller, D.E.2
Lambert, S.3
-
13
-
-
0028709436
-
The EUROGEM Map of Human Chromosome 10
-
Kapsetaki M, Kokkinaki M, Angelicheva D, Lubyova B, Mavraki H, Argyrokastritis A, Vergnaud G, Ferguson-Smith M, Rubinsztein DC, Lush M, Moschonas NK: The EUROGEM Map of Human Chromosome 10. Eur J hum Genet 2:222-223 (1994).
-
(1994)
Eur J Hum Genet
, vol.2
, pp. 222-223
-
-
Kapsetaki, M.1
Kokkinaki, M.2
Angelicheva, D.3
Lubyova, B.4
Mavraki, H.5
Argyrokastritis, A.6
Vergnaud, G.7
Ferguson-Smith, M.8
Rubinsztein, D.C.9
Lush, M.10
Moschonas, N.K.11
-
14
-
-
0026046616
-
HOX11, a homeobox-containing T-cell oncogene on human chromosome 10q24
-
Kennedy MA, Gonzalez-Sarmiento R, Kees UR, Lampert F, Dear N, Boehm T, Rabbitts TH: HOX11, a homeobox-containing T-cell oncogene on human chromosome 10q24. Proc natl Acad Sci, USA 88:8900-04 (1991).
-
(1991)
Proc Natl Acad Sci, USA
, vol.88
, pp. 8900-8904
-
-
Kennedy, M.A.1
Gonzalez-Sarmiento, R.2
Kees, U.R.3
Lampert, F.4
Dear, N.5
Boehm, T.6
Rabbitts, T.H.7
-
15
-
-
0028949229
-
Localization of multiple human dihydrodiol dehydrogenase (DDH1 and DDH2) and chlordecone reductase (CHDR) genes in chromosome 10 by the polymerase chain reaction and fluorescent in situ hybridization
-
Khanna M, Qin KN, Klisak I, Belkin S, Sparkes RS, Cheng KC: Localization of multiple human dihydrodiol dehydrogenase (DDH1 and DDH2) and chlordecone reductase (CHDR) genes in chromosome 10 by the polymerase chain reaction and fluorescent in situ hybridization. Genomics 25:588-590 (1995).
-
(1995)
Genomics
, vol.25
, pp. 588-590
-
-
Khanna, M.1
Qin, K.N.2
Klisak, I.3
Belkin, S.4
Sparkes, R.S.5
Cheng, K.C.6
-
16
-
-
0029064179
-
CHUK, a conserved helix-loop-helix ubiquitous kinase, maps to human chromosome 10 and mouse chromosome 19
-
Mock BA, Conelly MA, McBride OW, Kozak CA, Marcu KB: CHUK, a conserved helix-loop-helix ubiquitous kinase, maps to human chromosome 10 and mouse chromosome 19. Genomics 27:348-351 (1995).
-
(1995)
Genomics
, vol.27
, pp. 348-351
-
-
Mock, B.A.1
Conelly, M.A.2
McBride, O.W.3
Kozak, C.A.4
Marcu, K.B.5
-
17
-
-
0028949919
-
Random search for shared chromosomal regions in four affected individuals: The assignment of a new hereditary ataxia locus
-
Nikali K, Suomalainen A, Terwillinger J: Random search for shared chromosomal regions in four affected individuals: the assignment of a new hereditary ataxia locus. Am J hum Genet 56:1088-1095 (1995).
-
(1995)
Am J Hum Genet
, vol.56
, pp. 1088-1095
-
-
Nikali, K.1
Suomalainen, A.2
Terwillinger, J.3
-
18
-
-
0029116382
-
The cloning and chromosomal mapping of two novel human opioid-somatostatin-like receptor genes GPR7 and GPR8, expressed in discrete areas of the brain
-
O'Dowd BF, Scheideler MA, Nguyen T, Cheng R, Rasmussen JS, Marchese A, Zastawny R, Heng HHQ, Tsui LC, Shi XM: The cloning and chromosomal mapping of two novel human opioid-somatostatin-like receptor genes GPR7 and GPR8, expressed in discrete areas of the brain. Genomics 28:84-91 (1995).
-
(1995)
Genomics
, vol.28
, pp. 84-91
-
-
O'Dowd, B.F.1
Scheideler, M.A.2
Nguyen, T.3
Cheng, R.4
Rasmussen, J.S.5
Marchese, A.6
Zastawny, R.7
Heng, H.H.Q.8
Tsui, L.C.9
Shi, X.M.10
-
19
-
-
0029098705
-
Gene structure and amino acid sequence of the human cone photoreceptor cGMP-phosphodiesterase alpha subunit (PDEA2) and its chromosomal localization to 10q24
-
Piriev NI, Viczian AS, Ye JJ, Kerner B, Korenberg JR, Farber DB: Gene structure and amino acid sequence of the human cone photoreceptor cGMP-phosphodiesterase alpha subunit (PDEA2) and its chromosomal localization to 10q24. Genomics 28:429-435 (1995).
-
(1995)
Genomics
, vol.28
, pp. 429-435
-
-
Piriev, N.I.1
Viczian, A.S.2
Ye, J.J.3
Kerner, B.4
Korenberg, J.R.5
Farber, D.B.6
-
20
-
-
0029024891
-
Chromosome 10 deletion mapping in human gliomas: A common deletion region in 10q25
-
Rasheed BKA, McLendon RE, Friedman HS, Friedman AH, Fuchs HE, Bigner DD, Bigner SH: Chromosome 10 deletion mapping in human gliomas: a common deletion region in 10q25. Oncogene 10:2243-46 (1995).
-
(1995)
Oncogene
, vol.10
, pp. 2243-2246
-
-
Rasheed, B.K.A.1
McLendon, R.E.2
Friedman, H.S.3
Friedman, A.H.4
Fuchs, H.E.5
Bigner, D.D.6
Bigner, S.H.7
-
21
-
-
0027981524
-
Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome
-
Reardon W, Winter RM, Rutland P, Pulleyn LJ, Jones M, Malcolm S: Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome. Nature Genet 8:98-103 (1994).
-
(1994)
Nature Genet
, vol.8
, pp. 98-103
-
-
Reardon, W.1
Winter, R.M.2
Rutland, P.3
Pulleyn, L.J.4
Jones, M.5
Malcolm, S.6
-
22
-
-
0029109137
-
Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypes
-
Rutland P, Pulleyn U, Reardon W, Baraitser M, Hayward R, Jones B, Malcolm S, Winter RM, Oldridge M, Slaney SF, Poole MD, Wilkie AOM: Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypes. Nature Genet 9:173-176 (1995).
-
(1995)
Nature Genet
, vol.9
, pp. 173-176
-
-
Rutland, P.1
Pulleyn, U.2
Reardon, W.3
Baraitser, M.4
Hayward, R.5
Jones, B.6
Malcolm, S.7
Winter, R.M.8
Oldridge, M.9
Slaney, S.F.10
Poole, M.D.11
Wilkie, A.O.M.12
-
23
-
-
0028966947
-
Mutation of the PAX2 gene in a family with optic nerve colobomas, renal anomalies and vesicoureteral reflux
-
Sanyanusin P, Schimmenti LA, McNoe LA, Ward TA, Pierpont MEM, Sullivan MJ, Dobyns WB, Eccles MR: Mutation of the PAX2 gene in a family with optic nerve colobomas, renal anomalies and vesicoureteral reflux. Nature Genet 9:358-363 (1995).
-
(1995)
Nature Genet
, vol.9
, pp. 358-363
-
-
Sanyanusin, P.1
Schimmenti, L.A.2
McNoe, L.A.3
Ward, T.A.4
Pierpont, M.E.M.5
Sullivan, M.J.6
Dobyns, W.B.7
Eccles, M.R.8
-
24
-
-
0029099521
-
Structure and chromosomal localization of the human stromal cell-derived factor 1 (SDF1) gene
-
Shirozu M, Nakano T, Inazawa J, Tashiro K, Tada H, Shinohara T, Honjo T: Structure and chromosomal localization of the human stromal cell-derived factor 1 (SDF1) gene. Genomics 28:495-500 (1995).
-
(1995)
Genomics
, vol.28
, pp. 495-500
-
-
Shirozu, M.1
Nakano, T.2
Inazawa, J.3
Tashiro, K.4
Tada, H.5
Shinohara, T.6
Honjo, T.7
-
25
-
-
0029310532
-
Phylogenetic conservation and physical mapping of members of the H6 homeobox gene family
-
Stadler HS, Murray JC, Leysens NJ: Phylogenetic conservation and physical mapping of members of the H6 homeobox gene family. Mammal Genome 6:383-388 (1995).
-
(1995)
Mammal Genome
, vol.6
, pp. 383-388
-
-
Stadler, H.S.1
Murray, J.C.2
Leysens, N.J.3
-
26
-
-
0027533927
-
Chromosomal localization of seven PAX genes and cloning of a novel family member, PAX-9
-
Stapleton P, Weith A, Urbanek P, Kozmik Z, Busslinger M: Chromosomal localization of seven PAX genes and cloning of a novel family member, PAX-9. Nature Genet 3:292-298 (1993).
-
(1993)
Nature Genet
, vol.3
, pp. 292-298
-
-
Stapleton, P.1
Weith, A.2
Urbanek, P.3
Kozmik, Z.4
Busslinger, M.5
-
27
-
-
0028949383
-
The eukaryotic cofactor for the human immunodeficiency virus type 1 (HIV-1) rev protein, eIF-5A pseudogenes map to 10q23.3, 17q25, and 19q13.2
-
Steinkasserer A, Jones T, Sheer D: The eukaryotic cofactor for the human immunodeficiency virus type 1 (HIV-1) rev protein, eIF-5A pseudogenes map to 10q23.3, 17q25, and 19q13.2. Genomics 25:749-752 (1995).
-
(1995)
Genomics
, vol.25
, pp. 749-752
-
-
Steinkasserer, A.1
Jones, T.2
Sheer, D.3
-
28
-
-
0028833524
-
An autosomal locus predisposing to deletions of mitochondrial DNA
-
Suomalainen A, Kaukonen J, Amati P, Timonen R, Haltia M, Weissenbach J, Zeviani M, Somer H, Peltonen L: An autosomal locus predisposing to deletions of mitochondrial DNA Nature Genet 9:146-151 (1995).
-
(1995)
Nature Genet
, vol.9
, pp. 146-151
-
-
Suomalainen, A.1
Kaukonen, J.2
Amati, P.3
Timonen, R.4
Haltia, M.5
Weissenbach, J.6
Zeviani, M.7
Somer, H.8
Peltonen, L.9
-
29
-
-
0028959529
-
Human androgen-induced growth factor in prostate and breast cancer cells: It's molecular cloning and growth properties
-
Tanaka A, Miyamoto K, Matsuo H, Matsumoto K, Yoshida H: Human androgen-induced growth factor in prostate and breast cancer cells: It's molecular cloning and growth properties. FEBS Letters 363:226-230 (1995).
-
(1995)
FEBS Letters
, vol.363
, pp. 226-230
-
-
Tanaka, A.1
Miyamoto, K.2
Matsuo, H.3
Matsumoto, K.4
Yoshida, H.5
-
30
-
-
0028012821
-
Chromosomal location of two human genes encoding tetrahydrobiopterin-metabolizing enzymes: 6-pyruvoyl-tetrahydropterin synthase maps to 11q22.3-q23.3, and pterin-4 alpha-carbinolamine dehydratase maps to 10q22
-
Thony B, Heizmann CW, Mattei MG: Chromosomal location of two human genes encoding tetrahydrobiopterin-metabolizing enzymes: 6-pyruvoyl-tetrahydropterin synthase maps to 11q22.3-q23.3, and pterin-4 alpha-carbinolamine dehydratase maps to 10q22. Genomics 19:365-368 (1994).
-
(1994)
Genomics
, vol.19
, pp. 365-368
-
-
Thony, B.1
Heizmann, C.W.2
Mattei, M.G.3
-
31
-
-
0028956422
-
Chromosomal localization of mitochondrial transcription factor A (TCF6), single-stranded DNA-binding protein (SSBP), and endonuclease G (ENDOG), three human housekeeping genes involved in mitochondrial biogenesis
-
Tiranti V, Rossi E, Ruiz-Carillo A, Rossi G, Rocchi M, DiDonato S, Zuffardi O, Zeviani M: Chromosomal localization of mitochondrial transcription factor A (TCF6), single-stranded DNA-binding protein (SSBP), and endonuclease G (ENDOG), three human housekeeping genes involved in mitochondrial biogenesis. Genomics 25:559-564 (1995).
-
(1995)
Genomics
, vol.25
, pp. 559-564
-
-
Tiranti, V.1
Rossi, E.2
Ruiz-Carillo, A.3
Rossi, G.4
Rocchi, M.5
DiDonato, S.6
Zuffardi, O.7
Zeviani, M.8
-
32
-
-
0028798546
-
Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome
-
Wilkie AOM, Slaney SF, Oldridge M, Poole MD, Ashworth GJ, Hockley AD, Hayward RD, David DJ, Pulleyn LJ, Rutland P, Malcolm S, Winter RM, Reardon W: Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome. Nature Genet 9:165-172 (1995).
-
(1995)
Nature Genet
, vol.9
, pp. 165-172
-
-
Wilkie, A.O.M.1
Slaney, S.F.2
Oldridge, M.3
Poole, M.D.4
Ashworth, G.J.5
Hockley, A.D.6
Hayward, R.D.7
David, D.J.8
Pulleyn, L.J.9
Rutland, P.10
Malcolm, S.11
Winter, R.M.12
Reardon, W.13
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