-
1
-
-
0025836092
-
Genetic counselling in facioscapulohumeral muscular dystrophy
-
P.W. Lunt, and P.S. Harper Genetic counselling in facioscapulohumeral muscular dystrophy J Med Genet 28 1991 655 664
-
(1991)
J Med Genet
, vol.28
, pp. 655-664
-
-
Lunt, P.W.1
Harper, P.S.2
-
2
-
-
0027433246
-
Evidence for heterogeneity in facioscapulohumeral muscular dystrophy (FSHD)
-
J.R. Gilbert, J.M. Stajich, and S. Wall Evidence for heterogeneity in facioscapulohumeral muscular dystrophy (FSHD) Am J Hum Genet 53 1993 401 408
-
(1993)
Am J Hum Genet
, vol.53
, pp. 401-408
-
-
Gilbert, J.R.1
Stajich, J.M.2
Wall, S.3
-
3
-
-
0032055028
-
44th ENMC international workshop: Facioscapulohumeral muscular dystrophy: Molecular studies 19-21 July 1996, Naarden, the Netherlands
-
P.W. Lunt 44th ENMC international workshop: facioscapulohumeral muscular dystrophy: molecular studies 19-21 July 1996, Naarden, The Netherlands Neuromuscul Disord 8 1998 126 130
-
(1998)
Neuromuscul Disord
, vol.8
, pp. 126-130
-
-
Lunt, P.W.1
-
4
-
-
0034821243
-
Clinical studies in non-chromosome 4-linked facioscapulohumeral muscular dystrophy
-
R.W. Tim, J.R. Gilbert, and J.M. Stajich Clinical studies in non-chromosome 4-linked facioscapulohumeral muscular dystrophy J Clin Neuromuscul Dis 3 2001 1 7
-
(2001)
J Clin Neuromuscul Dis
, vol.3
, pp. 1-7
-
-
Tim, R.W.1
Gilbert, J.R.2
Stajich, J.M.3
-
5
-
-
0026922062
-
Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy
-
C. Wijmenga, J.E. Hewitt, and L.A. Sandkuijl Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy Nat Genet 2 1992 26 30
-
(1992)
Nat Genet
, vol.2
, pp. 26-30
-
-
Wijmenga, C.1
Hewitt, J.E.2
Sandkuijl, L.A.3
-
6
-
-
0037047439
-
Inappropriate gene activation in FSHD: A repressor complex binds a chromosomal repeat deleted in dystrophic muscle
-
D. Gabellini, M.R. Green, and R. Tupler Inappropriate gene activation in FSHD: a repressor complex binds a chromosomal repeat deleted in dystrophic muscle Cell 110 2002 339 348
-
(2002)
Cell
, vol.110
, pp. 339-348
-
-
Gabellini, D.1
Green, M.R.2
Tupler, R.3
-
7
-
-
0035281548
-
HMG1 and 2, and related 'architectural' DNA-binding proteins
-
J.O. Thomas, and A.A. Travers HMG1 and 2, and related 'architectural' DNA-binding proteins Trends Biochem Sci 26 2001 167 174
-
(2001)
Trends Biochem Sci
, vol.26
, pp. 167-174
-
-
Thomas, J.O.1
Travers, A.A.2
-
8
-
-
0032531280
-
Human hematopoietic cell specific nuclear protein MNDA interacts with the multifunctional transcription factor YY1 and stimulates YY1 DNA binding
-
J. Xie, J.A. Briggs, and R.C. Briggs Human hematopoietic cell specific nuclear protein MNDA interacts with the multifunctional transcription factor YY1 and stimulates YY1 DNA binding J Cell Biochem 70 1998 489 506
-
(1998)
J Cell Biochem
, vol.70
, pp. 489-506
-
-
Xie, J.1
Briggs, J.A.2
Briggs, R.C.3
-
9
-
-
0344875044
-
Expression profiling of FSHD muscle supports a defect in specific stages of myogenic differentiation
-
S.T. Winokur, Y.W. Chen, and P.S. Masny Expression profiling of FSHD muscle supports a defect in specific stages of myogenic differentiation Hum Mol Genet 12 2003 2895 2907
-
(2003)
Hum Mol Genet
, vol.12
, pp. 2895-2907
-
-
Winokur, S.T.1
Chen, Y.W.2
Masny, P.S.3
-
10
-
-
0344436078
-
Nucleotide sequence of the partially deleted D4Z4 locus in a patient with FSHD identifies a putative gene within each 3.3 kb element
-
J. Gabriels, M.C. Beckers, and H. Ding Nucleotide sequence of the partially deleted D4Z4 locus in a patient with FSHD identifies a putative gene within each 3.3 kb element Gene 236 1999 25 32
-
(1999)
Gene
, vol.236
, pp. 25-32
-
-
Gabriels, J.1
Beckers, M.C.2
Ding, H.3
-
11
-
-
0026702158
-
Regional mapping of facioscapulohumeral muscular dystrophy gene on 4q35: Combined analysis of an international consortium
-
M. Sarfarazi, C. Wijmenga, and B. Weiffenbach Regional mapping of facioscapulohumeral muscular dystrophy gene on 4q35: Combined analysis of an international consortium Am J Hum Genet 51 1992 396 403
-
(1992)
Am J Hum Genet
, vol.51
, pp. 396-403
-
-
Sarfarazi, M.1
Wijmenga, C.2
Weiffenbach, B.3
-
12
-
-
0028303398
-
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
-
S.T. Winokur, U. Bengtsson, and J. Feddersen 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 1994 225 234
-
(1994)
Chromosome Res
, vol.2
, pp. 225-234
-
-
Winokur, S.T.1
Bengtsson, U.2
Feddersen, J.3
-
13
-
-
0029155470
-
Exclusion mapping of chromosomal regions which cross hybridise to FSHD1A associated markers in FSHD1B
-
J.R. Gilbert, M.C. Speer, and J. Stajich Exclusion mapping of chromosomal regions which cross hybridise to FSHD1A associated markers in FSHD1B J Med Genet 32 1995 770 773
-
(1995)
J Med Genet
, vol.32
, pp. 770-773
-
-
Gilbert, J.R.1
Speer, M.C.2
Stajich, J.3
-
14
-
-
0030052273
-
Diagnostic, predictive, and prenatal testing for facioscapulohumeral muscular dystrophy: Diagnostic approach for sporadic and familial cases
-
E. Bakker, M.J. van der Wielen, and E. Voorhoeve Diagnostic, predictive, and prenatal testing for facioscapulohumeral muscular dystrophy: diagnostic approach for sporadic and familial cases J Med Genet 33 1996 29 35
-
(1996)
J Med Genet
, vol.33
, pp. 29-35
-
-
Bakker, E.1
Van Der Wielen, M.J.2
Voorhoeve, E.3
-
15
-
-
0031215409
-
Further exclusion of FSHD1B from the telomeric region of 10q
-
M.C. Speer, M.A. Pericak-Vance, and J.M. Stajich Further exclusion of FSHD1B from the telomeric region of 10q Neurogenetics 1 1997 151 152
-
(1997)
Neurogenetics
, vol.1
, pp. 151-152
-
-
Speer, M.C.1
Pericak-Vance, M.A.2
Stajich, J.M.3
-
16
-
-
0031612929
-
Recommendations for a nomenclature system for human gene mutations. Nomenclature working group
-
S.E. Antonarakis Recommendations for a nomenclature system for human gene mutations. Nomenclature working group Hum Mutat 11 1998 1 3
-
(1998)
Hum Mutat
, vol.11
, pp. 1-3
-
-
Antonarakis, S.E.1
-
17
-
-
0345257778
-
Hypomethylation of D4Z4 in 4q-linked and non-4q-linked facioscapulohumeral muscular dystrophy
-
P.G. van Overveld, R.J. Lemmers, and L.A. Sandkuijl Hypomethylation of D4Z4 in 4q-linked and non-4q-linked facioscapulohumeral muscular dystrophy Nat Genet 35 2003 315 317
-
(2003)
Nat Genet
, vol.35
, pp. 315-317
-
-
Van Overveld, P.G.1
Lemmers, R.J.2
Sandkuijl, L.A.3
-
18
-
-
0345238700
-
Evidence consistent with linkage to 15q of non-chromosome 4 linked FSHD family
-
B. Randolph-Anderson, J.M. Stajich, F.L. Graham, M.A. Pericak-Vance, M.C. Speer, and J.R. Gilbert Evidence consistent with linkage to 15q of non-chromosome 4 linked FSHD family Am J Hum Genet 71 2002 530
-
(2002)
Am J Hum Genet
, vol.71
, pp. 530
-
-
Randolph-Anderson, B.1
Stajich, J.M.2
Graham, F.L.3
Pericak-Vance, M.A.4
Speer, M.C.5
Gilbert, J.R.6
-
19
-
-
15944422749
-
Expression profiling: Is there a role for vascular smooth muscle dysfunction in facioscapulohumeral muscular dystrophy (FSHD)?
-
Los Angeles, CA
-
Venance SL, Henderson S, Sowden J, Welle S, Thornton CA, Tawil R. Expression profiling: is there a role for vascular smooth muscle dysfunction in facioscapulohumeral muscular dystrophy (FSHD)? FSHD international consortium meeting, Los Angeles, CA; 2003.
-
(2003)
FSHD International Consortium Meeting
-
-
Venance, S.L.1
Henderson, S.2
Sowden, J.3
Welle, S.4
Thornton, C.A.5
Tawil, R.6
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