-
1
-
-
0042632780
-
Vascular malformations: Localized defects in vascular morphogenesis
-
Brouillard P, Vikkula M (2003) Vascular malformations: localized defects in vascular morphogenesis. Clin Genet 63:340-351
-
(2003)
Clin Genet
, vol.63
, pp. 340-351
-
-
Brouillard, P.1
Vikkula, M.2
-
2
-
-
33749491894
-
Vascular update: Morphogenesis, tumors, malformations, and molecular dimensions
-
Cohen MM Jr (2006) Vascular update: morphogenesis, tumors, malformations, and molecular dimensions. Am J Med Genet A 140:2013-2038
-
(2006)
Am J Med Genet A
, vol.140
, pp. 2013-2038
-
-
Cohen Jr., M.M.1
-
3
-
-
0347362524
-
Capillary malformation-arteriovenous malformation, a new clinical and genetic disorder caused by RASA1 mutations
-
Eerola I, Boon LM, Mulliken JB, Burrows PE, Dompmartin A, Watanabe S, Vanwijck R, Vikkula M (2003) Capillary malformation-arteriovenous malformation, a new clinical and genetic disorder caused by RASA1 mutations. Am J Hum Genet 73:1240-1249
-
(2003)
Am J Hum Genet
, vol.73
, pp. 1240-1249
-
-
Eerola, I.1
Boon, L.M.2
Mulliken, J.B.3
Burrows, P.E.4
Dompmartin, A.5
Watanabe, S.6
Vanwijck, R.7
Vikkula, M.8
-
4
-
-
0027454104
-
Nonsense mutations in the C-terminal SH2 region of the GTPase activating protein (GAP) gene in human tumours
-
Friedman E, Gejman PV, Martin GA, McCormick F (1993) Nonsense mutations in the C-terminal SH2 region of the GTPase activating protein (GAP) gene in human tumours. Nat Genet 5:242-247
-
(1993)
Nat Genet
, vol.5
, pp. 242-247
-
-
Friedman, E.1
Gejman, P.V.2
Martin, G.A.3
McCormick, F.4
-
6
-
-
33847081209
-
Vascular malformations: Part I
-
quiz 371-354
-
Garzon MC, Huang JT, Enjolras O, Frieden IJ (2007) Vascular malformations: part I. J Am Acad Dermatol 56:353-370, quiz 371-354
-
(2007)
J Am Acad Dermatol
, vol.56
, pp. 353-370
-
-
Garzon, M.C.1
Huang, J.T.2
Enjolras, O.3
Frieden, I.J.4
-
7
-
-
0037138372
-
Organization and regulation of the human rasGAP gene
-
Glanzer JG, Liao L, Baker T, McMullen MH, Langan AS, Crandall LZ, Vorce RL (2002) Organization and regulation of the human rasGAP gene. Gene 285:149-156
-
(2002)
Gene
, vol.285
, pp. 149-156
-
-
Glanzer, J.G.1
Liao, L.2
Baker, T.3
McMullen, M.H.4
Langan, A.S.5
Crandall, L.Z.6
Vorce, R.L.7
-
8
-
-
33845254306
-
The G397A (E133K) change in the AGGF1 (VG5Q) gene is a single nucleotide polymorphism in the Spanish population
-
Gutierrez S, Magano L, Delicado A, Mori MA, de Torres ML, Fernandez L, Palomares M, Fernandez E, Tarduchy GR, Molano J, Gracia R, Pajares IL, Lapunzina P (2006) The G397A (E133K) change in the AGGF1 (VG5Q) gene is a single nucleotide polymorphism in the Spanish population. Am J Med Genet A 140:2832-2833
-
(2006)
Am J Med Genet a
, vol.140
, pp. 2832-2833
-
-
Gutierrez, S.1
Magano, L.2
Delicado, A.3
Mori, M.A.4
De Torres, M.L.5
Fernandez, L.6
Palomares, M.7
Fernandez, E.8
Tarduchy, G.R.9
Molano, J.10
Gracia, R.11
Pajares, I.L.12
Lapunzina, P.13
-
9
-
-
0028788570
-
Vascular system defects and neuronal apoptosis in mice lacking ras GTPase-activating protein
-
Henkemeyer M, Rossi DJ, Holmyard DP, Puri MC, Mbamalu G, Harpal K, Shih TS, Jacks T, Pawson T (1995) Vascular system defects and neuronal apoptosis in mice lacking ras GTPase-activating protein. Nature 377:695-701
-
(1995)
Nature
, vol.377
, pp. 695-701
-
-
Henkemeyer, M.1
Rossi, D.J.2
Holmyard, D.P.3
Puri, M.C.4
Mbamalu, G.5
Harpal, K.6
Shih, T.S.7
Jacks, T.8
Pawson, T.9
-
10
-
-
0031594873
-
Klippel-Trenaunay syndrome: Spectrum and management
-
Jacob AG, Driscoll DJ, Shaughnessy WJ, Stanson AW, Clay RP, Gloviczki P (1998) Klippel-Trenaunay syndrome: spectrum and management. Mayo Clin Proc 73:28-36
-
(1998)
Mayo Clin Proc
, vol.73
, pp. 28-36
-
-
Jacob, A.G.1
Driscoll, D.J.2
Shaughnessy, W.J.3
Stanson, A.W.4
Clay, R.P.5
Gloviczki, P.6
-
11
-
-
0017121616
-
The incidence of birthmarks in the neonate
-
Jacobs AH, Walton RG (1976) The incidence of birthmarks in the neonate. Pediatrics 58:218-222
-
(1976)
Pediatrics
, vol.58
, pp. 218-222
-
-
Jacobs, A.H.1
Walton, R.G.2
-
12
-
-
0034678368
-
Role of p120 Ras-GAP in directed cell movement
-
Kulkarni SV, Gish G, van der Geer P, Henkemeyer M, Pawson T (2000) Role of p120 Ras-GAP in directed cell movement. J Cell Biol 149:457-470
-
(2000)
J Cell Biol
, vol.149
, pp. 457-470
-
-
Kulkarni, S.V.1
Gish, G.2
Van Der Geer, P.3
Henkemeyer, M.4
Pawson, T.5
-
13
-
-
0038708339
-
Transgenic RNA interference in ES cell-derived embryos recapitulates a genetic null phenotype
-
Kunath T, Gish G, Lickert H, Jones N, Pawson T, Rossant J (2003) Transgenic RNA interference in ES cell-derived embryos recapitulates a genetic null phenotype. Nat Biotechnol 21:559-561
-
(2003)
Nat Biotechnol
, vol.21
, pp. 559-561
-
-
Kunath, T.1
Gish, G.2
Lickert, H.3
Jones, N.4
Pawson, T.5
Rossant, J.6
-
14
-
-
10744223472
-
Identification of an angiogenic factor that when mutated causes susceptibility to Klippel-Trenaunay syndrome
-
Tian XL, Kadaba R, You SA, Liu M, Timur AA, Yang L, Chen Q, Szafranski P, Rao S, Wu L, Housman DE, DiCorleto PE, Driscoll DJ, Borrow J, Wang Q (2004) Identification of an angiogenic factor that when mutated causes susceptibility to Klippel-Trenaunay syndrome. Nature 427:640-645
-
(2004)
Nature
, vol.427
, pp. 640-645
-
-
Tian, X.L.1
Kadaba, R.2
You, S.A.3
Liu, M.4
Timur, A.A.5
Yang, L.6
Chen, Q.7
Szafranski, P.8
Rao, S.9
Wu, L.10
Housman, D.E.11
Dicorleto, P.E.12
Driscoll, D.J.13
Borrow, J.14
Wang, Q.15
-
15
-
-
0023619575
-
A cytoplasmic protein stimulates normal N-ras p21 GTPase, but does not affect oncogenic mutants
-
Trahey M, McCormick F (1987) A cytoplasmic protein stimulates normal N-ras p21 GTPase, but does not affect oncogenic mutants. Science 238:542-545
-
(1987)
Science
, vol.238
, pp. 542-545
-
-
Trahey, M.1
McCormick, F.2
-
16
-
-
0024212303
-
Molecular cloning of two types of GAP complementary DNA from human placenta
-
Trahey M, Wong G, Halenbeck R, Rubinfeld B, Martin GA, Ladner M, Long CM, Crosier WJ, Watt K, Koths K et al (1988) Molecular cloning of two types of GAP complementary DNA from human placenta. Science 242:1697-1700
-
(1988)
Science
, vol.242
, pp. 1697-1700
-
-
Trahey, M.1
Wong, G.2
Halenbeck, R.3
Rubinfeld, B.4
Martin, G.A.5
Ladner, M.6
Long, C.M.7
Crosier, W.J.8
Watt, K.9
Koths, K.10
-
17
-
-
0028832284
-
Klippel-Trenaunay-Weber syndrome associated with a 5:11 balanced translocation
-
Whelan AJ, Watson MS, Porter FD, Steiner RD (1995) Klippel-Trenaunay- Weber syndrome associated with a 5:11 balanced translocation. Am J Med Genet 59:492-494
-
(1995)
Am J Med Genet
, vol.59
, pp. 492-494
-
-
Whelan, A.J.1
Watson, M.S.2
Porter, F.D.3
Steiner, R.D.4
-
18
-
-
0020534650
-
The proteus syndrome. Partial gigantism of the hands and/or feet, nevi, hemihypertrophy, subcutaneous tumors, macrocephaly or other skull anomalies and possible accelerated growth and visceral affections
-
Wiedemann HR, Burgio GR, Aldenhoff P, Kunze J, Kaufmann HJ, Schirg E (1983) The proteus syndrome. Partial gigantism of the hands and/or feet, nevi, hemihypertrophy, subcutaneous tumors, macrocephaly or other skull anomalies and possible accelerated growth and visceral affections. Eur J Pediatr 140:5-12
-
(1983)
Eur J Pediatr
, vol.140
, pp. 5-12
-
-
Wiedemann, H.R.1
Burgio, G.R.2
Aldenhoff, P.3
Kunze, J.4
Kaufmann, H.J.5
Schirg, E.6
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