-
1
-
-
0028920994
-
Localization of new genes and markers to the distal part of the human major histocompatiblilty complex (MHC) region and comparison with the mouse: New insights into the evolution of mammalian genomes
-
Amadou, C., M.T. Ribouchon, M.G. Mattel, N.A. Jenkins, D.J. Gilbert, N.G. Copeland, P. Avoustin, and P. Pontarotti. 1995. Localization of new genes and markers to the distal part of the human major histocompatiblilty complex (MHC) region and comparison with the mouse: New insights into the evolution of mammalian genomes. Genomics 26: 9-20.
-
(1995)
Genomics
, vol.26
, pp. 9-20
-
-
Amadou, C.1
Ribouchon, M.T.2
Mattel, M.G.3
Jenkins, N.A.4
Gilbert, D.J.5
Copeland, N.G.6
Avoustin, P.7
Pontarotti, P.8
-
2
-
-
0030253109
-
The first international workshop on comparative genome organisation
-
Andersson, L., A. Archibald, M. Ashburner, S. Audun, W. Barendse, J. Bitgood, C. Bottema, T. Broad, S. Brown, D. Burt et al. 1997. The first international workshop on comparative genome organisation. Mamm. Genome 7: 717-734.
-
(1997)
Mamm. Genome
, vol.7
, pp. 717-734
-
-
Andersson, L.1
Archibald, A.2
Ashburner, M.3
Audun, S.4
Barendse, W.5
Bitgood, J.6
Bottema, C.7
Broad, T.8
Brown, S.9
Burt, D.10
-
3
-
-
0025881630
-
X-chromosome inactivation may explain the difference in viability of XO humans and mice
-
Ashworth, A., S. Rastan, R. Lovell-Badge, and G. Kay. 1991. X-chromosome inactivation may explain the difference in viability of XO humans and mice. Nature 351: 406-408.
-
(1991)
Nature
, vol.351
, pp. 406-408
-
-
Ashworth, A.1
Rastan, S.2
Lovell-Badge, R.3
Kay, G.4
-
4
-
-
0028866218
-
A metric physical map of human chromosome 19
-
Ashworth, L.K., M.A. Batzer, B. Brandriff, E. Branscomb, P. dejong, E. Garcia, J. Garnes, L. Gordon, J.E. Lamerdin, G. Lennon et al. 1995. A metric physical map of human chromosome 19. Nature Genet. 11: 422-427.
-
(1995)
Nature Genet.
, vol.11
, pp. 422-427
-
-
Ashworth, L.K.1
Batzer, M.A.2
Brandriff, B.3
Branscomb, E.4
Dejong, P.5
Garcia, E.6
Garnes, J.7
Gordon, L.8
Lamerdin, J.E.9
Lennon, G.10
-
5
-
-
0031028759
-
Mouse models of human disease. Part II: Recent progress and future directions
-
Bedell, M.A., D.A. Largaespada, N.A. Jenkins, and N.G. Copeland. 1997. Mouse models of human disease. Part II: Recent progress and future directions. Genes & Dev. 11: 11-43.
-
(1997)
Genes & Dev.
, vol.11
, pp. 11-43
-
-
Bedell, M.A.1
Largaespada, D.A.2
Jenkins, N.A.3
Copeland, N.G.4
-
6
-
-
0028098241
-
New insights into the man-mouse comparative map of the X chromosome
-
Blair, H.J., V. Reed, S.H. Laval, and Y. Boyd. 1994. New insights into the man-mouse comparative map of the X chromosome. Genomics 19: 212-220.
-
(1994)
Genomics
, vol.19
, pp. 212-220
-
-
Blair, H.J.1
Reed, V.2
Laval, S.H.3
Boyd, Y.4
-
7
-
-
0029128281
-
High-resolution comparative mapping of the proximal region of the mouse X chromosome
-
Blair, H.J., M. Ho, A.P. Monaco, S. Fisher, I.W. Craig, and Y. Boyd. 1995. High-resolution comparative mapping of the proximal region of the mouse X chromosome. Genomics 28: 305-310.
-
(1995)
Genomics
, vol.28
, pp. 305-310
-
-
Blair, H.J.1
Ho, M.2
Monaco, A.P.3
Fisher, S.4
Craig, I.W.5
Boyd, Y.6
-
8
-
-
0031435290
-
Man and mouse - Lessons learned from the distal end of the X chromosome
-
this issue
-
Blaschke, R.J. and G.A. Rappold. 1997. Man and mouse - Lessons learned from the distal end of the X chromosome. Genome Res. (this issue).
-
(1997)
Genome Res.
-
-
Blaschke, R.J.1
Rappold, G.A.2
-
9
-
-
0027503479
-
Physical mapping of 2000 kb of the mouse X chromosome in the vicinity of the Xist locus
-
Cooper, P., J.T. Keer, V.M. McCabe, R.M. Hamvas, S.D. Brown, S. Rastan, and N. Brockdorff. 1993. Physical mapping of 2000 kb of the mouse X chromosome in the vicinity of the Xist locus. Genomics 15: 570-575.
-
(1993)
Genomics
, vol.15
, pp. 570-575
-
-
Cooper, P.1
Keer, J.T.2
McCabe, V.M.3
Hamvas, R.M.4
Brown, S.D.5
Rastan, S.6
Brockdorff, N.7
-
10
-
-
0027507490
-
A genetic linkage map of the mouse: Current applications and future prospects
-
Copeland, N.E., N.A. Jenkins, D.J. Gilbert, J.T. Eppig, L.J. Maltais, J.C. Miller, W.F. Dietrich, A. Weaver, S.E. Lincoln, R.G. Steen, L.D. Stein et al. 1993. A genetic linkage map of the mouse: Current applications and future prospects. Science 262: 57-66.
-
(1993)
Science
, vol.262
, pp. 57-66
-
-
Copeland, N.E.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
-
11
-
-
0030215347
-
Comparative mapping on the mouse X chromosome defines a myotubular myopathy equivalent region
-
de Gouyon, B., A. Chatterjee, A. Monaco, N. Quaderi, S.D. Brown, and G.E. Herman. 1996. Comparative mapping on the mouse X chromosome defines a myotubular myopathy equivalent region. Mamm. Genome 7: 575-579.
-
(1996)
Mamm. Genome
, vol.7
, pp. 575-579
-
-
Gouyon, B.1
Chatterjee, A.2
Monaco, A.3
Quaderi, N.4
Brown, S.D.5
Herman, G.E.6
-
12
-
-
0030012657
-
Human/mouse homology relationships
-
DeBry, R.W. and M.F. Seldin. 1996. Human/mouse homology relationships. Genomics 33: 337-351.
-
(1996)
Genomics
, vol.33
, pp. 337-351
-
-
DeBry, R.W.1
Seldin, M.F.2
-
13
-
-
0030200922
-
A new region of conservation is defined between human and mouse X chromosomes
-
Dinulos, M.B., M.T. Bassi, E.I. Rugarli, V. Chapman, A. Ballabio, and C.M. Disteche. 1996. A new region of conservation is defined between human and mouse X chromosomes. Genomics 35: 244-247.
-
(1996)
Genomics
, vol.35
, pp. 244-247
-
-
Dinulos, M.B.1
Bassi, M.T.2
Rugarli, E.I.3
Chapman, V.4
Ballabio, A.5
Disteche, C.M.6
-
14
-
-
0026907357
-
The human pseudoautosomal GM-CSF receptor a subunit gene is autosomal in mouse
-
Disteche, C.M., C.I. Brannan, A. Larsen, D.A. Adler, D.F. Schorderet, D. Gearing, N.G. Copeland, N.A. Jenkins, and L.S. Park. 1992. The human pseudoautosomal GM-CSF receptor a subunit gene is autosomal in mouse. Nature Genet. 1: 333-336.
-
(1992)
Nature Genet.
, vol.1
, pp. 333-336
-
-
Disteche, C.M.1
Brannan, C.I.2
Larsen, A.3
Adler, D.A.4
Schorderet, D.F.5
Gearing, D.6
Copeland, N.G.7
Jenkins, N.A.8
Park, L.S.9
-
15
-
-
0029831686
-
Unequal interchromosomal rearrangements may result in elastin gene deletions causing the Williams-Beuren syndrome
-
Dutly, F. and A. Schinzel. 1996. Unequal interchromosomal rearrangements may result in elastin gene deletions causing the Williams-Beuren syndrome. Hum. Mol. Genet. 5: 1893-1898.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 1893-1898
-
-
Dutly, F.1
Schinzel, A.2
-
16
-
-
0029678404
-
Rapid evolution of human pseudoautosomal genes and their mouse homologs
-
Ellison, J.W., X. Li, U. Francke, and L.J. Shapiro. 1996. Rapid evolution of human pseudoautosomal genes and their mouse homologs. Mamm. Genome 7: 25-30.
-
(1996)
Mamm. Genome
, vol.7
, pp. 25-30
-
-
Ellison, J.W.1
Li, X.2
Francke, U.3
Shapiro, L.J.4
-
17
-
-
0030877094
-
PHOG, a candidate gene for involvement in the short stature of Turner syndrome
-
Ellison, J.W., Z. Wardak, M.F. Young, P.G. Robey, M. Webster, and W. Chiong. 1997. PHOG, a candidate gene for involvement in the short stature of Turner syndrome. Hum. Mol. Genet. 8: 1341-1347.
-
(1997)
Hum. Mol. Genet.
, vol.8
, pp. 1341-1347
-
-
Ellison, J.W.1
Wardak, Z.2
Young, M.F.3
Robey, P.G.4
Webster, M.5
Chiong, W.6
-
18
-
-
0029587634
-
Comparative maps: The mammalian jigsaw puzzle
-
Eppig, J.T. and J.H. Nadeau. 1995. Comparative maps: The mammalian jigsaw puzzle. Curr. Opin. Genet. Dev. 5: 709-716.
-
(1995)
Curr. Opin. Genet. Dev.
, vol.5
, pp. 709-716
-
-
Eppig, J.T.1
Nadeau, J.H.2
-
19
-
-
0342887321
-
Mammals that break the rules: Genetics of marsupials and monotremes
-
Graves, J.A. 1996. Mammals that break the rules: Genetics of marsupials and monotremes. Annu. Rev. Genet. 30: 233-260.
-
(1996)
Annu. Rev. Genet.
, vol.30
, pp. 233-260
-
-
Graves, J.A.1
-
20
-
-
16944364045
-
A deletion in the bovine myostatin gene causes the double-muscled phenotype in cattle
-
Grobet, L., L.J. Martin, D. Poncelet, D. Pirottin, B. Brouwers, J. Riquet, A. Schoeberlein, S. Dunner, F. Menissier, J. Massabanda et al. 1997. A deletion in the bovine myostatin gene causes the double-muscled phenotype in cattle. Nature Genet. 17: 71-74.
-
(1997)
Nature Genet.
, vol.17
, pp. 71-74
-
-
Grobet, L.1
Martin, L.J.2
Poncelet, D.3
Pirottin, D.4
Brouwers, B.5
Riquet, J.6
Schoeberlein, A.7
Dunner, S.8
Menissier, F.9
Massabanda, J.10
-
21
-
-
9044240048
-
A radiation hybrid map of the human genome
-
Gyapay, G., K. Schmitt, C. Fizames, H. Jones, N. Vega-Czarny, D. Spillett, D. Muselet, J.F. Prud'Homme, C. Dib, C. Auffray et al. 1996. A radiation hybrid map of the human genome. Hum. Mol. Genet. 5: 339-346.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 339-346
-
-
Gyapay, G.1
Schmitt, K.2
Fizames, C.3
Jones, H.4
Vega-Czarny, N.5
Spillett, D.6
Muselet, D.7
Prud'Homme, J.F.8
Dib, C.9
Auffray, C.10
-
22
-
-
84979132203
-
The comparative genetics of color in rodents and carnivora
-
Haldane, J.B.S. 1927. The comparative genetics of color in rodents and carnivora. Biol. Rev. Camb. Philos. Soc. 2: 199-212.
-
(1927)
Biol. Rev. Camb. Philos. Soc.
, vol.2
, pp. 199-212
-
-
Haldane, J.B.S.1
-
23
-
-
0030627695
-
Mouse Chromosome 17
-
Hamvas, R.M.J., K. Artzt, K. Fisher-Lindahl, Z. Trachtulec, C. Vernet, and J. Forejt. 1997. Mouse Chromosome 17. Mamm. Genome 7:S274-294.
-
(1997)
Mamm. Genome
, vol.7
-
-
Hamvas, R.M.J.1
Artzt, K.2
Fisher-Lindahl, K.3
Trachtulec, Z.4
Vernet, C.5
Forejt, J.6
-
24
-
-
0025856958
-
Colinearity of novel genes in the class II regions of the MHC in mouse and human
-
Hanson, I.M. and J. Trowsdale. 1991. Colinearity of novel genes in the class II regions of the MHC in mouse and human. Immunogenetics 34: 5-11.
-
(1991)
Immunogenetics
, vol.34
, pp. 5-11
-
-
Hanson, I.M.1
Trowsdale, J.2
-
25
-
-
0022519469
-
Mapping of the class II region of the human major histocompatibility complex by pulsed-field gel electrophoresis
-
Hardy, D.A., J.I. Bell, E.O. Long, T. Lindsten, and H.O. McDevitt. 1986. Mapping of the class II region of the human major histocompatibility complex by pulsed-field gel electrophoresis. Nature 323: 453-455.
-
(1986)
Nature
, vol.323
, pp. 453-455
-
-
Hardy, D.A.1
Bell, J.I.2
Long, E.O.3
Lindsten, T.4
McDevitt, H.O.5
-
26
-
-
0027507405
-
Universal mapping probes and the origin of human chromosome 3
-
Hino, O., J.R. Testa, K.H. Buetow, T. Taguchi, J.Y. Zhou, M. Bremer, A. Bruzel, R. Yeung, G. Levan, K.K. Levan et al. 1993. Universal mapping probes and the origin of human chromosome 3. Proc. Natl. Acad. Sci. 90: 730-734.
-
(1993)
Proc. Natl. Acad. Sci.
, vol.90
, pp. 730-734
-
-
Hino, O.1
Testa, J.R.2
Buetow, K.H.3
Taguchi, T.4
Zhou, J.Y.5
Bremer, M.6
Bruzel, A.7
Yeung, R.8
Levan, G.9
Levan, K.K.10
-
27
-
-
0027856025
-
Human and mouse T-cell-receptor loci: The importance of comparative large-scale DNA sequence analyses
-
Hood, L., B.F. Koop, L. Rowen, and K. Wang. 1993. Human and mouse T-cell-receptor loci: The importance of comparative large-scale DNA sequence analyses. Cold Spring Harbor Symp. Quant. Biol. 58: 339-348.
-
(1993)
Cold Spring Harbor Symp. Quant. Biol.
, vol.58
, pp. 339-348
-
-
Hood, L.1
Koop, B.F.2
Rowen, L.3
Wang, K.4
-
28
-
-
0027058946
-
Characterization of the mouse apolipoprotein Apoa-1/Apoc-3 gene locus: Genomic, mRNA, and protein sequences with comparisons to other species
-
Januzzi, J.L., N. Azrolan, A. O'Connell, K. Aalto-Setala, and J.L. Breslow. 1992. Characterization of the mouse apolipoprotein Apoa-1/Apoc-3 gene locus: Genomic, mRNA, and protein sequences with comparisons to other species. Genomics 14: 1081-1088.
-
(1992)
Genomics
, vol.14
, pp. 1081-1088
-
-
Januzzi, J.L.1
Azrolan, N.2
O'Connell, A.3
Aalto-Setala, K.4
Breslow, J.L.5
-
29
-
-
0031153976
-
Gene homologs on human chromosome 15q21-q26 and a chicken microchromosome identify a new conserved segment
-
Jones, C.T., D.R. Morrice, I.R. Paton, and D.W. Burt. 1997. Gene homologs on human chromosome 15q21-q26 and a chicken microchromosome identify a new conserved segment. Mamm. Genome 8: 436-440.
-
(1997)
Mamm. Genome
, vol.8
, pp. 436-440
-
-
Jones, C.T.1
Morrice, D.R.2
Paton, I.R.3
Burt, D.W.4
-
30
-
-
0030818314
-
Mutations in myostatin (GDF8) in double-muscled Belgian blue cattle
-
Kambadur, R., M. Sharma, T.P.L. Smith, and J.J. Bass. 1997. Mutations in myostatin (GDF8) in double-muscled Belgian blue cattle. Genome Res. 7: 910-915.
-
(1997)
Genome Res.
, vol.7
, pp. 910-915
-
-
Kambadur, R.1
Sharma, M.2
Smith, T.P.L.3
Bass, J.J.4
-
31
-
-
0031025934
-
The second case of a t(17;22) in a family with neurofibromatosis type 1: Sequence analysis of the breakpoint regions
-
Kehrer-Sawatzki, H., J. Haussler, W. Krone, H. Bode, D.E. Jenne, K.U. Mehnert, U. Tummers, and G. Assum. 1997. The second case of a t(17;22) in a family with neurofibromatosis type 1: Sequence analysis of the breakpoint regions. Hum. Genet. 99: 237-247.
-
(1997)
Hum. Genet.
, vol.99
, pp. 237-247
-
-
Kehrer-Sawatzki, H.1
Haussler, J.2
Krone, W.3
Bode, H.4
Jenne, D.E.5
Mehnert, K.U.6
Tummers, U.7
Assum, G.8
-
32
-
-
0030919534
-
The human homolog of a mouse-imprinted gene, Peg3, maps to a zinc finger gene-rich region of human chromosome 19q13.4
-
Kim, J., L. Ashworth, E. Branscomb, and L. Stubbs. 1997. The human homolog of a mouse-imprinted gene, Peg3, maps to a zinc finger gene-rich region of human chromosome 19q13.4. Genome Res. 7: 532-540.
-
(1997)
Genome Res.
, vol.7
, pp. 532-540
-
-
Kim, J.1
Ashworth, L.2
Branscomb, E.3
Stubbs, L.4
-
33
-
-
0024420119
-
Physical mapping of a family of interferon-activated genes, serum amyloid P-component, and alpha-spectrin on mouse chromosome 1
-
Kingsmore, S.F., J. Snoddy, D. Choubey, P. Lengyel, and M.F. Seldin. 1989. Physical mapping of a family of interferon-activated genes, serum amyloid P-component, and alpha-spectrin on mouse chromosome 1. Immunogenetics 30: 169-174.
-
(1989)
Immunogenetics
, vol.30
, pp. 169-174
-
-
Kingsmore, S.F.1
Snoddy, J.2
Choubey, D.3
Lengyel, P.4
Seldin, M.F.5
-
34
-
-
0029944470
-
High frequency de novo alterations in the long-range genomic structure of the mouse pseudoautosomal region
-
Kipling, D., E.C. Salido, L.J. Shapiro, and H.J. Cooke. 1996. High frequency de novo alterations in the long-range genomic structure of the mouse pseudoautosomal region. Nature Genet. 13: 78-80.
-
(1996)
Nature Genet.
, vol.13
, pp. 78-80
-
-
Kipling, D.1
Salido, E.C.2
Shapiro, L.J.3
Cooke, H.J.4
-
35
-
-
0029278766
-
Homologs of genes and anonymous loci on human chromosome 13 map to mouse chromosomes 8 and 14
-
Koizumi, T., E. Hendel, P.A. Lalley, M.B. Tchetgen, and J.H. Nadeau. 1995. Homologs of genes and anonymous loci on human chromosome 13 map to mouse chromosomes 8 and 14. Mamm. Genome 6: 263-268.
-
(1995)
Mamm. Genome
, vol.6
, pp. 263-268
-
-
Koizumi, T.1
Hendel, E.2
Lalley, P.A.3
Tchetgen, M.B.4
Nadeau, J.H.5
-
36
-
-
0026706487
-
Organization, structure, and function of 95 kb of DNA spanning the murine T-cell receptor C alpha/C delta region
-
Koop, B.F., R.K. Wilson, K. Wang, B. Vernooij, D. Zallwer, C.L. Kuo, D. Seto, M. Toda, and L. Hood. 1992. Organization, structure, and function of 95 kb of DNA spanning the murine T-cell receptor C alpha/C delta region. Genomics 13: 1209-1230.
-
(1992)
Genomics
, vol.13
, pp. 1209-1230
-
-
Koop, B.F.1
Wilson, R.K.2
Wang, K.3
Vernooij, B.4
Zallwer, D.5
Kuo, C.L.6
Seto, D.7
Toda, M.8
Hood, L.9
-
37
-
-
0028203470
-
The human T-cell receptor TCRAC/TCRDC (C α/C δ) region: Organization, sequence, and evolution of 97.6 kb of DNA
-
Koop, B.F., L. Rowen, K. Wang, C.L. Kuo, D. Seto, J.A. Lenstra, S. Howard, W. Shan, P. Deshpande, and L. Hood. 1994. The human T-cell receptor TCRAC/TCRDC (C α/C δ) region: Organization, sequence, and evolution of 97.6 kb of DNA. Genomics 19: 478-493.
-
(1994)
Genomics
, vol.19
, pp. 478-493
-
-
Koop, B.F.1
Rowen, L.2
Wang, K.3
Kuo, C.L.4
Seto, D.5
Lenstra, J.A.6
Howard, S.7
Shan, W.8
Deshpande, P.9
Hood, L.10
-
38
-
-
0026766022
-
A deletion/inversion rearrangement of the beta-globin gene cluster in a Turkish family with delta beta zero-thalassemia intermedia
-
Kulozik, A.E., A. Bellan-Koch, E. Kohne, and E. Kleihauer. 1992. A deletion/inversion rearrangement of the beta-globin gene cluster in a Turkish family with delta beta zero-thalassemia intermedia. Blood 79: 2455-2459.
-
(1992)
Blood
, vol.79
, pp. 2455-2459
-
-
Kulozik, A.E.1
Bellan-Koch, A.2
Kohne, E.3
Kleihauer, E.4
-
39
-
-
0027261522
-
Pulsed-field map of Xq13 in the region of the human X inactivation center
-
Lafreniere, R.G. and H.F. Willard. 1993. Pulsed-field map of Xq13 in the region of the human X inactivation center. Genomics 17: 502-506.
-
(1993)
Genomics
, vol.17
, pp. 502-506
-
-
Lafreniere, R.G.1
Willard, H.F.2
-
40
-
-
0028968707
-
Genomic sequence comparison of the human and mouse XRCC1 DNA repair gene regions
-
Lamerdin, J.E., M.A. Montgomery, S.A. Stilwagen, L.K. Scheidecker, R.S. Tebbs, K.W. Brookman, L.H. Thompson and A.V. Carrano. 1995. Genomic sequence comparison of the human and mouse XRCC1 DNA repair gene regions. Genomics 25: 547-554.
-
(1995)
Genomics
, vol.25
, pp. 547-554
-
-
Lamerdin, J.E.1
Montgomery, M.A.2
Stilwagen, S.A.3
Scheidecker, L.K.4
Tebbs, R.S.5
Brookman, K.W.6
Thompson, L.H.7
Carrano, A.V.8
-
41
-
-
0030585760
-
Sequence analysis of the ERCC2 gene regions in human, mouse, and hamster reveals three linked genes
-
Lamerdin, J.E., S.A. Stilwagen, M.H. Ramirez, L. Stubbs, and A.V. Corrano. 1996. Sequence analysis of the ERCC2 gene regions in human, mouse, and hamster reveals three linked genes. Genomics 34: 399-409.
-
(1996)
Genomics
, vol.34
, pp. 399-409
-
-
Lamerdin, J.E.1
Stilwagen, S.A.2
Ramirez, M.H.3
Stubbs, L.4
Corrano, A.V.5
-
42
-
-
1842292786
-
Identification of an obesity quantitative trait locus on mouse chromosome 2 and evidence of linkage to body fat and insulin on the human homologous region 20q
-
Lembertas, A.V., L. Perusse, Y.C. Chagnon, J.S. Fisler, C.H. Warden, D.A. Purcell-Huynh, F.T. Dionne, J. Gagnon, A. Nadeau, A.J. Lusis, and C. Bouchard. 1997. Identification of an obesity quantitative trait locus on mouse chromosome 2 and evidence of linkage to body fat and insulin on the human homologous region 20q. J. Clin. Invest. 100: 1240-1247.
-
(1997)
J. Clin. Invest.
, vol.100
, pp. 1240-1247
-
-
Lembertas, A.V.1
Perusse, L.2
Chagnon, Y.C.3
Fisler, J.S.4
Warden, C.H.5
Purcell-Huynh, D.A.6
Dionne, F.T.7
Gagnon, J.8
Nadeau, A.9
Lusis, A.J.10
Bouchard, C.11
-
43
-
-
0028894943
-
Experimental design and error detection for polyploid radiation hybrid mapping
-
Lunetta K.L., M. Boehnke, K. Lange, and D.R. Cox. 1995. Experimental design and error detection for polyploid radiation hybrid mapping. Genome Res. 5: 151-163.
-
(1995)
Genome Res.
, vol.5
, pp. 151-163
-
-
Lunetta, K.L.1
Boehnke, M.2
Lange, K.3
Cox, D.R.4
-
44
-
-
0029760561
-
Selected locus and multiple panel models for radiation hybrid mapping
-
_. 1996. Selected locus and multiple panel models for radiation hybrid mapping. Am. J. Hum. Genet. 59: 717-725.
-
(1996)
Am. J. Hum. Genet.
, vol.59
, pp. 717-725
-
-
-
45
-
-
0031012314
-
Comparative anchor tagged sequences (CATS) for integrative mapping of mammalian genomes
-
Lyons, L.A., T.F. Laughlin, N.G. Copeland, N.A. Jenkins, J.E. Womack, and S.J. O'Brien. 1997. Comparative anchor tagged sequences (CATS) for integrative mapping of mammalian genomes. Nature Genet. 15: 47-56.
-
(1997)
Nature Genet.
, vol.15
, pp. 47-56
-
-
Lyons, L.A.1
Laughlin, T.F.2
Copeland, N.G.3
Jenkins, N.A.4
Womack, J.E.5
O'Brien, S.J.6
-
46
-
-
0030878110
-
Congenital leptin deficiency is associated with severe early-onset obesity in humans
-
Montague, C.T., I.S. Farooqi, J.P. Whitehead, M.A. Soos, H. Rau, N.J. Wareham, C.P. Sewter, J.E. Digby, S.N. Mohammed, J.A. Hurst et al. 1997. Congenital leptin deficiency is associated with severe early-onset obesity in humans. Nature 387: 903-908.
-
(1997)
Nature
, vol.387
, pp. 903-908
-
-
Montague, C.T.1
Farooqi, I.S.2
Whitehead, J.P.3
Soos, M.A.4
Rau, H.5
Wareham, N.J.6
Sewter, C.P.7
Digby, J.E.8
Mohammed, S.N.9
Hurst, J.A.10
-
47
-
-
0025721084
-
The conservation of dinucleotide microsatellites among mammalian genomes allows the use of heterologous PCR primer pairs in closely related species
-
Moore, S.S., L.L. Sargeant, T.J. King, J.S. Mattick, M. Georges, and D.J. Hetzel. 1991. The conservation of dinucleotide microsatellites among mammalian genomes allows the use of heterologous PCR primer pairs in closely related species. Genomics 10: 654-660.
-
(1991)
Genomics
, vol.10
, pp. 654-660
-
-
Moore, S.S.1
Sargeant, L.L.2
King, T.J.3
Mattick, J.S.4
Georges, M.5
Hetzel, D.J.6
-
48
-
-
0342920312
-
-
The Jackson Laboratory, Bar Harbor, Maine. August
-
Mouse Genome Database (MGD), Mouse Genome Informatics, The Jackson Laboratory, Bar Harbor, Maine. August 1997. http://www.informatics.jax.org/.
-
(1997)
Mouse Genome Database (MGD), Mouse Genome Informatics
-
-
-
49
-
-
0026040628
-
Genomic organization of adrenergic and serotonin receptors in the mouse: Linkage mapping of sequence-related genes provides a method for examining mammalian chromosome evolution
-
Oakey, R.J., M.G. Caron, R.J. Lefkowitz, and M.F. Seldin. 1991. Genomic organization of adrenergic and serotonin receptors in the mouse: Linkage mapping of sequence-related genes provides a method for examining mammalian chromosome evolution. Genomics 10: 338-344.
-
(1991)
Genomics
, vol.10
, pp. 338-344
-
-
Oakey, R.J.1
Caron, M.G.2
Lefkowitz, R.J.3
Seldin, M.F.4
-
50
-
-
0026951066
-
Construction of a physical map on mouse and human chromosome 1: Comparison of 13 Mb of mouse and 11 Mb of human DNA
-
Oakey, R.J., M.L. Watson, and M.F. Seldin. 1992. Construction of a physical map on mouse and human chromosome 1: Comparison of 13 Mb of mouse and 11 Mb of human DNA. Hum. Mol. Genet. 1: 613-620.
-
(1992)
Hum. Mol. Genet.
, vol.1
, pp. 613-620
-
-
Oakey, R.J.1
Watson, M.L.2
Seldin, M.F.3
-
51
-
-
0030966052
-
Large-scale comparative sequence analysis of the human and murine Bruton's tyrosine kinase loci reveals conserved regulatory domains
-
Oeltjen, J.C., T.M. Malley, D.M. Muzny, W. Miller, R.A. Gibbs, and J.W. Belmont. 1997. Large-scale comparative sequence analysis of the human and murine Bruton's tyrosine kinase loci reveals conserved regulatory domains. Genome Res 7: 315-329.
-
(1997)
Genome Res
, vol.7
, pp. 315-329
-
-
Oeltjen, J.C.1
Malley, T.M.2
Muzny, D.M.3
Miller, W.4
Gibbs, R.A.5
Belmont, J.W.6
-
53
-
-
0029111867
-
A contravention of Ohno's law in mice
-
Palmer, S., J. Perry, and A. Ashworth. 1995. A contravention of Ohno's law in mice. Nature Genet. 10: 472-476.
-
(1995)
Nature Genet.
, vol.10
, pp. 472-476
-
-
Palmer, S.1
Perry, J.2
Ashworth, A.3
-
54
-
-
0030137707
-
A detailed physical map of the porcine major histocompatibility complex (MHC) class III region: Comparison with human and mouse MHC class III regions
-
Peelman, L.J., P. Chardon, M. Vaiman, M. Mattheuws, A. Van Zeveren, A. Van de Weghe, Y. Bouquet, and R.D. Campbell. 1996. A detailed physical map of the porcine major histocompatibility complex (MHC) class III region: Comparison with human and mouse MHC class III regions. Mamm. Genome 7: 363-367.
-
(1996)
Mamm. Genome
, vol.7
, pp. 363-367
-
-
Peelman, L.J.1
Chardon, P.2
Vaiman, M.3
Mattheuws, M.4
Van Zeveren, A.5
Van De Weghe, A.6
Bouquet, Y.7
Campbell, R.D.8
-
55
-
-
0028966156
-
Comparative mapping of 50 human chromosome 9 loci in the laboratory mouse
-
Pilz, A., K. Woodward, S. Povey, and C. Abbott. 1995. Comparative mapping of 50 human chromosome 9 loci in the laboratory mouse. Genomics 25: 139-149.
-
(1995)
Genomics
, vol.25
, pp. 139-149
-
-
Pilz, A.1
Woodward, K.2
Povey, S.3
Abbott, C.4
-
56
-
-
0027970838
-
Chromosomal translocation in human cancer
-
Rabbitts, T.H. 1994. Chromosomal translocation in human cancer. Nature 372: 143-149.
-
(1994)
Nature
, vol.372
, pp. 143-149
-
-
Rabbitts, T.H.1
-
57
-
-
0030940217
-
Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome
-
Rao, E., B. Weiss, M. Fukami, A. Rump, B. Niesler, A. Mertz, K. Muroya, G. Binder, S. Kirsch, M. Winkelmann et al. 1997. Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome. Nature Genet. 16: 54-63.
-
(1997)
Nature Genet.
, vol.16
, pp. 54-63
-
-
Rao, E.1
Weiss, B.2
Fukami, M.3
Rump, A.4
Niesler, B.5
Mertz, A.6
Muroya, K.7
Binder, G.8
Kirsch, S.9
Winkelmann, M.10
-
58
-
-
0026524350
-
Comparison of mouse and human HOX-4 complexes defines conserved sequences involved in the regulation of Hox-4.4
-
Renucci, A., V. Zappavigna, J. Zakany, J.C. Izpisua-Belmonte, K. Burki, and D. Duboule. 1992. Comparison of mouse and human HOX-4 complexes defines conserved sequences involved in the regulation of Hox-4.4. EMBO J. 11: 1459-1468.
-
(1992)
EMBO J.
, vol.11
, pp. 1459-1468
-
-
Renucci, A.1
Zappavigna, V.2
Zakany, J.3
Izpisua-Belmonte, J.C.4
Burki, K.5
Duboule, D.6
-
59
-
-
0028862024
-
Characterization of a YAC contig spanning the pseudoautosomal region
-
Ried, K., A. Mertz, R. Nagaraja, M. Trusgnich, J.H. Riley, R. Anand, H. Lehrach, D. Page, J.W. Ellison, and G. Rappold. 1995. Characterization of a YAC contig spanning the pseudoautosomal region. Genomics 29: 787-792.
-
(1995)
Genomics
, vol.29
, pp. 787-792
-
-
Ried, K.1
Mertz, A.2
Nagaraja, R.3
Trusgnich, M.4
Riley, J.H.5
Anand, R.6
Lehrach, H.7
Page, D.8
Ellison, J.W.9
Rappold, G.10
-
60
-
-
0027058727
-
Isolation and expression of linked zinc finger gene clusters on human chromosome 11q
-
Saleh, M., L. Selleri, P.F. Little, and G.A. Evans. 1992. Isolation and expression of linked zinc finger gene clusters on human chromosome 11q. Genomics 14: 970-978.
-
(1992)
Genomics
, vol.14
, pp. 970-978
-
-
Saleh, M.1
Selleri, L.2
Little, P.F.3
Evans, G.A.4
-
61
-
-
0028306521
-
Comparative chromosome painting discloses homologous segments in distantly related mammals
-
Scherthan, H., T. Cremer, U. Arnason, H.U. Weier, A. Lima-de-Faria, and L. Fronick. 1994. Comparative chromosome painting discloses homologous segments in distantly related mammals. Nature Genet. 6: 342-347.
-
(1994)
Nature Genet.
, vol.6
, pp. 342-347
-
-
Scherthan, H.1
Cremer, T.2
Arnason, U.3
Weier, H.U.4
Lima-de-Faria, A.5
Fronick, L.6
-
62
-
-
0029924743
-
Construction of a mouse whole-genome radiation hybrid panel and application to MMU11
-
Schmitt, K., J.W. Foster, R.W. Feakes, C. Knights, M.E. Davis, D.J. Spillett, and P.N. Goodfellow. 1996. Construction of a mouse whole-genome radiation hybrid panel and application to MMU11. Genomics 34: 193-197.
-
(1996)
Genomics
, vol.34
, pp. 193-197
-
-
Schmitt, K.1
Foster, J.W.2
Feakes, R.W.3
Knights, C.4
Davis, M.E.5
Spillett, D.J.6
Goodfellow, P.N.7
-
63
-
-
0028012820
-
The human serum amyloid A protein (SAA) superfamily gene cluster: Mapping to chromosome 11p15.1 by physical and genetic linkage analysis
-
Sellar, G.C., S.A. Jordan, W.A. Bickmore, J.A. Fantes, V. van Heyningen, and A.S. Whitehead. 1994. The human serum amyloid A protein (SAA) superfamily gene cluster: Mapping to chromosome 11p15.1 by physical and genetic linkage analysis. Genomics 19: 221-227.
-
(1994)
Genomics
, vol.19
, pp. 221-227
-
-
Sellar, G.C.1
Jordan, S.A.2
Bickmore, W.A.3
Fantes, J.A.4
Van Heyningen, V.5
Whitehead, A.S.6
-
64
-
-
2642669464
-
Tandem zinc-finger gene families in mammals: Insights and unanswered questions
-
in press
-
Shannon, M., J. Kim, L.K. Ashworth, E. Branscomb, and L. Stubbs. 1997. Tandem zinc-finger gene families in mammals: Insights and unanswered questions. Gene Sequence (in press).
-
(1997)
Gene Sequence
-
-
Shannon, M.1
Kim, J.2
Ashworth, L.K.3
Branscomb, E.4
Stubbs, L.5
-
65
-
-
0021732612
-
Tracts of high or low sequence divergence in the mouse major histocompatibility complex
-
Steinmetz, M., M. Malissen, L. Hood. A. Orn, R.A. Maki, G.R. Dastoornikoo, D. Stephan, E. Gibb, and R. Romaniuk. 1984. Tracts of high or low sequence divergence in the mouse major histocompatibility complex. EMBO J. 3: 2995-3003.
-
(1984)
EMBO J.
, vol.3
, pp. 2995-3003
-
-
Steinmetz, M.1
Malissen, M.2
Hood, L.3
Orn, A.4
Maki, R.A.5
Dastoornikoo, G.R.6
Stephan, D.7
Gibb, E.8
Romaniuk, R.9
-
66
-
-
0025174888
-
Clusters of intragenic Alu repeats predispose the human C1 inhibitor locus to deleterious rearrangements
-
Stoppa-Lyonnet, D., P.E. Carter, T. Meo, and M. Tosi. 1990. Clusters of intragenic Alu repeats predispose the human C1 inhibitor locus to deleterious rearrangements. Proc. Natl. Acad. Sci. 87: 1551-1555.
-
(1990)
Proc. Natl. Acad. Sci.
, vol.87
, pp. 1551-1555
-
-
Stoppa-Lyonnet, D.1
Carter, P.E.2
Meo, T.3
Tosi, M.4
-
67
-
-
0028587896
-
Clustering of six human 11p15 gene homologs within a 500-kb interval of proximal mouse chromosome 7
-
Stubbs, L., E.M. Rinchik, E. Goldberg, B. Rudy, M.A. Handel, and D. Johnson. 1994. Clustering of six human 11p15 gene homologs within a 500-kb interval of proximal mouse chromosome 7. Genomics 24: 324-332.
-
(1994)
Genomics
, vol.24
, pp. 324-332
-
-
Stubbs, L.1
Rinchik, E.M.2
Goldberg, E.3
Rudy, B.4
Handel, M.A.5
Johnson, D.6
-
68
-
-
0030219837
-
Detailed comparative map of human chromosome 19q and related regions of the mouse genome
-
Stubbs, L., E.A. Carver, M.E. Shannon, J. Kim, J. Geisler, E.E. Generoso, B.G. Stanford, W.C. Dunn, H. Mohrenweiser, W. Zimmermann et al. 1996. Detailed comparative map of human chromosome 19q and related regions of the mouse genome. Genomics 35: 499-508.
-
(1996)
Genomics
, vol.35
, pp. 499-508
-
-
Stubbs, L.1
Carver, E.A.2
Shannon, M.E.3
Kim, J.4
Geisler, J.5
Generoso, E.E.6
Stanford, B.G.7
Dunn, W.C.8
Mohrenweiser, H.9
Zimmermann, W.10
-
69
-
-
0029827344
-
Evidence for subtelomeric exchange of 3.3 kb tandemly repeated units between chromosomes 4q35 and 10q26: Implications for genetic counseling and etiology of FSHD1
-
van Deutekom, J.C., E. Bakker, R.J. Lemmers, M.J. van der Wielen, E. Bik, M.H. Hofker, G.W. Padberg, and R.R. Frants. 1996. Evidence for subtelomeric exchange of 3.3 kb tandemly repeated units between chromosomes 4q35 and 10q26: Implications for genetic counseling and etiology of FSHD1. Hum. Mol. Genet. 5: 1997-2003.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 1997-2003
-
-
Van Deutekom, J.C.1
Bakker, E.2
Lemmers, R.J.3
Van Der Wielen, M.J.4
Bik, E.5
Hofker, M.H.6
Padberg, G.W.7
Frants, R.R.8
-
70
-
-
0031568899
-
Genetic mapping of 21 genes on mouse chromosome 11 reveals disruptions in linkage conservation with human chromosome 5
-
Watkins-Chow, D.E., M.S. Buckwalter, M.M. Newhouse, A.C. Lossie, M.L. Brinkmeier, and S.A. Camper. 1997. Genetic mapping of 21 genes on mouse chromosome 11 reveals disruptions in linkage conservation with human chromosome 5. Genomics 40: 114-122.
-
(1997)
Genomics
, vol.40
, pp. 114-122
-
-
Watkins-Chow, D.E.1
Buckwalter, M.S.2
Newhouse, M.M.3
Lossie, A.C.4
Brinkmeier, M.L.5
Camper, S.A.6
-
71
-
-
0021150525
-
Organization and evolution of the class I gene family in the major histocompatibility complex of the C57BL/10 mouse
-
Weiss, E.H., L. Golden, K. Fahrner, A.L. Mellor, J.J. Devlin, H. Bullman, H. Tiddens, H. Bud, and R.A. Flavell. 1984. Organization and evolution of the class I gene family in the major histocompatibility complex of the C57BL/10 mouse. Nature 310: 650-655.
-
(1984)
Nature
, vol.310
, pp. 650-655
-
-
Weiss, E.H.1
Golden, L.2
Fahrner, K.3
Mellor, A.L.4
Devlin, J.J.5
Bullman, H.6
Tiddens, H.7
Bud, H.8
Flavell, R.A.9
-
72
-
-
0029939509
-
Fine mapping of the 1q21 breakpoint of the papillary renal cell carcinoma-associated (X;1) translocation
-
Weterman, M.A., M. Wilbrink, T. Dijkhuizen, E. van den Berg, and A. Geurts van Kessel. 1996. Fine mapping of the 1q21 breakpoint of the papillary renal cell carcinoma-associated (X;1) translocation. Hum. Genet. 98: 16-21.
-
(1996)
Hum. Genet.
, vol.98
, pp. 16-21
-
-
Weterman, M.A.1
Wilbrink, M.2
Dijkhuizen, T.3
Van Den Berg, E.4
Van Geurts Kessel, A.5
-
73
-
-
0029585512
-
Chromosome painting in mammals as an approach to comparative genomics
-
Wienberg, J. and R. Stanyon. 1995. Chromosome painting in mammals as an approach to comparative genomics. Curr. Opin. Genet. Dev. 5: 792-797.
-
(1995)
Curr. Opin. Genet. Dev.
, vol.5
, pp. 792-797
-
-
Wienberg, J.1
Stanyon, R.2
-
74
-
-
0027936475
-
Report and abstracts of the fifth international workshop on human X chromosome mapping 1994
-
Willard, H.F., F. Cremers, J.L. Mandel, A.P. Monaco, D.L. Nelson, and D. Schlessinger. 1994. Report and abstracts of the fifth international workshop on human X chromosome mapping 1994. Cytogenet. Cell Genet. 67: 295-358.
-
(1994)
Cytogenet. Cell Genet.
, vol.67
, pp. 295-358
-
-
Willard, H.F.1
Cremers, F.2
Mandel, J.L.3
Monaco, A.P.4
Nelson, D.L.5
Schlessinger, D.6
|