-
1
-
-
34250305402
-
Genetic basis for congenital heart defects: current knowledge: a scientific statement from the American Heart Association Congenital Cardiac Defects Committee, Council on Cardiovascular Disease in the Young: endorsed by the American Academy of Pediatrics
-
Pierpont ME, Basson CT, Benson DW Jr, Gelb BD, Giglia TM, et al. (2007) Genetic basis for congenital heart defects: current knowledge: a scientific statement from the American Heart Association Congenital Cardiac Defects Committee, Council on Cardiovascular Disease in the Young: endorsed by the American Academy of Pediatrics. Circulation 115: 3015-3038.
-
(2007)
Circulation
, vol.115
, pp. 3015-3038
-
-
Pierpont, M.E.1
Basson, C.T.2
Benson Jr., D.W.3
Gelb, B.D.4
Giglia, T.M.5
-
2
-
-
77952328830
-
Cardiovascular anomalies associated with chromosome 22q11.2 deletion syndrome
-
Momma K, (2010) Cardiovascular anomalies associated with chromosome 22q11.2 deletion syndrome. Am J Cardiol 105: 1617-1624.
-
(2010)
Am J Cardiol
, vol.105
, pp. 1617-1624
-
-
Momma, K.1
-
3
-
-
0035096508
-
Deconstructing DiGeorge syndrome
-
Schinke M, Izumo S, (2001) Deconstructing DiGeorge syndrome. Nat Genet 27: 238-240.
-
(2001)
Nat Genet
, vol.27
, pp. 238-240
-
-
Schinke, M.1
Izumo, S.2
-
4
-
-
33751201822
-
Cardiovascular anomalies associated with chromosome 22q11.2 deletion
-
Momma K, (2007) Cardiovascular anomalies associated with chromosome 22q11.2 deletion. Int J Cardiol 114: 147-149.
-
(2007)
Int J Cardiol
, vol.114
, pp. 147-149
-
-
Momma, K.1
-
5
-
-
77957130806
-
Genomic profile of copy number variants on the short arm of human chromosome 8
-
Yu S, Fiedler S, Stegner A, Graf WD, (2010) Genomic profile of copy number variants on the short arm of human chromosome 8. Eur J Hum Genet 18: 1114-1120.
-
(2010)
Eur J Hum Genet
, vol.18
, pp. 1114-1120
-
-
Yu, S.1
Fiedler, S.2
Stegner, A.3
Graf, W.D.4
-
6
-
-
1542579983
-
The application of region-specific probes for the resolution of duplication 8p: a case report and a review of the literature
-
Pabst B, Arslan-Kirchner M, Schmidtke J, Miller K, (2003) The application of region-specific probes for the resolution of duplication 8p: a case report and a review of the literature. Cytogenet Genome Res 103: 3-7.
-
(2003)
Cytogenet Genome Res
, vol.103
, pp. 3-7
-
-
Pabst, B.1
Arslan-Kirchner, M.2
Schmidtke, J.3
Miller, K.4
-
7
-
-
34247599683
-
Two classes of low-copy repeats comediate a new recurrent rearrangement consisting of duplication at 8p23.1 and triplication at 8p23.2
-
Giorda R, Ciccone R, Gimelli G, Pramparo T, Beri S, et al. (2007) Two classes of low-copy repeats comediate a new recurrent rearrangement consisting of duplication at 8p23.1 and triplication at 8p23.2. Hum Mutat 28: 459-468.
-
(2007)
Hum Mutat
, vol.28
, pp. 459-468
-
-
Giorda, R.1
Ciccone, R.2
Gimelli, G.3
Pramparo, T.4
Beri, S.5
-
8
-
-
0033365295
-
Delineation of the critical deletion region for congenital heart defects, on chromosome 8p23.1
-
Devriendt K, Matthijs G, Van Dael R, Gewillig M, Eyskens B, et al. (1999) Delineation of the critical deletion region for congenital heart defects, on chromosome 8p23.1. Am J Hum Genet 64: 1119-1126.
-
(1999)
Am J Hum Genet
, vol.64
, pp. 1119-1126
-
-
Devriendt, K.1
Matthijs, G.2
Van Dael, R.3
Gewillig, M.4
Eyskens, B.5
-
9
-
-
83755228903
-
Detecting 22q11.2 deletion in Chinese children with conotruncal heart defects and single nucleotide polymorphisms in the haploid TBX1 locus
-
Xu YJ, Wang J, Xu R, Zhao PJ, Wang XK, et al. (2011) Detecting 22q11.2 deletion in Chinese children with conotruncal heart defects and single nucleotide polymorphisms in the haploid TBX1 locus. BMC Med Genet 12: 169.
-
(2011)
BMC Med Genet
, vol.12
, pp. 169
-
-
Xu, Y.J.1
Wang, J.2
Xu, R.3
Zhao, P.J.4
Wang, X.K.5
-
10
-
-
37349129016
-
Genetic insights into normal and abnormal heart development
-
Nemer M, (2008) Genetic insights into normal and abnormal heart development. Cardiovasc Pathol 17: 48-54.
-
(2008)
Cardiovasc Pathol
, vol.17
, pp. 48-54
-
-
Nemer, M.1
-
11
-
-
36248986199
-
Association of single-nucleotide polymorphisms in MTMR9 gene with obesity
-
Yanagiya T, Tanabe A, Iida A, Saito S, Sekine A, et al. (2007) Association of single-nucleotide polymorphisms in MTMR9 gene with obesity. Hum Mol Genet 16: 3017-3026.
-
(2007)
Hum Mol Genet
, vol.16
, pp. 3017-3026
-
-
Yanagiya, T.1
Tanabe, A.2
Iida, A.3
Saito, S.4
Sekine, A.5
-
12
-
-
80052575003
-
Integrative analysis of array-comparative genomic hybridisation and matched gene expression profiling data reveals novel genes with prognostic significance in oesophageal adenocarcinoma
-
Goh XY, Rees JR, Paterson AL, Chin SF, Marioni JC, et al. (2011) Integrative analysis of array-comparative genomic hybridisation and matched gene expression profiling data reveals novel genes with prognostic significance in oesophageal adenocarcinoma. Gut 60: 1317-1326.
-
(2011)
Gut
, vol.60
, pp. 1317-1326
-
-
Goh, X.Y.1
Rees, J.R.2
Paterson, A.L.3
Chin, S.F.4
Marioni, J.C.5
-
13
-
-
84877850718
-
Lipid phosphatases identified by screening a mouse phosphatase shRNA library regulate T-cell differentiation and Protein kinase B AKT signaling
-
Guo L, Martens C, Bruno D, Porcella SF, Yamane H, et al. (2013) Lipid phosphatases identified by screening a mouse phosphatase shRNA library regulate T-cell differentiation and Protein kinase B AKT signaling. Proc Natl Acad Sci U S A 110: E1849-1856.
-
(2013)
Proc Natl Acad Sci U S A
, vol.110
-
-
Guo, L.1
Martens, C.2
Bruno, D.3
Porcella, S.F.4
Yamane, H.5
-
14
-
-
62549137023
-
Copy number variation of beta-defensins and relevance to disease
-
Hollox EJ, (2008) Copy number variation of beta-defensins and relevance to disease. Cytogenet Genome Res 123: 148-155.
-
(2008)
Cytogenet Genome Res
, vol.123
, pp. 148-155
-
-
Hollox, E.J.1
-
15
-
-
84861477402
-
Higher DEFB4 genomic copy number in SLE and ANCA-associated small vasculitis
-
Zhou XJ, Cheng FJ, Lv JC, Luo H, Yu F, et al. (2012) Higher DEFB4 genomic copy number in SLE and ANCA-associated small vasculitis. Rheumatology (Oxford) 51: 992-995.
-
(2012)
Rheumatology (Oxford)
, vol.51
, pp. 992-995
-
-
Zhou, X.J.1
Cheng, F.J.2
Lv, J.C.3
Luo, H.4
Yu, F.5
-
16
-
-
58849117701
-
Allelic recombination between distinct genomic locations generates copy number diversity in human beta-defensins
-
Abu Bakar S, Hollox EJ, Armour JA, (2009) Allelic recombination between distinct genomic locations generates copy number diversity in human beta-defensins. Proc Natl Acad Sci U S A 106: 853-858.
-
(2009)
Proc Natl Acad Sci U S A
, vol.106
, pp. 853-858
-
-
Abu Bakar, S.1
Hollox, E.J.2
Armour, J.A.3
-
17
-
-
55549113578
-
Defensins and the dynamic genome: what we can learn from structural variation at human chromosome band 8p23.1
-
Hollox EJ, Barber JC, Brookes AJ, Armour JA, (2008) Defensins and the dynamic genome: what we can learn from structural variation at human chromosome band 8p23.1. Genome Res 18: 1686-1697.
-
(2008)
Genome Res
, vol.18
, pp. 1686-1697
-
-
Hollox, E.J.1
Barber, J.C.2
Brookes, A.J.3
Armour, J.A.4
-
18
-
-
37549033125
-
Psoriasis is associated with increased beta-defensin genomic copy number
-
Hollox EJ, Huffmeier U, Zeeuwen PL, Palla R, Lascorz J, et al. (2008) Psoriasis is associated with increased beta-defensin genomic copy number. Nat Genet 40: 23-25.
-
(2008)
Nat Genet
, vol.40
, pp. 23-25
-
-
Hollox, E.J.1
Huffmeier, U.2
Zeeuwen, P.L.3
Palla, R.4
Lascorz, J.5
-
19
-
-
77950954883
-
Haplotyping and copy number estimation of the highly polymorphic human beta-defensin locus on 8p23 by 454 amplicon sequencing
-
Taudien S, Groth M, Huse K, Petzold A, Szafranski K, et al. (2010) Haplotyping and copy number estimation of the highly polymorphic human beta-defensin locus on 8p23 by 454 amplicon sequencing. BMC Genomics 11: 252.
-
(2010)
BMC Genomics
, vol.11
, pp. 252
-
-
Taudien, S.1
Groth, M.2
Huse, K.3
Petzold, A.4
Szafranski, K.5
-
20
-
-
0042387792
-
Extensive normal copy number variation of a beta-defensin antimicrobial-gene cluster
-
Hollox EJ, Armour JA, Barber JC, (2003) Extensive normal copy number variation of a beta-defensin antimicrobial-gene cluster. Am J Hum Genet 73: 591-600.
-
(2003)
Am J Hum Genet
, vol.73
, pp. 591-600
-
-
Hollox, E.J.1
Armour, J.A.2
Barber, J.C.3
-
21
-
-
0035071955
-
Olfactory receptor-gene clusters, genomic-inversion polymorphisms, and common chromosome rearrangements
-
Giglio S, Broman KW, Matsumoto N, Calvari V, Gimelli G, et al. (2001) Olfactory receptor-gene clusters, genomic-inversion polymorphisms, and common chromosome rearrangements. Am J Hum Genet 68: 874-883.
-
(2001)
Am J Hum Genet
, vol.68
, pp. 874-883
-
-
Giglio, S.1
Broman, K.W.2
Matsumoto, N.3
Calvari, V.4
Gimelli, G.5
-
22
-
-
10744228785
-
Complex low-copy repeats associated with a common polymorphic inversion at human chromosome 8p23
-
Sugawara H, Harada N, Ida T, Ishida T, Ledbetter DH, et al. (2003) Complex low-copy repeats associated with a common polymorphic inversion at human chromosome 8p23. Genomics 82: 238-244.
-
(2003)
Genomics
, vol.82
, pp. 238-244
-
-
Sugawara, H.1
Harada, N.2
Ida, T.3
Ishida, T.4
Ledbetter, D.H.5
-
23
-
-
0034713818
-
Deletion of a 5-cM region at chromosome 8p23 is associated with a spectrum of congenital heart defects
-
Giglio S, Graw SL, Gimelli G, Pirola B, Varone P, et al. (2000) Deletion of a 5-cM region at chromosome 8p23 is associated with a spectrum of congenital heart defects. Circulation 102: 432-437.
-
(2000)
Circulation
, vol.102
, pp. 432-437
-
-
Giglio, S.1
Graw, S.L.2
Gimelli, G.3
Pirola, B.4
Varone, P.5
-
24
-
-
35348956454
-
Prenatal diagnosis of Fryns syndrome associated with a microdeletion at 8p23.1
-
Chen CP, Wang TH, Chen YJ, Chang TY, Liu YP, et al. (2007) Prenatal diagnosis of Fryns syndrome associated with a microdeletion at 8p23.1. Prenat Diagn 27: 967-969.
-
(2007)
Prenat Diagn
, vol.27
, pp. 967-969
-
-
Chen, C.P.1
Wang, T.H.2
Chen, Y.J.3
Chang, T.Y.4
Liu, Y.P.5
-
25
-
-
19144369894
-
The same molecular mechanism at the maternal meiosis I produces mono- and dicentric 8p duplications
-
Floridia G, Piantanida M, Minelli A, Dellavecchia C, Bonaglia C, et al. (1996) The same molecular mechanism at the maternal meiosis I produces mono- and dicentric 8p duplications. Am J Hum Genet 58: 785-796.
-
(1996)
Am J Hum Genet
, vol.58
, pp. 785-796
-
-
Floridia, G.1
Piantanida, M.2
Minelli, A.3
Dellavecchia, C.4
Bonaglia, C.5
-
26
-
-
0034013088
-
A case of inv dup(8p) with early onset breast cancer
-
Seltmann M, Harrington P, Ponder BA, (2000) A case of inv dup(8p) with early onset breast cancer. J Med Genet 37: 70-71.
-
(2000)
J Med Genet
, vol.37
, pp. 70-71
-
-
Seltmann, M.1
Harrington, P.2
Ponder, B.A.3
-
27
-
-
79959564757
-
[Two cases of partial trisomy 8p derived from paternal reciprocal translocation or maternal insertion translocation: clinical features and genetic abnormalities]
-
Xiao B, Zhang JM, Ji X, Jiang WT, Hu J, et al. (2011) [Two cases of partial trisomy 8p derived from paternal reciprocal translocation or maternal insertion translocation: clinical features and genetic abnormalities]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi 28: 247-250.
-
(2011)
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
, vol.28
, pp. 247-250
-
-
Xiao, B.1
Zhang, J.M.2
Ji, X.3
Jiang, W.T.4
Hu, J.5
-
28
-
-
79951952181
-
Genotype-phenotype correlations in a new case of 8p23.1 deletion and review of the literature
-
Ballarati L, Cereda A, Caselli R, Selicorni A, Recalcati MP, et al. (2011) Genotype-phenotype correlations in a new case of 8p23.1 deletion and review of the literature. Eur J Med Genet 54: 55-59.
-
(2011)
Eur J Med Genet
, vol.54
, pp. 55-59
-
-
Ballarati, L.1
Cereda, A.2
Caselli, R.3
Selicorni, A.4
Recalcati, M.P.5
-
29
-
-
84862128193
-
Human gene copy number spectra analysis in congenital heart malformations
-
Tomita-Mitchell A, Mahnke DK, Struble CA, Tuffnell ME, Stamm KD, et al. (2012) Human gene copy number spectra analysis in congenital heart malformations. Physiol Genomics 44: 518-541.
-
(2012)
Physiol Genomics
, vol.44
, pp. 518-541
-
-
Tomita-Mitchell, A.1
Mahnke, D.K.2
Struble, C.A.3
Tuffnell, M.E.4
Stamm, K.D.5
-
30
-
-
77955877152
-
[Cytogenetic and molecular genetic study of a case with 8p inverted duplication deletion syndrome]
-
Han X, Zhang JM, Jiang WT, Hu Q, Tao J, (2010) [Cytogenetic and molecular genetic study of a case with 8p inverted duplication deletion syndrome]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi 27: 361-366.
-
(2010)
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
, vol.27
, pp. 361-366
-
-
Han, X.1
Zhang, J.M.2
Jiang, W.T.3
Hu, Q.4
Tao, J.5
-
31
-
-
27144474963
-
Duplications and copy number variants of 8p23.1 are cytogenetically indistinguishable but distinct at the molecular level
-
Barber JC, Maloney V, Hollox EJ, Stuke-Sontheimer A, du Bois G, et al. (2005) Duplications and copy number variants of 8p23.1 are cytogenetically indistinguishable but distinct at the molecular level. Eur J Hum Genet 13: 1131-1136.
-
(2005)
Eur J Hum Genet
, vol.13
, pp. 1131-1136
-
-
Barber, J.C.1
Maloney, V.2
Hollox, E.J.3
Stuke-Sontheimer, A.4
du Bois, G.5
-
32
-
-
77949470049
-
8p23.1 duplication syndrome differentiated from copy number variation of the defensin cluster at prenatal diagnosis in four new families
-
Barber JC, Bunyan D, Curtis M, Robinson D, Morlot S, et al. (2010) 8p23.1 duplication syndrome differentiated from copy number variation of the defensin cluster at prenatal diagnosis in four new families. Mol Cytogenet 3: 3.
-
(2010)
Mol Cytogenet
, vol.3
, pp. 3
-
-
Barber, J.C.1
Bunyan, D.2
Curtis, M.3
Robinson, D.4
Morlot, S.5
-
33
-
-
37249022274
-
8p23.1 duplication syndrome; a novel genomic condition with unexpected complexity revealed by array CGH
-
Barber JC, Maloney VK, Huang S, Bunyan DJ, Cresswell L, et al. (2008) 8p23.1 duplication syndrome; a novel genomic condition with unexpected complexity revealed by array CGH. Eur J Hum Genet 16: 18-27.
-
(2008)
Eur J Hum Genet
, vol.16
, pp. 18-27
-
-
Barber, J.C.1
Maloney, V.K.2
Huang, S.3
Bunyan, D.J.4
Cresswell, L.5
-
34
-
-
84868449650
-
Decreased expression of SOX7 is correlated with poor prognosis in lung adenocarcinoma patients
-
Li B, Ge Z, Song S, Zhang S, Yan H, et al. (2012) Decreased expression of SOX7 is correlated with poor prognosis in lung adenocarcinoma patients. Pathol Oncol Res 18: 1039-1045.
-
(2012)
Pathol Oncol Res
, vol.18
, pp. 1039-1045
-
-
Li, B.1
Ge, Z.2
Song, S.3
Zhang, S.4
Yan, H.5
-
35
-
-
53349141350
-
Sox7 Is an independent checkpoint for beta-catenin function in prostate and colon epithelial cells
-
Guo L, Zhong D, Lau S, Liu X, Dong XY, et al. (2008) Sox7 Is an independent checkpoint for beta-catenin function in prostate and colon epithelial cells. Mol Cancer Res 6: 1421-1430.
-
(2008)
Mol Cancer Res
, vol.6
, pp. 1421-1430
-
-
Guo, L.1
Zhong, D.2
Lau, S.3
Liu, X.4
Dong, X.Y.5
-
36
-
-
0030580370
-
Cloning and characterization of Xenopus laevis xSox7 cDNA
-
Shiozawa M, Hiraoka Y, Komatsu N, Ogawa M, Sakai Y, et al. (1996) Cloning and characterization of Xenopus laevis xSox7 cDNA. Biochim Biophys Acta 1309: 73-76.
-
(1996)
Biochim Biophys Acta
, vol.1309
, pp. 73-76
-
-
Shiozawa, M.1
Hiraoka, Y.2
Komatsu, N.3
Ogawa, M.4
Sakai, Y.5
-
37
-
-
0033553650
-
Isolation and characterization of a mouse SRY-related cDNA, mSox7
-
Taniguchi K, Hiraoka Y, Ogawa M, Sakai Y, Kido S, et al. (1999) Isolation and characterization of a mouse SRY-related cDNA, mSox7. Biochim Biophys Acta 1445: 225-231.
-
(1999)
Biochim Biophys Acta
, vol.1445
, pp. 225-231
-
-
Taniguchi, K.1
Hiraoka, Y.2
Ogawa, M.3
Sakai, Y.4
Kido, S.5
-
38
-
-
76549099062
-
SoxF genes: Key players in the development of the cardio-vascular system
-
Francois M, Koopman P, Beltrame M, (2010) SoxF genes: Key players in the development of the cardio-vascular system. Int J Biochem Cell Biol 42: 445-448.
-
(2010)
Int J Biochem Cell Biol
, vol.42
, pp. 445-448
-
-
Francois, M.1
Koopman, P.2
Beltrame, M.3
-
39
-
-
0035503920
-
SOX7 transcription factor: sequence, chromosomal localisation, expression, transactivation and interference with Wnt signalling
-
Takash W, Canizares J, Bonneaud N, Poulat F, Mattei MG, et al. (2001) SOX7 transcription factor: sequence, chromosomal localisation, expression, transactivation and interference with Wnt signalling. Nucleic Acids Res 29: 4274-4283.
-
(2001)
Nucleic Acids Res
, vol.29
, pp. 4274-4283
-
-
Takash, W.1
Canizares, J.2
Bonneaud, N.3
Poulat, F.4
Mattei, M.G.5
-
40
-
-
28444446266
-
SOX7 and SOX18 are essential for cardiogenesis in Xenopus
-
Zhang C, Basta T, Klymkowsky MW, (2005) SOX7 and SOX18 are essential for cardiogenesis in Xenopus. Dev Dyn 234: 878-891.
-
(2005)
Dev Dyn
, vol.234
, pp. 878-891
-
-
Zhang, C.1
Basta, T.2
Klymkowsky, M.W.3
-
41
-
-
12944324694
-
SOX7 is an immediate-early target of VegT and regulates Nodal-related gene expression in Xenopus
-
Zhang C, Basta T, Fawcett SR, Klymkowsky MW, (2005) SOX7 is an immediate-early target of VegT and regulates Nodal-related gene expression in Xenopus. Dev Biol 278: 526-541.
-
(2005)
Dev Biol
, vol.278
, pp. 526-541
-
-
Zhang, C.1
Basta, T.2
Fawcett, S.R.3
Klymkowsky, M.W.4
-
43
-
-
0346429839
-
Enhanced cardiogenesis in embryonic stem cells overexpressing the GATA-4 transcription factor
-
Grepin C, Nemer G, Nemer M, (1997) Enhanced cardiogenesis in embryonic stem cells overexpressing the GATA-4 transcription factor. Development 124: 2387-2395.
-
(1997)
Development
, vol.124
, pp. 2387-2395
-
-
Grepin, C.1
Nemer, G.2
Nemer, M.3
-
44
-
-
0031032654
-
Over-expression of GATA-6 in Xenopus embryos blocks differentiation of heart precursors
-
Gove C, Walmsley M, Nijjar S, Bertwistle D, Guille M, et al. (1997) Over-expression of GATA-6 in Xenopus embryos blocks differentiation of heart precursors. EMBO J 16: 355-368.
-
(1997)
EMBO J
, vol.16
, pp. 355-368
-
-
Gove, C.1
Walmsley, M.2
Nijjar, S.3
Bertwistle, D.4
Guille, M.5
-
45
-
-
0037043688
-
Wnt-11 activation of a non-canonical Wnt signalling pathway is required for cardiogenesis
-
Pandur P, Lasche M, Eisenberg LM, Kuhl M, (2002) Wnt-11 activation of a non-canonical Wnt signalling pathway is required for cardiogenesis. Nature 418: 636-641.
-
(2002)
Nature
, vol.418
, pp. 636-641
-
-
Pandur, P.1
Lasche, M.2
Eisenberg, L.M.3
Kuhl, M.4
-
46
-
-
34347254242
-
Array-based functional screening for genes that regulate vascular endothelial differentiation of Flk1-positive progenitors derived from embryonic stem cells
-
Yamauchi F, Okada M, Kato K, Jakt LM, Iwata H, (2007) Array-based functional screening for genes that regulate vascular endothelial differentiation of Flk1-positive progenitors derived from embryonic stem cells. Biochim Biophys Acta 1770: 1085-1097.
-
(2007)
Biochim Biophys Acta
, vol.1770
, pp. 1085-1097
-
-
Yamauchi, F.1
Okada, M.2
Kato, K.3
Jakt, L.M.4
Iwata, H.5
-
47
-
-
61749096984
-
Lineage specification of Flk-1+ progenitors is associated with divergent Sox7 expression in cardiopoiesis
-
Nelson TJ, Chiriac A, Faustino RS, Crespo-Diaz RJ, Behfar A, et al. (2009) Lineage specification of Flk-1+ progenitors is associated with divergent Sox7 expression in cardiopoiesis. Differentiation 77: 248-255.
-
(2009)
Differentiation
, vol.77
, pp. 248-255
-
-
Nelson, T.J.1
Chiriac, A.2
Faustino, R.S.3
Crespo-Diaz, R.J.4
Behfar, A.5
-
48
-
-
74049094042
-
Sox7-sustained expression alters the balance between proliferation and differentiation of hematopoietic progenitors at the onset of blood specification
-
Gandillet A, Serrano AG, Pearson S, Lie ALM, Lacaud G, et al. (2009) Sox7-sustained expression alters the balance between proliferation and differentiation of hematopoietic progenitors at the onset of blood specification. Blood 114: 4813-4822.
-
(2009)
Blood
, vol.114
, pp. 4813-4822
-
-
Gandillet, A.1
Serrano, A.G.2
Pearson, S.3
Lie, A.L.M.4
Lacaud, G.5
-
49
-
-
84859317394
-
SOX7 regulates the expression of VE-cadherin in the haemogenic endothelium at the onset of haematopoietic development
-
Costa G, Mazan A, Gandillet A, Pearson S, Lacaud G, et al. (2012) SOX7 regulates the expression of VE-cadherin in the haemogenic endothelium at the onset of haematopoietic development. Development 139: 1587-1598.
-
(2012)
Development
, vol.139
, pp. 1587-1598
-
-
Costa, G.1
Mazan, A.2
Gandillet, A.3
Pearson, S.4
Lacaud, G.5
-
50
-
-
48149098737
-
Establishment of endoderm progenitors by SOX transcription factor expression in human embryonic stem cells
-
Seguin CA, Draper JS, Nagy A, Rossant J, (2008) Establishment of endoderm progenitors by SOX transcription factor expression in human embryonic stem cells. Cell Stem Cell 3: 182-195.
-
(2008)
Cell Stem Cell
, vol.3
, pp. 182-195
-
-
Seguin, C.A.1
Draper, J.S.2
Nagy, A.3
Rossant, J.4
-
51
-
-
77955290927
-
Endogenous Wnt/beta-catenin signaling is required for cardiac differentiation in human embryonic stem cells
-
Paige SL, Osugi T, Afanasiev OK, Pabon L, Reinecke H, et al. (2010) Endogenous Wnt/beta-catenin signaling is required for cardiac differentiation in human embryonic stem cells. PLoS One 5: e11134.
-
(2010)
PLoS One
, vol.5
-
-
Paige, S.L.1
Osugi, T.2
Afanasiev, O.K.3
Pabon, L.4
Reinecke, H.5
-
52
-
-
79960832802
-
Geometric control of cardiomyogenic induction in human pluripotent stem cells
-
Bauwens CL, Song H, Thavandiran N, Ungrin M, Masse S, et al. (2011) Geometric control of cardiomyogenic induction in human pluripotent stem cells. Tissue Eng Part A 17: 1901-1909.
-
(2011)
Tissue Eng Part A
, vol.17
, pp. 1901-1909
-
-
Bauwens, C.L.1
Song, H.2
Thavandiran, N.3
Ungrin, M.4
Masse, S.5
-
53
-
-
68049097102
-
Chromosome 8p23.1 deletions as a cause of complex congenital heart defects and diaphragmatic hernia
-
Wat MJ, Shchelochkov OA, Holder AM, Breman AM, Dagli A, et al. (2009) Chromosome 8p23.1 deletions as a cause of complex congenital heart defects and diaphragmatic hernia. Am J Med Genet A 149A: 1661-1677.
-
(2009)
Am J Med Genet A
, vol.149 A
, pp. 1661-1677
-
-
Wat, M.J.1
Shchelochkov, O.A.2
Holder, A.M.3
Breman, A.M.4
Dagli, A.5
-
54
-
-
8644267516
-
Sox7 plays crucial roles in parietal endoderm differentiation in F9 embryonal carcinoma cells through regulating Gata-4 and Gata-6 expression
-
Futaki S, Hayashi Y, Emoto T, Weber CN, Sekiguchi K, (2004) Sox7 plays crucial roles in parietal endoderm differentiation in F9 embryonal carcinoma cells through regulating Gata-4 and Gata-6 expression. Mol Cell Biol 24: 10492-10503.
-
(2004)
Mol Cell Biol
, vol.24
, pp. 10492-10503
-
-
Futaki, S.1
Hayashi, Y.2
Emoto, T.3
Weber, C.N.4
Sekiguchi, K.5
-
55
-
-
77952112456
-
The molecular genetics of congenital heart disease: a review of recent developments
-
Wolf M, Basson CT, (2010) The molecular genetics of congenital heart disease: a review of recent developments. Curr Opin Cardiol 25: 192-197.
-
(2010)
Curr Opin Cardiol
, vol.25
, pp. 192-197
-
-
Wolf, M.1
Basson, C.T.2
-
56
-
-
84871167873
-
Newborn screening for critical congenital heart disease: essential public health roles for birth defects monitoring programs
-
Olney RS, Botto LD, (2012) Newborn screening for critical congenital heart disease: essential public health roles for birth defects monitoring programs. Birth Defects Res A Clin Mol Teratol 94: 965-969.
-
(2012)
Birth Defects Res A Clin Mol Teratol
, vol.94
, pp. 965-969
-
-
Olney, R.S.1
Botto, L.D.2
-
57
-
-
84860732683
-
The Polish National Registry for Fetal Cardiac Pathology: organization, diagnoses, management, educational aspects and telemedicine endeavors
-
Slodki M, Szymkiewicz-Dangel J, Tobota Z, Seligman NS, Weiner S, et al. (2012) The Polish National Registry for Fetal Cardiac Pathology: organization, diagnoses, management, educational aspects and telemedicine endeavors. Prenat Diagn 32: 456-460.
-
(2012)
Prenat Diagn
, vol.32
, pp. 456-460
-
-
Slodki, M.1
Szymkiewicz-Dangel, J.2
Tobota, Z.3
Seligman, N.S.4
Weiner, S.5
-
58
-
-
84858663594
-
Fetal cardiac screening and variation in prenatal detection rates of congenital heart disease: why bother with screening at all?
-
Sharland G, (2012) Fetal cardiac screening and variation in prenatal detection rates of congenital heart disease: why bother with screening at all? Future Cardiol 8: 189-202.
-
(2012)
Future Cardiol
, vol.8
, pp. 189-202
-
-
Sharland, G.1
-
59
-
-
34548454381
-
Fetal echocardiographic screening in twins for congenital heart diseases
-
Li H, Meng T, Shang T, Guan YP, Zhou WW, et al. (2007) Fetal echocardiographic screening in twins for congenital heart diseases. Chin Med J (Engl) 120: 1391-1394.
-
(2007)
Chin Med J (Engl)
, vol.120
, pp. 1391-1394
-
-
Li, H.1
Meng, T.2
Shang, T.3
Guan, Y.P.4
Zhou, W.W.5
-
60
-
-
68249139764
-
Incidence of congenital heart disease in Beijing, China
-
Yang XY, Li XF, Lu XD, Liu YL, (2009) Incidence of congenital heart disease in Beijing, China. Chin Med J (Engl) 122: 1128-1132.
-
(2009)
Chin Med J (Engl)
, vol.122
, pp. 1128-1132
-
-
Yang, X.Y.1
Li, X.F.2
Lu, X.D.3
Liu, Y.L.4
-
61
-
-
84860318096
-
MLPA: a prenatal diagnostic tool for the study of congenital heart defects?
-
Mademont-Soler I, Morales C, Soler A, Clusellas N, Margarit E, et al. (2012) MLPA: a prenatal diagnostic tool for the study of congenital heart defects? Gene 500: 151-154.
-
(2012)
Gene
, vol.500
, pp. 151-154
-
-
Mademont-Soler, I.1
Morales, C.2
Soler, A.3
Clusellas, N.4
Margarit, E.5
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