-
1
-
-
0027383692
-
Sutural biology and the correlates of craniosynostosis
-
8266985 10.1002/ajmg.1320470507
-
Cohen MM Jr (1993) Sutural biology and the correlates of craniosynostosis. Am J Med Genet 47(5):581-616
-
(1993)
Am J Med Genet
, vol.47
, Issue.5
, pp. 581-616
-
-
Cohen, Jr.M.M.1
-
2
-
-
34547642377
-
Clinical dividends from the molecular genetic diagnosis of craniosynostosis
-
17621648 10.1002/ajmg.a.31905
-
Wilkie AO, Bochukova EG, Hansen RM, Taylor IB, Rannan-Eliya SV, Byren JC, Wall SA, Ramos L, Venâncio M, Hurst JA, O'rourke AW, Williams LJ, Seller A, Lester T (2007) Clinical dividends from the molecular genetic diagnosis of craniosynostosis. Am J Med Genet A 143A(16):1941-1949
-
(2007)
Am J Med Genet A
, vol.143
, Issue.16
, pp. 1941-1949
-
-
Wilkie, A.O.1
Bochukova, E.G.2
Hansen, R.M.3
Taylor, I.B.4
Rannan-Eliya, S.V.5
Byren, J.C.6
Wall, S.A.7
Ramos, L.8
Venâncio, M.9
Hurst, J.A.10
O'Rourke, A.W.11
Williams, L.J.12
Seller, A.13
Lester, T.14
-
3
-
-
77955481154
-
Prevalence and complications of single-gene and chromosomal disorders in craniosynostosis
-
20643727 10.1542/peds.2009-3491
-
Wilkie AO, Byren JC, Hurst JA, Jayamohan J, Johnson D, Knight SJ, Lester T, Richards PG, Twigg SR, Wall SA (2010) Prevalence and complications of single-gene and chromosomal disorders in craniosynostosis. Pediatrics 126(2):e391-400
-
(2010)
Pediatrics
, vol.126
, Issue.2
, pp. 391-400
-
-
Wilkie, A.O.1
Byren, J.C.2
Hurst, J.A.3
Jayamohan, J.4
Johnson, D.5
Knight, S.J.6
Lester, T.7
Richards, P.G.8
Twigg, S.R.9
Wall, S.A.10
-
4
-
-
80051863260
-
Evaluation and management of nonsyndromic craniosynostosis
-
21457300 10.1111/j.1651-2227.2011.02299.x 1:STN:280: DC%2BC3MjmtlOgtA%3D%3D
-
Ursitti F, Fadda T, Papetti L, Pagnoni M, Nicita F, Iannetti G, Spalice A (2011) Evaluation and management of nonsyndromic craniosynostosis. Acta Paediatr 100(9):1185-1194
-
(2011)
Acta Paediatr
, vol.100
, Issue.9
, pp. 1185-1194
-
-
Ursitti, F.1
Fadda, T.2
Papetti, L.3
Pagnoni, M.4
Nicita, F.5
Iannetti, G.6
Spalice, A.7
-
5
-
-
0023853515
-
Nosographic identification and classification of plagiocephaly
-
3401869
-
Di Rocco C, Velardi F (1988) Nosographic identification and classification of plagiocephaly. Childs Nerv Syst 4(1):9-15
-
(1988)
Childs Nerv Syst
, vol.4
, Issue.1
, pp. 9-15
-
-
Di Rocco, C.1
Velardi, F.2
-
6
-
-
67349121905
-
The increase of metopic synostosis: A pan-European observation
-
19326483 10.1097/SCS.0b013e31818436be
-
van der Meulen J, van der Hulst R, van Adrichem L, Arnaud E, Chin-Shong D, Duncan C, Habets E, Hinojosa J, Mathijssen I, May P, Morritt D, Nishikawa H, Noons P, Richardson D, Wall S, van der Vlugt J, Renier D (2009) The increase of metopic synostosis: a pan-European observation. J Craniofac Surg 20(2):283-286
-
(2009)
J Craniofac Surg
, vol.20
, Issue.2
, pp. 283-286
-
-
Van Der Meulen, J.1
Van Der Hulst, R.2
Van Adrichem, L.3
Arnaud, E.4
Chin-Shong, D.5
Duncan, C.6
Habets, E.7
Hinojosa, J.8
Mathijssen, I.9
May, P.10
Morritt, D.11
Nishikawa, H.12
Noons, P.13
Richardson, D.14
Wall, S.15
Van Der Vlugt, J.16
Renier, D.17
-
7
-
-
67349229415
-
The changing epidemiologic spectrum of single-suture synostoses
-
18626371 10.1097/PRS.0b013e31817d548c 1:CAS:528:DC%2BD1cXpt1Whtbw%3D
-
Selber J, Reid RR, Chike-Obi CJ, Sutton LN, Zackai EH, McDonald-McGinn D, Sonnad SS, Whitaker LA, Bartlett SP (2008) The changing epidemiologic spectrum of single-suture synostoses. Plast Reconstr Surg 122(2):527-533
-
(2008)
Plast Reconstr Surg
, vol.122
, Issue.2
, pp. 527-533
-
-
Selber, J.1
Reid, R.R.2
Chike-Obi, C.J.3
Sutton, L.N.4
Zackai, E.H.5
McDonald-Mcginn, D.6
Sonnad, S.S.7
Whitaker, L.A.8
Bartlett, S.P.9
-
8
-
-
67650149722
-
Evolution in the frequency of nonsyndromic craniosynostosis
-
19569905 10.3171/2009.3.PEDS08355
-
Di Rocco F, Arnaud E, Renier D (2009) Evolution in the frequency of nonsyndromic craniosynostosis. J Neurosurg Pediatr 4(1):21-25
-
(2009)
J Neurosurg Pediatr
, vol.4
, Issue.1
, pp. 21-25
-
-
Di Rocco, F.1
Arnaud, E.2
Renier, D.3
-
9
-
-
0021341288
-
Trigonocephaly: A new familial syndrome
-
6741996 10.1002/ajmg.1320180109 1:STN:280:DyaL2c3ltlynsg%3D%3D
-
Frydman M, Kauschansky A, Elian E (1984) Trigonocephaly: a new familial syndrome. Am J Med Genet 18(1):55-59
-
(1984)
Am J Med Genet
, vol.18
, Issue.1
, pp. 55-59
-
-
Frydman, M.1
Kauschansky, A.2
Elian, E.3
-
10
-
-
0029879970
-
Genetic study of scaphocephaly
-
8882788 10.1002/(SICI)1096-8628(19960329)62:3<282: AID-AJMG15>3.0.CO;2-G 1:STN:280:DyaK2s%2FjslWnsw%3D%3D
-
Lajeunie E, Le Merrer M, Bonaïti-Pellie C, Marchac D, Renier D (1996) Genetic study of scaphocephaly. Am J Med Genet 62(3):282-285
-
(1996)
Am J Med Genet
, vol.62
, Issue.3
, pp. 282-285
-
-
Lajeunie, E.1
Le Merrer, M.2
Bonaïti-Pellie, C.3
Marchac, D.4
Renier, D.5
-
11
-
-
0031963105
-
Syndromal and nonsyndromal primary trigonocephaly: Analysis of a series of 237 patients
-
9450889 10.1002/(SICI)1096-8628(19980113)75:2<211: AID-AJMG19>3.0.CO;2-S 1:STN:280:DyaK1c7htFeltw%3D%3D
-
Lajeunie E, Le Merrer M, Marchac D, Renier D (1998) Syndromal and nonsyndromal primary trigonocephaly: analysis of a series of 237 patients. Am J Med Genet 75(2):211-215
-
(1998)
Am J Med Genet
, vol.75
, Issue.2
, pp. 211-215
-
-
Lajeunie, E.1
Le Merrer, M.2
Marchac, D.3
Renier, D.4
-
12
-
-
0034485778
-
An unusual FGFR1 mutation (fibroblast growth factor receptor 1 mutation) in a girl with non-syndromic trigonocephaly
-
11173846 10.1159/000056834 1:STN:280:DC%2BD3M7otFynsw%3D%3D
-
Kress W, Petersen B, Collmann H, Grimm T (2000) An unusual FGFR1 mutation (fibroblast growth factor receptor 1 mutation) in a girl with non-syndromic trigonocephaly. Cytogenet Cell Genet 91(1-4):138-140
-
(2000)
Cytogenet Cell Genet
, vol.91
, Issue.1-4
, pp. 138-140
-
-
Kress, W.1
Petersen, B.2
Collmann, H.3
Grimm, T.4
-
13
-
-
0041819790
-
Clinical and genetic aspects of trigonocephaly: A study of 25 cases
-
12567409
-
Azimi C, Kennedy SJ, Chitayat D, Chakraborty P, Clarke JT, Forrest C, Teebi AS (2003) Clinical and genetic aspects of trigonocephaly: a study of 25 cases. Am J Med Genet A 117A(2):127-135
-
(2003)
Am J Med Genet A
, vol.117
, Issue.2
, pp. 127-135
-
-
Azimi, C.1
Kennedy, S.J.2
Chitayat, D.3
Chakraborty, P.4
Clarke, J.T.5
Forrest, C.6
Teebi, A.S.7
-
14
-
-
23744461534
-
Familial scaphocephaly syndrome caused by a novel mutation in the FGFR2 tyrosine kinase domain
-
16061565 10.1136/jmg.2004.027888 1:CAS:528:DC%2BD2MXhtVSltrjL
-
McGillivray G, Savarirayan R, Cox TC, Stojkoski C, McNeil R, Bankier A, Bateman JF, Roscioli T, Gardner RJ, Lamandé SR (2005) Familial scaphocephaly syndrome caused by a novel mutation in the FGFR2 tyrosine kinase domain. J Med Genet 42(8):656-662
-
(2005)
J Med Genet
, vol.42
, Issue.8
, pp. 656-662
-
-
McGillivray, G.1
Savarirayan, R.2
Cox, T.C.3
Stojkoski, C.4
McNeil, R.5
Bankier, A.6
Bateman, J.F.7
Roscioli, T.8
Gardner, R.J.9
Lamandé, S.R.10
-
15
-
-
77956118641
-
Copy number variation analysis in single-suture craniosynostosis: Multiple rare variants including RUNX2 duplication in two cousins with metopic craniosynostosis
-
20683987 10.1002/ajmg.a.33557
-
Mefford HC, Shafer N, Antonacci F, Tsai JM, Park SS, Hing AV, Rieder MJ, Smyth MD, Speltz ML, Eichler EE, Cunningham ML (2010) Copy number variation analysis in single-suture craniosynostosis: multiple rare variants including RUNX2 duplication in two cousins with metopic craniosynostosis. Am J Med Genet A 152A(9):2203-2210
-
(2010)
Am J Med Genet A
, vol.152
, Issue.9
, pp. 2203-2210
-
-
Mefford, H.C.1
Shafer, N.2
Antonacci, F.3
Tsai, J.M.4
Park, S.S.5
Hing, A.V.6
Rieder, M.J.7
Smyth, M.D.8
Speltz, M.L.9
Eichler, E.E.10
Cunningham, M.L.11
-
16
-
-
0018668892
-
Sagittal craniostenosis: Fetal head constraint as one possible cause
-
490245
-
Graham JM Jr, deSaxe M, Smith DW (1979) Sagittal craniostenosis: fetal head constraint as one possible cause. J Pediatr 95(5 Pt 1):747-750
-
(1979)
J Pediatr
, vol.95
, Issue.5 PART 1
, pp. 747-750
-
-
Graham, Jr.J.M.1
Desaxe, M.2
Smith, D.W.3
-
17
-
-
0028146437
-
Increased risk of craniosynostosis with maternal cigarette smoking during pregnancy
-
7974250 10.1002/tera.1420500103 1:STN:280:DyaK2M%2FmsVGlsw%3D%3D
-
Alderman BW, Bradley CM, Greene C, Fernbach SK, Barón AE (1994) Increased risk of craniosynostosis with maternal cigarette smoking during pregnancy. Teratology 50(1):13-18
-
(1994)
Teratology
, vol.50
, Issue.1
, pp. 13-18
-
-
Alderman, B.W.1
Bradley, C.M.2
Greene, C.3
Fernbach, S.K.4
Barón, A.E.5
-
18
-
-
0031888582
-
Maternal exposure to prescription and non-prescription pharmaceuticals or drugs of abuse and risk of craniosynostosis
-
9563695 10.1093/ije/27.1.64 1:STN:280:DyaK1c3itlWrtg%3D%3D
-
Gardner JS, Guyard-Boileau B, Alderman BW, Fernbach SK, Greene C, Mangione EJ (1998) Maternal exposure to prescription and non-prescription pharmaceuticals or drugs of abuse and risk of craniosynostosis. Int J Epidemiol 27(1):64-67
-
(1998)
Int J Epidemiol
, vol.27
, Issue.1
, pp. 64-67
-
-
Gardner, J.S.1
Guyard-Boileau, B.2
Alderman, B.W.3
Fernbach, S.K.4
Greene, C.5
Mangione, E.J.6
-
19
-
-
0035043261
-
Toward an understanding of nonsyndromic craniosynostosis: Altered patterns of TGF-beta receptor and FGF receptor expression induced by intrauterine head constraint
-
11352430 10.1097/00000637-200105000-00015 1:STN:280: DC%2BD3M3lsVSqsw%3D%3D
-
Hunenko O, Karmacharya J, Ong G, Kirschner RE (2001) Toward an understanding of nonsyndromic craniosynostosis: altered patterns of TGF-beta receptor and FGF receptor expression induced by intrauterine head constraint. Ann Plast Surg 46(5):546-553
-
(2001)
Ann Plast Surg
, vol.46
, Issue.5
, pp. 546-553
-
-
Hunenko, O.1
Karmacharya, J.2
Ong, G.3
Kirschner, R.E.4
-
20
-
-
0034034560
-
Growth restriction of cranial sutures in the fetal lamb causes deformational changes, not craniosynostosis
-
10845296 10.1097/00006534-200006000-00017 1:STN:280: DC%2BD3czgtF2jtA%3D%3D
-
Bradley JP, Shahinian H, Levine JP, Rowe N, Longaker MT (2000) Growth restriction of cranial sutures in the fetal lamb causes deformational changes, not craniosynostosis. Plast Reconstr Surg 105(7):2416-2423
-
(2000)
Plast Reconstr Surg
, vol.105
, Issue.7
, pp. 2416-2423
-
-
Bradley, J.P.1
Shahinian, H.2
Levine, J.P.3
Rowe, N.4
Longaker, M.T.5
-
21
-
-
0029042409
-
Increased risk of craniosynostosis with higher antenatal maternal altitude
-
7635605 10.1093/ije/24.2.420 1:STN:280:DyaK2Mzmt1equg%3D%3D
-
Alderman BW, Zamudio S, Barón AE, Joshua SC, Fernbach SK, Greene C, Mangione EJ (1995) Increased risk of craniosynostosis with higher antenatal maternal altitude. Int J Epidemiol 24(2):420-426
-
(1995)
Int J Epidemiol
, vol.24
, Issue.2
, pp. 420-426
-
-
Alderman, B.W.1
Zamudio, S.2
Barón, A.E.3
Joshua, S.C.4
Fernbach, S.K.5
Greene, C.6
Mangione, E.J.7
-
22
-
-
0344069730
-
Maternal smoking and craniosynostosis
-
10471899 10.1002/(SICI)1096-9926(199909)60:3<146: AID-TERA10>3.0. CO;2-3
-
Källén K (1999) Maternal smoking and craniosynostosis. Teratology 60(3):146-150
-
(1999)
Teratology
, vol.60
, Issue.3
, pp. 146-150
-
-
Källén, K.1
-
23
-
-
40049091130
-
Craniosynostosis and maternal smoking
-
National Birth Defects Prevention Study 18050313 10.1002/bdra.20426 1:CAS:528:DC%2BD1cXjtlKmsLk%3D
-
Carmichael SL, Ma C, Rasmussen SA, Honein MA, Lammer EJ, Shaw GM, National Birth Defects Prevention Study (2008) Craniosynostosis and maternal smoking. Birth Defects Res A Clin Mol Teratol 82(2):78-85
-
(2008)
Birth Defects Res A Clin Mol Teratol
, vol.82
, Issue.2
, pp. 78-85
-
-
Carmichael, S.L.1
Ma, C.2
Rasmussen, S.A.3
Honein, M.A.4
Lammer, E.J.5
Shaw, G.M.6
-
24
-
-
80051925984
-
Maternal smoking in pregnancy and birth defects: A systematic review based on 173,687 malformed cases and 11.7 million controls
-
21747128 10.1093/humupd/dmr022 1:CAS:528:DC%2BC3MXhtVyntr3F
-
Hackshaw A, Rodeck C, Boniface S (2011) Maternal smoking in pregnancy and birth defects: a systematic review based on 173,687 malformed cases and 11.7 million controls. Hum Reprod Update 17(5):589-604
-
(2011)
Hum Reprod Update
, vol.17
, Issue.5
, pp. 589-604
-
-
Hackshaw, A.1
Rodeck, C.2
Boniface, S.3
-
25
-
-
0032934535
-
Decreased proliferation and altered differentiation in osteoblasts from genetically and clinically distinct craniosynostotic disorders
-
10329600 10.1016/S0002-9440(10)65401-6 1:STN:280:DyaK1M3mtlersQ%3D%3D
-
Fragale A, Tartaglia M, Bernardini S, Di Stasi AM, Di Rocco C, Velardi F, Teti A, Battaglia PA, Migliaccio S (1999) Decreased proliferation and altered differentiation in osteoblasts from genetically and clinically distinct craniosynostotic disorders. Am J Pathol 154(5):1465-1477
-
(1999)
Am J Pathol
, vol.154
, Issue.5
, pp. 1465-1477
-
-
Fragale, A.1
Tartaglia, M.2
Bernardini, S.3
Di Stasi, A.M.4
Di Rocco, C.5
Velardi, F.6
Teti, A.7
Battaglia, P.A.8
Migliaccio, S.9
-
26
-
-
28444453646
-
Growth of the normal skull vault and its alteration in craniosynostosis: Insights from human genetics and experimental studies
-
16313397 10.1111/j.1469-7580.2005.00475.x
-
Morriss-Kay GM, Wilkie AO (2005) Growth of the normal skull vault and its alteration in craniosynostosis: insights from human genetics and experimental studies. J Anat 207(5):637-653
-
(2005)
J Anat
, vol.207
, Issue.5
, pp. 637-653
-
-
Morriss-Kay, G.M.1
Wilkie, A.O.2
-
27
-
-
0031048450
-
Age-related changes in bone formation, osteoblastic cell proliferation, and differentiation during postnatal osteogenesis in human calvaria
-
9015761 10.1002/(SICI)1097-4644(199701)64:1<128: AID-JCB15>3.0. CO;2-H
-
de Pollak C, Arnaud E, Renier D, Marie PJ (1997) Age-related changes in bone formation, osteoblastic cell proliferation, and differentiation during postnatal osteogenesis in human calvaria. J Cell Biochem 64(1):128-139
-
(1997)
J Cell Biochem
, vol.64
, Issue.1
, pp. 128-139
-
-
De Pollak, C.1
Arnaud, E.2
Renier, D.3
Marie, P.J.4
-
28
-
-
0038688373
-
The complexities of skeletal biology
-
12748648 10.1038/nature01654 1:CAS:528:DC%2BD3sXjs1ynu7w%3D
-
Karsenty G (2003) The complexities of skeletal biology. Nature 423(6937):316-318
-
(2003)
Nature
, vol.423
, Issue.6937
, pp. 316-318
-
-
Karsenty, G.1
-
29
-
-
0017879438
-
Sutural closure in rabbit and man: A morphological and histochemical study
-
624680 1:STN:280:DyaE1c7gvFagsA%3D%3D
-
Persson M, Magnusson BC, Thilander B (1978) Sutural closure in rabbit and man: a morphological and histochemical study. J Anat 125(Pt 2):313-321
-
(1978)
J Anat
, vol.125
, Issue.PART 2
, pp. 313-321
-
-
Persson, M.1
Magnusson, B.C.2
Thilander, B.3
-
30
-
-
0027383692
-
Sutural biology and the correlates of craniosynostosis
-
8266985 10.1002/ajmg.1320470507
-
Cohen MM Jr (1993) Sutural biology and the correlates of craniosynostosis. Am J Med Genet 47(5):581-616
-
(1993)
Am J Med Genet
, vol.47
, Issue.5
, pp. 581-616
-
-
Cohen, Jr.M.M.1
-
31
-
-
35748968230
-
Cell fate specification during calvarial bone and suture development
-
17931618 10.1016/j.ydbio.2007.08.028 1:CAS:528:DC%2BD2sXht1yltrrE
-
Lana-Elola E, Rice R, Grigoriadis AE, Rice DP (2007) Cell fate specification during calvarial bone and suture development. Dev Biol 311(2):335-346
-
(2007)
Dev Biol
, vol.311
, Issue.2
, pp. 335-346
-
-
Lana-Elola, E.1
Rice, R.2
Grigoriadis, A.E.3
Rice, D.P.4
-
32
-
-
33645810601
-
Cell mixing at a neural crest-mesoderm boundary and deficient ephrin-Eph signaling in the pathogenesis of craniosynostosis
-
16540516 10.1093/hmg/ddl052 1:CAS:528:DC%2BD28XjtV2gtbs%3D
-
Merrill AE, Bochukova EG, Brugger SM, Ishii M, Pilz DT, Wall SA, Lyons KM, Wilkie AO, Maxson RE Jr (2006) Cell mixing at a neural crest-mesoderm boundary and deficient ephrin-Eph signaling in the pathogenesis of craniosynostosis. Hum Mol Genet 15(8):1319-1328
-
(2006)
Hum Mol Genet
, vol.15
, Issue.8
, pp. 1319-1328
-
-
Merrill, A.E.1
Bochukova, E.G.2
Brugger, S.M.3
Ishii, M.4
Pilz, D.T.5
Wall, S.A.6
Lyons, K.M.7
Wilkie, A.O.8
Maxson, Jr.R.E.9
-
33
-
-
84866080873
-
Genes and molecular pathways of the osteogenic process
-
Lin Y(ed) InTech
-
Lattanzi W, Bernardini C (2011) Genes and molecular pathways of the osteogenic process. In: Lin Y(ed) Osteogenesis, InTech, Available at http://www.intechopen.com/books/osteogenesis/genes-and-molecular-pathways-of- the-osteogenic-process
-
(2011)
Osteogenesis
-
-
Lattanzi, W.1
Bernardini, C.2
-
34
-
-
0031755753
-
LMP-1, a LIM-domain protein, mediates BMP-6 effects on bone formation
-
9832452 10.1210/en.139.12.5125 1:CAS:528:DyaK1cXns1ehtb8%3D
-
Boden SD, Liu Y, Hair GA, Helms JA, Hu D, Racine M, Nanes MS, Titus L (1998) LMP-1, a LIM-domain protein, mediates BMP-6 effects on bone formation. Endocrinology 139(12):5125-5134
-
(1998)
Endocrinology
, vol.139
, Issue.12
, pp. 5125-5134
-
-
Boden, S.D.1
Liu, Y.2
Hair, G.A.3
Helms, J.A.4
Hu, D.5
Racine, M.6
Nanes, M.S.7
Titus, L.8
-
35
-
-
78549251452
-
Early transcriptional events during osteogenic differentiation of human bone marrow stromal cells induced by Lim mineralization protein 3
-
21061915 10.3727/105221610X12819686555097 1:CAS:528:DC%2BC3cXhsF2qsr%2FJ
-
Bernardini C, Saulnier N, Parrilla C, Pola E, Gambotto A, Michetti F, Robbins PD, Lattanzi W (2010) Early transcriptional events during osteogenic differentiation of human bone marrow stromal cells induced by Lim mineralization protein 3. Gene Expr 15(1):27-42
-
(2010)
Gene Expr
, vol.15
, Issue.1
, pp. 27-42
-
-
Bernardini, C.1
Saulnier, N.2
Parrilla, C.3
Pola, E.4
Gambotto, A.5
Michetti, F.6
Robbins, P.D.7
Lattanzi, W.8
-
37
-
-
0036821229
-
Expression profiles of craniosynostosis-derived fibroblasts
-
12477974 1:CAS:528:DC%2BD38Xps1OltLg%3D
-
Carinci F, Bodo M, Tosi L, Francioso F, Evangelisti R, Pezzetti F, Scapoli L, Martinelli M, Baroni T, Stabellini G, Carinci P, Bellucci C, Lilli C, Volinia S (2002) Expression profiles of craniosynostosis-derived fibroblasts. Mol Med 8(10):638-644
-
(2002)
Mol Med
, vol.8
, Issue.10
, pp. 638-644
-
-
Carinci, F.1
Bodo, M.2
Tosi, L.3
Francioso, F.4
Evangelisti, R.5
Pezzetti, F.6
Scapoli, L.7
Martinelli, M.8
Baroni, T.9
Stabellini, G.10
Carinci, P.11
Bellucci, C.12
Lilli, C.13
Volinia, S.14
-
38
-
-
38849198460
-
Unravelling the molecular control of calvarial suture fusion in children with craniosynostosis
-
18076769 10.1186/1471-2164-8-458
-
Coussens AK, Wilkinson CR, Hughes IP, Morris CP, van Daal A, Anderson PJ, Powell BC (2007) Unravelling the molecular control of calvarial suture fusion in children with craniosynostosis. BMC Genomics 8:458
-
(2007)
BMC Genomics
, vol.8
, pp. 458
-
-
Coussens, A.K.1
Wilkinson, C.R.2
Hughes, I.P.3
Morris, C.P.4
Van Daal, A.5
Anderson, P.J.6
Powell, B.C.7
-
39
-
-
34548492521
-
Apert p.Ser252Trp mutation in FGFR2 alters osteogenic potential and gene expression of cranial periosteal cells
-
17622301 1:CAS:528:DC%2BD2sXhtVynsrjF
-
Fanganiello RD, Sertié AL, Reis EM, Yeh E, Oliveira NA, Bueno DF, Kerkis I, Alonso N, Cavalheiro S, Matsushita H, Freitas R, Verjovski-Almeida S, Passos-Bueno MR (2007) Apert p.Ser252Trp mutation in FGFR2 alters osteogenic potential and gene expression of cranial periosteal cells. Mol Med 13(7-8):422-442
-
(2007)
Mol Med
, vol.13
, Issue.7-8
, pp. 422-442
-
-
Fanganiello, R.D.1
Sertié, A.L.2
Reis, E.M.3
Yeh, E.4
Oliveira, N.A.5
Bueno, D.F.6
Kerkis, I.7
Alonso, N.8
Cavalheiro, S.9
Matsushita, H.10
Freitas, R.11
Verjovski-Almeida, S.12
Passos-Bueno, M.R.13
-
40
-
-
44249101629
-
Identification of genes differentially expressed by prematurely fused human sutures using a novel in vivo-in vitro approach
-
18093228 10.1111/j.1432-0436.2007.00244.x 1:CAS:528:DC%2BD1cXnsVyntLw%3D
-
Coussens AK, Hughes IP, Wilkinson CR, Morris CP, Anderson PJ, Powell BC, van Daal A (2008) Identification of genes differentially expressed by prematurely fused human sutures using a novel in vivo-in vitro approach. Differentiation 76(5):531-545
-
(2008)
Differentiation
, vol.76
, Issue.5
, pp. 531-545
-
-
Coussens, A.K.1
Hughes, I.P.2
Wilkinson, C.R.3
Morris, C.P.4
Anderson, P.J.5
Powell, B.C.6
Van Daal, A.7
-
41
-
-
78649618915
-
Scalp fibroblasts have a shared expression profile in monogenic craniosynostosis
-
19755431 10.1136/jmg.2009.069617 1:CAS:528:DC%2BC3MXhtVKrtLk%3D
-
Bochukova EG, Soneji S, Wall SA, Wilkie AO (2010) Scalp fibroblasts have a shared expression profile in monogenic craniosynostosis. J Med Genet 47(12):803-808
-
(2010)
J Med Genet
, vol.47
, Issue.12
, pp. 803-808
-
-
Bochukova, E.G.1
Soneji, S.2
Wall, S.A.3
Wilkie, A.O.4
-
42
-
-
80054787803
-
Differential expression of extracellular matrix-mediated pathways in single-suture craniosynostosis
-
22028906 10.1371/journal.pone.0026557 1:CAS:528:DC%2BC3MXhsVCrsrvI
-
Stamper BD, Park SS, Beyer RP, Bammler TK, Farin FM, Mecham B, Cunningham ML (2011) Differential expression of extracellular matrix-mediated pathways in single-suture craniosynostosis. PLoS One 6(10):e26557
-
(2011)
PLoS One
, vol.6
, Issue.10
, pp. 26557
-
-
Stamper, B.D.1
Park, S.S.2
Beyer, R.P.3
Bammler, T.K.4
Farin, F.M.5
Mecham, B.6
Cunningham, M.L.7
-
43
-
-
2942560339
-
Mutations of ephrin-B1 (EFNB1), a marker of tissue boundary formation, cause craniofrontonasal syndrome
-
15166289 10.1073/pnas.0402819101 1:CAS:528:DC%2BD2cXltFKksLw%3D
-
Twigg SR, Kan R, Babbs C, Bochukova EG, Robertson SP, Wall SA, Morriss-Kay GM, Wilkie AO (2004) Mutations of ephrin-B1 (EFNB1), a marker of tissue boundary formation, cause craniofrontonasal syndrome. Proc Natl Acad Sci U S A 101(23):8652-8657
-
(2004)
Proc Natl Acad Sci U S A
, vol.101
, Issue.23
, pp. 8652-8657
-
-
Twigg, S.R.1
Kan, R.2
Babbs, C.3
Bochukova, E.G.4
Robertson, S.P.5
Wall, S.A.6
Morriss-Kay, G.M.7
Wilkie, A.O.8
-
44
-
-
0033198844
-
Impaired retinal function and vitamin A availability in mice lacking retinol-binding protein
-
10469643 10.1093/emboj/18.17.4633 1:CAS:528:DyaK1MXmt1yisLg%3D
-
Quadro L, Blaner WS, Salchow DJ, Vogel S, Piantedosi R, Gouras P, Freeman S, Cosma MP, Colantuoni V, Gottesman ME (1999) Impaired retinal function and vitamin A availability in mice lacking retinol-binding protein. EMBO J 18:4633-4644
-
(1999)
EMBO J
, vol.18
, pp. 4633-4644
-
-
Quadro, L.1
Blaner, W.S.2
Salchow, D.J.3
Vogel, S.4
Piantedosi, R.5
Gouras, P.6
Freeman, S.7
Cosma, M.P.8
Colantuoni, V.9
Gottesman, M.E.10
-
45
-
-
12544251542
-
The loss of glypican-3 induces alterations in Wnt signaling
-
15537637 10.1074/jbc.M410090200 1:CAS:528:DC%2BD2MXksVWgtg%3D%3D
-
Song HH, Shi W, Xiang YY, Filmus J (2005) The loss of glypican-3 induces alterations in Wnt signaling. J Biol Chem 280:2116-2125
-
(2005)
J Biol Chem
, vol.280
, pp. 2116-2125
-
-
Song, H.H.1
Shi, W.2
Xiang, Y.Y.3
Filmus, J.4
-
46
-
-
0034284766
-
Glypican-3 controls cellular responses to Bmp4 in limb patterning and skeletal development
-
10964473 10.1006/dbio.2000.9831 1:CAS:528:DC%2BD3cXmtVGgu7c%3D
-
Paine-Saunders S, Viviano BL, Zupicich J, Skarnes WC, Saunders S (2000) glypican-3 controls cellular responses to Bmp4 in limb patterning and skeletal development. Dev Biol 225:179-187
-
(2000)
Dev Biol
, vol.225
, pp. 179-187
-
-
Paine-Saunders, S.1
Viviano, B.L.2
Zupicich, J.3
Skarnes, W.C.4
Saunders, S.5
-
47
-
-
0242593885
-
Processing by proprotein convertases is required for glypican-3 modulation of cell survival, Wnt signaling, and gastrulation movements
-
14610063 10.1083/jcb.200302152
-
De Cat B, Muyldermans SY, Coomans C, Degeest G, Vanderschueren B, Creemers J, Biemar F, Peers B, David G (2003) Processing by proprotein convertases is required for glypican-3 modulation of cell survival, Wnt signaling, and gastrulation movements. J Cell Biol 163:625-635
-
(2003)
J Cell Biol
, vol.163
, pp. 625-635
-
-
De Cat, B.1
Muyldermans, S.Y.2
Coomans, C.3
Degeest, G.4
Vanderschueren, B.5
Creemers, J.6
Biemar, F.7
Peers, B.8
David, G.9
-
48
-
-
0037428667
-
Glypican-3, overexpressed in hepatocellular carcinoma, modulates FGF2 and BMP-7 signaling
-
12478660 10.1002/ijc.10856 1:CAS:528:DC%2BD3sXhvVOjug%3D%3D
-
Midorikawa Y, Ishikawa S, Iwanari H, Imamura T, Sakamoto H, Miyazono K, Kodama T, Makuuchi M, Aburatani H (2003) Glypican-3, overexpressed in hepatocellular carcinoma, modulates FGF2 and BMP-7 signaling. Int J Cancer 103:455-465
-
(2003)
Int J Cancer
, vol.103
, pp. 455-465
-
-
Midorikawa, Y.1
Ishikawa, S.2
Iwanari, H.3
Imamura, T.4
Sakamoto, H.5
Miyazono, K.6
Kodama, T.7
Makuuchi, M.8
Aburatani, H.9
-
49
-
-
13344261391
-
Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome
-
8589713 10.1038/ng0396-241 1:CAS:528:DyaK28XhvVSgtL4%3D
-
Pilia G, Hughes-Benzie RM, MacKenzie A, Baybayan P, Chen EY, Huber R, Neri G, Cao A, Forabosco A, Schlessinger D (1996) Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome. Nat Genet 12:241-247
-
(1996)
Nat Genet
, vol.12
, pp. 241-247
-
-
Pilia, G.1
Hughes-Benzie, R.M.2
MacKenzie, A.3
Baybayan, P.4
Chen, E.Y.5
Huber, R.6
Neri, G.7
Cao, A.8
Forabosco, A.9
Schlessinger, D.10
-
50
-
-
30344461303
-
Cartducin, a paralog of Acrp30/adiponectin, is induced during chondrogenic differentiation and promotes proliferation of chondrogenic precursors and chondrocytes
-
16155912 10.1002/jcp.20493 1:CAS:528:DC%2BD28XlslGhug%3D%3D
-
Maeda T, Jikko A, Abe M, Yokohama-Tamaki T, Akiyama H, Furukawa S, Takigawa M, Wakisaka S (2006) Cartducin, a paralog of Acrp30/adiponectin, is induced during chondrogenic differentiation and promotes proliferation of chondrogenic precursors and chondrocytes. J Cell Physiol 206:537-544
-
(2006)
J Cell Physiol
, vol.206
, pp. 537-544
-
-
Maeda, T.1
Jikko, A.2
Abe, M.3
Yokohama-Tamaki, T.4
Akiyama, H.5
Furukawa, S.6
Takigawa, M.7
Wakisaka, S.8
-
51
-
-
70350646899
-
Activating mutations in FGFR3 and HRAS reveal a shared genetic origin for congenital disorders and testicular tumors
-
19855393 10.1038/ng.470 1:CAS:528:DC%2BD1MXhtlSqsbzE
-
Goriely A, Hansen RM, Taylor IB, Olesen IA, Jacobsen GK, McGowan SJ, Pfeifer SP, McVean GA, Rajpert-De Meyts E, Wilkie AO (2009) Activating mutations in FGFR3 and HRAS reveal a shared genetic origin for congenital disorders and testicular tumors. Nat Genet 41(11):1247-1252
-
(2009)
Nat Genet
, vol.41
, Issue.11
, pp. 1247-1252
-
-
Goriely, A.1
Hansen, R.M.2
Taylor, I.B.3
Olesen, I.A.4
Jacobsen, G.K.5
McGowan, S.J.6
Pfeifer, S.P.7
McVean, G.A.8
Rajpert-De Meyts, E.9
Wilkie, A.O.10
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