-
2
-
-
0023626634
-
Genetic linkage map of human chromosome 7 with 63 DNA markers
-
Barker D, Green P, Knowlton R, Schumm J, Lander E, Oliphant A, Willard H, Akots G, Brown V, Gravius T, Helms C, Nelson C, Parker C, Rediker K, Rising M, Watt D, Weiffenbach B, Donis-Keller H (1987) Genetic linkage map of human chromosome 7 with 63 DNA markers. Proc Natl Acad Sci USA 84: 8006-8010
-
(1987)
Proc Natl Acad Sci USA
, vol.84
, pp. 8006-8010
-
-
Barker, D.1
Green, P.2
Knowlton, R.3
Schumm, J.4
Lander, E.5
Oliphant, A.6
Willard, H.7
Akots, G.8
Brown, V.9
Gravius, T.10
Helms, C.11
Nelson, C.12
Parker, C.13
Rediker, K.14
Rising, M.15
Watt, D.16
Weiffenbach, B.17
Donis-Keller, H.18
-
3
-
-
0026668037
-
Localization of the photoreceptor gene ROM1 to human chromosome 11 and mouse chromosome 19: Sublocalization to human 11q13 between PGA and PYGM
-
Bascom RA, García-Heras J, Hseih C-L, Gerhard DS, Jones C, Francke U, Willard HF, Ledbetter DH, McInnes RR (1992) Localization of the photoreceptor gene ROM1 to human chromosome 11 and mouse chromosome 19: sublocalization to human 11q13 between PGA and PYGM. Am J Hum Genet 51:1028-1035
-
(1992)
Am J Hum Genet
, vol.51
, pp. 1028-1035
-
-
Bascom, R.A.1
García-Heras, J.2
Hseih, C.-L.3
Gerhard, D.S.4
Jones, C.5
Francke, U.6
Willard, H.F.7
Ledbetter, D.H.8
McInnes, R.R.9
-
4
-
-
0025845424
-
cDNA cloning and chromosomal localization of the human B-adrenergic receptor kinase
-
Benovic JL, Stone WC, Huebner K, Croce C, Caron MG, Lefkowitz RJ (1991) cDNA cloning and chromosomal localization of the human B-adrenergic receptor kinase. FEBS Lett 283:122-126
-
(1991)
FEBS Lett
, vol.283
, pp. 122-126
-
-
Benovic, J.L.1
Stone, W.C.2
Huebner, K.3
Croce, C.4
Caron, M.G.5
Lefkowitz, R.J.6
-
5
-
-
0025766230
-
Hypervariable polymorphism in the APOC3 gene
-
Bhattacharya S, Wilson TME, Wojciechowski AP, Volpe CP, Scott J (1991) Hypervariable polymorphism in the APOC3 gene. Nucleic Acids Res 19:4799
-
(1991)
Nucleic Acids Res
, vol.19
, pp. 4799
-
-
Bhattacharya, S.1
Wilson, T.M.E.2
Wojciechowski, A.P.3
Volpe, C.P.4
Scott, J.5
-
6
-
-
0024550229
-
Mammalian chromosome bandins - An expression of genome organisation
-
Bickmore WA, Sumner AT (1989) Mammalian chromosome bandins - an expression of genome organisation. Trends Genet 5: 144-148
-
(1989)
Trends Genet
, vol.5
, pp. 144-148
-
-
Bickmore, W.A.1
Sumner, A.T.2
-
7
-
-
0026564551
-
p microsatellites with degenerate sequencing primers
-
p microsatellites with degenerate sequencing primers. Nucleic Acids Res 20:141
-
(1992)
Nucleic Acids Res
, vol.20
, pp. 141
-
-
Browne, D.L.1
Litt, M.2
-
8
-
-
0022910321
-
A highly polymorphic locus on chromosome 16q revealed by a probe from a chromosome-specific cosmid library
-
Bufton L, Mohandas TK, Magenis RE, Sheehy R, Bestwick RK, Litt M (1986) A highly polymorphic locus on chromosome 16q revealed by a probe from a chromosome-specific cosmid library. Hum Genet 74:425-431
-
(1986)
Hum Genet
, vol.74
, pp. 425-431
-
-
Bufton, L.1
Mohandas, T.K.2
Magenis, R.E.3
Sheehy, R.4
Bestwick, R.K.5
Litt, M.6
-
9
-
-
0028356291
-
Differential sensitivity of FOS and JUN family members to calpains
-
Carillo S, Pariat M, Steff A-M, Roux P, Etienne-Julan M, Lorca T, Piechaczyk M (1994) Differential sensitivity of FOS and JUN family members to calpains. Oncogene 9: 1679-1689
-
(1994)
Oncogene
, vol.9
, pp. 1679-1689
-
-
Carillo, S.1
Pariat, M.2
Steff, A.-M.3
Roux, P.4
Etienne-Julan, M.5
Lorca, T.6
Piechaczyk, M.7
-
10
-
-
0026600132
-
Primary structure of NuMA, an intranuclear protein that defines a novel pathway for segregation of proteins at mitosis
-
Compton DA, Szilak I, Cleveland DW (1992) Primary structure of NuMA, an intranuclear protein that defines a novel pathway for segregation of proteins at mitosis. J Cell Biol 116:1395-1408
-
(1992)
J Cell Biol
, vol.116
, pp. 1395-1408
-
-
Compton, D.A.1
Szilak, I.2
Cleveland, D.W.3
-
11
-
-
0024364317
-
The aniridia-Wilms' tumour association: Molecular and genetic analysis of chromosome deletions on the short arm of chromosome 11
-
Cowell JK, Wadey RB, Buckle BB, Pritchard J (1989) The aniridia-Wilms' tumour association: molecular and genetic analysis of chromosome deletions on the short arm of chromosome 11. Hum Genet 82:123-126
-
(1989)
Hum Genet
, vol.82
, pp. 123-126
-
-
Cowell, J.K.1
Wadey, R.B.2
Buckle, B.B.3
Pritchard, J.4
-
12
-
-
0028301317
-
The distribution of CpG islands in mammalian chromosomes
-
Craig JM, Bickmore WA (1994) The distribution of CpG islands in mammalian chromosomes. Nat Genet 7:376-381
-
(1994)
Nat Genet
, vol.7
, pp. 376-381
-
-
Craig, J.M.1
Bickmore, W.A.2
-
13
-
-
0027933734
-
A genome-wide search for human type 1 diabetes susceptibility genes
-
Davies JL, Kaawaguchi 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 (1994) A genome-wide search for human type 1 diabetes susceptibility genes. Nature 371:130-136
-
(1994)
Nature
, vol.371
, pp. 130-136
-
-
Davies, J.L.1
Kaawaguchi, 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
-
14
-
-
0025644837
-
Irradiation microcell-mediated chromosome transfer (XMMCT): The generation of specific chromosomal arm deletions
-
Dowdy SF, Scanlon DJ, Fasching CL, Casey G, Stanbridge EJ (1990) Irradiation microcell-mediated chromosome transfer (XMMCT): the generation of specific chromosomal arm deletions. Genes Chromosom Cancer 2:318-327
-
(1990)
Genes Chromosom Cancer
, vol.2
, pp. 318-327
-
-
Dowdy, S.F.1
Scanlon, D.J.2
Fasching, C.L.3
Casey, G.4
Stanbridge, E.J.5
-
15
-
-
0025947340
-
Isolation, localization, and physical mapping of a highly polymorphic locus on human chromosome 11q13
-
Eubanks JH, Selleri L, Hart, R Rosette C, Evans GA (1991) Isolation, localization, and physical mapping of a highly polymorphic locus on human chromosome 11q13. Genomics 11:720-729
-
(1991)
Genomics
, vol.11
, pp. 720-729
-
-
Eubanks, J.H.1
Selleri, L.2
Hart, R.3
Rosette, C.4
Evans, G.A.5
-
16
-
-
0024399727
-
Clonality of parathyroid tumors in familial multiple endocrine neoplasia type 1
-
Friedman E, Sakaguchi K, Bale AE, Falchetti A, Streeten E, Zimering MB, Weinstein LS, McBride WO, Nakamura Y, Brandi M-L, Norton JA, Auerbach GD, Spiegel AM, Marx SJ (1989) Clonality of parathyroid tumors in familial multiple endocrine neoplasia type 1. N Engl J Med 321:213-218
-
(1989)
N Engl J Med
, vol.321
, pp. 213-218
-
-
Friedman, E.1
Sakaguchi, K.2
Bale, A.E.3
Falchetti, A.4
Streeten, E.5
Zimering, M.B.6
Weinstein, L.S.7
McBride, W.O.8
Nakamura, Y.9
Brandi, M.-L.10
Norton, J.A.11
Auerbach, G.D.12
Spiegel, A.M.13
Marx, S.J.14
-
17
-
-
0026714811
-
Isolation of 1001 new markers from human chromosome 11, excluding the region of 11p13-p15.5, and their sublocalization by a new series of radiation-reduced somatic cell hybrids
-
Gerhard DS, Lawrence E, Wu J, Chua H, Ma N, Bland S, Jones C (1992) Isolation of 1001 new markers from human chromosome 11, excluding the region of 11p13-p15.5, and their sublocalization by a new series of radiation-reduced somatic cell hybrids. Genomics 13:1133-1142
-
(1992)
Genomics
, vol.13
, pp. 1133-1142
-
-
Gerhard, D.S.1
Lawrence, E.2
Wu, J.3
Chua, H.4
Ma, N.5
Bland, S.6
Jones, C.7
-
18
-
-
0027480155
-
Irradiation hybrids for human chromosome 11: Characterization and use for generating region-specific markers in 11q14-q23
-
Gillett GT, McConville CM, Byrd PJ, Stankovic T, Taylor AM, Hunt DM, West LF, Fox MF, Povey S, Benham FJ (1993) Irradiation hybrids for human chromosome 11: characterization and use for generating region-specific markers in 11q14-q23. Genomics 15:332-341
-
(1993)
Genomics
, vol.15
, pp. 332-341
-
-
Gillett, G.T.1
McConville, C.M.2
Byrd, P.J.3
Stankovic, T.4
Taylor, A.M.5
Hunt, D.M.6
West, L.F.7
Fox, M.F.8
Povey, S.9
Benham, F.J.10
-
19
-
-
0024797779
-
A fine-structure deletion map of chromosome 11p: Analysis of J1 series hybrids
-
Glaser T, Housman D, Lewis WH, Gerhard D, Jones C (1989) A fine-structure deletion map of chromosome 11p: analysis of J1 series hybrids. Somat Cell Mol Genet 15:477-501
-
(1989)
Somat Cell Mol Genet
, vol.15
, pp. 477-501
-
-
Glaser, T.1
Housman, D.2
Lewis, W.H.3
Gerhard, D.4
Jones, C.5
-
20
-
-
0028231090
-
The 1993-94 Généthon human genetic linkage map
-
Gyapay G, Morissette J, Vignal A, Dib C, Fizames C, Millasseau P, Marc S, Bernardi G, Lathrop M, Weissenbach J (1994) The 1993-94 Généthon human genetic linkage map. Nat Genet 7:246-339
-
(1994)
Nat Genet
, vol.7
, pp. 246-339
-
-
Gyapay, G.1
Morissette, J.2
Vignal, A.3
Dib, C.4
Fizames, C.5
Millasseau, P.6
Marc, S.7
Bernardi, G.8
Lathrop, M.9
Weissenbach, J.10
-
21
-
-
0028070552
-
Genetic mapping of a susceptibility locus for insulin-dependent diabetes mellirus on chromosome 11q
-
Hashimoto L, Habita C, Beressi JP, Detepine M, Besse C, Cambon-Thomsen A, Deschamps I, Rotter JI, Djoulah S, James MR, Froguel P, Weissenbach J, Lathrop GM, Julier C (1994) Genetic mapping of a susceptibility locus for insulin-dependent diabetes mellirus on chromosome 11q. Nature 371:161-164
-
(1994)
Nature
, vol.371
, pp. 161-164
-
-
Hashimoto, L.1
Habita, C.2
Beressi, J.P.3
Detepine, M.4
Besse, C.5
Cambon-Thomsen, A.6
Deschamps, I.7
Rotter, J.I.8
Djoulah, S.9
James, M.R.10
Froguel, P.11
Weissenbach, J.12
Lathrop, G.M.13
Julier, C.14
-
22
-
-
0026523066
-
A minisatellite and a microsatellite polymorphism within 1.5 kb at the human muscle glycogen phosphorylase (PYGM) locus can be amplified by PCR and have combined informativeness of PIC 0.95
-
Iwasaki H, Stewart PW, William GD, Holt MS, Steinbrueck TD, Wells Jr SA, Donis-Keller H (1992) A minisatellite and a microsatellite polymorphism within 1.5 kb at the human muscle glycogen phosphorylase (PYGM) locus can be amplified by PCR and have combined informativeness of PIC 0.95. Genomics 13: 7-15
-
(1992)
Genomics
, vol.13
, pp. 7-15
-
-
Iwasaki, H.1
Stewart, P.W.2
William, G.D.3
Holt, M.S.4
Steinbrueck, T.D.5
Wells Jr., S.A.6
Donis-Keller, H.7
-
23
-
-
20244377832
-
A radiation hybrid map of 506 STS markers spanning human chromosome 11
-
James MR, Richard III CW, Schott J-J, Yousry C, Clark K, Bell J, Terwilliger JD, Hazan J, Dubay C, Vignal A, Agrapart M, Imai T, Nakamura Y, Polymeropoulos M, Weissenbach J, Cox DR, Lathrop GM (1994) A radiation hybrid map of 506 STS markers spanning human chromosome 11. Nat Genet 8:70-76
-
(1994)
Nat Genet
, vol.8
, pp. 70-76
-
-
James, M.R.1
Richard III, C.W.2
Schott, J.-J.3
Yousry, C.4
Clark, K.5
Bell, J.6
Terwilliger, J.D.7
Hazan, J.8
Dubay, C.9
Vignal, A.10
Agrapart, M.11
Imai, T.12
Nakamura, Y.13
Polymeropoulos, M.14
Weissenbach, J.15
Cox, D.R.16
Lathrop, G.M.17
-
24
-
-
0025836654
-
Detailed physical map of human chromosomal region 11q12-13 shows high meiotic recombination rate around the MEN1 locus
-
Janson M, Larsson C, Werelius B, Jones C, Glaser T, Nakamura Y, Jones CP, Nordenskjold M (1991) Detailed physical map of human chromosomal region 11q12-13 shows high meiotic recombination rate around the MEN1 locus. Proc Natl Acad Sci USA 88:10609-10613
-
(1991)
Proc Natl Acad Sci USA
, vol.88
, pp. 10609-10613
-
-
Janson, M.1
Larsson, C.2
Werelius, B.3
Jones, C.4
Glaser, T.5
Nakamura, Y.6
Jones, C.P.7
Nordenskjold, M.8
-
25
-
-
0021125404
-
Relationships between genes on human chromosome 11 encoding cell-surface antigens
-
Jones C, Bill J, Larizza L, Pym B, Goodfellow P, Tunnacliffe A (1984) Relationships between genes on human chromosome 11 encoding cell-surface antigens. Somat Cell Mol Genet 10:423-428
-
(1984)
Somat Cell Mol Genet
, vol.10
, pp. 423-428
-
-
Jones, C.1
Bill, J.2
Larizza, L.3
Pym, B.4
Goodfellow, P.5
Tunnacliffe, A.6
-
26
-
-
0025041497
-
A detailed genetic map of the long arm of chromosome 11
-
Julier C, Nakamura Y, Lathrop M, O'Connell P, Leppert M, Litt M, Mohandas T, Lalouel JM, White R (1990) A detailed genetic map of the long arm of chromosome 11. Genomics 7:335-345
-
(1990)
Genomics
, vol.7
, pp. 335-345
-
-
Julier, C.1
Nakamura, Y.2
Lathrop, M.3
O'Connell, P.4
Leppert, M.5
Litt, M.6
Mohandas, T.7
Lalouel, J.M.8
White, R.9
-
27
-
-
0017087583
-
Genetics of somatic mammalian cells: Genetic, immunologic, and biochemical analysis with Chinese hamster cell hybrids containing selected human chromosomes
-
Kao F-T, Jones C, Puck TT (1976) Genetics of somatic mammalian cells: genetic, immunologic, and biochemical analysis with Chinese hamster cell hybrids containing selected human chromosomes. Proc Natl Acad Sci USA 73:193-197
-
(1976)
Proc Natl Acad Sci USA
, vol.73
, pp. 193-197
-
-
Kao, F.-T.1
Jones, C.2
Puck, T.T.3
-
28
-
-
0027219551
-
Assignment of the human FAU gene to a subregion of chromosome 11q13
-
Kas K, Schoenmakers E, Ven W van de, Weber G, Nordenskjöld M, Michiels L, Merregaert J, Larsson C (1993) Assignment of the human FAU gene to a subregion of chromosome 11q13. Genomics 17:387-392
-
(1993)
Genomics
, vol.17
, pp. 387-392
-
-
Kas, K.1
Schoenmakers, E.2
Van De Ven, W.3
Weber, G.4
Nordenskjöld, M.5
Michiels, L.6
Merregaert, J.7
Larsson, C.8
-
29
-
-
0027058412
-
Linkage of Usher syndrome type 1 (USHB1) to the long arm of chromosome 11
-
Kimberling WJ, Möller CG, Davenport S, Priluck IA, Beighton PH, Greenberg J, Reardon W, Weston MD, Kenyon JB, Grunkemeyer JA, Pieke Dahl S, Overbeck LD, Blackwood DJ, Brower AM, Hoover DM, Rowland P, Smith RJH (1992) Linkage of Usher syndrome type 1 (USHB1) to the long arm of chromosome 11. Genomics 14:988-994
-
(1992)
Genomics
, vol.14
, pp. 988-994
-
-
Kimberling, W.J.1
Möller, C.G.2
Davenport, S.3
Priluck, I.A.4
Beighton, P.H.5
Greenberg, J.6
Reardon, W.7
Weston, M.D.8
Kenyon, J.B.9
Grunkemeyer, J.A.10
Pieke Dahl, S.11
Overbeck, L.D.12
Blackwood, D.J.13
Brower, A.M.14
Hoover, D.M.15
Rowland, P.16
Smith, R.J.H.17
-
30
-
-
0024515583
-
Limited proteolysis of protein kinase C subspecies by calcium-dependent neutral protease (calpain)
-
Kishimoto A, Mikawa K, Hashimoto K, Yasuda I, Tanaka S, Tominaga M, Kuroda T, Nishizuka Y (1989) Limited proteolysis of protein kinase C subspecies by calcium-dependent neutral protease (calpain) J. Biol. Chem 264:4088-4092
-
(1989)
J. Biol. Chem
, vol.264
, pp. 4088-4092
-
-
Kishimoto, A.1
Mikawa, K.2
Hashimoto, K.3
Yasuda, I.4
Tanaka, S.5
Tominaga, M.6
Kuroda, T.7
Nishizuka, Y.8
-
31
-
-
0027212389
-
D11S971 CATT polymorphism (RC27) located near the MEN1 locus at 11q13
-
Krebs CJ, Horton JH, Mullins CM, Paradee WJ, Taggart RT (1993) D11S971 CATT polymorphism (RC27) located near the MEN1 locus at 11q13. Hum Mol Genet 2:825
-
(1993)
Hum Mol Genet
, vol.2
, pp. 825
-
-
Krebs, C.J.1
Horton, J.H.2
Mullins, C.M.3
Paradee, W.J.4
Taggart, R.T.5
-
32
-
-
0023828816
-
Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma
-
Larsson C, Skogseid B, Öberg K, Nakamura Y, Nordenskjöld MC (1988) Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma. Nature 332:85-87
-
(1988)
Nature
, vol.332
, pp. 85-87
-
-
Larsson, C.1
Skogseid, B.2
Öberg, K.3
Nakamura, Y.4
Nordenskjöld, M.C.5
-
33
-
-
0026734478
-
Predictive testing for multiple endocrine neoplasia type 1 using DNA polymorphisms
-
Larsson C, Shepherd J, Nakamura Y, Blomberg C, Weber G, Werelius B, Hayward N, Teh B, Tokino T, Seizinger B, Skogseid B, Öberg K, Nordenskjöld M (1992) Predictive testing for multiple endocrine neoplasia type 1 using DNA polymorphisms. J Clin Invest 89:1344-1349
-
(1992)
J Clin Invest
, vol.89
, pp. 1344-1349
-
-
Larsson, C.1
Shepherd, J.2
Nakamura, Y.3
Blomberg, C.4
Weber, G.5
Werelius, B.6
Hayward, N.7
Teh, B.8
Tokino, T.9
Seizinger, B.10
Skogseid, B.11
Öberg, K.12
Nordenskjöld, M.13
-
34
-
-
0021344005
-
Easy calculation of LOD scores and genetic risk on small computers
-
Lathrop GM, Lalouel JM (1984) Easy calculation of LOD scores and genetic risk on small computers. Am J Hum Genet 36: 460-465
-
(1984)
Am J Hum Genet
, vol.36
, pp. 460-465
-
-
Lathrop, G.M.1
Lalouel, J.M.2
-
36
-
-
0028128537
-
Bardet-Biedl syndrome is linked to DNA markers on chromosome 11q and is genetically heterogeneous
-
Leppert M, Baird L, Anderson KL, Otterud B, Lupski JR, Lewis RA (1994) Bardet-Biedl syndrome is linked to DNA markers on chromosome 11q and is genetically heterogeneous. Nature Genetics 7: 108-111
-
(1994)
Nature Genetics
, vol.7
, pp. 108-111
-
-
Leppert, M.1
Baird, L.2
Anderson, K.L.3
Otterud, B.4
Lupski, J.R.5
Lewis, R.A.6
-
37
-
-
0027256846
-
Human ciliary neurotrophic factor: Localization to the proximal region of the long arm of chromosome 11 and association with CA/GT dinucleotide repeat
-
Lev AA, Rosen DR, Kos C, Clifford E, Landes G, Hauser SL, Brown Jr RH (1993) Human ciliary neurotrophic factor: localization to the proximal region of the long arm of chromosome 11 and association with CA/GT dinucleotide repeat. Genomics 16:539-541
-
(1993)
Genomics
, vol.16
, pp. 539-541
-
-
Lev, A.A.1
Rosen, D.R.2
Kos, C.3
Clifford, E.4
Landes, G.5
Hauser, S.L.6
Brown Jr., R.H.7
-
38
-
-
0026756530
-
The autosomal dominant familial exudative vitreoretinopathy locus maps on 11q and is closely linked to D11S533
-
Li Y, Müller B, Fuhrmann C, Nouhuys E van, Laqua H, Humphries P, Schwinger E, Gal A (1992) The autosomal dominant familial exudative vitreoretinopathy locus maps on 11q and is closely linked to D11S533. Am J Hum Genet 51:749-754
-
(1992)
Am J Hum Genet
, vol.51
, pp. 749-754
-
-
Li, Y.1
Müller, B.2
Fuhrmann, C.3
Van Nouhuys, E.4
Laqua, H.5
Humphries, P.6
Schwinger, E.7
Gal, A.8
-
39
-
-
13344286321
-
A common molecular basis for three inherited kidney stone diseases
-
Lloyd SE, Pearce SHS, Fisher SE, Steinmeyer K, Schwappach B, Scheinman SJ, Harding B, Bolino A, Devoto M, Goodyer P, Rigden SPA, Wrong O, Jentsch TJ, Craig IW, Thakker RV (1996) A common molecular basis for three inherited kidney stone diseases. Nature 379:445-449
-
(1996)
Nature
, vol.379
, pp. 445-449
-
-
Lloyd, S.E.1
Pearce, S.H.S.2
Fisher, S.E.3
Steinmeyer, K.4
Schwappach, B.5
Scheinman, S.J.6
Harding, B.7
Bolino, A.8
Devoto, M.9
Goodyer, P.10
Rigden, S.P.A.11
Wrong, O.12
Jentsch, T.J.13
Craig, I.W.14
Thakker, R.V.15
-
41
-
-
0027468554
-
Dinucleotide repeat polymorphism at the D11S480 locus
-
Moffatt MF (1993) Dinucleotide repeat polymorphism at the D11S480 locus. Hum Mol Genet 2:492
-
(1993)
Hum Mol Genet
, vol.2
, pp. 492
-
-
Moffatt, M.F.1
-
42
-
-
0019272411
-
Expression of an X-linked gene from an inactive human X chromosome in mouse-human hybrid cells: Further evidence for the noninactivation of the steroid sulfatase locus in man
-
Mohandas T, Sparkes RS, Hellkuhl B, Grzeschik KH, Shapiro LJ (1980) Expression of an X-linked gene from an inactive human X chromosome in mouse-human hybrid cells: further evidence for the noninactivation of the steroid sulfatase locus in man. Proc Natl Acad Sci USA 77:6759-6763
-
(1980)
Proc Natl Acad Sci USA
, vol.77
, pp. 6759-6763
-
-
Mohandas, T.1
Sparkes, R.S.2
Hellkuhl, B.3
Grzeschik, K.H.4
Shapiro, L.J.5
-
43
-
-
0024605060
-
Direct detection of point mutations by mismatch analysis: Application to haemophilia B
-
Montandon AJ, Green PM, Gianelli F, Bentley DR (1989) Direct detection of point mutations by mismatch analysis: application to haemophilia B. Nucleic Acids Res 17:3347-3358
-
(1989)
Nucleic Acids Res
, vol.17
, pp. 3347-3358
-
-
Montandon, A.J.1
Green, P.M.2
Gianelli, F.3
Bentley, D.R.4
-
44
-
-
0028180063
-
Refining the locus for Best vitelliform macular dystrophy and mutation analysis of the candidate sene ROM1
-
Nichols BE, Bascom RA, Litt M, McInnes R, Sheffield VC, Stone EM (1994) Refining the locus for Best vitelliform macular dystrophy and mutation analysis of the candidate sene ROM1. Am J Hum Genet 54:95-103
-
(1994)
Am J Hum Genet
, vol.54
, pp. 95-103
-
-
Nichols, B.E.1
Bascom, R.A.2
Litt, M.3
McInnes, R.4
Sheffield, V.C.5
Stone, E.M.6
-
45
-
-
0027258640
-
pp60src is an endogenous substrate for calpain in human blood platelets
-
Oda A, Druker BJ, Ariyoshi H, Smith M, Salzman EW (1993) pp60src is an endogenous substrate for calpain in human blood platelets. J Biol Chem 268:12603-12608
-
(1993)
J Biol Chem
, vol.268
, pp. 12603-12608
-
-
Oda, A.1
Druker, B.J.2
Ariyoshi, H.3
Smith, M.4
Salzman, E.W.5
-
46
-
-
0025183807
-
Four genes for the calpain family locate on four distinct human chromosomes
-
Ohno S, Minoshima S, Kudoh J, Fukuyama R, Shimizu Y, Ohmi-Imajoh S, Shizimu N, Suzuki K (1990) Four genes for the calpain family locate on four distinct human chromosomes. Cytogenet Cell Genet 53:225-229
-
(1990)
Cytogenet Cell Genet
, vol.53
, pp. 225-229
-
-
Ohno, S.1
Minoshima, S.2
Kudoh, J.3
Fukuyama, R.4
Shimizu, Y.5
Ohmi-Imajoh, S.6
Shizimu, N.7
Suzuki, K.8
-
47
-
-
0027032545
-
Molecular genetic mapping of the multiple endocrine neoplasia type 1 (MEN1) locus
-
Pang JT, Pook MA, Eubanks JH, Jones C, Van Heyningen V, Evans GA, Thakker RV (1992) Molecular genetic mapping of the multiple endocrine neoplasia type 1 (MEN1) locus. Henry Ford Hosp Med J 40:162-166
-
(1992)
Henry Ford Hosp Med J
, vol.40
, pp. 162-166
-
-
Pang, J.T.1
Pook, M.A.2
Eubanks, J.H.3
Jones, C.4
Van Heyningen, V.5
Evans, G.A.6
Thakker, R.V.7
-
48
-
-
0027537482
-
Removal of the carboxyl-terminal of phospholipase C-β1 by calpain abolishes activation by Gαq
-
Park D, Jhon D-Y, Lee C-W, Ryu SH, Rhee SG (1993) Removal of the carboxyl-terminal of phospholipase C-β1 by calpain abolishes activation by Gαq. J Biol Chem 268:3710-3714
-
(1993)
J Biol Chem
, vol.268
, pp. 3710-3714
-
-
Park, D.1
Jhon, D.-Y.2
Lee, C.-W.3
Ryu, S.H.4
Rhee, S.G.5
-
49
-
-
0026865130
-
A donor splice site mutation in the parathyroid hormone gene is associated with autosomal recessive hypoparathyroidism
-
Parkinson DB, Thakker RV (1992) A donor splice site mutation in the parathyroid hormone gene is associated with autosomal recessive hypoparathyroidism. Nature Genet 1:149-152
-
(1992)
Nature Genet
, vol.1
, pp. 149-152
-
-
Parkinson, D.B.1
Thakker, R.V.2
-
51
-
-
0028848215
-
Calcium-sensing receptor mutations in familial benign hypercalcemia and neonatal hyperparathyroidism
-
Pearce SHS, Trump D, Wooding C, Besser GM, Chew SL, Grant DB, Heath DA, Hughes IA, Paterson CR, Whyte MP, Thakker RV (1995) Calcium-sensing receptor mutations in familial benign hypercalcemia and neonatal hyperparathyroidism. J Clin Invest 96:2683-2692
-
(1995)
J Clin Invest
, vol.96
, pp. 2683-2692
-
-
Pearce, S.H.S.1
Trump, D.2
Wooding, C.3
Besser, G.M.4
Chew, S.L.5
Grant, D.B.6
Heath, D.A.7
Hughes, I.A.8
Paterson, C.R.9
Whyte, M.P.10
Thakker, R.V.11
-
53
-
-
15844362454
-
EagI and NotI linking clones from human chromosomes 11 and Xp
-
Pook MA, Thakrar R, Pottinger B, Harding B, Porteous D, Heyningen V van, Cowell J, Jones C, Povey S, Davies KE, Thakker RV (1996) EagI and NotI linking clones from human chromosomes 11 and Xp. Hum Genet 97:742-749
-
(1996)
Hum Genet
, vol.97
, pp. 742-749
-
-
Pook, M.A.1
Thakrar, R.2
Pottinger, B.3
Harding, B.4
Porteous, D.5
Van Heyningen, V.6
Cowell, J.7
Jones, C.8
Povey, S.9
Davies, K.E.10
Thakker, R.V.11
-
54
-
-
0024763058
-
Human-mouse hybrids carrying fragments of single chromosomes selected by tumor growth
-
Poneous DJ, Wilkinson MM, Retcher JM, Van Heyningen V (1989) Human-mouse hybrids carrying fragments of single chromosomes selected by tumor growth. Genomics 5:680-684
-
(1989)
Genomics
, vol.5
, pp. 680-684
-
-
Poneous, D.J.1
Wilkinson, M.M.2
Retcher, J.M.3
Van Heyningen, V.4
-
55
-
-
0028020605
-
Spinocerebellar ataxia type 5 in a family descended from the grandparents of President Lincoln maps to chromosome 11
-
Ranum LPW, Schut LJ, Lundgren JK, Orr HT, Livingston DM (1994) Spinocerebellar ataxia type 5 in a family descended from the grandparents of President Lincoln maps to chromosome 11. Nat Genet 8:280-284
-
(1994)
Nat Genet
, vol.8
, pp. 280-284
-
-
Ranum, L.P.W.1
Schut, L.J.2
Lundgren, J.K.3
Orr, H.T.4
Livingston, D.M.5
-
56
-
-
0026340029
-
A radiation hybrid map of the proximal long arm of human chromosome 11 containing the multiple endocrine neoplasia type 1 (MEN-1) and bcl-1 disease loci
-
Richard III CW, Withers DA, Meeker TC, Maurer S, Evans GA, Myers RM, Cox DR (1991) A radiation hybrid map of the proximal long arm of human chromosome 11 containing the multiple endocrine neoplasia type 1 (MEN-1) and bcl-1 disease loci. Am J Hum Genet 49.1189-1196
-
(1991)
Am J Hum Genet
, vol.49
, pp. 1189-1196
-
-
Richard III, C.W.1
Withers, D.A.2
Meeker, T.C.3
Maurer, S.4
Evans, G.A.5
Myers, R.M.6
Cox, D.R.7
-
57
-
-
0027177179
-
Mapping the gene causing X-linked recessive nephrolithiasis to Xp 11.22 by linkage studies
-
Scheinman SJ, Pook MA, Wooding C, Pang JT, Frymoyer PA, Thakker RV (1993) Mapping the gene causing X-linked recessive nephrolithiasis to Xp 11.22 by linkage studies. J Clin Invest 91:2351-2357
-
(1993)
J Clin Invest
, vol.91
, pp. 2351-2357
-
-
Scheinman, S.J.1
Pook, M.A.2
Wooding, C.3
Pang, J.T.4
Frymoyer, P.A.5
Thakker, R.V.6
-
58
-
-
0027058291
-
Localisation of two genes for Usher syndrome tvpe 1 to chromosome 11
-
Smith RJH, Lee EC, Kimberling WJ, Daiger SP, Pelias MZ, Keats BJB, Jay M, Bird A, Reardon W, Guest M, Ayyagari R, Hejtmancik (1992) Localisation of two genes for Usher syndrome tvpe 1 to chromosome 11. Genomics 14:995-1002.
-
(1992)
Genomics
, vol.14
, pp. 995-1002
-
-
Smith, R.J.H.1
Lee, E.C.2
Kimberling, W.J.3
Daiger, S.P.4
Pelias, M.Z.5
Bjb, K.6
Jay, M.7
Bird, A.8
Reardon, W.9
Guest, M.10
Ayyagari, R.11
Hejtmancik12
-
59
-
-
0027180467
-
A sequence-tagged site map of human chromosome 11
-
Smith MW, Clark SP, Hutchinson JS, Wei YH, Chrukian AC, Daniels LB, Diggle KL, Gen MW, Romo AJ, Lin Y, Selleri L, McElligott DL, Evans GA (1993) A sequence-tagged site map of human chromosome 11. Genomics 17:699-725
-
(1993)
Genomics
, vol.17
, pp. 699-725
-
-
Smith, M.W.1
Clark, S.P.2
Hutchinson, J.S.3
Wei, Y.H.4
Chrukian, A.C.5
Daniels, L.B.6
Diggle, K.L.7
Gen, M.W.8
Romo, A.J.9
Lin, Y.10
Selleri, L.11
McElligott, D.L.12
Evans, G.A.13
-
60
-
-
0026895234
-
Genetic linkage of vitelliform macular degeneration (Best's disease) to chromosome 11q13
-
Stone EM, Nichols BE, Streb LM, Kimura AE, Sheffield VC (1992a) Genetic linkage of vitelliform macular degeneration (Best's disease) to chromosome 11q13. Nat Genetics 1:246-250
-
(1992)
Nat Genetics
, vol.1
, pp. 246-250
-
-
Stone, E.M.1
Nichols, B.E.2
Streb, L.M.3
Kimura, A.E.4
Sheffield, V.C.5
-
61
-
-
0027018441
-
Genetic linkage of autosomal dominant neovascular inflammatory vitreoretinopathy to chromosome 11q13
-
Stone EM, Kimura AE, Folk JC, Bennett SR, Nichols BE, Streb LM, Sheffield VC (1992b) Genetic linkage of autosomal dominant neovascular inflammatory vitreoretinopathy to chromosome 11q13. Hum Mol Genet 1:685-689
-
(1992)
Hum Mol Genet
, vol.1
, pp. 685-689
-
-
Stone, E.M.1
Kimura, A.E.2
Folk, J.C.3
Bennett, S.R.4
Nichols, B.E.5
Streb, L.M.6
Sheffield, V.C.7
-
62
-
-
0027204595
-
Mapping genes according to their amplification status in tumour cells: Contribution to the map of 11q13
-
Szepetowski P, Perucca-Lostanlen D, Gaudray P (1993) Mapping genes according to their amplification status in tumour cells: contribution to the map of 11q13. Genomics 16:745-750
-
(1993)
Genomics
, vol.16
, pp. 745-750
-
-
Szepetowski, P.1
Perucca-Lostanlen, D.2
Gaudray, P.3
-
63
-
-
15744366444
-
D11S970 CATT polymorphism (RC29) located near the MEN1 locus at 11q13
-
Tassart RT, Krebs CJ, Mullins CM, Horton JH, Paradee WJ, Slusher R (1993) D11S970 CATT polymorphism (RC29) located near the MEN1 locus at 11q13. Hum Mol Genet 2:336
-
(1993)
Hum Mol Genet
, vol.2
, pp. 336
-
-
Tassart, R.T.1
Krebs, C.J.2
Mullins, C.M.3
Horton, J.H.4
Paradee, W.J.5
Slusher, R.6
-
64
-
-
0027397923
-
The molecular genetics of multiple endocrine neoplasia syndromes
-
Thakker RV (1993) The molecular genetics of multiple endocrine neoplasia syndromes. Clin Endocrinol 38:1-14
-
(1993)
Clin Endocrinol
, vol.38
, pp. 1-14
-
-
Thakker, R.V.1
-
65
-
-
0024394627
-
Association of parathyroid tumors in multiple endocrine neoplasia type 1 with loss of alleles on chromosome 11
-
Thakker RV, Bouloux P, Wooding C, Chotai K, Broad PM, Spurr NK, Besser GM, O'Riordan JLH (1989) Association of parathyroid tumors in multiple endocrine neoplasia type 1 with loss of alleles on chromosome 11. N Engl J Med 321:218-224
-
(1989)
N Engl J Med
, vol.321
, pp. 218-224
-
-
Thakker, R.V.1
Bouloux, P.2
Wooding, C.3
Chotai, K.4
Broad, P.M.5
Spurr, N.K.6
Besser, G.M.7
O'Riordan, J.L.H.8
-
66
-
-
0025332731
-
Mapping the gene causing X-linked recessive idiopathic hypoparathyroidism to Xq26-Xq27 by linkage studies
-
Thakker RV, Davies KE, Whyte MP, Wooding C, O'Riordan JLH (1990) Mapping the gene causing X-linked recessive idiopathic hypoparathyroidism to Xq26-Xq27 by linkage studies. J Clin Invest 86:40-45
-
(1990)
J Clin Invest
, vol.86
, pp. 40-45
-
-
Thakker, R.V.1
Davies, K.E.2
Whyte, M.P.3
Wooding, C.4
O'Riordan, J.L.H.5
-
67
-
-
0027284675
-
Linkage analysis of 7 polymorphic markers at chromosome 11p11.2-11q13 in 27 multiple endocrine neoplasia type 1 families
-
Thakker RV, Wooding C, Pang JT, Farren B, Harding B, Anderson DC, Besser GM, Bouloux P, Brenton DP, Buchanan KD, Edwards CR, Heath DA, Jackson CE, Jansen S, Lips K, Norum RA, Sampson J, Shalet SM, Taggart RT, Tailor D, Wheeler MH, Woollard PM, Yates J (1993a) Linkage analysis of 7 polymorphic markers at chromosome 11p11.2-11q13 in 27 multiple endocrine neoplasia type 1 families. Ann Hum Genet 57:17-25
-
(1993)
Ann Hum Genet
, vol.57
, pp. 17-25
-
-
Thakker, R.V.1
Wooding, C.2
Pang, J.T.3
Farren, B.4
Harding, B.5
Anderson, D.C.6
Besser, G.M.7
Bouloux, P.8
Brenton, D.P.9
Buchanan, K.D.10
Edwards, C.R.11
Heath, D.A.12
Jackson, C.E.13
Jansen, S.14
Lips, K.15
Norum, R.A.16
Sampson, J.17
Shalet, S.M.18
Taggart, R.T.19
Tailor, D.20
Wheeler, M.H.21
Woollard, P.M.22
Yates, J.23
more..
-
68
-
-
0027161684
-
Association of somatotrophinomas with loss of alleles on chromosome 11 and with gsp mutations
-
Thakker RV, Pook MA, Wooding C, Boscaro M, Scanarini M, Clayton RN (1993b) Association of somatotrophinomas with loss of alleles on chromosome 11 and with gsp mutations. J Clin Invest 91:2815-2821
-
(1993)
J Clin Invest
, vol.91
, pp. 2815-2821
-
-
Thakker, R.V.1
Pook, M.A.2
Wooding, C.3
Boscaro, M.4
Scanarini, M.5
Clayton, R.N.6
-
69
-
-
0028258069
-
Isolation and characterisation of a novel gene encoding nuclear protein at a locus (D11S636) tightly linked to multiple endocrine neoplasia type 1 (MEN1)
-
Toda T, Iida A, Miwa T, Nakamura Y, Imai T (1994) Isolation and characterisation of a novel gene encoding nuclear protein at a locus (D11S636) tightly linked to multiple endocrine neoplasia type 1 (MEN1). Hum Mol Genet 3:465-470
-
(1994)
Hum Mol Genet
, vol.3
, pp. 465-470
-
-
Toda, T.1
Iida, A.2
Miwa, T.3
Nakamura, Y.4
Imai, T.5
-
70
-
-
0026061721
-
Isolation and mapping of 62 new RFLP markers on human chromosome 11
-
Tokino T, Takahashi E, Mori M, Tanigami A, Glaser T, Park JW, Jones C, Hori T, Nakamura Y (1991) Isolation and mapping of 62 new RFLP markers on human chromosome 11. Am J Hum Genet 48:258-268
-
(1991)
Am J Hum Genet
, vol.48
, pp. 258-268
-
-
Tokino, T.1
Takahashi, E.2
Mori, M.3
Tanigami, A.4
Glaser, T.5
Park, J.W.6
Jones, C.7
Hori, T.8
Nakamura, Y.9
-
71
-
-
13344275870
-
Construction of a YAC contig and an STS map spanning 3.6 megabase pairs in Xp22.1
-
Trump D, Pilia G, Dixon PH, Wooding C, Thakrar R, Leigh SEA, Nagaraja Ramaiah, Whyte MP, Schlessinger D, Thakker RV (1996) Construction of a YAC contig and an STS map spanning 3.6 megabase pairs in Xp22.1. Hum Genet 97:60-69
-
(1996)
Hum Genet
, vol.97
, pp. 60-69
-
-
Trump, D.1
Pilia, G.2
Dixon, P.H.3
Wooding, C.4
Thakrar, R.5
Leigh, S.E.A.6
Ramaiah, N.7
Whyte, M.P.8
Schlessinger, D.9
Thakker, R.V.10
-
72
-
-
0028170327
-
The phospholipase C β3 gene located in the MEN1 region shows loss of expression in endocrine tumours
-
Weber G, Friedman E, Grimmond S, Hayward NK, Phelan C, Skogseid B, Gobl A, Zedenius J, Sandelin K, Teh BT, Carson E, White I, Öbere K, Shepherd J, Nordenskjöld M, Larsson C (1994) The phospholipase C β3 gene located in the MEN1 region shows loss of expression in endocrine tumours. Hum Mol Genet 3:1775-1781
-
(1994)
Hum Mol Genet
, vol.3
, pp. 1775-1781
-
-
Weber, G.1
Friedman, E.2
Grimmond, S.3
Hayward, N.K.4
Phelan, C.5
Skogseid, B.6
Gobl, A.7
Zedenius, J.8
Sandelin, K.9
Teh, B.T.10
Carson, E.11
White, I.12
Öbere, K.13
Shepherd, J.14
Nordenskjöld, M.15
Larsson, C.16
-
73
-
-
0026337065
-
Report for the DNA Committee and catalogues of the cloned and mapped genes, markers formulated for PCR and DNA polymorphisms
-
Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Ceverha P, Chipperfield M, Cooper DN, Coutelle C, Hewitt J, Klinger K, Langley K, Beckmann J, Tolley M, Maidak B (1991) Report for the DNA Committee and catalogues of the cloned and mapped genes, markers formulated for PCR and DNA polymorphisms. Cytogenet Cell Genet 58:1190-1832
-
(1991)
Cytogenet Cell Genet
, vol.58
, pp. 1190-1832
-
-
Williamson, R.1
Bowcock, A.2
Kidd, K.3
Pearson, P.4
Schmidtke, J.5
Ceverha, P.6
Chipperfield, M.7
Cooper, D.N.8
Coutelle, C.9
Hewitt, J.10
Klinger, K.11
Langley, K.12
Beckmann, J.13
Tolley, M.14
Maidak, B.15
-
74
-
-
0026589155
-
Conformation of genetic linkage between atopic immunoglobulin E responses and chromosome 11q13
-
Young RP, Sharp PA, Lynch JR, Faux JA, Lathrop GM, Cookson WOCM, Hopkin JM (1992) Conformation of genetic linkage between atopic immunoglobulin E responses and chromosome 11q13. J Med Genet 29:236-238
-
(1992)
J Med Genet
, vol.29
, pp. 236-238
-
-
Young, R.P.1
Sharp, P.A.2
Lynch, J.R.3
Faux, J.A.4
Lathrop, G.M.5
Cookson, W.O.C.M.6
Hopkin, J.M.7
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