-
1
-
-
0035279221
-
Congenital disorders of glycosylation: Genetic model systems lead the way
-
M. Aebi, and T. Hennet Congenital disorders of glycosylation: genetic model systems lead the way Trends Cell Biol. 11 3 2001 136 141
-
(2001)
Trends Cell Biol.
, vol.11
, Issue.3
, pp. 136-141
-
-
Aebi, M.1
Hennet, T.2
-
2
-
-
0038782391
-
Pannier and pointed P2 act sequentially to regulate Drosophila heart development
-
A.D. Alvarez, W. Shi, B.A. Wilson, and J.B. Skeath Pannier and pointed P2 act sequentially to regulate Drosophila heart development Development 130 13 2003 3015 3026
-
(2003)
Development
, vol.130
, Issue.13
, pp. 3015-3026
-
-
Alvarez, A.D.1
Shi, W.2
Wilson, B.A.3
Skeath, J.B.4
-
3
-
-
0034958793
-
Exo1-Dependent mutator mutations: Model system for studying functional interactions in mismatch repair
-
N.S. Amin, M.N. Nguyen, S. Oh, and R.D. Kolodner exo1-Dependent mutator mutations: model system for studying functional interactions in mismatch repair Mol. Cell. Biol. 21 15 2001 5142 5155
-
(2001)
Mol. Cell. Biol.
, vol.21
, Issue.15
, pp. 5142-5155
-
-
Amin, N.S.1
Nguyen, M.N.2
Oh, S.3
Kolodner, R.D.4
-
4
-
-
0142104970
-
Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome
-
S.J. Ansley, J.L. Badano, O.E. Blacque, J. Hill, B.E. Hoskins, C.C. Leitch, J.C. Kim, A.J. Ross, E.R. Eichers, T.M. Teslovich, A.K. Mah, R.C. Johnsen, J.C. Cavender, and R.A. Lewis Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome Nature 425 6958 2003 628 633
-
(2003)
Nature
, vol.425
, Issue.6958
, pp. 628-633
-
-
Ansley, S.J.1
Badano, J.L.2
Blacque, O.E.3
Hill, J.4
Hoskins, B.E.5
Leitch, C.C.6
Kim, J.C.7
Ross, A.J.8
Eichers, E.R.9
Teslovich, T.M.10
Mah, A.K.11
Johnsen, R.C.12
Cavender, J.C.13
Lewis, R.A.14
-
5
-
-
0027237596
-
Tinman and bagpipe: Two homeobox genes that determine cell fates in the dorsal mesoderm of Drosophila
-
N. Azpiazu, and M. Frasch Tinman and bagpipe: two homeobox genes that determine cell fates in the dorsal mesoderm of Drosophila Genes Dev. 7 1993 1325 1340
-
(1993)
Genes Dev.
, vol.7
, pp. 1325-1340
-
-
Azpiazu, N.1
Frasch, M.2
-
6
-
-
0030636780
-
Mutations in human TBX5 cause limb and cardiac malformation in Holt-Oram syndrome
-
C.T. Basson, D.R. Bachinsky, R.C. Lin, T. Levi, J.A. Elkins, J. Soults, D. Grayzel, E. Kroumpouzou, T.A. Traill, J. Leblanc-Straceski, B. Renault, R. Kucherlapati, J.G. Seidman, and C.E. Seidman Mutations in human TBX5 cause limb and cardiac malformation in Holt-Oram syndrome Nat. Genet. 15 1 1997 30 35
-
(1997)
Nat. Genet.
, vol.15
, Issue.1
, pp. 30-35
-
-
Basson, C.T.1
Bachinsky, D.R.2
Lin, R.C.3
Levi, T.4
Elkins, J.A.5
Soults, J.6
Grayzel, D.7
Kroumpouzou, E.8
Traill, T.A.9
Leblanc-Straceski, J.10
Renault, B.11
Kucherlapati, R.12
Seidman, J.G.13
Seidman, C.E.14
-
7
-
-
7644238411
-
Chapter 3. Model organisms in the study of development and disease
-
R.P.E.C.J. Epstein A. Wynshaw-Boris Oxford University Press New York
-
E. Bier, and W. McGinnis Chapter 3. Model organisms in the study of development and disease R.P.E.C.J. Epstein A. Wynshaw-Boris Molecular Basis of Inborn Errors of Development 2004 Oxford University Press New York 25 45
-
(2004)
Molecular Basis of Inborn Errors of Development
, pp. 25-45
-
-
Bier, E.1
McGinnis, W.2
-
8
-
-
0027282774
-
The gene tinman is required for specification of the heart and visceral muscles in Drosophila
-
R. Bodmer The gene tinman is required for specification of the heart and visceral muscles in Drosophila Development 118 3 1993 719 729
-
(1993)
Development
, vol.118
, Issue.3
, pp. 719-729
-
-
Bodmer, R.1
-
9
-
-
0028959673
-
Heart development in Drosophila and its relationship to vertebrate systems
-
R. Bodmer Heart development in Drosophila and its relationship to vertebrate systems Trends Cardiovasc. Med. 5 1995 21 28
-
(1995)
Trends Cardiovasc. Med.
, vol.5
, pp. 21-28
-
-
Bodmer, R.1
-
10
-
-
0002453643
-
Genetic determination of Drosophila heart development
-
N. Rosenthal R. Harvey Academic Press San Diego
-
R. Bodmer, and M. Frasch Genetic determination of Drosophila heart development N. Rosenthal R. Harvey Heart Development 1999 Academic Press San Diego 65 90
-
(1999)
Heart Development
, pp. 65-90
-
-
Bodmer, R.1
Frasch, M.2
-
11
-
-
0031805934
-
Heart development in Drosophila and vertebrates: Conservation of molecular mechanisms
-
R. Bodmer, and T.V. Venkatesh Heart development in Drosophila and vertebrates: conservation of molecular mechanisms Dev. Genet. 22 3 1998 181 186
-
(1998)
Dev. Genet.
, vol.22
, Issue.3
, pp. 181-186
-
-
Bodmer, R.1
Venkatesh, T.V.2
-
12
-
-
0037418307
-
Sex- and age-dependent human transcriptome variability: Implications for chronic heart failure
-
K.R. Boheler, M. Volkova, C. Morrell, R. Garg, Y. Zhu, K. Margulies, A.M. Seymour, and E.G. Lakatta Sex- and age-dependent human transcriptome variability: implications for chronic heart failure Proc. Natl. Acad. Sci. U. S. A. 100 5 2003 2754 2759
-
(2003)
Proc. Natl. Acad. Sci. U. S. A.
, vol.100
, Issue.5
, pp. 2754-2759
-
-
Boheler, K.R.1
Volkova, M.2
Morrell, C.3
Garg, R.4
Zhu, Y.5
Margulies, K.6
Seymour, A.M.7
Lakatta, E.G.8
-
13
-
-
0027160708
-
Targeted gene expression as a means of altering cell fates and generating dominant phenotypes
-
A.H. Brand, and N. Perrimon Targeted gene expression as a means of altering cell fates and generating dominant phenotypes Development 118 2 1993 401 415
-
(1993)
Development
, vol.118
, Issue.2
, pp. 401-415
-
-
Brand, A.H.1
Perrimon, N.2
-
14
-
-
0034028904
-
Mutations in the human delta homologue, DLL3, cause axial skeletal defects in spondylocostal dysostosis
-
M.P. Bulman, K. Kusumi, T.M. Frayling, C. McKeown, C. Garrett, E.S. Lander, R. Krumlauf, A.T. Hattersley, S. Ellard, and P.D. Turnpenny Mutations in the human delta homologue, DLL3, cause axial skeletal defects in spondylocostal dysostosis Nat. Genet. 24 4 2000 438 441
-
(2000)
Nat. Genet.
, vol.24
, Issue.4
, pp. 438-441
-
-
Bulman, M.P.1
Kusumi, K.2
Frayling, T.M.3
McKeown, C.4
Garrett, C.5
Lander, E.S.6
Krumlauf, R.7
Hattersley, A.T.8
Ellard, S.9
Turnpenny, P.D.10
-
15
-
-
0035929315
-
Genetics. The land between Mendelian and multifactorial inheritance
-
A.H. Burghes, H.E. Vaessin, and A. de La Chapelle Genetics. The land between Mendelian and multifactorial inheritance Science 293 5538 2001 2213 2214
-
(2001)
Science
, vol.293
, Issue.5538
, pp. 2213-2214
-
-
Burghes, A.H.1
Vaessin, H.E.2
De La Chapelle, A.3
-
16
-
-
0026075602
-
Early-onset Alzheimer's disease caused by mutations at codon 717 of the beta-amyloid precursor protein gene
-
M.C. Chartier-Harlin, F. Crawford, H. Houlden, A. Warren, D. Hughes, L. Fidani, A. Goate, M. Rossor, P. Roques, and J. Hardy Early-onset Alzheimer's disease caused by mutations at codon 717 of the beta-amyloid precursor protein gene Nature 353 6347 1991 844 846
-
(1991)
Nature
, vol.353
, Issue.6347
, pp. 844-846
-
-
Chartier-Harlin, M.C.1
Crawford, F.2
Houlden, H.3
Warren, A.4
Hughes, D.5
Fidani, L.6
Goate, A.7
Rossor, M.8
Roques, P.9
Hardy, J.10
-
17
-
-
0034283842
-
Genetics of heart development
-
J.N. Chen, and M.C. Fishman Genetics of heart development Trends Genet. 16 9 2000 383 388
-
(2000)
Trends Genet.
, vol.16
, Issue.9
, pp. 383-388
-
-
Chen, J.N.1
Fishman, M.C.2
-
18
-
-
0036081081
-
Homophila: Human disease gene cognates in Drosophila
-
S. Chien, L.T. Reiter, E. Bier, and M. Gribskov Homophila: human disease gene cognates in Drosophila Nucleic Acids Res. 30 1 2002 149 151
-
(2002)
Nucleic Acids Res.
, vol.30
, Issue.1
, pp. 149-151
-
-
Chien, S.1
Reiter, L.T.2
Bier, E.3
Gribskov, M.4
-
19
-
-
0036071021
-
Episodic coronary artery vasospasm and hypertension develop in the absence of Sur2 K(ATP) channels
-
W.A. Chutkow, J. Pu, M.T. Wheeler, T. Wada, J.C. Makielski, C.F. Burant, and E.M. McNally Episodic coronary artery vasospasm and hypertension develop in the absence of Sur2 K(ATP) channels J. Clin. Invest. 110 2 2002 203 208
-
(2002)
J. Clin. Invest.
, vol.110
, Issue.2
, pp. 203-208
-
-
Chutkow, W.A.1
Pu, J.2
Wheeler, M.T.3
Wada, T.4
Makielski, J.C.5
Burant, C.F.6
McNally, E.M.7
-
20
-
-
0036608009
-
Control of cardiac development by an evolutionarily conserved transcriptional network
-
R.M. Cripps, and E.N. Olson Control of cardiac development by an evolutionarily conserved transcriptional network Dev. Biol. 246 1 2002 14 28
-
(2002)
Dev. Biol.
, vol.246
, Issue.1
, pp. 14-28
-
-
Cripps, R.M.1
Olson, E.N.2
-
21
-
-
0028914969
-
A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome
-
M.E. Curran, I. Splawski, K.W. Timothy, G.M. Vincent, E.D. Green, and M.T. Keating A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome Cell 80 5 1995 795 803
-
(1995)
Cell
, vol.80
, Issue.5
, pp. 795-803
-
-
Curran, M.E.1
Splawski, I.2
Timothy, K.W.3
Vincent, G.M.4
Green, E.D.5
Keating, M.T.6
-
22
-
-
0141593589
-
Evolutionary origins of the vertebrate heart: Specification of the cardiac lineage in Ciona intestinalis
-
B. Davidson, and M. Levine Evolutionary origins of the vertebrate heart: specification of the cardiac lineage in Ciona intestinalis Proc. Natl. Acad. Sci. U. S. A. 100 20 2003 11469 11473
-
(2003)
Proc. Natl. Acad. Sci. U. S. A.
, vol.100
, Issue.20
, pp. 11469-11473
-
-
Davidson, B.1
Levine, M.2
-
23
-
-
0029440590
-
A congenital heart defect in Drosophila caused by an action-potential mutation
-
H. Dowse, J. Ringo, J. Power, E. Johnson, K. Kinney, and L. White A congenital heart defect in Drosophila caused by an action-potential mutation J. Neurogenet. 10 3 1995 153 168
-
(1995)
J. Neurogenet.
, vol.10
, Issue.3
, pp. 153-168
-
-
Dowse, H.1
Ringo, J.2
Power, J.3
Johnson, E.4
Kinney, K.5
White, L.6
-
24
-
-
0036741796
-
GAL4 system in Drosophila: A fly geneticist's Swiss army knife
-
J.B. Duffy GAL4 system in Drosophila: a fly geneticist's Swiss army knife Genesis 34 1-2 2002 1 15
-
(2002)
Genesis
, vol.34
, Issue.12
, pp. 1-15
-
-
Duffy, J.B.1
-
25
-
-
0028903248
-
Induction of visceral and cardiac mesoderm by ectodermal Dpp in early Drosophila embryo
-
M. Frasch Induction of visceral and cardiac mesoderm by ectodermal Dpp in early Drosophila embryo Nature 374 1995 464 467
-
(1995)
Nature
, vol.374
, pp. 464-467
-
-
Frasch, M.1
-
26
-
-
0033942996
-
Genetic analysis of ion channel dysfunction in Drosophila
-
B. Ganetzky Genetic analysis of ion channel dysfunction in Drosophila Kidney Int. 57 3 2000 766 771
-
(2000)
Kidney Int.
, vol.57
, Issue.3
, pp. 766-771
-
-
Ganetzky, B.1
-
27
-
-
0043267988
-
GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5
-
V. Garg, I.S. Kathiriya, R. Barnes, M.K. Schluterman, I.N. King, C.A. Butler, C.R. Rothrock, R.S. Eapen, K. Hirayama-Yamada, K. Joo, R. Matsuoka, J.C. Cohen, and D. Srivastava GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5 Nature 424 6947 2003 443 447
-
(2003)
Nature
, vol.424
, Issue.6947
, pp. 443-447
-
-
Garg, V.1
Kathiriya, I.S.2
Barnes, R.3
Schluterman, M.K.4
King, I.N.5
Butler, C.A.6
Rothrock, C.R.7
Eapen, R.S.8
Hirayama-Yamada, K.9
Joo, K.10
Matsuoka, R.11
Cohen, J.C.12
Srivastava, D.13
-
28
-
-
0032005387
-
Shaping animal body plans in development and evolution by modulation of Hox expression patterns
-
G. Gellon, and W. McGinnis Shaping animal body plans in development and evolution by modulation of Hox expression patterns BioEssays 20 2 1998 116 125
-
(1998)
BioEssays
, vol.20
, Issue.2
, pp. 116-125
-
-
Gellon, G.1
McGinnis, W.2
-
29
-
-
79959503826
-
The international HapMap project
-
R.A. Gibbs, J.W. Belmont, P. Hardenbol, T.D. Willis, F. Yu, H. Yang, L.Y. Ch'ang, W. Huang, B. Liu, Y. Shen, P.K. Tam, L.C. Tsui, M.M. Waye, and J.T. Wong The international HapMap project Nature 426 6968 2003 789 796
-
(2003)
Nature
, vol.426
, Issue.6968
, pp. 789-796
-
-
Gibbs, R.A.1
Belmont, J.W.2
Hardenbol, P.3
Willis, T.D.4
Yu, F.5
Yang, H.6
Ch'Ang, L.Y.7
Huang, W.8
Liu, B.9
Shen, Y.10
Tam, P.K.11
Tsui, L.C.12
Waye, M.M.13
Wong, J.T.14
-
30
-
-
0026088977
-
Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease
-
A. Goate, M.C. Chartier-Harlin, M. Mullan, J. Brown, F. Crawford, L. Fidani, L. Giuffra, A. Haynes, N. Irving, and L. James Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease Nature 349 6311 1991 704 706
-
(1991)
Nature
, vol.349
, Issue.6311
, pp. 704-706
-
-
Goate, A.1
Chartier-Harlin, M.C.2
Mullan, M.3
Brown, J.4
Crawford, F.5
Fidani, L.6
Giuffra, L.7
Haynes, A.8
Irving, N.9
James, L.10
-
31
-
-
1542329546
-
Deficiency of the first mannosylation step in the N-glycosylation pathway causes congenital disorder of glycosylation type Ik
-
C.E. Grubenmann, C.G. Frank, A.J. Hulsmeier, E. Schollen, G. Matthijs, E. Mayatepek, E.G. Berger, M. Aebi, and T. Hennet Deficiency of the first mannosylation step in the N-glycosylation pathway causes congenital disorder of glycosylation type Ik Hum. Mol. Genet. 13 2004 535 542
-
(2004)
Hum. Mol. Genet.
, vol.13
, pp. 535-542
-
-
Grubenmann, C.E.1
Frank, C.G.2
Hulsmeier, A.J.3
Schollen, E.4
Matthijs, G.5
Mayatepek, E.6
Berger, E.G.7
Aebi, M.8
Hennet, T.9
-
32
-
-
10744224341
-
Expression profiling of human idiopathic dilated cardiomyopathy
-
R. Grzeskowiak, H. Witt, M. Drungowski, R. Thermann, S. Hennig, A. Perrot, K.J. Osterziel, D. Klingbiel, S. Scheid, R. Spang, H. Lehrach, and P. Ruiz Expression profiling of human idiopathic dilated cardiomyopathy Cardiovasc. Res. 59 2 2003 400 411
-
(2003)
Cardiovasc. Res.
, vol.59
, Issue.2
, pp. 400-411
-
-
Grzeskowiak, R.1
Witt, H.2
Drungowski, M.3
Thermann, R.4
Hennig, S.5
Perrot, A.6
Osterziel, K.J.7
Klingbiel, D.8
Scheid, S.9
Spang, R.10
Lehrach, H.11
Ruiz, P.12
-
33
-
-
0037133619
-
A screen for dominant mutations applied to components in the Drosophila EGF-R pathway
-
A. Guichard, S. Srinivasan, G. Zimm, and E. Bier A screen for dominant mutations applied to components in the Drosophila EGF-R pathway Proc. Natl. Acad. Sci. U. S. A. 99 6 2002 3752 3757
-
(2002)
Proc. Natl. Acad. Sci. U. S. A.
, vol.99
, Issue.6
, pp. 3752-3757
-
-
Guichard, A.1
Srinivasan, S.2
Zimm, G.3
Bier, E.4
-
34
-
-
0035098436
-
Mice lacking the homologue of the human 22q11.2 gene CRKL phenocopy neurocristopathies of DiGeorge syndrome
-
D.L. Guris, J. Fantes, D. Tara, B.J. Druker, and A. Imamoto Mice lacking the homologue of the human 22q11.2 gene CRKL phenocopy neurocristopathies of DiGeorge syndrome Nat. Genet. 27 3 2001 293 298
-
(2001)
Nat. Genet.
, vol.27
, Issue.3
, pp. 293-298
-
-
Guris, D.L.1
Fantes, J.2
Tara, D.3
Druker, B.J.4
Imamoto, A.5
-
35
-
-
0038782384
-
Myogenic cells fates are antagonized by Notch only in asymmetric lineages of the Drosophila heart, with or without cell division
-
Z. Han, and R. Bodmer Myogenic cells fates are antagonized by Notch only in asymmetric lineages of the Drosophila heart, with or without cell division Development 130 13 2003 3039 3051
-
(2003)
Development
, vol.130
, Issue.13
, pp. 3039-3051
-
-
Han, Z.1
Bodmer, R.2
-
36
-
-
0036937281
-
Transcriptional integration of competence modulated by mutual repression generates cell-type specificity within the cardiogenic mesoderm
-
Z. Han, M. Fujioka, M. Su, M. Liu, J.B. Jaynes, and R. Bodmer Transcriptional integration of competence modulated by mutual repression generates cell-type specificity within the cardiogenic mesoderm Dev. Biol. 252 2 2002 225 240
-
(2002)
Dev. Biol.
, vol.252
, Issue.2
, pp. 225-240
-
-
Han, Z.1
Fujioka, M.2
Su, M.3
Liu, M.4
Jaynes, J.B.5
Bodmer, R.6
-
37
-
-
0032574767
-
Rescue of Caenorhabditis elegans pharyngeal development by a vertebrate heart specification gene
-
C. Haun, J. Alexander, D.Y. Stainier, and P.G. Okkema Rescue of Caenorhabditis elegans pharyngeal development by a vertebrate heart specification gene Proc. Natl. Acad. Sci. U. S. A. 95 9 1998 5072 5075
-
(1998)
Proc. Natl. Acad. Sci. U. S. A.
, vol.95
, Issue.9
, pp. 5072-5075
-
-
Haun, C.1
Alexander, J.2
Stainier, D.Y.3
Okkema, P.G.4
-
38
-
-
0037333508
-
AmphiNk2-tin, an amphioxus homeobox gene expressed in myocardial progenitors: Insights into evolution of the vertebrate heart
-
N.D. Holland, T.V. Venkatesh, L.Z. Holland, D.K. Jacobs, and R. Bodmer AmphiNk2-tin, an amphioxus homeobox gene expressed in myocardial progenitors: insights into evolution of the vertebrate heart Dev. Biol. 255 1 2003 128 137
-
(2003)
Dev. Biol.
, vol.255
, Issue.1
, pp. 128-137
-
-
Holland, N.D.1
Venkatesh, T.V.2
Holland, L.Z.3
Jacobs, D.K.4
Bodmer, R.5
-
39
-
-
0033536073
-
A mutation in the human ortholog of the Saccharomyces cerevisiae ALG6 gene causes carbohydrate-deficient glycoprotein syndrome type-Ic
-
T. Imbach, P. Burda, P. Kuhnert, R.A. Wevers, M. Aebi, E.G. Berger, and T. Hennet A mutation in the human ortholog of the Saccharomyces cerevisiae ALG6 gene causes carbohydrate-deficient glycoprotein syndrome type-Ic Proc. Natl. Acad. Sci. U. S. A. 96 12 1999 6982 6987
-
(1999)
Proc. Natl. Acad. Sci. U. S. A.
, vol.96
, Issue.12
, pp. 6982-6987
-
-
Imbach, T.1
Burda, P.2
Kuhnert, P.3
Wevers, R.A.4
Aebi, M.5
Berger, E.G.6
Hennet, T.7
-
40
-
-
0033968250
-
Deficiency of dolichol-phosphate-mannose synthase-1 causes congenital disorder of glycosylation type Ie
-
T. Imbach, B. Schenk, E. Schollen, P. Burda, A. Stutz, S. Grunewald, N.M. Bailie, M.D. King, J. Jaeken, G. Matthijs, E.G. Berger, M. Aebi, and T. Hennet Deficiency of dolichol-phosphate-mannose synthase-1 causes congenital disorder of glycosylation type Ie J. Clin. Invest. 105 2 2000 233 239
-
(2000)
J. Clin. Invest.
, vol.105
, Issue.2
, pp. 233-239
-
-
Imbach, T.1
Schenk, B.2
Schollen, E.3
Burda, P.4
Stutz, A.5
Grunewald, S.6
Bailie, N.M.7
King, M.D.8
Jaeken, J.9
Matthijs, G.10
Berger, E.G.11
Aebi, M.12
Hennet, T.13
-
41
-
-
0031858797
-
Genetic and pharmacological identification of ion channels central to the Drosophila cardiac pacemaker
-
E. Johnson, J. Ringo, N. Bray, and H. Dowse Genetic and pharmacological identification of ion channels central to the Drosophila cardiac pacemaker J. Neurogenet. 12 1 1998 1 24
-
(1998)
J. Neurogenet.
, vol.12
, Issue.1
, pp. 1-24
-
-
Johnson, E.1
Ringo, J.2
Bray, N.3
Dowse, H.4
-
42
-
-
34250134008
-
Mutations affecting the pattern of the larval cuticle in Drosophila melanogaster: II. Zygotic loci on the third chromosome
-
G. Jurgens, E. Wieschaus, C. Nusslein-Volhard, and H. Kluding Mutations affecting the pattern of the larval cuticle in Drosophila melanogaster: II. Zygotic loci on the third chromosome Roux's Arch. Dev. Biol. 193 1984 283 295
-
(1984)
Roux's Arch. Dev. Biol.
, vol.193
, pp. 283-295
-
-
Jurgens, G.1
Wieschaus, E.2
Nusslein-Volhard, C.3
Kluding, H.4
-
43
-
-
0035475115
-
Exploring the molecular basis of Bardet-Biedl syndrome
-
N. Katsanis, J.R. Lupski, and P.L. Beales Exploring the molecular basis of Bardet-Biedl syndrome Hum. Mol. Genet. 10 20 2001 2293 2299
-
(2001)
Hum. Mol. Genet.
, vol.10
, Issue.20
, pp. 2293-2299
-
-
Katsanis, N.1
Lupski, J.R.2
Beales, P.L.3
-
44
-
-
0035929273
-
Triallelic inheritance in Bardet-Biedl syndrome, a Mendelian recessive disorder
-
N. Katsanis, S.J. Ansley, J.L. Badano, E.R. Eichers, R.A. Lewis, B.E. Hoskins, P.J. Scambler, W.S. Davidson, P.L. Beales, and J.R. Lupski Triallelic inheritance in Bardet-Biedl syndrome, a Mendelian recessive disorder Science 293 5538 2001 2256 2259
-
(2001)
Science
, vol.293
, Issue.5538
, pp. 2256-2259
-
-
Katsanis, N.1
Ansley, S.J.2
Badano, J.L.3
Eichers, E.R.4
Lewis, R.A.5
Hoskins, B.E.6
Scambler, P.J.7
Davidson, W.S.8
Beales, P.L.9
Lupski, J.R.10
-
45
-
-
0038444550
-
Gata factor Pannier is required to establish competence for heart progenitor formation
-
S.L. Klinedinst, and R. Bodmer Gata factor Pannier is required to establish competence for heart progenitor formation Development 130 13 2003 3027 3038
-
(2003)
Development
, vol.130
, Issue.13
, pp. 3027-3038
-
-
Klinedinst, S.L.1
Bodmer, R.2
-
46
-
-
0028867842
-
Mismatch repair: Mechanisms and relationship to cancer susceptibility
-
R.D. Kolodner Mismatch repair: mechanisms and relationship to cancer susceptibility Trends Biochem. Sci. 20 10 1995 397 401
-
(1995)
Trends Biochem. Sci.
, vol.20
, Issue.10
, pp. 397-401
-
-
Kolodner, R.D.1
-
47
-
-
0344118852
-
Group 6: Pleiotropy and multivariate analysis
-
P. Kraft, and M. De Andrade Group 6: pleiotropy and multivariate analysis Genet. Epidemiol. 25 Suppl. 1 2003 S50 S56
-
(2003)
Genet. Epidemiol.
, vol.25
, Issue.1
-
-
Kraft, P.1
De Andrade, M.2
-
48
-
-
0034212710
-
Notch signaling is essential for vascular morphogenesis in mice
-
L.T. Krebs, Y. Xue, C.R. Norton, J.R. Shutter, M. Maguire, J.P. Sundberg, D. Gallahan, V. Closson, J. Kitajewski, R. Callahan, G.H. Smith, K.L. Stark, and T. Gridley Notch signaling is essential for vascular morphogenesis in mice Genes Dev. 14 11 2000 1343 1352
-
(2000)
Genes Dev.
, vol.14
, Issue.11
, pp. 1343-1352
-
-
Krebs, L.T.1
Xue, Y.2
Norton, C.R.3
Shutter, J.R.4
Maguire, M.5
Sundberg, J.P.6
Gallahan, D.7
Closson, V.8
Kitajewski, J.9
Callahan, R.10
Smith, G.H.11
Stark, K.L.12
Gridley, T.13
-
49
-
-
0028797783
-
Identification and characterization of a spinal muscular atrophy-determining gene
-
S. Lefebvre, L. Burglen, S. Reboullet, O. Clermont, P. Burlet, L. Viollet, B. Benichou, C. Cruaud, P. Millasseau, and M. Zeviani Identification and characterization of a spinal muscular atrophy-determining gene Cell 80 1 1995 155 165
-
(1995)
Cell
, vol.80
, Issue.1
, pp. 155-165
-
-
Lefebvre, S.1
Burglen, L.2
Reboullet, S.3
Clermont, O.4
Burlet, P.5
Viollet, L.6
Benichou, B.7
Cruaud, C.8
Millasseau, P.9
Zeviani, M.10
-
50
-
-
0029150716
-
A familial Alzheimer's disease locus on chromosome 1
-
E. Levy-Lahad, E.M. Wijsman, E. Nemens, L. Anderson, K.A. Goddard, J.L. Weber, T.D. Bird, and G.D. Schellenberg A familial Alzheimer's disease locus on chromosome 1 Science 269 5226 1995 970 973
-
(1995)
Science
, vol.269
, Issue.5226
, pp. 970-973
-
-
Levy-Lahad, E.1
Wijsman, E.M.2
Nemens, E.3
Anderson, L.4
Goddard, K.A.5
Weber, J.L.6
Bird, T.D.7
Schellenberg, G.D.8
-
51
-
-
0030804005
-
Elastin point mutations cause an obstructive vascular disease, supravalvular aortic stenosis
-
D.Y. Li, A.E. Toland, B.B. Boak, D.L. Atkinson, G.J. Ensing, C.A. Morris, and M.T. Keating Elastin point mutations cause an obstructive vascular disease, supravalvular aortic stenosis Hum. Mol. Genet. 6 7 1997 1021 1028
-
(1997)
Hum. Mol. Genet.
, vol.6
, Issue.7
, pp. 1021-1028
-
-
Li, D.Y.1
Toland, A.E.2
Boak, B.B.3
Atkinson, D.L.4
Ensing, G.J.5
Morris, C.A.6
Keating, M.T.7
-
52
-
-
0029968116
-
A transcription map in the CATCH22 critical region: Identification, mapping, and ordering of four novel transcripts expressed in heart
-
E.A. Lindsay, P. Rizzu, R. Antonacci, V. Jurecic, J. Delmas-Mata, C.C. Lee, U.J. Kim, P.J. Scambler, and A. Baldini A transcription map in the CATCH22 critical region: identification, mapping, and ordering of four novel transcripts expressed in heart Genomics 32 1 1996 104 112
-
(1996)
Genomics
, vol.32
, Issue.1
, pp. 104-112
-
-
Lindsay, E.A.1
Rizzu, P.2
Antonacci, R.3
Jurecic, V.4
Delmas-Mata, J.5
Lee, C.C.6
Kim, U.J.7
Scambler, P.J.8
Baldini, A.9
-
53
-
-
0035263599
-
Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice
-
E.A. Lindsay, F. Vitelli, H. Su, M. Morishima, T. Huynh, T. Pramparo, V. Jurecic, G. Ogunrinu, H.F. Sutherland, P.J. Scambler, A. Bradley, and A. Baldini Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice Nature 410 6824 2001 97 101
-
(2001)
Nature
, vol.410
, Issue.6824
, pp. 97-101
-
-
Lindsay, E.A.1
Vitelli, F.2
Su, H.3
Morishima, M.4
Huynh, T.5
Pramparo, T.6
Jurecic, V.7
Ogunrinu, G.8
Sutherland, H.F.9
Scambler, P.J.10
Bradley, A.11
Baldini, A.12
-
54
-
-
0034967570
-
A role for the COUP-TF-related gene seven-up in the diversification of cardioblast identities in the dorsal vessel of Drosophila
-
P.C. Lo, and M. Frasch A role for the COUP-TF-related gene seven-up in the diversification of cardioblast identities in the dorsal vessel of Drosophila Mech. Dev. 104 1-2 2001 49 60
-
(2001)
Mech. Dev.
, vol.104
, Issue.12
, pp. 49-60
-
-
Lo, P.C.1
Frasch, M.2
-
55
-
-
0036011238
-
The patterns of wingless, decapentaplegic, and tinman position the Drosophila heart
-
W.K. Lockwood, and R. Bodmer The patterns of wingless, decapentaplegic, and tinman position the Drosophila heart Mech. Dev. 114 1-2 2002 13 26
-
(2002)
Mech. Dev.
, vol.114
, Issue.12
, pp. 13-26
-
-
Lockwood, W.K.1
Bodmer, R.2
-
56
-
-
0036849903
-
The Hox gene abdominal-A specifies heart cell fate in the Drosophila dorsal vessel
-
T.L. Lovato, T.P. Nguyen, M.R. Molina, and R.M. Cripps The Hox gene abdominal-A specifies heart cell fate in the Drosophila dorsal vessel Development 129 21 2002 5019 5027
-
(2002)
Development
, vol.129
, Issue.21
, pp. 5019-5027
-
-
Lovato, T.L.1
Nguyen, T.P.2
Molina, M.R.3
Cripps, R.M.4
-
57
-
-
0036368287
-
Molecular analysis of spinal muscular atrophy and modification of the phenotype by SMN2
-
M.D. Mailman, J.W. Heinz, A.C. Papp, P.J. Snyder, M.S. Sedra, B. Wirth, A.H. Burghes, and T.W. Prior Molecular analysis of spinal muscular atrophy and modification of the phenotype by SMN2 Genet. Med. 4 1 2002 20 26
-
(2002)
Genet. Med.
, vol.4
, Issue.1
, pp. 20-26
-
-
Mailman, M.D.1
Heinz, J.W.2
Papp, A.C.3
Snyder, P.J.4
Sedra, M.S.5
Wirth, B.6
Burghes, A.H.7
Prior, T.W.8
-
58
-
-
0034766036
-
Ostia, the inflow tracts of the Drosophila heart, develop from a genetically distinct subset of cardial cells
-
M.R. Molina, and R.M. Cripps Ostia, the inflow tracts of the Drosophila heart, develop from a genetically distinct subset of cardial cells Mech. Dev. 109 1 2001 51 59
-
(2001)
Mech. Dev.
, vol.109
, Issue.1
, pp. 51-59
-
-
Molina, M.R.1
Cripps, R.M.2
-
59
-
-
0025950987
-
A mutation in the amyloid precursor protein associated with hereditary Alzheimer's disease
-
J. Murrell, M. Farlow, B. Ghetti, and M.D. Benson A mutation in the amyloid precursor protein associated with hereditary Alzheimer's disease Science 254 5028 1991 97 99
-
(1991)
Science
, vol.254
, Issue.5028
, pp. 97-99
-
-
Murrell, J.1
Farlow, M.2
Ghetti, B.3
Benson, M.D.4
-
60
-
-
0032830934
-
A novel sulfonylurea receptor family member expressed in the embryonic Drosophila dorsal vessel and tracheal system
-
I. Nasonkin, A. Alikasifoglu, C. Ambrose, P. Cahill, M. Cheng, A. Sarniak, M. Egan, and P.M. Thomas A novel sulfonylurea receptor family member expressed in the embryonic Drosophila dorsal vessel and tracheal system J. Biol. Chem. 274 41 1999 29420 29425
-
(1999)
J. Biol. Chem.
, vol.274
, Issue.41
, pp. 29420-29425
-
-
Nasonkin, I.1
Alikasifoglu, A.2
Ambrose, C.3
Cahill, P.4
Cheng, M.5
Sarniak, A.6
Egan, M.7
Thomas, P.M.8
-
61
-
-
0019133661
-
Mutations affecting segment number and polarity in Drosophila
-
C. Nusslein-Volhard, and E. Wieschaus Mutations affecting segment number and polarity in Drosophila Nature 287 1980 795 801
-
(1980)
Nature
, vol.287
, pp. 795-801
-
-
Nusslein-Volhard, C.1
Wieschaus, E.2
-
62
-
-
0008125299
-
Mutations affecting the pattern of the larval cuticle in Drosophila melanogaster: I. Zygotic loci on the second chromosome
-
C. Nusslein-Volhard, E. Wieschaus, and H. Kluding Mutations affecting the pattern of the larval cuticle in Drosophila melanogaster: I. Zygotic loci on the second chromosome Roux's Arch. Dev. Biol. 193 1984 267 282
-
(1984)
Roux's Arch. Dev. Biol.
, vol.193
, pp. 267-282
-
-
Nusslein-Volhard, C.1
Wieschaus, E.2
Kluding, H.3
-
63
-
-
0035947742
-
Age-associated cardiac dysfunction in Drosophila melanogaster
-
G. Paternostro, C. Vignola, D.U. Bartsch, J.H. Omens, A.D. McCulloch, and J.C. Reed Age-associated cardiac dysfunction in Drosophila melanogaster Circ. Res. 88 10 2001 1053 1058
-
(2001)
Circ. Res.
, vol.88
, Issue.10
, pp. 1053-1058
-
-
Paternostro, G.1
Vignola, C.2
Bartsch, D.U.3
Omens, J.H.4
McCulloch, A.D.5
Reed, J.C.6
-
64
-
-
0035992788
-
Developmental paradigms in heart disease: Insights from tinman
-
O.W. Prall, D.A. Elliott, and R.P. Harvey Developmental paradigms in heart disease: insights from tinman Ann. Med. 34 3 2002 148 156
-
(2002)
Ann. Med.
, vol.34
, Issue.3
, pp. 148-156
-
-
Prall, O.W.1
Elliott, D.A.2
Harvey, R.P.3
-
65
-
-
12244276719
-
A genome scan for hypertension susceptibility loci in populations of Chinese and Japanese origins
-
K. Ranade, D. Hinds, C.A. Hsiung, L.M. Chuang, M.S. Chang, Y.T. Chen, R. Pesich, J. Hebert, Y.D. Chen, V. Dzau, R. Olshen, D. Curb, D. Botstein, and D.R. Cox A genome scan for hypertension susceptibility loci in populations of Chinese and Japanese origins Am. J. Hypertens. 16 2 2003 158 162
-
(2003)
Am. J. Hypertens.
, vol.16
, Issue.2
, pp. 158-162
-
-
Ranade, K.1
Hinds, D.2
Hsiung, C.A.3
Chuang, L.M.4
Chang, M.S.5
Chen, Y.T.6
Pesich, R.7
Hebert, J.8
Chen, Y.D.9
Dzau, V.10
Olshen, R.11
Curb, D.12
Botstein, D.13
Cox, D.R.14
-
66
-
-
0034837386
-
A systematic analysis of human disease-associated gene sequences in Drosophila melanogaster
-
L.T. Reiter, L. Potocki, S. Chien, M. Gribskov, and E. Bier A systematic analysis of human disease-associated gene sequences in Drosophila melanogaster Genome Res. 11 6 2001 1114 1125
-
(2001)
Genome Res.
, vol.11
, Issue.6
, pp. 1114-1125
-
-
Reiter, L.T.1
Potocki, L.2
Chien, S.3
Gribskov, M.4
Bier, E.5
-
67
-
-
0029101491
-
Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene
-
E.I. Rogaev, R. Sherrington, E.A. Rogaeva, G. Levesque, M. Ikeda, Y. Liang, H. Chi, C. Lin, K. Holman, and T. Tsuda Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene Nature 376 6543 1995 775 778
-
(1995)
Nature
, vol.376
, Issue.6543
, pp. 775-778
-
-
Rogaev, E.I.1
Sherrington, R.2
Rogaeva, E.A.3
Levesque, G.4
Ikeda, M.5
Liang, Y.6
Chi, H.7
Lin, C.8
Holman, K.9
Tsuda, T.10
-
68
-
-
0032479573
-
Congenital heart disease caused by mutations in the transcription factor NKX2-5
-
J.J. Schott, D.W. Benson, C.T. Basson, W. Pease, G.M. Silberbach, J.P. Moak, B.J. Maron, C.E. Seidman, and J.G. Seidman Congenital heart disease caused by mutations in the transcription factor NKX2-5 Science 281 5373 1998 108 111
-
(1998)
Science
, vol.281
, Issue.5373
, pp. 108-111
-
-
Schott, J.J.1
Benson, D.W.2
Basson, C.T.3
Pease, W.4
Silberbach, G.M.5
Moak, J.P.6
Maron, B.J.7
Seidman, C.E.8
Seidman, J.G.9
-
69
-
-
0031018002
-
A role for bone morphogenetic proteins in the induction of cardiac myogenesis
-
T.M. Schultheiss, J.B. Burch, and A.B. Lassar A role for bone morphogenetic proteins in the induction of cardiac myogenesis Genes Dev. 11 4 1997 451 462
-
(1997)
Genes Dev.
, vol.11
, Issue.4
, pp. 451-462
-
-
Schultheiss, T.M.1
Burch, J.B.2
Lassar, A.B.3
-
71
-
-
0029004341
-
Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease
-
R. Sherrington, E.I. Rogaev, Y. Liang, E.A. Rogaeva, G. Levesque, M. Ikeda, H. Chi, C. Lin, G. Li, and K. Holman Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease Nature 375 6534 1995 754 760
-
(1995)
Nature
, vol.375
, Issue.6534
, pp. 754-760
-
-
Sherrington, R.1
Rogaev, E.I.2
Liang, Y.3
Rogaeva, E.A.4
Levesque, G.5
Ikeda, M.6
Chi, H.7
Lin, C.8
Li, G.9
Holman, K.10
-
72
-
-
0025997867
-
Ras1 and a putative guanine nucleotide exchange factor perform crucial steps in signaling by the sevenless tyrosine kinase
-
M.A. Simon, D.D.L. Bowtell, G.S. Dodson, T.R. Laverty, and G.M. Rubin Ras1 and a putative guanine nucleotide exchange factor perform crucial steps in signaling by the sevenless tyrosine kinase Cell 67 1991 701 716
-
(1991)
Cell
, vol.67
, pp. 701-716
-
-
Simon, M.A.1
Bowtell, D.D.L.2
Dodson, G.S.3
Laverty, T.R.4
Rubin, G.M.5
-
73
-
-
18544383162
-
Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia
-
I. Splawski, K.W. Timothy, M. Tateyama, C.E. Clancy, A. Malhotra, A.H. Beggs, F.P. Cappuccio, G.A. Sagnella, R.S. Kass, and M.T. Keating Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia Science 297 5585 2002 1333 1336
-
(2002)
Science
, vol.297
, Issue.5585
, pp. 1333-1336
-
-
Splawski, I.1
Timothy, K.W.2
Tateyama, M.3
Clancy, C.E.4
Malhotra, A.5
Beggs, A.H.6
Cappuccio, F.P.7
Sagnella, G.A.8
Kass, R.S.9
Keating, M.T.10
-
74
-
-
0035047622
-
Genetic assembly of the heart: Implications for congenital heart disease
-
D. Srivastava Genetic assembly of the heart: implications for congenital heart disease Annu. Rev. Physiol. 63 2001 451 469
-
(2001)
Annu. Rev. Physiol.
, vol.63
, pp. 451-469
-
-
Srivastava, D.1
-
75
-
-
7644230718
-
-
National Vital Statistics Report Hyattsville, MD
-
Statistics, N.C.f.H. Preliminary Data for 1998 1999 National Vital Statistics Report Hyattsville, MD 99 107
-
(1999)
Preliminary Data for 1998
, pp. 99-107
-
-
Statistics1
F. H, N.C.2
-
76
-
-
0030752982
-
Elastin: Genomic structure and point mutations in patients with supravalvular aortic stenosis
-
M. Tassabehji, K. Metcalfe, D. Donnai, J. Hurst, W. Reardon, M. Burch, and A.P. Read Elastin: genomic structure and point mutations in patients with supravalvular aortic stenosis Hum. Mol. Genet. 6 7 1997 1029 1036
-
(1997)
Hum. Mol. Genet.
, vol.6
, Issue.7
, pp. 1029-1036
-
-
Tassabehji, M.1
Metcalfe, K.2
Donnai, D.3
Hurst, J.4
Reardon, W.5
Burch, M.6
Read, A.P.7
-
77
-
-
0037562916
-
Novel mutations in DLL3, a somitogenesis gene encoding a ligand for the Notch signalling pathway, cause a consistent pattern of abnormal vertebral segmentation in spondylocostal dysostosis
-
P.D. Turnpenny, N. Whittock, J. Duncan, S. Dunwoodie, K. Kusumi, and S. Ellard Novel mutations in DLL3, a somitogenesis gene encoding a ligand for the Notch signalling pathway, cause a consistent pattern of abnormal vertebral segmentation in spondylocostal dysostosis J. Med. Genet. 40 5 2003 333 339
-
(2003)
J. Med. Genet.
, vol.40
, Issue.5
, pp. 333-339
-
-
Turnpenny, P.D.1
Whittock, N.2
Duncan, J.3
Dunwoodie, S.4
Kusumi, K.5
Ellard, S.6
-
78
-
-
0036308551
-
Connection between elastin haploinsufficiency and increased cell proliferation in patients with supravalvular aortic stenosis and Williams-Beuren syndrome
-
Z. Urban, S. Riazi, T.L. Seidl, J. Katahira, L.B. Smoot, D. Chitayat, C.D. Boyd, and A. Hinek Connection between elastin haploinsufficiency and increased cell proliferation in patients with supravalvular aortic stenosis and Williams-Beuren syndrome Am. J. Hum. Genet. 71 1 2002 30 44
-
(2002)
Am. J. Hum. Genet.
, vol.71
, Issue.1
, pp. 30-44
-
-
Urban, Z.1
Riazi, S.2
Seidl, T.L.3
Katahira, J.4
Smoot, L.B.5
Chitayat, D.6
Boyd, C.D.7
Hinek, A.8
-
79
-
-
0033635818
-
Characterization of a novel subset of cardiac cells and their progenitors in the Drosophila embryo
-
E.J. Ward, and J.B. Skeath Characterization of a novel subset of cardiac cells and their progenitors in the Drosophila embryo Development 127 22 2000 4959 4969
-
(2000)
Development
, vol.127
, Issue.22
, pp. 4959-4969
-
-
Ward, E.J.1
Skeath, J.B.2
-
80
-
-
0036501072
-
A frequent mild mutation in ALG6 may exacerbate the clinical severity of patients with congenital disorder of glycosylation Ia (CDG-Ia) caused by phosphomannomutase deficiency
-
V. Westphal, S. Kjaergaard, E. Schollen, K. Martens, S. Grunewald, M. Schwartz, G. Matthijs, and H.H. Freeze A frequent mild mutation in ALG6 may exacerbate the clinical severity of patients with congenital disorder of glycosylation Ia (CDG-Ia) caused by phosphomannomutase deficiency Hum. Mol. Genet. 11 5 2002 599 604
-
(2002)
Hum. Mol. Genet.
, vol.11
, Issue.5
, pp. 599-604
-
-
Westphal, V.1
Kjaergaard, S.2
Schollen, E.3
Martens, K.4
Grunewald, S.5
Schwartz, M.6
Matthijs, G.7
Freeze, H.H.8
-
81
-
-
34250136181
-
Mutations affecting the pattern of the larval cuticle of Drosophila melanogaster: III. Zygotic loci on the X-chromosome and fourth chromosome
-
E. Wieschaus, C. Nusslein-Volhard, and G. Jurgens Mutations affecting the pattern of the larval cuticle of Drosophila melanogaster: III. Zygotic loci on the X-chromosome and fourth chromosome Roux's Arch. Dev. Biol. 193 1984 296 307
-
(1984)
Roux's Arch. Dev. Biol.
, vol.193
, pp. 296-307
-
-
Wieschaus, E.1
Nusslein-Volhard, C.2
Jurgens, G.3
-
82
-
-
10744223651
-
Role of TBX1 in human del22q11.2 syndrome
-
H. Yagi, Y. Furutani, H. Hamada, T. Sasaki, S. Asakawa, S. Minoshima, F. Ichida, K. Joo, M. Kimura, S. Imamura, N. Kamatani, K. Momma, A. Takao, and M. Nakazawa Role of TBX1 in human del22q11.2 syndrome Lancet 362 9393 2003 1366 1373
-
(2003)
Lancet
, vol.362
, Issue.9393
, pp. 1366-1373
-
-
Yagi, H.1
Furutani, Y.2
Hamada, H.3
Sasaki, T.4
Asakawa, S.5
Minoshima, S.6
Ichida, F.7
Joo, K.8
Kimura, M.9
Imamura, S.10
Kamatani, N.11
Momma, K.12
Takao, A.13
Nakazawa, M.14
-
83
-
-
0037144658
-
Early signals in cardiac development
-
S. Zaffran, and M. Frasch Early signals in cardiac development Circ. Res. 91 6 2002 457 469
-
(2002)
Circ. Res.
, vol.91
, Issue.6
, pp. 457-469
-
-
Zaffran, S.1
Frasch, M.2
|