-
1
-
-
0027460737
-
Physical and genetic mapping of the dipeptidase gene DPEP1 to 16q24.3
-
Austruy E, Jeanpierre C, Antignac C, Whitmore SA, Van Cong N, Bernheim A, Callen DP, Junien C: Physical and genetic mapping of the dipeptidase gene DPEP1 to 16q24.3. Genomics 15:684-687 (1993).
-
(1993)
Genomics
, vol.15
, pp. 684-687
-
-
Austruy, E.1
Jeanpierre, C.2
Antignac, C.3
Whitmore, S.A.4
Van Cong, N.5
Bernheim, A.6
Callen, D.P.7
Junien, C.8
-
2
-
-
6844241328
-
Assignment of muscle cadherin (MCAD) to human chromosome 16q24-qter and to mouse chromosome 8, and of placental cadherin (PCAD)-like sequences PCADL1 to 16q22.1 and PCADL2 to 16q24-qter
-
Becker-Follmann J, Kaupmann K, Vestweber D, Jochusch H, Starzinski-Powitz A, Scherer G: Assignment of muscle cadherin (MCAD) to human chromosome 16q24-qter and to mouse chromosome 8, and of placental cadherin (PCAD)-like sequences PCADL1 to 16q22.1 and PCADL2 to 16q24-qter. Cytogenet Cell Genet 60:168 (1992).
-
(1992)
Cytogenet Cell Genet
, vol.60
, pp. 168
-
-
Becker-Follmann, J.1
Kaupmann, K.2
Vestweber, D.3
Jochusch, H.4
Starzinski-Powitz, A.5
Scherer, G.6
-
3
-
-
85087585903
-
E-cadherin is a tumour/invasion suppressor gene mutated in human lobular breast cancers
-
in press
-
Berx G, Cleton-Jansen A-M, Nollet F, De Leeuw WJF, Van de Vijver MJ, Cornelisse CJ, Van Roy F: E-cadherin is a tumour/invasion suppressor gene mutated in human lobular breast cancers. EMBO J (in press).
-
EMBO J
-
-
Berx, G.1
Cleton-Jansen, A.-M.2
Nollet, F.3
De Leeuw, W.J.F.4
Van De Vijver, M.J.5
Cornelisse, C.J.6
Van Roy, F.7
-
4
-
-
0028788975
-
Familial cylindromatosis (turban tumour syndrome) gene localized to chromosome 16q12-q13: Evidence for its role as a tumour supressor gene
-
Biggs PJ, Wooster R, Ford D, Chapman P, Mangion J, Quirk Y, Easton DE, Burn J, Stratton MR: Familial cylindromatosis (turban tumour syndrome) gene localized to chromosome 16q12-q13: evidence for its role as a tumour supressor gene. Nature Genetics 11:441-443 (1995).
-
(1995)
Nature Genetics
, vol.11
, pp. 441-443
-
-
Biggs, P.J.1
Wooster, R.2
Ford, D.3
Chapman, P.4
Mangion, J.5
Quirk, Y.6
Easton, D.E.7
Burn, J.8
Stratton, M.R.9
-
5
-
-
0028879076
-
Epithelial sodium channel genes SCNN1B and SCNN1G are closely linked on distal mouse chromosome 7
-
Brooker DR, Kozak CA, Kleyman TR: Epithelial sodium channel genes SCNN1B and SCNN1G are closely linked on distal mouse chromosome 7. Genomics 29:784-786 (1995).
-
(1995)
Genomics
, vol.29
, pp. 784-786
-
-
Brooker, D.R.1
Kozak, C.A.2
Kleyman, T.R.3
-
6
-
-
9244252171
-
Report of the committee on the genetic constituency of chromosome 16
-
Cuticchia AJ (ed): The Johns Hopkins University Press, Baltimore
-
Callen DF, Doggett NA; Report of the committee on the genetic constituency of chromosome 16, in Cuticchia AJ (ed): Human Gene Mapping 1994, A Compendium, pp 559-646 (The Johns Hopkins University Press, Baltimore 1995).
-
(1995)
Human Gene Mapping 1994, A Compendium
, pp. 559-646
-
-
Callen, D.F.1
Doggett, N.A.2
-
7
-
-
0029118377
-
Integration of transcript and genetic maps of chromosome 16 at near 1 Mb resolution: Demonstration of a 'hot-spot' for recombination at 16p12
-
Callen DF, Lane SA, Kozman H, Kremmidiotis G, Whitmore SA, Lowenstein M, Doggett NA, Kenmochi N, Page DC, Maglott DR, Nierman WC, Murakawa K, Berry R, Sikela JM, Houlgatte R, Auffray C, Sutherland GR: Integration of transcript and genetic maps of chromosome 16 at near 1 Mb resolution: Demonstration of a 'hot-spot' for recombination at 16p12. Genomics 29:503-511 (1995).
-
(1995)
Genomics
, vol.29
, pp. 503-511
-
-
Callen, D.F.1
Lane, S.A.2
Kozman, H.3
Kremmidiotis, G.4
Whitmore, S.A.5
Lowenstein, M.6
Doggett, N.A.7
Kenmochi, N.8
Page, D.C.9
Maglott, D.R.10
Nierman, W.C.11
Murakawa, K.12
Berry, R.13
Sikela, J.M.14
Houlgatte, R.15
Auffray, C.16
Sutherland, G.R.17
-
8
-
-
0027078247
-
Localization of the human gene for mu-crystallin to chromosome 16p
-
Chen H, Phillips HA, Callen DF, Kim RY, Wistow GJ, Antonarakis SE: Localization of the human gene for mu-crystallin to chromosome 16p. Genomics 14:1115-1116 (1992).
-
(1992)
Genomics
, vol.14
, pp. 1115-1116
-
-
Chen, H.1
Phillips, H.A.2
Callen, D.F.3
Kim, R.Y.4
Wistow, G.J.5
Antonarakis, S.E.6
-
9
-
-
0027095653
-
Overexpression of a transporter gene in a multidrug-resistant human lung cancer cell line
-
Cole SPC, Bhardwaj G, Gerlach JH, Mackie JE, Grent CE, Almquist KC, Stewart AJ, Kurz EU, Duncan AMV, Deeley RG: Overexpression of a transporter gene in a multidrug-resistant human lung cancer cell line. Science 258:1650-1654 (1992).
-
(1992)
Science
, vol.258
, pp. 1650-1654
-
-
Cole, S.P.C.1
Bhardwaj, G.2
Gerlach, J.H.3
Mackie, J.E.4
Grent, C.E.5
Almquist, K.C.6
Stewart, A.J.7
Kurz, E.U.8
Duncan, A.M.V.9
Deeley, R.G.10
-
10
-
-
0027507490
-
A genetic linkage map of the mouse: Current applications and future prospects
-
Copeland NG, Jenkins NA, Gilbert DJ, Eppig JT, Maltais LJ, Miller JC, Dietrich WF, Weaver A, Lincoln SE, Steen RG, Stein LD, Nadeau JH, Lander ES: A genetic linkage map of the mouse: current applications and future prospects. Science 262:57-66 (1993).
-
(1993)
Science
, vol.262
, pp. 57-66
-
-
Copeland, N.G.1
Jenkins, N.A.2
Gilbert, D.J.3
Eppig, J.T.4
Maltais, L.J.5
Miller, J.C.6
Dietrich, W.F.7
Weaver, A.8
Lincoln, S.E.9
Steen, R.G.10
Stein, L.D.11
Nadeau, J.H.12
Lander, E.S.13
-
11
-
-
0027517493
-
Smooth muscle myosin heavy chain locus (MYH11) maps to 16p13.13-p13.12 and establishes a new region of conserved synteny between human 16p and mouse 16
-
Deng ZM, Liu P, Marlton P, Claxton DF, Lane S, Callen DF, Collins FS, Siciliano MJ: Smooth muscle myosin heavy chain locus (MYH11) maps to 16p13.13-p13.12 and establishes a new region of conserved synteny between human 16p and mouse 16. Genomics 18:156-159 (1993).
-
(1993)
Genomics
, vol.18
, pp. 156-159
-
-
Deng, Z.M.1
Liu, P.2
Marlton, P.3
Claxton, D.F.4
Lane, S.5
Callen, D.F.6
Collins, F.S.7
Siciliano, M.J.8
-
12
-
-
0028915805
-
Report of the third international workshop on human chromosome 16 mapping 1994
-
Doggett NA, Callen DF: Report of the third international workshop on human chromosome 16 mapping 1994. Cytogenet Cell Genet 68:165-184 (1995).
-
(1995)
Cytogenet Cell Genet
, vol.68
, pp. 165-184
-
-
Doggett, N.A.1
Callen, D.F.2
-
13
-
-
0029653645
-
An integrated physical map of human chromosome 16
-
Doggett NA, Good win LA, Tesmer JG, Meincke LJ, Bruce DC, Clark LM, Altherr MR, Ford AA, Chi H-C, Marrone BL, Longmire JL, Lane SA, Whitmore SA, Lowenstein MG, Sutherland RD, Mundt MO, Knill EH, Bruno WJ, Macken CA, Tomey DC, Wu JR, Griffith J, Sutherland GR, Deaven LL, Callen DF, Moyzis RK: An integrated physical map of human chromosome 16. Nature 377: Suppl:335-365 (1995).
-
(1995)
Nature
, vol.377
, Issue.SUPPL.
, pp. 335-365
-
-
Doggett, N.A.1
Good Win, L.A.2
Tesmer, J.G.3
Meincke, L.J.4
Bruce, D.C.5
Clark, L.M.6
Altherr, M.R.7
Ford, A.A.8
Chi, H.-C.9
Marrone, B.L.10
Longmire, J.L.11
Lane, S.A.12
Whitmore, S.A.13
Lowenstein, M.G.14
Sutherland, R.D.15
Mundt, M.O.16
Knill, E.H.17
Bruno, W.J.18
Macken, C.A.19
Tomey, D.C.20
Wu, J.R.21
Griffith, J.22
Sutherland, G.R.23
Deaven, L.L.24
Callen, D.F.25
Moyzis, R.K.26
more..
-
14
-
-
0027485239
-
Mapping of the phenol sulfotransferase gene (STP) to human chromosome 16p12.1-p11.2 and to mouse chromosome 7
-
Dooley TP, Obermoeller RD, Leiter EH, Chapman HD, Falany CN, Deng Z, Siciliano MJ: Mapping of the phenol sulfotransferase gene (STP) to human chromosome 16p12.1-p11.2 and to mouse chromosome 7. Genomics 18:440-443 (1993).
-
(1993)
Genomics
, vol.18
, pp. 440-443
-
-
Dooley, T.P.1
Obermoeller, R.D.2
Leiter, E.H.3
Chapman, H.D.4
Falany, C.N.5
Deng, Z.6
Siciliano, M.J.7
-
15
-
-
0027167456
-
Cloning and characterization of a mouse 3-methyladenine/7-methylguanine/3-methylguanine DNA glycosylase cDNA whose gene maps to chromosome 11
-
Engelward BP, Boosalis MS, Chen BJ, Deng ZM, Siciliano MJ, Samson L: Cloning and characterization of a mouse 3-methyladenine/7-methylguanine/3-methylguanine DNA glycosylase cDNA whose gene maps to chromosome 11. Carcinogenesis 14:175-181 (1993).
-
(1993)
Carcinogenesis
, vol.14
, pp. 175-181
-
-
Engelward, B.P.1
Boosalis, M.S.2
Chen, B.J.3
Deng, Z.M.4
Siciliano, M.J.5
Samson, L.6
-
16
-
-
0028091349
-
Mapping of the gene encoding the melanocortin-1 (alpha-melanocyte stimulating hormone) receptor (MC1R) to human chromosome 16q24.3 by fluorescence in situ hybridization
-
Gantz I, Yamada T, Tashiro T, Konda Y, Shimoto Y, Miwa H, Trent JM: Mapping of the gene encoding the melanocortin-1 (alpha-melanocyte stimulating hormone) receptor (MC1R) to human chromosome 16q24.3 by fluorescence in situ hybridization. Genomics 19:394-5 (1994).
-
(1994)
Genomics
, vol.19
, pp. 394-395
-
-
Gantz, I.1
Yamada, T.2
Tashiro, T.3
Konda, Y.4
Shimoto, Y.5
Miwa, H.6
Trent, J.M.7
-
17
-
-
0028849277
-
E-cadherin expression is silenced by DNA hypermethylation in human breast and prostate carcinomas
-
Graff JR, Herman JG, Lapidus RG, Chopra H, Xu R, Jarrard DF, Isaacs WB, Pitha PM, Davidson NE, Baylin SB: E-cadherin expression is silenced by DNA hypermethylation in human breast and prostate carcinomas. Cancer Research 55:5195-5199 (1995).
-
(1995)
Cancer Research
, vol.55
, pp. 5195-5199
-
-
Graff, J.R.1
Herman, J.G.2
Lapidus, R.G.3
Chopra, H.4
Xu, R.5
Jarrard, D.F.6
Isaacs, W.B.7
Pitha, P.M.8
Davidson, N.E.9
Baylin, S.B.10
-
18
-
-
0029004047
-
Structure of the leukemia-associated human CBFB gene
-
Hajra A, Collins FS: Structure of the leukemia-associated human CBFB gene. Genomics 26:571-579 (1995).
-
(1995)
Genomics
, vol.26
, pp. 571-579
-
-
Hajra, A.1
Collins, F.S.2
-
19
-
-
0029092801
-
Hypertension caused by a truncated epithelial sodium channel subunit: Genetic heterogeneity of Liddle syndrome
-
Hansson JH, Nelson-Williams C, Suzuki H, Schild L, Shimkets R, Lu Y, Canessa C, Iwasaki T, Rossier B, Lifton RP: Hypertension caused by a truncated epithelial sodium channel subunit: genetic heterogeneity of Liddle syndrome. Nature Genetics 11:76-82 (1995).
-
(1995)
Nature Genetics
, vol.11
, pp. 76-82
-
-
Hansson, J.H.1
Nelson-Williams, C.2
Suzuki, H.3
Schild, L.4
Shimkets, R.5
Lu, Y.6
Canessa, C.7
Iwasaki, T.8
Rossier, B.9
Lifton, R.P.10
-
20
-
-
0025880195
-
Genomic organization and chromosomal mapping of the mouse P-cadherin gene
-
Hatta M, Miyatani S, Copeland NG, Gilbert DJ, Jenkins NA, Takeichi M: Genomic organization and chromosomal mapping of the mouse P-cadherin gene. Nucl Acids Res 19:4437-4441 (1991).
-
(1991)
Nucl Acids Res
, vol.19
, pp. 4437-4441
-
-
Hatta, M.1
Miyatani, S.2
Copeland, N.G.3
Gilbert, D.J.4
Jenkins, N.A.5
Takeichi, M.6
-
21
-
-
0028049934
-
Mapping the gene that encodes phosphatidylinositol-specific phospholipase C-gamma 2 in the human and the mouse
-
Hernandez D, Egan SE, Yulug IG, Fisher EMC: Mapping the gene that encodes phosphatidylinositol-specific phospholipase C-gamma 2 in the human and the mouse. Genomics 23:504-7 (1994).
-
(1994)
Genomics
, vol.23
, pp. 504-507
-
-
Hernandez, D.1
Egan, S.E.2
Yulug, I.G.3
Fisher, E.M.C.4
-
22
-
-
0026509388
-
Human-mouse homologies in the region of the polycystic kidney disease gene (PKD1)
-
Himmelbauer H, Pohlschmidt M, Snarey A, Germino GG, Weinstat-Saslow D, Soinlo S, Reeders ST, Frischauf A: Human-mouse homologies in the region of the polycystic kidney disease gene (PKD1). Genomics 13:35-38 (1992).
-
(1992)
Genomics
, vol.13
, pp. 35-38
-
-
Himmelbauer, H.1
Pohlschmidt, M.2
Snarey, A.3
Germino, G.G.4
Weinstat-Saslow, D.5
Soinlo, S.6
Reeders, S.T.7
Frischauf, A.8
-
23
-
-
0029069583
-
The polycystic kidney disease 1 (PKD1) gene encodes a novel protein with multiple cell recognition domains
-
Hughes J, Ward CJ, Peral B, Aspinwall R, Clark K, San Millán JL, Gamble V, Harris PC: The polycystic kidney disease 1 (PKD1) gene encodes a novel protein with multiple cell recognition domains. Nature Genetics 10:151-160 (1995).
-
(1995)
Nature Genetics
, vol.10
, pp. 151-160
-
-
Hughes, J.1
Ward, C.J.2
Peral, B.3
Aspinwall, R.4
Clark, K.5
San Millán, J.L.6
Gamble, V.7
Harris, P.C.8
-
24
-
-
0029164859
-
YAC and cosmid contigs spanning the Batten disease region (CLN3) at 16p12.1-p11.2
-
Järvelä IE, Mitchison HM, O'Rawe AM, Munroe PB, Taschner PEM, de Vos N, Lemer TJ, D'Arigo KL, Callen DE, Thompson AD, Knight M, Marrone BL, Mundt MO, Meincke L, Breuning MH, Gardiner RM, Doggett NA, Mole SE: YAC and cosmid contigs spanning the Batten disease region (CLN3) at 16p12.1-p11.2. Genomics 29:478-489 (1995).
-
(1995)
Genomics
, vol.29
, pp. 478-489
-
-
Järvelä, I.E.1
Mitchison, H.M.2
O'Rawe, A.M.3
Munroe, P.B.4
Taschner, P.E.M.5
De Vos, N.6
Lemer, T.J.7
D'Arigo, K.L.8
Callen, D.E.9
Thompson, A.D.10
Knight, M.11
Marrone, B.L.12
Mundt, M.O.13
Meincke, L.14
Breuning, M.H.15
Gardiner, R.M.16
Doggett, N.A.17
Mole, S.E.18
-
25
-
-
0027468074
-
Chromosomal assignment of the uromodulin gene (UMOD) to 16p13.11
-
Jeanpierre C, Whitmore SA, Austruy E, Cohen-Salmon M, Callen DF, Junien C: Chromosomal assignment of the uromodulin gene (UMOD) to 16p13.11 Cytogenet Cell Genet 62:185-187 (1993).
-
(1993)
Cytogenet Cell Genet
, vol.62
, pp. 185-187
-
-
Jeanpierre, C.1
Whitmore, S.A.2
Austruy, E.3
Cohen-Salmon, M.4
Callen, D.F.5
Junien, C.6
-
26
-
-
0028830856
-
A germline insertion in the tuberous sclerosis (TSC2) gene gives rise to the Eker rat model of dominantly inherited cancer
-
Kobayashi T, Hirayama Y, Kobayashi E, Kubo Y, Hino O: A germline insertion in the tuberous sclerosis (TSC2) gene gives rise to the Eker rat model of dominantly inherited cancer. Nature Genetics 9:70-74 (1995).
-
(1995)
Nature Genetics
, vol.9
, pp. 70-74
-
-
Kobayashi, T.1
Hirayama, Y.2
Kobayashi, E.3
Kubo, Y.4
Hino, O.5
-
27
-
-
0028485229
-
Mapping of the ACTH, MSH, and neural (MC3 and MC4) melanocortin receptors in the mouse and human
-
Magenis RE, Smith L, Nadeau JH, Johnson KR, Mountjoy KG, Cone RD: Mapping of the ACTH, MSH, and neural (MC3 and MC4) melanocortin receptors in the mouse and human. Mammal Genome 5:503-8 (1994).
-
(1994)
Mammal Genome
, vol.5
, pp. 503-508
-
-
Magenis, R.E.1
Smith, L.2
Nadeau, J.H.3
Johnson, K.R.4
Mountjoy, K.G.5
Cone, R.D.6
-
28
-
-
0001363246
-
Report of the committee on comparative gene mapping
-
Cuticchia AJ, Pearson PL, Klinger HP (eds): S Karger, Basel
-
O'Brien SJ, Peters J, Searle A, Womack J, Marshall-Graves J: Report of the committee on comparative gene mapping, in Cuticchia AJ, Pearson PL, Klinger HP (eds): Chromosome Coordinating Meeting 1992, pp 758-809 (S Karger, Basel 1993).
-
(1993)
Chromosome Coordinating Meeting 1992
, pp. 758-809
-
-
O'Brien, S.J.1
Peters, J.2
Searle, A.3
Womack, J.4
Marshall-Graves, J.5
-
30
-
-
0028939384
-
The mouse homologue of the tuberin gene (TSC2) maps to a conserved synteny group between mouse chromosome 17 and human 16p13.3
-
Olsson PG, Sutherland HF, Nowicka U, Kom B, Poustka A, Frischauf AM: The mouse homologue of the tuberin gene (TSC2) maps to a conserved synteny group between mouse chromosome 17 and human 16p13.3. Genomics 25:339-340 (1995).
-
(1995)
Genomics
, vol.25
, pp. 339-340
-
-
Olsson, P.G.1
Sutherland, H.F.2
Nowicka, U.3
Kom, B.4
Poustka, A.5
Frischauf, A.M.6
-
31
-
-
0028207313
-
CD19 maps to a region of conservation between human chromosome 16 and mouse chromosome 7
-
Ord DC, Edelhoff S, Dushkin H, Zhou LJ, Beier DR, Disteche C, Tedder TF: CD19 maps to a region of conservation between human chromosome 16 and mouse chromosome 7. Immunogenetics 39-322-8 (1994),
-
(1994)
Immunogenetics
, vol.39
, pp. 322-328
-
-
Ord, D.C.1
Edelhoff, S.2
Dushkin, H.3
Zhou, L.J.4
Beier, D.R.5
Disteche, C.6
Tedder, T.F.7
-
32
-
-
0026708517
-
Mapping of the human GSPT1 gene, a human homolog of the yeast GST1 gene, to chromosomal band 16p13.1 Somat Cell molec
-
Ozawa K, Murakami Y, Eki T, Yokoyama K, Soeda E, Hoshino S, Ui M, Hanaoka F: Mapping of the human GSPT1 gene, a human homolog of the yeast GST1 gene, to chromosomal band 16p13.1 Somat Cell molec Genet 18:189-194 (1992).
-
(1992)
Genet
, vol.18
, pp. 189-194
-
-
Ozawa, K.1
Murakami, Y.2
Eki, T.3
Yokoyama, K.4
Soeda, E.5
Hoshino, S.6
Ui, M.7
Hanaoka, F.8
-
33
-
-
0026631182
-
MT-III a brain-specific member of the metallothionein gene family
-
Palmiter RD, Findley SD, Whitmore TE, Dumam DM: MT-III a brain-specific member of the metallothionein gene family. Proc natl Acad Sci, USA 89:6333-6337 (1992).
-
(1992)
Proc Natl Acad Sci, USA
, vol.89
, pp. 6333-6337
-
-
Palmiter, R.D.1
Findley, S.D.2
Whitmore, T.E.3
Dumam, D.M.4
-
34
-
-
0029022770
-
Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP
-
Petrij F, Giles RH, Dauwerse HG, Saris JJ, Hennekam RCM, Masuno M, Tommerup N, vanOmmen G-JB, Goodman RH, Peters DJM, Breuning MH: Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP. Nature 376:348-351 (1995).
-
(1995)
Nature
, vol.376
, pp. 348-351
-
-
Petrij, F.1
Giles, R.H.2
Dauwerse, H.G.3
Saris, J.J.4
Hennekam, R.C.M.5
Masuno, M.6
Tommerup, N.7
VanOmmen, G.-J.B.8
Goodman, R.H.9
Peters, D.J.M.10
Breuning, M.H.11
-
35
-
-
0028969225
-
The mouse homologue of the human tuberous sclerosis 2 (TSC2) gene maps to chromosome 17, but does not fall within the t(w18) or t(h20) deletions
-
Pilz A, Glenister P, Povey S, Lyon M, Abbott C: The mouse homologue of the human tuberous sclerosis 2 (TSC2) gene maps to chromosome 17, but does not fall within the t(w18) or t(h20) deletions. Genomics 26:420-21 (1995).
-
(1995)
Genomics
, vol.26
, pp. 420-421
-
-
Pilz, A.1
Glenister, P.2
Povey, S.3
Lyon, M.4
Abbott, C.5
-
36
-
-
0004402555
-
A paracentric inversion of 16q in a patient with anus, hand, and ear anomalies: Further evidence for a Townes-Brocks syndrome gene at 16q12.1
-
Powell CM, Reitnauer PJ, Kaiser-Rogers KA, Rao KW: A paracentric inversion of 16q in a patient with anus, hand, and ear anomalies: further evidence for a Townes-Brocks syndrome gene at 16q12.1. Am J hum Genet 57:suppl:A100 (1995).
-
(1995)
Am J Hum Genet
, vol.57
, Issue.SUPPL.
-
-
Powell, C.M.1
Reitnauer, P.J.2
Kaiser-Rogers, K.A.3
Rao, K.W.4
-
37
-
-
0028840709
-
Localization of the Fanconi anaemia, complementation group A gene to chromosome 16q24.3
-
Pronk JC, Gibson RA, Savoia A, Wijker M, Morgan NV, Melchionda S, Ford D, Temtamy S, Onega JJ, Jansen S, Havenga C, Cohn RJ, de Ravel TJ, Roberts I, Westerveld A, Easton DP, Joenje H, Mathew CO, Arwert F: Localization of the Fanconi anaemia, complementation group A gene to chromosome 16q24.3. Nature Genetics 11:338-340 (1995).
-
(1995)
Nature Genetics
, vol.11
, pp. 338-340
-
-
Pronk, J.C.1
Gibson, R.A.2
Savoia, A.3
Wijker, M.4
Morgan, N.V.5
Melchionda, S.6
Ford, D.7
Temtamy, S.8
Onega, J.J.9
Jansen, S.10
Havenga, C.11
Cohn, R.J.12
De Ravel, T.J.13
Roberts, I.14
Westerveld, A.15
Easton, D.P.16
Joenje, H.17
Mathew, C.O.18
Arwert, F.19
-
38
-
-
0025990209
-
Cloning and characterization of a 3-melhyladenine DNA glycosylase cDNA from human cells whose gene maps to chromosome 16
-
Samson L, Derfler B, Boosalis M, Call K: Cloning and characterization of a 3-melhyladenine DNA glycosylase cDNA from human cells whose gene maps to chromosome 16. Prot natl Acad Sci, USA 88:9127-9131 (1991).
-
(1991)
Prot Natl Acad Sci, USA
, vol.88
, pp. 9127-9131
-
-
Samson, L.1
Derfler, B.2
Boosalis, M.3
Call, K.4
-
39
-
-
0027287258
-
Purification and molecular cloning of mouse renal dipeptidase
-
Satoh S, Keida Y, Konta Y, Maeda M, Matsumoto Y, Niwa M, Kohsaka M: Purification and molecular cloning of mouse renal dipeptidase. Biochem biophys Acta 1163:234-42 (1993).
-
(1993)
Biochem Biophys Acta
, vol.1163
, pp. 234-242
-
-
Satoh, S.1
Keida, Y.2
Konta, Y.3
Maeda, M.4
Matsumoto, Y.5
Niwa, M.6
Kohsaka, M.7
-
40
-
-
84951605684
-
Genomic rearrangement of the alpha-globin gene complex during mamalian evolution
-
Tan H, Whitney JB: Genomic rearrangement of the alpha-globin gene complex during mamalian evolution. Biochem Genet 31:473-84 (1993).
-
(1993)
Biochem Genet
, vol.31
, pp. 473-484
-
-
Tan, H.1
Whitney, J.B.2
-
41
-
-
0028942745
-
Analysis of the genomic sequence for the autosomal dominant polycystic kidney diesase (PKD1) gene predicts the presence of a leucine-rich repeat
-
The American PKD1 Consortium: Burn TC, Connors TD, Dackowski WR, Petry LR, Van Raay TJ, Millholland JM, Venet M, Miller G, Hakim RM, Landes GM, Klinger KW, Qian F, Onuchic LF, Watnick T, Germino GG, Doggett NA: Analysis of the genomic sequence for the autosomal dominant polycystic kidney diesase (PKD1) gene predicts the presence of a leucine-rich repeat Hum molec Genet 4:575-582 (1995).
-
(1995)
Hum Molec Genet
, vol.4
, pp. 575-582
-
-
Burn, T.C.1
Connors, T.D.2
Dackowski, W.R.3
Petry, L.R.4
Van Raay, T.J.5
Millholland, J.M.6
Venet, M.7
Miller, G.8
Hakim, R.M.9
Landes, G.M.10
Klinger, K.W.11
Qian, F.12
Onuchic, L.F.13
Watnick, T.14
Germino, G.G.15
Doggett, N.A.16
-
42
-
-
0029147298
-
Isolation of a novel gene underlying Batten disease CLN3
-
The International Batten Disease Consortium: Lemer TJ, Boustany R-MN, Anderson JW, D'Arigo KL, Schlumpf K, Buckler AJ, Gusella JF, Haines JL, Kremmidiotis G, Lensink IL, Sutherland GR, Callen DF, Taschner PEM, de Vos N, van Ommen G-JB, Breuning MH, Doggett NA, Meincke LJ, Liu Z-Y, Goodwin LA, Tesmer JG, Mitchison HM, O'Rawe A, Munroe PB, Järvelä E, Gardiner RM, Mole SE: Isolation of a novel gene underlying Batten disease CLN3. Cell 82:849-957 (1995).
-
(1995)
Cell
, vol.82
, pp. 849-957
-
-
Lemer, T.J.1
Boustany, R.-M.N.2
Anderson, J.W.3
D'Arigo, K.L.4
Schlumpf, K.5
Buckler, A.J.6
Gusella, J.F.7
Haines, J.L.8
Kremmidiotis, G.9
Lensink, I.L.10
Sutherland, G.R.11
Callen, D.F.12
Taschner, P.E.M.13
De Vos, N.14
Van Ommen, G.-J.B.15
Breuning, M.H.16
Doggett, N.A.17
Meincke, L.J.18
Liu, Z.-Y.19
Goodwin, L.A.20
Tesmer, J.G.21
Mitchison, H.M.22
O'Rawe, A.23
Munroe, P.B.24
Järvelä, E.25
Gardiner, R.M.26
Mole, S.E.27
more..
-
43
-
-
0028786945
-
Variants of the melanocyte-stimulating hormone receptor gene are associated with red hair and fair skin in humans
-
Valverde P, Healy E, Jackson I, Rees JL, Thody AJ: Variants of the melanocyte-stimulating hormone receptor gene are associated with red hair and fair skin in humans. Nature Genetics 11:328-330 (1995).
-
(1995)
Nature Genetics
, vol.11
, pp. 328-330
-
-
Valverde, P.1
Healy, E.2
Jackson, I.3
Rees, J.L.4
Thody, A.J.5
-
44
-
-
11944269657
-
Evolution of the mammalian G protein alpha subunit multigene family
-
Wilkie TM, Gilbert DJ, Olsen AS, Chen XN, Amatruda TT, Korenberg JR, Trask BJ, de Jong P, Reed RR, Simon MI, Jenkins NA, Copeland NG: Evolution of the mammalian G protein alpha subunit multigene family. Nature Genetics 1:85-91 (1992).
-
(1992)
Nature Genetics
, vol.1
, pp. 85-91
-
-
Wilkie, T.M.1
Gilbert, D.J.2
Olsen, A.S.3
Chen, X.N.4
Amatruda, T.T.5
Korenberg, J.R.6
Trask, B.J.7
De Jong, P.8
Reed, R.R.9
Simon, M.I.10
Jenkins, N.A.11
Copeland, N.G.12
-
45
-
-
0029114538
-
Silencing of the E-cadherin invasion-suppressor gene by CpG methylation in human carcinomas
-
Yoshiura K, Kanai Y, Ochiai A, Shimoyama Y, Sugimura T, Hirohashi S: Silencing of the E-cadherin invasion-suppressor gene by CpG methylation in human carcinomas. Proc natl Acad Sci, USA 92:7416-7419 (1995).
-
(1995)
Proc Natl Acad Sci, USA
, vol.92
, pp. 7416-7419
-
-
Yoshiura, K.1
Kanai, Y.2
Ochiai, A.3
Shimoyama, Y.4
Sugimura, T.5
Hirohashi, S.6
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