-
1
-
-
0029195881
-
Efforts toward understanding the molecular basis of facioseapulohumeral dystrophy
-
Altherr MR, Bengtsson U, Markovich RP,Winokur ST (1995) Efforts toward understanding the molecular basis of facioseapulohumeral dystrophy. Muscle Nerve 2 (Suppl.), S32-S38
-
(1995)
Muscle Nerve
, vol.2
, Issue.SUPPL.
-
-
Altherr, M.R.1
Bengtsson, U.2
Markovich, R.P.3
Winokur, S.T.4
-
2
-
-
0028353367
-
PCM-1, a 228kD centrosome autoantigen with a distinct cell cycle distribution
-
Balczon R, Bao L, and Zimmer WE (1994) PCM-1, a 228kD centrosome autoantigen with a distinct cell cycle distribution. J Cell Biol 124, 783-793
-
(1994)
J Cell Biol
, vol.124
, pp. 783-793
-
-
Balczon, R.1
Bao, L.2
Zimmer, W.E.3
-
3
-
-
0025891440
-
Gene structure and chromosomal localization of plasma kallikrein
-
Beaubien G, Rosinski-Chupin I, Mbikay M, Chretien M, and Seidah NG (1991) Gene structure and chromosomal localization of plasma kallikrein. Biochemistry 30, 1628-1635
-
(1991)
Biochemistry
, vol.30
, pp. 1628-1635
-
-
Beaubien, G.1
Rosinski-Chupin, I.2
Mbikay, M.3
Chretien, M.4
Seidah, N.G.5
-
4
-
-
0028214722
-
Towards high resolution maps of the mouse and human genomes - a facility for ordering markers to 0.1cM resolution
-
Breen M, Deakin L, B, M, Miller S, Sibson R, Tarttelin E et al. (1994) Towards high resolution maps of the mouse and human genomes - a facility for ordering markers to 0.1cM resolution. Hum Mol Genet 3, 621-627
-
(1994)
Hum Mol Genet
, vol.3
, pp. 621-627
-
-
Breen, M.1
Deakin, L.B.M.2
Miller, S.3
Sibson, R.4
Tarttelin, E.5
-
5
-
-
0030248545
-
Chromosomal mapping of cell death proteases CPP32, MCH2 and MCH3
-
Bullrich F, Fernandes-Alnemri T, Litwack G, Alnemri ES, Croce CM (1996) Chromosomal mapping of cell death proteases CPP32, MCH2 and MCH3. Genomics 36, 362-365
-
(1996)
Genomics
, vol.36
, pp. 362-365
-
-
Bullrich, F.1
Fernandes-Alnemri, T.2
Litwack, G.3
Alnemri, E.S.4
Croce, C.M.5
-
6
-
-
0025284845
-
Structure, comparison with rat gene, and assignment to the long arm of chromosome 4
-
Cassard AM, Bouillaud F, Mattei MG, Hentz E, Raimbault S, et al. (1990) Structure, comparison with rat gene, and assignment to the long arm of chromosome 4. J Cell Biochem 43, 255-264
-
(1990)
J Cell Biochem
, vol.43
, pp. 255-264
-
-
Cassard, A.M.1
Bouillaud, F.2
Mattei, M.G.3
Hentz, E.4
Raimbault, S.5
-
7
-
-
0030625101
-
Mouse Chromosome 8
-
Ceci JD, Mills KA (1997) Mouse Chromosome 8. Mamm Genome 7 (Suppl), S143-S158
-
(1997)
Mamm Genome
, vol.7
, Issue.SUPPL.
-
-
Ceci, J.D.1
Mills, K.A.2
-
8
-
-
0028221036
-
Molecular basis of splotch and Waardenburg Pax-3 mutations
-
Chalepakis G, Goulding M, Read AP, Strachan T, Gruss P (1994) Molecular basis of splotch and Waardenburg Pax-3 mutations. Proc Natl Acad Sci USA 91, 3685-3689
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 3685-3689
-
-
Chalepakis, G.1
Goulding, M.2
Read, A.P.3
Strachan, T.4
Gruss, P.5
-
9
-
-
0028302127
-
A genetic map of the mouse with 4,006 simple sequence polymorphisms
-
Dietrich WF, Miller JC, Steen RG, Merchant M, Damron D et al. (1994) A genetic map of the mouse with 4,006 simple sequence polymorphisms. Natl Genet 7, 220-245
-
(1994)
Natl Genet
, vol.7
, pp. 220-245
-
-
Dietrich, W.F.1
Miller, J.C.2
Steen, R.G.3
Merchant, M.4
Damron, D.5
-
10
-
-
13344287050
-
A comprehensive genetic map of the mouse genome
-
Dietrich WF, Miller J, Steen R, Merchant MA, Damron-Boles D (1996) A comprehensive genetic map of the mouse genome. Nature 380, 149-152
-
(1996)
Nature
, vol.380
, pp. 149-152
-
-
Dietrich, W.F.1
Miller, J.2
Steen, R.3
Merchant, M.A.4
Damron-Boles, D.5
-
11
-
-
0028844745
-
Molecular cloning and tissue expression of FAT, the human homologue of the Drosophila fat gene that is located on chromosome 4q34-q35 and encodes a putative adhesion molecule
-
Dunne J, Hanby AM, Poulsom R, Jones TA, Sheer D et al. (1995) Molecular cloning and tissue expression of FAT, the human homologue of the Drosophila fat gene that is located on chromosome 4q34-q35 and encodes a putative adhesion molecule. Genomics 30, 207-223
-
(1995)
Genomics
, vol.30
, pp. 207-223
-
-
Dunne, J.1
Hanby, A.M.2
Poulsom, R.3
Jones, T.A.4
Sheer, D.5
-
12
-
-
0025925068
-
2H), a mutation affecting development of the mouse neural tube, shows a deletion with the paired homeodomain of Pax-3
-
2H), a mutation affecting development of the mouse neural tube, shows a deletion with the paired homeodomain of Pax-3. Cell 67, 767-774
-
(1991)
Cell
, vol.67
, pp. 767-774
-
-
Epstein, D.J.1
Vekemans, M.2
Gros, P.3
-
13
-
-
0028860302
-
The shaker-1 mouse deafness mutation encodes a myosin-VII motor
-
Gibson F, Walsh J, Mburu P, Varela A, Brown KA et al. (1995) The shaker-1 mouse deafness mutation encodes a myosin-VII motor. Nature 374, 62-64
-
(1995)
Nature
, vol.374
, pp. 62-64
-
-
Gibson, F.1
Walsh, J.2
Mburu, P.3
Varela, A.4
Brown, K.A.5
-
14
-
-
0031133964
-
Fath, the murine homologue of the Drosophila fat tumor suppressor gene maps to chromosome 8
-
Grewal PK, Hewitt JE (1997) Fath, the murine homologue of the Drosophila fat tumor suppressor gene maps to chromosome 8. Mamm Genome 8, 383-384
-
(1997)
Mamm Genome
, vol.8
, pp. 383-384
-
-
Grewal, P.K.1
Hewitt, J.E.2
-
15
-
-
0031153982
-
The mouse homolog of FRG1, a candidate gene for FSHD, maps proximal to the myodystrophy mutation on chromosome 8
-
Grewal PK, van Deutekom JCT, Mills KA, Lemmers JLF, Mathews KD et al. (1997) The mouse homolog of FRG1, a candidate gene for FSHD, maps proximal to the myodystrophy mutation on chromosome 8. Mamm Genome 8, 394-398
-
(1997)
Mamm Genome
, vol.8
, pp. 394-398
-
-
Grewal, P.K.1
Van Deutekom, J.C.T.2
Mills, K.A.3
Lemmers, J.L.F.4
Mathews, K.D.5
-
16
-
-
0030253127
-
A comprehensive large-insert yeast artificial chromosome library for physical mapping of the mouse genome
-
Haldi ML, Strickland C, Lim P, Van Berkel V, Chen XN et al. (1996) A comprehensive large-insert yeast artificial chromosome library for physical mapping of the mouse genome. Mamm Genome 7, 767-769
-
(1996)
Mamm Genome
, vol.7
, pp. 767-769
-
-
Haldi, M.L.1
Strickland, C.2
Lim, P.3
Van Berkel, V.4
Chen, X.N.5
-
17
-
-
0027415747
-
Assignment of the human carboxypeptidase E (CPE) gene to chromosome 4
-
Hall C, Manser E, Spurr NS, Lim L (1993) Assignment of the human carboxypeptidase E (CPE) gene to chromosome 4. Genomics 15, 461-463
-
(1993)
Genomics
, vol.15
, pp. 461-463
-
-
Hall, C.1
Manser, E.2
Spurr, N.S.3
Lim, L.4
-
18
-
-
0028040601
-
Analysis of the tandem repeat locus D4Z4 associated with facioscapulohumeral muscular dystrophy
-
Hewitt JE, Lyle R, Clark LN, Valleley EM, Wright TJ et al. (1994) Analysis of the tandem repeat locus D4Z4 associated with facioscapulohumeral muscular dystrophy. Hum Mol Genet 3, 1287-1295
-
(1994)
Hum Mol Genet
, vol.3
, pp. 1287-1295
-
-
Hewitt, J.E.1
Lyle, R.2
Clark, L.N.3
Valleley, E.M.4
Wright, T.J.5
-
19
-
-
0031568869
-
Identification and genetic mapping of a new polycystic kidney disease gene on mouse chromosome 8
-
Janaswami PM, Birkenmeier EH, Cook SA, Rowe LB, Bronson RT et al. (1997) Identification and genetic mapping of a new polycystic kidney disease gene on mouse chromosome 8. Genomics 40, 101-107
-
(1997)
Genomics
, vol.40
, pp. 101-107
-
-
Janaswami, P.M.1
Birkenmeier, E.H.2
Cook, S.A.3
Rowe, L.B.4
Bronson, R.T.5
-
20
-
-
0017087803
-
Myodystrophy, a new myopathy on chromosome 8 of the mouse
-
Lane PW, Beamer TC, Myers DD (1976) Myodystrophy, a new myopathy on chromosome 8 of the mouse. J Hered 67, 135-138
-
(1976)
J Hered
, vol.67
, pp. 135-138
-
-
Lane, P.W.1
Beamer, T.C.2
Myers, D.D.3
-
21
-
-
0031149053
-
Neuropeptide Y receptor genes on human chromosome 4q31-q32 map to conserved linkage groups on mouse chromosomes 3 and 8
-
Lutz CM, Frankel WN, Richards JE, Thompson DA (1997) Neuropeptide Y receptor genes on human chromosome 4q31-q32 map to conserved linkage groups on mouse chromosomes 3 and 8. Genomics 41, 498-500
-
(1997)
Genomics
, vol.41
, pp. 498-500
-
-
Lutz, C.M.1
Frankel, W.N.2
Richards, J.E.3
Thompson, D.A.4
-
22
-
-
0027355585
-
A Macintosh program for storage and analysis of experimental genetic mapping data
-
Manly KF, (1993) A Macintosh program for storage and analysis of experimental genetic mapping data. Mamm Genome 4, 303-313
-
(1993)
Mamm Genome
, vol.4
, pp. 303-313
-
-
Manly, K.F.1
-
23
-
-
0029958021
-
The molecular genetics of human facioscapulohumeral muscular dystrophy and the myodystrophy mouse
-
Mathews KD, Mills KA (1996) The molecular genetics of human facioscapulohumeral muscular dystrophy and the myodystrophy mouse. Curr Opin Neurol 9, 394-399
-
(1996)
Curr Opin Neurol
, vol.9
, pp. 394-399
-
-
Mathews, K.D.1
Mills, K.A.2
-
24
-
-
0028929385
-
Mouse myodystrophy (myd) mutation: Refined mapping in an interval flanked by homology with distal human 4q
-
Mathews KD, Mills KA, Bailey H, Schelper R, Murray J (1995a) Mouse myodystrophy (myd) mutation: refined mapping in an interval flanked by homology with distal human 4q. Muscle Nerve 2 (Suppl.), S98-S102
-
(1995)
Muscle Nerve
, vol.2
, Issue.SUPPL.
-
-
Mathews, K.D.1
Mills, K.A.2
Bailey, H.3
Schelper, R.4
Murray, J.5
-
25
-
-
0029015822
-
Phenotypic and pathological evaluation of the myd mouse, a candidate model for facioscapulohumeral dystrophy
-
Mathews KD, Rapisarda D, Bailey HL, Murray JC, Schleper RL et al. (1995b) Phenotypic and pathological evaluation of the myd mouse, a candidate model for facioscapulohumeral dystrophy. J Neuropathol Exp Neurol 54, 601-606
-
(1995)
J Neuropathol Exp Neurol
, vol.54
, pp. 601-606
-
-
Mathews, K.D.1
Rapisarda, D.2
Bailey, H.L.3
Murray, J.C.4
Schleper, R.L.5
-
26
-
-
0029278925
-
Genetic mapping near the myd locus on mouse chromosome 8
-
Mills KA, Mathews KD, Scherpbier-Heddema T, Schleper RL, Schmalzel R et al. (1995) Genetic mapping near the myd locus on mouse chromosome 8. Mamm Genome 6, 278-280
-
(1995)
Mamm Genome
, vol.6
, pp. 278-280
-
-
Mills, K.A.1
Mathews, K.D.2
Scherpbier-Heddema, T.3
Schleper, R.L.4
Schmalzel, R.5
-
27
-
-
0030249979
-
Genetic and physical mapping of a voltage-ddpendent chloride channel gene to human 4q32 and to mouse 8
-
Mills KA, Mathews KD, Scherpbier-Heddema T, Buetow KH, Baldini A et al. (1996) Genetic and physical mapping of a voltage-ddpendent chloride channel gene to human 4q32 and to mouse 8. Genomics 36, 374-376
-
(1996)
Genomics
, vol.36
, pp. 374-376
-
-
Mills, K.A.1
Mathews, K.D.2
Scherpbier-Heddema, T.3
Buetow, K.H.4
Baldini, A.5
-
28
-
-
0003928480
-
-
Mouse Genome Informatics, The Jackson Laboratory, Bar Harbor, ME Data retrieval, January
-
Mouse Genome Database (MGD). Mouse Genome Informatics, The Jackson Laboratory, Bar Harbor, ME (http://www.informatics.jax.org/). Data retrieval, January 1998
-
(1998)
Mouse Genome Database (MGD)
-
-
-
30
-
-
0024595101
-
Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms
-
Orita M, Iwahana H, Kanazawa H, Hayashi K, Sekiya T (1989) Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms. Proc Natl Acad Sci USA 86, 2766-2770
-
(1989)
Proc Natl Acad Sci USA
, vol.86
, pp. 2766-2770
-
-
Orita, M.1
Iwahana, H.2
Kanazawa, H.3
Hayashi, K.4
Sekiya, T.5
-
31
-
-
0028307353
-
Genetic linkage analysis of the AKI, Col5a1, Epb7.2, Fpgs, Grp78, Pbx3, and Notch1 genes in the region of mouse chromosome 2 homologous to human chromosome 9q
-
Pilz A, Prohaska R, Peters J, Abbott C (1994) Genetic linkage analysis of the AKI, Col5a1, Epb7.2, Fpgs, Grp78, Pbx3, and Notch1 genes in the region of mouse chromosome 2 homologous to human chromosome 9q. Genomics 21, 104-109
-
(1994)
Genomics
, vol.21
, pp. 104-109
-
-
Pilz, A.1
Prohaska, R.2
Peters, J.3
Abbott, C.4
-
32
-
-
0030249306
-
Assignment of the genes encoding the human chloride channel CLCNKA and CLCNKB to 1p36 and of CLCN3 to 4q32-q33 by in situ hybridisation
-
Saito-Ohara F, Uchida S, Takeuchi Y, Sasaki S, Hayashi A et al. (1996) Assignment of the genes encoding the human chloride channel CLCNKA and CLCNKB to 1p36 and of CLCN3 to 4q32-q33 by in situ hybridisation. Genomics 36, 372-374
-
(1996)
Genomics
, vol.36
, pp. 372-374
-
-
Saito-Ohara, F.1
Uchida, S.2
Takeuchi, Y.3
Sasaki, S.4
Hayashi, A.5
-
33
-
-
0029929954
-
Characterization of a novel gene product (mammalian Tolloid-like) with high sequence similarity to mammalian Tolloid/bone morphogenetic protein-1
-
Takahara K, Brevard R, Hoffman GG, Suzuki N, Greenspan DS (1996) Characterization of a novel gene product (mammalian Tolloid-like) with high sequence similarity to mammalian Tolloid/bone morphogenetic protein-1. Genomics 34, 157-165
-
(1996)
Genomics
, vol.34
, pp. 157-165
-
-
Takahara, K.1
Brevard, R.2
Hoffman, G.G.3
Suzuki, N.4
Greenspan, D.S.5
-
34
-
-
0026602124
-
Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene
-
Tassabehji M, Read AP, Newton VE, Harris R, Balling R et al. (1992) Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene. Nature 355, 635-636
-
(1992)
Nature
, vol.355
, pp. 635-636
-
-
Tassabehji, M.1
Read, A.P.2
Newton, V.E.3
Harris, R.4
Balling, R.5
-
35
-
-
0027744223
-
FSHD associated rearrangements are due to deletion of integral copies of a 3.2kb tandemly repeated unit
-
van Deutekom JCT, Wijmenga C, van Tienhoven EAE, Gruter A-M, Hewitt JE et al. (1993) FSHD associated rearrangements are due to deletion of integral copies of a 3.2kb tandemly repeated unit. Hum Mol Genet 2, 2037-2042
-
(1993)
Hum Mol Genet
, vol.2
, pp. 2037-2042
-
-
Van Deutekom, J.C.T.1
Wijmenga, C.2
Van Tienhoven, E.A.E.3
Gruter, A.-M.4
Hewitt, J.E.5
-
36
-
-
0029180264
-
Search for the FSHD gene using cDNA selection in a region spanning 100 kb on chromosome 4q35
-
van Deutekom JCT, Hofker MH, Romberg S, van Geel M, Rommens J et al. (1995) Search for the FSHD gene using cDNA selection in a region spanning 100 kb on chromosome 4q35. Muscle Nerve 2 (Suppl.), S19-S26
-
(1995)
Muscle Nerve
, vol.2
, Issue.SUPPL.
-
-
Van Deutekom, J.C.T.1
Hofker, M.H.2
Romberg, S.3
Van Geel, M.4
Rommens, J.5
-
37
-
-
9244232833
-
Identification of the first gene (FRG1) from the FSHD region on human chromosome 4q35
-
van Deutekom JCT, Lemmers RJLF, Grewal PK, van Geel M, Romberg S et al. (1996) Identification of the first gene (FRG1) from the FSHD region on human chromosome 4q35. Hum Mol Genet 5, 581-589
-
(1996)
Hum Mol Genet
, vol.5
, pp. 581-589
-
-
Van Deutekom, J.C.T.1
Lemmers, R.J.L.F.2
Grewal, P.K.3
Van Geel, M.4
Romberg, S.5
-
38
-
-
0028815440
-
Defective myosin-VIIA gene responsible for Usher syndrome type 1B
-
Weil D, Blanchard S, Kaplan J, Guilford P, Gibson F et al. (1995) Defective myosin-VIIA gene responsible for Usher syndrome type 1B. Nature 374, 60-61
-
(1995)
Nature
, vol.374
, pp. 60-61
-
-
Weil, D.1
Blanchard, S.2
Kaplan, J.3
Guilford, P.4
Gibson, F.5
-
39
-
-
0026922062
-
Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy
-
Wijmenga C, Hewitt JE, Sandkuijl LA, Clark LN, Wright TJ et al. (1992) Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy. Nat Genet 2, 26-30
-
(1992)
Nat Genet
, vol.2
, pp. 26-30
-
-
Wijmenga, C.1
Hewitt, J.E.2
Sandkuijl, L.A.3
Clark, L.N.4
Wright, T.J.5
-
40
-
-
0027179549
-
The human skeletal muscle adenine nucleotide translocator gene maps to chromosome 4q35 in the region of the facioscapulohumeral muscular dystrophy locus
-
Wijmenga C, Winokur ST, Padberg GW, Skraastad MI, Altherr MR, et al. (1993) The human skeletal muscle adenine nucleotide translocator gene maps to chromosome 4q35 in the region of the facioscapulohumeral muscular dystrophy locus. Hum Genet 92, 198-203
-
(1993)
Hum Genet
, vol.92
, pp. 198-203
-
-
Wijmenga, C.1
Winokur, S.T.2
Padberg, G.W.3
Skraastad, M.I.4
Altherr, M.R.5
-
41
-
-
0028303398
-
The DNA rearrangement associated with facioscapulohumeral muscular dystrophy involves a heterochromatin-associated repetitive element: Implications for a role of chromatin structure in the pathogenesis of the disease
-
Winokur ST, Bengtsson U, Feddersen J, Mathews KD, Weiffenbach B et al. (1994) The DNA rearrangement associated with facioscapulohumeral muscular dystrophy involves a heterochromatin-associated repetitive element: implications for a role of chromatin structure in the pathogenesis of the disease. Chromosome Res 2, 225-234
-
(1994)
Chromosome Res
, vol.2
, pp. 225-234
-
-
Winokur, S.T.1
Bengtsson, U.2
Feddersen, J.3
Mathews, K.D.4
Weiffenbach, B.5
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