-
1
-
-
0031710557
-
PAK3 mutation in nonsyndromic X-linked mental retardation
-
Allen, K.M., J.G. Gleeson, S. Bagrodia, M.W. Partington, J.C. MacMillan, R.A. Cerione, J.C. Mulley, and C.A. Walsh. 1998. PAK3 mutation in nonsyndromic X-linked mental retardation. Nat. Genet. 20: 25-30.
-
(1998)
Nat. Genet.
, vol.20
, pp. 25-30
-
-
Allen, K.M.1
Gleeson, J.G.2
Bagrodia, S.3
Partington, M.W.4
MacMillan, J.C.5
Cerione, R.A.6
Mulley, J.C.7
Walsh, C.A.8
-
2
-
-
0031865393
-
Mind the GAP, Rho, Rab and GDI
-
Antonarakis, S.E. and L. Van Aelst. 1998. Mind the GAP, Rho, Rab and GDI. Nat. Genet. 19: 106-108.
-
(1998)
Nat. Genet.
, vol.19
, pp. 106-108
-
-
Antonarakis, S.E.1
Van Aelst, L.2
-
3
-
-
0023802705
-
Linkage analysis suggests at least two loci for X-linked nonspecific mental retardation
-
Arveiler, B., Y. Alembik, A. Hanauer, P. Jacobs, L. Tranebjaerg, M. Mikkelsen, H. Puissant, L.L. Piet, and J.L. Mandel. 1988. Linkage analysis suggests at least two loci for X-linked nonspecific mental retardation. Am. J. Med. Genet. 30: 473-483.
-
(1988)
Am. J. Med. Genet.
, vol.30
, pp. 473-483
-
-
Arveiler, B.1
Alembik, Y.2
Hanauer, A.3
Jacobs, P.4
Tranebjaerg, L.5
Mikkelsen, M.6
Puissant, H.7
Piet, L.L.8
Mandel, J.L.9
-
4
-
-
0028875683
-
Cdc42 and PAK-mediated signaling leads to Jun kinase and p38 mitogen- Activated protein kinase activation
-
Bagrodia, S., B. Derijard, R.J. Davis, and R.A. Cerione. 1995. Cdc42 and PAK-mediated signaling leads to Jun kinase and p38 mitogen- activated protein kinase activation. J. Biol. Chem. 270: 27995-27998.
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 27995-27998
-
-
Bagrodia, S.1
Derijard, B.2
Davis, R.J.3
Cerione, R.A.4
-
5
-
-
0033606802
-
Characterization of integrin-tetraspanin adhesion complexes: Role of tetraspanins in integrin signaling
-
Berditchevski, F. and E. Odintsova. 1999. Characterization of integrin-tetraspanin adhesion complexes: Role of tetraspanins in integrin signaling. J. Cell Biol. 146: 477-492.
-
(1999)
J. Cell Biol.
, vol.146
, pp. 477-492
-
-
Berditchevski, F.1
Odintsova, E.2
-
6
-
-
0032418301
-
Oligophrenin 1 encodes a rho GAP protein involved in X-linked mental retardation
-
Paris
-
Billuart, P., T. Bienvenu, N. Ronce, V. des Portes, M.C. Vinet, R. Zemni, A. Carrie, C. Beldjord, A. Kahn, C. Moraine, and J. Chelly. 1998. Oligophrenin 1 encodes a rho GAP protein involved in X-linked mental retardation. Pathol. Biol. (Paris) 46: 678.
-
(1998)
Pathol. Biol.
, vol.46
, pp. 678
-
-
Billuart, P.1
Bienvenu, T.2
Ronce, N.3
Des Portes, V.4
Vinet, M.C.5
Zemni, R.6
Carrie, A.7
Beldjord, C.8
Kahn, A.9
Moraine, C.10
Chelly, J.11
-
7
-
-
0027476024
-
A synaptic model of memory: Long-term potentiation in the hippocampus
-
Bliss, T.V. and G.L. Collingridge. 1993. A synaptic model of memory: Long-term potentiation in the hippocampus. Nature 361: 31-39.
-
(1993)
Nature
, vol.361
, pp. 31-39
-
-
Bliss, T.V.1
Collingridge, G.L.2
-
8
-
-
0032819848
-
A new member of the IL-1 receptor family highly expressed in hippocampus and involved in X-linked mental retardation
-
Carrie, A., L. Jun, T. Bienvenu, M.C. Vinet, N. McDonell, P. Couvert, R. Zemni, A. Cardona, G. Van Buggenhout, S. Frints et al. 1999. A new member of the IL-1 receptor family highly expressed in hippocampus and involved in X-linked mental retardation. Nat. Genet. 23: 25-31.
-
(1999)
Nat. Genet.
, vol.23
, pp. 25-31
-
-
Carrie, A.1
Jun, L.2
Bienvenu, T.3
Vinet, M.C.4
McDonell, N.5
Couvert, P.6
Zemni, R.7
Cardona, A.8
Van Buggenhout, G.9
Frints, S.10
-
9
-
-
0032872234
-
Breakthroughs in molecular and cellular mechanisms underlying X-linked mental retardation
-
Chelly, J. 1999. Breakthroughs in molecular and cellular mechanisms underlying X-linked mental retardation. Hum. Mol. Genet. 8: 1833-1838.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 1833-1838
-
-
Chelly, J.1
-
10
-
-
0031922095
-
Recurrence risks in mental retardation
-
Crow, Y.J. and J.L. Tolmie. 1998. Recurrence risks in mental retardation. J. Med. Genet. 35: 177-182.
-
(1998)
J. Med. Genet.
, vol.35
, pp. 177-182
-
-
Crow, Y.J.1
Tolmie, J.L.2
-
11
-
-
17344369362
-
Mutations in GDI1 are responsible for X linked nonspecific mental retardation
-
D'Adamo, P., A. Menegon, C. Lo Nigro, M. Grasso, M. Gulisano, F. Tamanini, T. Bienvenu, A.K. Gedeon, B. Oostra, S.K. Wu, A. Tandon, F. Valtorta, W.E. Balch, J. Chelly, and D. Toniolo. 1998. Mutations in GDI1 are responsible for X linked nonspecific mental retardation. Nat. Genet. 19: 134-139.
-
(1998)
Nat. Genet.
, vol.19
, pp. 134-139
-
-
D'Adamo, P.1
Menegon, A.2
Lo Nigro, C.3
Grasso, M.4
Gulisano, M.5
Tamanini, F.6
Bienvenu, T.7
Gedeon, A.K.8
Oostra, B.9
Wu, S.K.10
Tandon, A.11
Valtorta, F.12
Balch, W.E.13
Chelly, J.14
Toniolo, D.15
-
12
-
-
0028798545
-
The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation
-
Flint, J., A.O. Wilkie, V.J. Buckle, R.M. Winter, A.J. Holland, and H.E. McDermid. 1995. The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation. Nat. Genet. 9: 132-140.
-
(1995)
Nat. Genet.
, vol.9
, pp. 132-140
-
-
Flint, J.1
Wilkie, A.O.2
Buckle, V.J.3
Winter, R.M.4
Holland, A.J.5
McDermid, H.E.6
-
13
-
-
0030137717
-
Identification of the gene FMR2, associated with FRAXE mental retardation
-
Gécz, J., A.K. Gedeon, G.R. Sutherland, and J.C. Mulley. 1996. Identification of the gene FMR2, associated with FRAXE mental retardation. Nat. Genet. 13: 105-108.
-
(1996)
Nat. Genet.
, vol.13
, pp. 105-108
-
-
Gécz, J.1
Gedeon, A.K.2
Sutherland, G.R.3
Mulley, J.C.4
-
14
-
-
0031239275
-
Gene structure and subcellular localization of FMR2, a member of a new family of putative transcription activators
-
Gécz, J., S. Bielby, G.R. Sutherland, and J.C. Mulley. 1997a. Gene structure and subcellular localization of FMR2, a member of a new family of putative transcription activators. Genomics 44: 201-213.
-
(1997)
Genomics
, vol.44
, pp. 201-213
-
-
Gécz, J.1
Bielby, S.2
Sutherland, G.R.3
Mulley, J.C.4
-
15
-
-
0031044516
-
FMR2 expression in families with FRAXE mental retardation
-
Gécz, J., B.A. Oostra, A. Hockey, P. Carbonell, G. Turner, E.A. Haan, G.R. Sutherland, and J.C. Mulley. 1997b. FMR2 expression in families with FRAXE mental retardation. Hum. Mol. Genet. 6: 435-441.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 435-441
-
-
Gécz, J.1
Oostra, B.A.2
Hockey, A.3
Carbonell, P.4
Turner, G.5
Haan, E.A.6
Sutherland, G.R.7
Mulley, J.C.8
-
16
-
-
4244196836
-
Characterization of the human glutamate receptor subunit 3 gene (GRIA3), a candidate for bipolar disorder and nonspecific X-linked mental retardation
-
in press
-
Gécz, J., S. Barnett, J. Liu, G. Hollway, A. Donnelly, H. Eyre, H.S. Eshkevari, R. Baltazar, A. Grunn, R. Nagaraja et al. 2000. Characterization of the human glutamate receptor subunit 3 gene (GRIA3), a candidate for bipolar disorder and nonspecific X-linked mental retardation. Genomics (in press).
-
(2000)
Genomics
-
-
Gécz, J.1
Barnett, S.2
Liu, J.3
Hollway, G.4
Donnelly, A.5
Eyre, H.6
Eshkevari, H.S.7
Baltazar, R.8
Grunn, A.9
Nagaraja, R.10
-
17
-
-
0030580974
-
How many X-linked genes for nonspecific mental retardation (MRX) are there?
-
Gedeon, A.K., A.J. Donnelly, J.C. Mulley, B. Kerr, and G. Turner. 1996. How many X-linked genes for nonspecific mental retardation (MRX) are there? [letter]. Am. J. Med. Genet. 64: 158-162.
-
(1996)
Am. J. Med. Genet.
, vol.64
, pp. 158-162
-
-
Gedeon, A.K.1
Donnelly, A.J.2
Mulley, J.C.3
Kerr, B.4
Turner, G.5
-
18
-
-
0025817417
-
X linked mental retardation
-
Glass, I.A. 1991. X linked mental retardation. J. Med. Genet. 28: 361-371.
-
(1991)
J. Med. Genet.
, vol.28
, pp. 361-371
-
-
Glass, I.A.1
-
19
-
-
0030138905
-
Identification of FMR2, a novel gene associated with the Fraxe Ccg repeat and Cpg island
-
Gu, Y.H., Y. Shen, R.A. Gibbs, and D.J. Nelson. 1996. Identification of FMR2, a novel gene associated with the Fraxe Ccg repeat and Cpg island. Nat. Genet. 13: 109-113.
-
(1996)
Nat. Genet.
, vol.13
, pp. 109-113
-
-
Gu, Y.H.1
Shen, Y.2
Gibbs, R.A.3
Nelson, D.J.4
-
20
-
-
0029007354
-
Sex differences in mental test scores, variability, and numbers of high-scoring individuals
-
Hedges, L.V. and A. Nowell. 1995. Sex differences in mental test scores, variability, and numbers of high-scoring individuals. Science 269: 41-45.
-
(1995)
Science
, vol.269
, pp. 41-45
-
-
Hedges, L.V.1
Nowell, A.2
-
21
-
-
0031720629
-
Integrin associated proteins
-
Hemler, M.E. 1998. Integrin associated proteins. Curr. Opin. Cell. Biol. 10: 578-585.
-
(1998)
Curr. Opin. Cell. Biol.
, vol.10
, pp. 578-585
-
-
Hemler, M.E.1
-
22
-
-
0025765855
-
Nonspecific X linked mental retardation
-
Kerr, B., G. Turner, J. Mulley, A. Gedeon, and M. Partington. 1991. Nonspecific X linked mental retardation. J. Med. Genet. 28: 378-382.
-
(1991)
J. Med. Genet.
, vol.28
, pp. 378-382
-
-
Kerr, B.1
Turner, G.2
Mulley, J.3
Gedeon, A.4
Partington, M.5
-
23
-
-
0015336653
-
Theory of X-linkage of major intellectual traits
-
Lehrke, R. 1972. Theory of X-linkage of major intellectual traits. Am. J. Ment. Defic. 76: 611-619.
-
(1972)
Am. J. Ment. Defic.
, vol.76
, pp. 611-619
-
-
Lehrke, R.1
-
24
-
-
0033515499
-
XLMR genes: Update 1998
-
Lubs, H., P. Chiurazzi, J. Arena, C. Schwartz, L. Tranebjaerg, and G. Neri. 1999. XLMR genes: Update 1998. Am. J. Med. Genet. 83: 237-247.
-
(1999)
Am. J. Med. Genet.
, vol.83
, pp. 237-247
-
-
Lubs, H.1
Chiurazzi, P.2
Arena, J.3
Schwartz, C.4
Tranebjaerg, L.5
Neri, G.6
-
25
-
-
0028242904
-
Towards identification of X-linked mental retardation genes: A proposal
-
Mandel, J.L. 1994. Towards identification of X-linked mental retardation genes: A proposal. Am. J. Med. Genet. 51: 550-552.
-
(1994)
Am. J. Med. Genet.
, vol.51
, pp. 550-552
-
-
Mandel, J.L.1
-
26
-
-
0023640087
-
Review of recent epidemiological studies of mental retardation: Prevalence, associated disorders, and etiology
-
McLaren, J. and S.E. Bryson. 1987. Review of recent epidemiological studies of mental retardation: Prevalence, associated disorders, and etiology. Am. J. Ment. Retard. 92: 243-254.
-
(1987)
Am. J. Ment. Retard.
, vol.92
, pp. 243-254
-
-
McLaren, J.1
Bryson, S.E.2
-
27
-
-
0032910443
-
A missense mutation in RPS6KA3 (RSK2) responsible for nonspecific mental retardation
-
Merienne, K., S. Jacquot, S. Pannetier, M. Zeniou, A. Bankier, J. Gécz, J.L. Mandel, J. Mulley, P. Sassone-Corsi, and A. Hanauer. 1999. A missense mutation in RPS6KA3 (RSK2) responsible for nonspecific mental retardation [letter]. Nat. Genet. 22: 13-14.
-
(1999)
Nat. Genet.
, vol.22
, pp. 13-14
-
-
Merienne, K.1
Jacquot, S.2
Pannetier, S.3
Zeniou, M.4
Bankier, A.5
Gécz, J.6
Mandel, J.L.7
Mulley, J.8
Sassone-Corsi, P.9
Hanauer, A.10
-
28
-
-
0039180894
-
Effect of inbreeding on IQ and mental retardation
-
Morton, N.E. 1978. Effect of inbreeding on IQ and mental retardation. Proc. Natl. Acad. Sci. 75: 3906-3908.
-
(1978)
Proc. Natl. Acad. Sci.
, vol.75
, pp. 3906-3908
-
-
Morton, N.E.1
-
29
-
-
0026569472
-
Genes for intelligence on the X chromosome
-
_. 1992. Genes for intelligence on the X chromosome. J. Med. Genet. 29: 71.
-
(1992)
J. Med. Genet.
, vol.29
, pp. 71
-
-
-
30
-
-
0017359223
-
Colchester revisited: A genetic study of mental defect
-
Morton, N.E., D.C. Rao, H. Lang-Brown, C.J. Maclean, R.D. Bart, and R. Lew. 1977. Colchester revisited: A genetic study of mental defect. J. Med. Genet. 14: 1-9.
-
(1977)
J. Med. Genet.
, vol.14
, pp. 1-9
-
-
Morton, N.E.1
Rao, D.C.2
Lang-Brown, H.3
Maclean, C.J.4
Bart, R.D.5
Lew, R.6
-
31
-
-
0026683988
-
Nomenclature guidelines for X-linked mental retardation
-
Mulley, J.C., B. Kerr, R. Stevenson, and H. Lubs. 1992. Nomenclature guidelines for X-linked mental retardation. Am. J. Med. Genet. 43: 383-391.
-
(1992)
Am. J. Med. Genet.
, vol.43
, pp. 383-391
-
-
Mulley, J.C.1
Kerr, B.2
Stevenson, R.3
Lubs, H.4
-
32
-
-
0342558952
-
A mouse model of FRAXE mental retardation provides detailed study of normal expression and sliowes behavioral abnormalities
-
Strasbourg, France
-
Nelson, D.L., Y. Gu, K. Yamagata, K. Mcllwain, R. Payor, and H. Zoghby. 1999. A mouse model of FRAXE mental retardation provides detailed study of normal expression and sliowes behavioral abnormalities. Ninth International Workshop on Fragile Syndrome and X Linked Mental Retardation, Strasbourg, France p. 75.
-
(1999)
Ninth International Workshop on Fragile Syndrome and X Linked Mental Retardation
, pp. 75
-
-
Nelson, D.L.1
Gu, Y.2
Yamagata, K.3
Mcllwain, K.4
Payor, R.5
Zoghby, H.6
-
35
-
-
0031912995
-
Glutamate receptors in the mammalian central nervous system
-
Ozawa, S., H. Kamiya, and K. Tsuzuki. 1998. Glutamate receptors in the mammalian central nervous system. Prog. Neurobiol. 54: 581-618.
-
(1998)
Prog. Neurobiol.
, vol.54
, pp. 581-618
-
-
Ozawa, S.1
Kamiya, H.2
Tsuzuki, K.3
-
37
-
-
0029981623
-
The genetic basis for mental retardation
-
Raynham, H., R. Gibbons, J. Flint, and D. Higgs. 1996. The genetic basis for mental retardation. Q.J. Med. 89: 169-175.
-
(1996)
Q.J. Med.
, vol.89
, pp. 169-175
-
-
Raynham, H.1
Gibbons, R.2
Flint, J.3
Higgs, D.4
-
38
-
-
0031105660
-
Human p21-activated kinase (Pak1) regulates actin organization in mammalian cells
-
Sells, M.A., U.G. Knaus, S. Bagrodia, D.M. Ambrose, G.M. Bokoch, and J. Chernoff. 1997. Human p21-activated kinase (Pak1) regulates actin organization in mammalian cells. Curr. Biol. 7: 202-210.
-
(1997)
Curr. Biol.
, vol.7
, pp. 202-210
-
-
Sells, M.A.1
Knaus, U.G.2
Bagrodia, S.3
Ambrose, D.M.4
Bokoch, G.M.5
Chernoff, J.6
-
39
-
-
0033546052
-
Rapid spine delivery and redistribution of AMPA receptors after synaptic NMDA receptor activation
-
Shi, S.H., Y. Hayashi, R.S. Petralia, S.H. Zaman, R.J. Wenthold, K. Svoboda, and R. Malinow. 1999. Rapid spine delivery and redistribution of AMPA receptors after synaptic NMDA receptor activation. Science 284: 1811-1816.
-
(1999)
Science
, vol.284
, pp. 1811-1816
-
-
Shi, S.H.1
Hayashi, Y.2
Petralia, R.S.3
Zaman, S.H.4
Wenthold, R.J.5
Svoboda, K.6
Malinow, R.7
-
40
-
-
0032901062
-
Screening for submicroscopic chromosome rearrangements in children with idiopathic mental retardation using microsatellite markers for the chromosome telomeres
-
Slavotinek, A., M. Rosenberg, S. Knight, L. Gaunt, W. Fergusson, C. Killoran, J. Clayton Smith, H. Kingston, R.H. Campbell, J. Flint, D. Donnai, and L. Biesecker. 1999. Screening for submicroscopic chromosome rearrangements in children with idiopathic mental retardation using microsatellite markers for the chromosome telomeres. J. Med. Genet. 36: 405-411.
-
(1999)
J. Med. Genet.
, vol.36
, pp. 405-411
-
-
Slavotinek, A.1
Rosenberg, M.2
Knight, S.3
Gaunt, L.4
Fergusson, W.5
Killoran, C.6
Smith, J.C.7
Kingston, H.8
Campbell, R.H.9
Flint, J.10
Donnai, D.11
Biesecker, L.12
-
41
-
-
0002011789
-
Making sense of gene-expression data
-
Somogyi, R. 1999. Making sense of gene-expression data. Trends Genet. (Suppl.): 17-24.
-
(1999)
Trends Genet. (Suppl.)
, pp. 17-24
-
-
Somogyi, R.1
-
42
-
-
0032836974
-
Forward genetics in mammalian cells: Functional approaches to gene discovery
-
Stark, G.R. and A.V. Gudkov. 1999. Forward genetics in mammalian cells: Functional approaches to gene discovery. Hum. Mol. Genet. 8: 1925-1938.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 1925-1938
-
-
Stark, G.R.1
Gudkov, A.V.2
-
43
-
-
0023766711
-
A non-syndromal form of X-linked mental retardation (XLMR) is linked to DXS14
-
Suthers, G.K., G. Turner, and J.C. Mulley. 1988. A non-syndromal form of X-linked mental retardation (XLMR) is linked to DXS14. Am. J. Med. Genet. 30: 485-491.
-
(1988)
Am. J. Med. Genet.
, vol.30
, pp. 485-491
-
-
Suthers, G.K.1
Turner, G.2
Mulley, J.C.3
-
44
-
-
0033517366
-
Genetic enhancement of learning and memory in mice
-
Tang, Y.P., E. Shimizu, G.R. Dube, C. Rampon, G.A. Kerchner, M. Zhuo, G. Liu, and J.Z. Tsien. 1999. Genetic enhancement of learning and memory in mice. Nature 401: 63-99.
-
(1999)
Nature
, vol.401
, pp. 63-99
-
-
Tang, Y.P.1
Shimizu, E.2
Dube, G.R.3
Rampon, C.4
Kerchner, G.A.5
Zhuo, M.6
Liu, G.7
Tsien, J.Z.8
-
45
-
-
0029832136
-
Mutations in the kinase Rsk-2 associated with Coffin-Lowry syndrome
-
Trivier, E., D. De Cesare, S. Jacquot, S. Pannetier, E. Zackai, I. Young, J.L. Mandel, P. Sassone-Corsi, and A. Hanauer. 1996. Mutations in the kinase Rsk-2 associated with Coffin-Lowry syndrome. Nature 384: 567-570.
-
(1996)
Nature
, vol.384
, pp. 567-570
-
-
Trivier, E.1
De Cesare, D.2
Jacquot, S.3
Pannetier, S.4
Zackai, E.5
Young, I.6
Mandel, J.L.7
Sassone-Corsi, P.8
Hanauer, A.9
-
46
-
-
0029786254
-
Intelligence and the X chromosome
-
Turner, G. 1996. Intelligence and the X chromosome. Lancet 347: 1814-1815.
-
(1996)
Lancet
, vol.347
, pp. 1814-1815
-
-
Turner, G.1
-
47
-
-
0025832873
-
Genes for intelligence on the X chromosome
-
Turner, G. and M.W. Partington. 1991. Genes for intelligence on the X chromosome [letter] J. Med. Genet. 28: 429.
-
(1991)
J. Med. Genet.
, vol.28
, pp. 429
-
-
Turner, G.1
Partington, M.W.2
-
48
-
-
0029924873
-
Prevalence of fragile X syndrome
-
Turner, G., T. Webb, S. Wake, and H. Robinson. 1996. Prevalence of fragile X syndrome. Am. J. Med. Genet. 64: 196-197.
-
(1996)
Am. J. Med. Genet.
, vol.64
, pp. 196-197
-
-
Turner, G.1
Webb, T.2
Wake, S.3
Robinson, H.4
-
49
-
-
0030968580
-
Rho GTPases and signaling networks
-
Van Aelst, L. and C. D'Souza-Schorey. 1997. Rho GTPases and signaling networks. Genes & Dev. 11: 2295-2322.
-
(1997)
Genes & Dev.
, vol.11
, pp. 2295-2322
-
-
Van Aelst, L.1
D'Souza-Schorey, C.2
-
50
-
-
0030016056
-
Cloning and characterization of DXS6673E, a candidate gene for X-linked mental retardation in Xq13.1
-
van der Maarel, S.M., I.H. Scholten, I. Huber, C. Philippe, R.F. Suijkerbuijk, S. Gilgenkrantz, J. Kere, F.P. Cremers, and H.H. Ropers. 1996. Cloning and characterization of DXS6673E, a candidate gene for X-linked mental retardation in Xq13.1. Hum. Mol. Genet. 5: 887-897.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 887-897
-
-
Van Der Maarel, S.M.1
Scholten, I.H.2
Huber, I.3
Philippe, C.4
Suijkerbuijk, R.F.5
Gilgenkrantz, S.6
Kere, J.7
Cremers, F.P.8
Ropers, H.H.9
-
51
-
-
0032904148
-
Systematic characterisation of disease associated balanced chromosome rearrangements by FISH: Cytogenetically and genetically anchored YACs identify microdeletions and candidate regions tor mental retardation genes
-
Wirth, J., H.G. Nothwang, S. van der Maarel, C, Menzel, G. Borck, I. Lopez-Pajares, K. Brondum-Nielsen, N. Tommerup, M. Bugge, H.H. Ropers, and T. Haaf. 1999. Systematic characterisation of disease associated balanced chromosome rearrangements by FISH: Cytogenetically and genetically anchored YACs identify microdeletions and candidate regions tor mental retardation genes. J. Med. Genet. 36: 271-278.
-
(1999)
J. Med. Genet.
, vol.36
, pp. 271-278
-
-
Wirth, J.1
Nothwang, H.G.2
Van Der Maarel, S.3
Menzel, C.4
Borck, G.5
Lopez-Pajares, I.6
Brondum-Nielsen, K.7
Tommerup, N.8
Bugge, M.9
Ropers, H.H.10
Haaf, T.11
-
52
-
-
0029789643
-
Coupling of the RAS-MAPK pathway to gene activation by RSK2, a growth factor-regulated CREB kinase
-
Xing, J., D.D. Ginty, and M.E. Greenberg. 1996. Coupling of the RAS-MAPK pathway to gene activation by RSK2, a growth factor-regulated CREB kinase. Science 273: 959-963.
-
(1996)
Science
, vol.273
, pp. 959-963
-
-
Xing, J.1
Ginty, D.D.2
Greenberg, M.E.3
-
53
-
-
0343864561
-
Identification of a novel gene involved in X-linked mental retardation through investigation of an X;2 balanced translocation
-
in press, 2000
-
Zemni, R., T. Bienvenu, M.C. Vinet, A. Sefiani, A. Carrie, P. Billuart, N. McDonell, P. Couvert, F. Francis, P. Chafey, F. Fauchereau, G. Friocourt, V. des Portes, A. Cardona, S. Frints, A. Meindl, O. Brandau, N. Ronce, C. Moraine, H. van Bokhoven, H.H. Ropers, R. Sudbrak, A. Kahn, J.P. Fryns, C. Beldjord, and J. Chelly. 2000. Identification of a novel gene involved in X-linked mental retardation through investigation of an X;2 balanced translocation.Nat. Genet. (in press, 2000)
-
(2000)
Nat. Genet.
-
-
Zemni, R.1
Bienvenu, T.2
Vinet, M.C.3
Sefiani, A.4
Carrie, A.5
Billuart, P.6
McDonell, N.7
Couvert, P.8
Francis, F.9
Chafey, P.10
Fauchereau, F.11
Friocourt, G.12
Des Portes, V.13
Cardona, A.14
Frints, S.15
Meindl, A.16
Brandau, O.17
Ronce, N.18
Moraine, C.19
Van Bokhoven, H.20
Ropers, H.H.21
Sudbrak, R.22
Kahn, A.23
Fryns, J.P.24
Beldjord, C.25
Chelly, J.26
more..
-
54
-
-
0032863227
-
Large-scale gene expression data analysis: A new challenge to computational biologists
-
Zhang, M.Q. 1999. Large-scale gene expression data analysis: A new challenge to computational biologists. Genome Res. 9: 681-688.
-
(1999)
Genome Res.
, vol.9
, pp. 681-688
-
-
Zhang, M.Q.1
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