-
1
-
-
34249063569
-
Overview of epidemiology, genetics, birth defects, and chromosome abnormalities associated with CDH
-
Pober BR, (2007) Overview of epidemiology, genetics, birth defects, and chromosome abnormalities associated with CDH. Am J Med Genet C Semin Med Genet 145C, 158-171.
-
(2007)
Am J Med Genet C Semin Med Genet
, vol.145 C
, pp. 158-171
-
-
Pober, B.R.1
-
2
-
-
33749185118
-
Cardiopulmonary support in duchenne muscular dystrophy
-
Finsterer J, (2006) Cardiopulmonary support in duchenne muscular dystrophy. Lung 184, 205-215.
-
(2006)
Lung
, vol.184
, pp. 205-215
-
-
Finsterer, J.1
-
3
-
-
65349110431
-
Henry Gray's anatomy
-
Pearce JM, (2009) Henry Gray's anatomy. Clin Anat 22, 291-295.
-
(2009)
Clin Anat
, vol.22
, pp. 291-295
-
-
Pearce, J.M.1
-
4
-
-
0030906363
-
Embryogenesis of the phrenic nerve and diaphragm in the fetal rat
-
Allan DW, &, Greer JJ, (1997) Embryogenesis of the phrenic nerve and diaphragm in the fetal rat. J Comp Neurol 382, 459-468.
-
(1997)
J Comp Neurol
, vol.382
, pp. 459-468
-
-
Allan, D.W.1
Greer, J.J.2
-
5
-
-
84867672921
-
A contemporary atlas of the mouse diaphragm: Myogenicity, vascularity, and the Pax3 connection
-
Stuelsatz P, Keire P, Almuly R, &, Yablonka-Reuveni Z, (2012) A contemporary atlas of the mouse diaphragm: myogenicity, vascularity, and the Pax3 connection. J Histochem Cytochem 60, 638-657.
-
(2012)
J Histochem Cytochem
, vol.60
, pp. 638-657
-
-
Stuelsatz, P.1
Keire, P.2
Almuly, R.3
Yablonka-Reuveni, Z.4
-
7
-
-
0017258379
-
Diaphragm function and alveolar hypoventilation
-
Davis J, Goldman M, Loh L, &, Casson M, (1976) Diaphragm function and alveolar hypoventilation. Q J Med 45, 87-100.
-
(1976)
Q J Med
, vol.45
, pp. 87-100
-
-
Davis, J.1
Goldman, M.2
Loh, L.3
Casson, M.4
-
8
-
-
0023103816
-
Selective factors in the origin of the mammalian diaphragm
-
Ruben JA, Bennett AF, &, Hisaw FL, (1987) Selective factors in the origin of the mammalian diaphragm. Paleobiology 13, 54-59.
-
(1987)
Paleobiology
, vol.13
, pp. 54-59
-
-
Ruben, J.A.1
Bennett, A.F.2
Hisaw, F.L.3
-
9
-
-
0023518535
-
Effect of acute diaphragm paralysis on ventilation in awake and sleeping dogs
-
Stradling JR, Kozar LF, Dark J, Kirby T, Andrey SM, &, Phillipson EA, (1987) Effect of acute diaphragm paralysis on ventilation in awake and sleeping dogs. Am Rev Respir Dis 136, 633-637.
-
(1987)
Am Rev Respir Dis
, vol.136
, pp. 633-637
-
-
Stradling, J.R.1
Kozar, L.F.2
Dark, J.3
Kirby, T.4
Andrey, S.M.5
Phillipson, E.A.6
-
10
-
-
0036773226
-
The diaphragm: Two physiological muscles in one
-
Pickering M, &, Jones JF, (2002) The diaphragm: two physiological muscles in one. J Anat 201, 305-312.
-
(2002)
J Anat
, vol.201
, pp. 305-312
-
-
Pickering, M.1
Jones, J.F.2
-
11
-
-
84865852484
-
Fixed cervical count and the origin of the mammalian diaphragm
-
Buchholtz EA, Bailin HG, Laves SA, Yang JT, Chan MY, &, Drozd LE, (2012) Fixed cervical count and the origin of the mammalian diaphragm. Evolution & Development 14, 399-411.
-
(2012)
Evolution & Development
, vol.14
, pp. 399-411
-
-
Buchholtz, E.A.1
Bailin, H.G.2
Laves, S.A.3
Yang, J.T.4
Chan, M.Y.5
Drozd, L.E.6
-
12
-
-
77949774355
-
The evolutionary origin of the mammalian diaphragm
-
Perry SF, Similowski T, Klein W, &, Codd JR, (2010) The evolutionary origin of the mammalian diaphragm. Respir Physiol Neurobiol 171, 1-16.
-
(2010)
Respir Physiol Neurobiol
, vol.171
, pp. 1-16
-
-
Perry, S.F.1
Similowski, T.2
Klein, W.3
Codd, J.R.4
-
14
-
-
0032033316
-
Msg1 and Mrg1, founding members of a gene family, show distinct patterns of gene expression during mouse embryogenesis
-
Dunwoodie SL, Rodriguez TA, &, Beddington RS, (1998) Msg1 and Mrg1, founding members of a gene family, show distinct patterns of gene expression during mouse embryogenesis. Mech Dev 72, 27-40.
-
(1998)
Mech Dev
, vol.72
, pp. 27-40
-
-
Dunwoodie, S.L.1
Rodriguez, T.A.2
Beddington, R.S.3
-
15
-
-
0034747394
-
Alpha4 integrin is expressed in a subset of cranial neural crest cells and in epicardial progenitor cells during early mouse development
-
Pinco KA, Liu S, &, Yang JT, (2001) Alpha4 integrin is expressed in a subset of cranial neural crest cells and in epicardial progenitor cells during early mouse development. Mech Dev 100, 99-103.
-
(2001)
Mech Dev
, vol.100
, pp. 99-103
-
-
Pinco, K.A.1
Liu, S.2
Yang, J.T.3
-
16
-
-
33746289068
-
Spatio-temporal expression of Pbx3 during mouse organogenesis
-
Di Giacomo G, Koss M, Capellini TD, Brendolan A, Popperl H, &, Selleri L, (2006) Spatio-temporal expression of Pbx3 during mouse organogenesis. Gene Expr Patterns 6, 747-757.
-
(2006)
Gene Expr Patterns
, vol.6
, pp. 747-757
-
-
Di Giacomo, G.1
Koss, M.2
Capellini, T.D.3
Brendolan, A.4
Popperl, H.5
Selleri, L.6
-
17
-
-
0021251745
-
Experimental study on embryogenesis of congenital diaphragmatic hernia
-
Iritani I, (1984) Experimental study on embryogenesis of congenital diaphragmatic hernia. Anat Embryol (Berl) 169, 133-139.
-
(1984)
Anat Embryol (Berl)
, vol.169
, pp. 133-139
-
-
Iritani, I.1
-
18
-
-
0029845472
-
Embryology of congenital diaphragmatic hernia
-
Kluth D, Keijzer R, Hertl M, &, Tibboel D, (1996) Embryology of congenital diaphragmatic hernia. Semin Pediatr Surg 5, 224-233.
-
(1996)
Semin Pediatr Surg
, vol.5
, pp. 224-233
-
-
Kluth, D.1
Keijzer, R.2
Hertl, M.3
Tibboel, D.4
-
19
-
-
0027415197
-
The natural history of congenital diaphragmatic hernia and pulmonary hypoplasia in the embryo
-
discussion 462-463
-
Kluth D, Tenbrinck R, von Ekesparre M, Kangah R, Reich P, Brandsma A, Tibboel D, &, Lambrecht W, (1993) The natural history of congenital diaphragmatic hernia and pulmonary hypoplasia in the embryo. J Pediatr Surg 28, 456-462; discussion 462-463.
-
(1993)
J Pediatr Surg
, vol.28
, pp. 456-462
-
-
Kluth, D.1
Tenbrinck, R.2
Von Ekesparre, M.3
Kangah, R.4
Reich, P.5
Brandsma, A.6
Tibboel, D.7
Lambrecht, W.8
-
20
-
-
42049119837
-
Gene expression in the developing diaphragm: Significance for congenital diaphragmatic hernia
-
Clugston RD, Zhang W, &, Greer JJ, (2008) Gene expression in the developing diaphragm: significance for congenital diaphragmatic hernia. Am J Physiol Lung Cell Mol Physiol 294, L665-L675.
-
(2008)
Am J Physiol Lung Cell Mol Physiol
, vol.294
-
-
Clugston, R.D.1
Zhang, W.2
Greer, J.J.3
-
21
-
-
0032961872
-
The role of SF/HGF and c-Met in the development of skeletal muscle
-
Dietrich S, Abou-Rebyeh F, Brohmann H, Bladt F, Sonnenberg-Riethmacher E, Yamaai T, Lumsden A, Brand-Saberi B, &, Birchmeier C, (1999) The role of SF/HGF and c-Met in the development of skeletal muscle. Development 126, 1621-1629.
-
(1999)
Development
, vol.126
, pp. 1621-1629
-
-
Dietrich, S.1
Abou-Rebyeh, F.2
Brohmann, H.3
Bladt, F.4
Sonnenberg-Riethmacher, E.5
Yamaai, T.6
Lumsden, A.7
Brand-Saberi, B.8
Birchmeier, C.9
-
22
-
-
0037454617
-
Embryological origins and development of the rat diaphragm
-
Babiuk RP, Zhang W, Clugston R, Allan DW, &, Greer JJ, (2003) Embryological origins and development of the rat diaphragm. J Comp Neurol 455, 477-487.
-
(2003)
J Comp Neurol
, vol.455
, pp. 477-487
-
-
Babiuk, R.P.1
Zhang, W.2
Clugston, R.3
Allan, D.W.4
Greer, J.J.5
-
23
-
-
34447287334
-
Skeletal muscle progenitor cells and the role of Pax genes
-
Buckingham M, (2007) Skeletal muscle progenitor cells and the role of Pax genes. C R Biol 330, 530-533.
-
(2007)
C R Biol
, vol.330
, pp. 530-533
-
-
Buckingham, M.1
-
24
-
-
2442604538
-
Divergent functions of murine Pax3 and Pax7 in limb muscle development
-
Relaix F, Rocancourt D, Mansouri A, &, Buckingham M, (2004) Divergent functions of murine Pax3 and Pax7 in limb muscle development. Genes Dev 18, 1088-1105.
-
(2004)
Genes Dev
, vol.18
, pp. 1088-1105
-
-
Relaix, F.1
Rocancourt, D.2
Mansouri, A.3
Buckingham, M.4
-
25
-
-
0030018672
-
Expression of the met receptor tyrosine kinase in muscle progenitor cells in somites and limbs is absent in Splotch mice
-
Yang XM, Vogan K, Gros P, &, Park M, (1996) Expression of the met receptor tyrosine kinase in muscle progenitor cells in somites and limbs is absent in Splotch mice. Development 122, 2163-2171.
-
(1996)
Development
, vol.122
, pp. 2163-2171
-
-
Yang, X.M.1
Vogan, K.2
Gros, P.3
Park, M.4
-
26
-
-
0029134104
-
Essential role for the c-met receptor in the migration of myogenic precursor cells into the limb bud
-
Bladt F, Riethmacher D, Isenmann S, Aguzzi A, &, Birchmeier C, (1995) Essential role for the c-met receptor in the migration of myogenic precursor cells into the limb bud. Nature 376, 768-771.
-
(1995)
Nature
, vol.376
, pp. 768-771
-
-
Bladt, F.1
Riethmacher, D.2
Isenmann, S.3
Aguzzi, A.4
Birchmeier, C.5
-
27
-
-
0030891169
-
Redefining the genetic hierarchies controlling skeletal myogenesis: Pax-3 and Myf-5 act upstream of MyoD
-
Tajbakhsh S, Rocancourt D, Cossu G, &, Buckingham M, (1997) Redefining the genetic hierarchies controlling skeletal myogenesis: Pax-3 and Myf-5 act upstream of MyoD. Cell 89, 127-138.
-
(1997)
Cell
, vol.89
, pp. 127-138
-
-
Tajbakhsh, S.1
Rocancourt, D.2
Cossu, G.3
Buckingham, M.4
-
28
-
-
0032212771
-
A crucial role for Pax3 in the development of the hypaxial musculature and the long-range migration of muscle precursors
-
Tremblay P, Dietrich S, Mericskay M, Schubert FR, Li Z, &, Paulin D, (1998) A crucial role for Pax3 in the development of the hypaxial musculature and the long-range migration of muscle precursors. Dev Biol 203, 49-61.
-
(1998)
Dev Biol
, vol.203
, pp. 49-61
-
-
Tremblay, P.1
Dietrich, S.2
Mericskay, M.3
Schubert, F.R.4
Li, Z.5
Paulin, D.6
-
29
-
-
0032536527
-
Polysialylated NCAM expression during motor axon outgrowth and myogenesis in the fetal rat
-
Allan DW, &, Greer JJ, (1998) Polysialylated NCAM expression during motor axon outgrowth and myogenesis in the fetal rat. J Comp Neurol 391, 275-292.
-
(1998)
J Comp Neurol
, vol.391
, pp. 275-292
-
-
Allan, D.W.1
Greer, J.J.2
-
30
-
-
0030297898
-
Uncoupling of Grb2 from the Met receptor in vivo reveals complex roles in muscle development
-
Maina F, Casagranda F, Audero E, Simeone A, Comoglio PM, Klein R, &, Ponzetto C, (1996) Uncoupling of Grb2 from the Met receptor in vivo reveals complex roles in muscle development. Cell 87, 531-542.
-
(1996)
Cell
, vol.87
, pp. 531-542
-
-
Maina, F.1
Casagranda, F.2
Audero, E.3
Simeone, A.4
Comoglio, P.M.5
Klein, R.6
Ponzetto, C.7
-
31
-
-
0001517943
-
Hepatocyte growth factor/scatter factor is an axonal chemoattractant and a neurotrophic factor for spinal motor neurons
-
Ebens A, Brose K, Leonardo ED, Hanson MG Jr, Bladt F, Birchmeier C, Barres BA, &, Tessier-Lavigne M, (1996) Hepatocyte growth factor/scatter factor is an axonal chemoattractant and a neurotrophic factor for spinal motor neurons. Neuron 17, 1157-1172.
-
(1996)
Neuron
, vol.17
, pp. 1157-1172
-
-
Ebens, A.1
Brose, K.2
Leonardo, E.D.3
Hanson, Jr.M.G.4
Bladt, F.5
Birchmeier, C.6
Barres, B.A.7
Tessier-Lavigne, M.8
-
32
-
-
0030865088
-
Hepatocyte growth factor (HGF/SF) is a muscle-derived survival factor for a subpopulation of embryonic motoneurons
-
Yamamoto Y, Livet J, Pollock RA, Garces A, Arce V, deLapeyriere O, &, Henderson CE, (1997) Hepatocyte growth factor (HGF/SF) is a muscle-derived survival factor for a subpopulation of embryonic motoneurons. Development 124, 2903-2913.
-
(1997)
Development
, vol.124
, pp. 2903-2913
-
-
Yamamoto, Y.1
Livet, J.2
Pollock, R.A.3
Garces, A.4
Arce, V.5
Delapeyriere, O.6
Henderson, C.E.7
-
33
-
-
79957468814
-
Origin of vertebrate limb muscle: The role of progenitor and myoblast populations
-
Murphy M, &, Kardon G, (2011) Origin of vertebrate limb muscle: the role of progenitor and myoblast populations. Curr Top Dev Biol 96, 1-32.
-
(2011)
Curr Top Dev Biol
, vol.96
, pp. 1-32
-
-
Murphy, M.1
Kardon, G.2
-
34
-
-
0036893391
-
Diaphragm defects occur in a CDH hernia model independently of myogenesis and lung formation
-
Babiuk RP, &, Greer JJ, (2002) Diaphragm defects occur in a CDH hernia model independently of myogenesis and lung formation. Am J Physiol Lung Cell Mol Physiol 283, L1310-L1314.
-
(2002)
Am J Physiol Lung Cell Mol Physiol
, vol.283
-
-
Babiuk, R.P.1
Greer, J.J.2
-
35
-
-
33745231769
-
Mammalian motoneuron axon targeting requires receptor protein tyrosine phosphatases sigma and delta
-
Uetani N, Chagnon MJ, Kennedy TE, Iwakura Y, &, Tremblay ML, (2006) Mammalian motoneuron axon targeting requires receptor protein tyrosine phosphatases sigma and delta. J Neurosci 26, 5872-5880.
-
(2006)
J Neurosci
, vol.26
, pp. 5872-5880
-
-
Uetani, N.1
Chagnon, M.J.2
Kennedy, T.E.3
Iwakura, Y.4
Tremblay, M.L.5
-
36
-
-
84870564931
-
Sustained Hox5 gene activity is required for respiratory motor neuron development
-
Philippidou P, Walsh CM, Aubin J, Jeannotte L, &, Dasen JS, (2012) Sustained Hox5 gene activity is required for respiratory motor neuron development. Nat Neurosci 15, 1636-1644.
-
(2012)
Nat Neurosci
, vol.15
, pp. 1636-1644
-
-
Philippidou, P.1
Walsh, C.M.2
Aubin, J.3
Jeannotte, L.4
Dasen, J.S.5
-
37
-
-
0019393575
-
Muscle nerve branches do not develop in chick wings devoid of muscle
-
Lewis J, Chevallier A, Kieny M, &, Wolpert L, (1981) Muscle nerve branches do not develop in chick wings devoid of muscle. J Embryol Exp Morphol 64, 211-232.
-
(1981)
J Embryol Exp Morphol
, vol.64
, pp. 211-232
-
-
Lewis, J.1
Chevallier, A.2
Kieny, M.3
Wolpert, L.4
-
38
-
-
39749119832
-
Retrograde regulation of motoneuron differentiation by muscle beta-catenin
-
Li XM, Dong XP, Luo SW, Zhang B, Lee DH, Ting AK, Neiswender H, Kim CH, Carpenter-Hyland E, Gao TM, et al,. (2008) Retrograde regulation of motoneuron differentiation by muscle beta-catenin. Nat Neurosci 11, 262-268.
-
(2008)
Nat Neurosci
, vol.11
, pp. 262-268
-
-
Li, X.M.1
Dong, X.P.2
Luo, S.W.3
Zhang, B.4
Lee, D.H.5
Ting, A.K.6
Neiswender, H.7
Kim, C.H.8
Carpenter-Hyland, E.9
Gao, T.M.10
-
39
-
-
84861991275
-
Beta-Catenin gain of function in muscles impairs neuromuscular junction formation
-
Wu H, Lu Y, Barik A, Joseph A, Taketo MM, Xiong WC, &, Mei L, (2012) beta-Catenin gain of function in muscles impairs neuromuscular junction formation. Development 139, 2392-2404.
-
(2012)
Development
, vol.139
, pp. 2392-2404
-
-
Wu, H.1
Lu, Y.2
Barik, A.3
Joseph, A.4
Taketo, M.M.5
Xiong, W.C.6
Mei, L.7
-
40
-
-
79955009131
-
SnapShot: Neuromuscular junction
-
e1
-
Burden SJ, (2011) SnapShot: neuromuscular junction. Cell 144, 826-826 e1.
-
(2011)
Cell
, vol.144
, pp. 826-826
-
-
Burden, S.J.1
-
41
-
-
77950462859
-
To build a synapse: Signaling pathways in neuromuscular junction assembly
-
Wu H, Xiong WC, &, Mei L, (2010) To build a synapse: signaling pathways in neuromuscular junction assembly. Development 137, 1017-1033.
-
(2010)
Development
, vol.137
, pp. 1017-1033
-
-
Wu, H.1
Xiong, W.C.2
Mei, L.3
-
42
-
-
33645867658
-
Fog2 is required for normal diaphragm and lung development in mice and humans
-
Ackerman KG, Herron BJ, Vargas SO, Huang H, Tevosian SG, Kochilas L, Rao C, Pober BR, Babiuk RP, Epstein JA, et al,. (2005) Fog2 is required for normal diaphragm and lung development in mice and humans. PLoS Genet 1, 58-65.
-
(2005)
PLoS Genet
, vol.1
, pp. 58-65
-
-
Ackerman, K.G.1
Herron, B.J.2
Vargas, S.O.3
Huang, H.4
Tevosian, S.G.5
Kochilas, L.6
Rao, C.7
Pober, B.R.8
Babiuk, R.P.9
Epstein, J.A.10
-
43
-
-
33846044214
-
Impaired mesenchymal cell function in Gata4 mutant mice leads to diaphragmatic hernias and primary lung defects
-
Jay PY, Bielinska M, Erlich JM, Mannisto S, Pu WT, Heikinheimo M, &, Wilson DB, (2007) Impaired mesenchymal cell function in Gata4 mutant mice leads to diaphragmatic hernias and primary lung defects. Dev Biol 301, 602-614.
-
(2007)
Dev Biol
, vol.301
, pp. 602-614
-
-
Jay, P.Y.1
Bielinska, M.2
Erlich, J.M.3
Mannisto, S.4
Pu, W.T.5
Heikinheimo, M.6
Wilson, D.B.7
-
44
-
-
34249031797
-
Congenital diaphragmatic hernia and pulmonary hypoplasia: New insights from developmental biology and genetics
-
Ackerman KG, &, Pober BR, (2007) Congenital diaphragmatic hernia and pulmonary hypoplasia: new insights from developmental biology and genetics. Am J Med Genet C Semin Med Genet 145C, 105-108.
-
(2007)
Am J Med Genet C Semin Med Genet
, vol.145 C
, pp. 105-108
-
-
Ackerman, K.G.1
Pober, B.R.2
-
45
-
-
34249096430
-
Antenatal and postnatal lung and vascular anatomic and functional studies in congenital diaphragmatic hernia: Implications for clinical management
-
Keller RL, (2007) Antenatal and postnatal lung and vascular anatomic and functional studies in congenital diaphragmatic hernia: implications for clinical management. Am J Med Genet C Semin Med Genet 145C, 184-200.
-
(2007)
Am J Med Genet C Semin Med Genet
, vol.145 C
, pp. 184-200
-
-
Keller, R.L.1
-
46
-
-
0028013621
-
A prospective study of the outcome for fetuses with diaphragmatic hernia
-
Harrison MR, Adzick NS, Estes JM, &, Howell LJ, (1994) A prospective study of the outcome for fetuses with diaphragmatic hernia. JAMA 271, 382-384.
-
(1994)
JAMA
, vol.271
, pp. 382-384
-
-
Harrison, M.R.1
Adzick, N.S.2
Estes, J.M.3
Howell, L.J.4
-
47
-
-
0027092777
-
A population-based study of congenital diaphragmatic hernia
-
Torfs CP, Curry CJ, Bateson TF, &, Honore LH, (1992) A population-based study of congenital diaphragmatic hernia. Teratology 46, 555-565.
-
(1992)
Teratology
, vol.46
, pp. 555-565
-
-
Torfs, C.P.1
Curry, C.J.2
Bateson, T.F.3
Honore, L.H.4
-
48
-
-
0025934667
-
Unusual varieties of diaphragmatic herniae
-
Stokes KB, (1991) Unusual varieties of diaphragmatic herniae. Prog Pediatr Surg 27, 127-147.
-
(1991)
Prog Pediatr Surg
, vol.27
, pp. 127-147
-
-
Stokes, K.B.1
-
49
-
-
34249043527
-
Development of the diaphragm and genetic mouse models of diaphragmatic defects
-
Ackerman KG, &, Greer JJ, (2007) Development of the diaphragm and genetic mouse models of diaphragmatic defects. Am J Med Genet C Semin Med Genet 145C, 109-116.
-
(2007)
Am J Med Genet C Semin Med Genet
, vol.145 C
, pp. 109-116
-
-
Ackerman, K.G.1
Greer, J.J.2
-
50
-
-
38949218052
-
Denys-Drash syndrome and congenital diaphragmatic hernia: Another case with the 1097G > A(Arg366His) mutation
-
Antonius T, van Bon B, Eggink A, van der Burgt I, Noordam K, &, van Heijst A, (2008) Denys-Drash syndrome and congenital diaphragmatic hernia: another case with the 1097G > A(Arg366His) mutation. Am J Med Genet A 146A, 496-499.
-
(2008)
Am J Med Genet A
, vol.146 A
, pp. 496-499
-
-
Antonius, T.1
Van Bon, B.2
Eggink, A.3
Van Der Burgt, I.4
Noordam, K.5
Van Heijst, A.6
-
51
-
-
81955161806
-
Causes of death and autopsy findings in a large study cohort of individuals with Cornelia de Lange syndrome and review of the literature
-
Schrier SA, Sherer I, Deardorff MA, Clark D, Audette L, Gillis L, Kline AD, Ernst L, Loomes K, Krantz ID, et al,. (2011) Causes of death and autopsy findings in a large study cohort of individuals with Cornelia de Lange syndrome and review of the literature. Am J Med Genet A 155A, 3007-3024.
-
(2011)
Am J Med Genet A
, vol.155 A
, pp. 3007-3024
-
-
Schrier, S.A.1
Sherer, I.2
Deardorff, M.A.3
Clark, D.4
Audette, L.5
Gillis, L.6
Kline, A.D.7
Ernst, L.8
Loomes, K.9
Krantz, I.D.10
-
52
-
-
0027371034
-
Diaphragmatic hernia, exomphalos, absent corpus callosum, hypertelorism, myopia, and sensorineural deafness: A newly recognized autosomal recessive disorder?
-
Donnai D, &, Barrow M, (1993) Diaphragmatic hernia, exomphalos, absent corpus callosum, hypertelorism, myopia, and sensorineural deafness: a newly recognized autosomal recessive disorder? Am J Med Genet 47, 679-682.
-
(1993)
Am J Med Genet
, vol.47
, pp. 679-682
-
-
Donnai, D.1
Barrow, M.2
-
53
-
-
78049282023
-
Congenital diaphragmatic hernia and a complex heart defect in association with Wolf-Hirschhorn syndrome
-
Tautz J, Veenma D, Eussen B, Joosen L, Poddighe P, Tibboel D, de Klein A, &, Schaible T, (2010) Congenital diaphragmatic hernia and a complex heart defect in association with Wolf-Hirschhorn syndrome. Am J Med Genet A 152A, 2891-2894.
-
(2010)
Am J Med Genet A
, vol.152 A
, pp. 2891-2894
-
-
Tautz, J.1
Veenma, D.2
Eussen, B.3
Joosen, L.4
Poddighe, P.5
Tibboel, D.6
De Klein, A.7
Schaible, T.8
-
54
-
-
33746435818
-
Recurrent congenital diaphragmatic hernia in Ehlers-Danlos syndrome
-
Lin IC, Ko SF, Shieh CS, Huang CF, Chien SJ, &, Liang CD, (2006) Recurrent congenital diaphragmatic hernia in Ehlers-Danlos syndrome. Cardiovasc Intervent Radiol 29, 920-923.
-
(2006)
Cardiovasc Intervent Radiol
, vol.29
, pp. 920-923
-
-
Lin, I.C.1
Ko, S.F.2
Shieh, C.S.3
Huang, C.F.4
Chien, S.J.5
Liang, C.D.6
-
55
-
-
79955009384
-
Co-occurrence of severe Goltz-Gorlin syndrome and pentalogy of Cantrell - Case report and review of the literature
-
Smigiel R, Jakubiak A, Lombardi MP, Jaworski W, Slezak R, Patkowski D, &, Hennekam RC, (2011) Co-occurrence of severe Goltz-Gorlin syndrome and pentalogy of Cantrell-Case report and review of the literature. Am J Med Genet A 155A, 1102-1105.
-
(2011)
Am J Med Genet A
, vol.155 A
, pp. 1102-1105
-
-
Smigiel, R.1
Jakubiak, A.2
Lombardi, M.P.3
Jaworski, W.4
Slezak, R.5
Patkowski, D.6
Hennekam, R.C.7
-
56
-
-
0942279747
-
Fryns syndrome: A review of the phenotype and diagnostic guidelines
-
Slavotinek AM, (2004) Fryns syndrome: a review of the phenotype and diagnostic guidelines. Am J Med Genet A 124A, 427-433.
-
(2004)
Am J Med Genet A
, vol.124 A
, pp. 427-433
-
-
Slavotinek, A.M.1
-
57
-
-
0042887607
-
A significant reduction of the diaphragm in mdx:MyoD-/-(9th) embryos suggests a role for MyoD in the diaphragm development
-
Inanlou MR, Dhillon GS, Belliveau AC, Reid GA, Ying C, Rudnicki MA, &, Kablar B, (2003) A significant reduction of the diaphragm in mdx:MyoD-/-(9th) embryos suggests a role for MyoD in the diaphragm development. Dev Biol 261, 324-336.
-
(2003)
Dev Biol
, vol.261
, pp. 324-336
-
-
Inanlou, M.R.1
Dhillon, G.S.2
Belliveau, A.C.3
Reid, G.A.4
Ying, C.5
Rudnicki, M.A.6
Kablar, B.7
-
58
-
-
0034082323
-
Pulmonary hypoplasia in the myogenin null mouse embryo
-
Tseng BS, Cavin ST, Booth FW, Olson EN, Marin MC, McDonnell TJ, &, Butler IJ, (2000) Pulmonary hypoplasia in the myogenin null mouse embryo. Am J Respir Cell Mol Biol 22, 304-315.
-
(2000)
Am J Respir Cell Mol Biol
, vol.22
, pp. 304-315
-
-
Tseng, B.S.1
Cavin, S.T.2
Booth, F.W.3
Olson, E.N.4
Marin, M.C.5
McDonnell, T.J.6
Butler, I.J.7
-
59
-
-
0038529805
-
Lysyl oxidase is required for vascular and diaphragmatic development in mice
-
Hornstra IK, Birge S, Starcher B, Bailey AJ, Mecham RP, &, Shapiro SD, (2003) Lysyl oxidase is required for vascular and diaphragmatic development in mice. J Biol Chem 278, 14387-14393.
-
(2003)
J Biol Chem
, vol.278
, pp. 14387-14393
-
-
Hornstra, I.K.1
Birge, S.2
Starcher, B.3
Bailey, A.J.4
Mecham, R.P.5
Shapiro, S.D.6
-
60
-
-
0025111022
-
Nitrofen-induced diaphragmatic hernias in rats: An animal model
-
Kluth D, Kangah R, Reich P, Tenbrinck R, Tibboel D, &, Lambrecht W, (1990) Nitrofen-induced diaphragmatic hernias in rats: an animal model. J Pediatr Surg 25, 850-854.
-
(1990)
J Pediatr Surg
, vol.25
, pp. 850-854
-
-
Kluth, D.1
Kangah, R.2
Reich, P.3
Tenbrinck, R.4
Tibboel, D.5
Lambrecht, W.6
-
61
-
-
0030878969
-
Pathogenesis of nitrofen-induced congenital diaphragmatic hernia in fetal rats
-
Allan DW, &, Greer JJ, (1997) Pathogenesis of nitrofen-induced congenital diaphragmatic hernia in fetal rats. J Appl Physiol 83, 338-347.
-
(1997)
J Appl Physiol
, vol.83
, pp. 338-347
-
-
Allan, D.W.1
Greer, J.J.2
-
62
-
-
77249097944
-
Understanding abnormal retinoid signaling as a causative mechanism in congenital diaphragmatic hernia
-
Clugston RD, Zhang W, Alvarez S, de Lera AR, &, Greer JJ, (2010) Understanding abnormal retinoid signaling as a causative mechanism in congenital diaphragmatic hernia. Am J Respir Cell Mol Biol 42, 276-285.
-
(2010)
Am J Respir Cell Mol Biol
, vol.42
, pp. 276-285
-
-
Clugston, R.D.1
Zhang, W.2
Alvarez, S.3
De Lera, A.R.4
Greer, J.J.5
-
63
-
-
66749088100
-
Phenotypic spectrum of STRA6 mutations: From Matthew-Wood syndrome to non-lethal anophthalmia
-
Chassaing N, Golzio C, Odent S, Lequeux L, Vigouroux A, Martinovic-Bouriel J, Tiziano FD, Masini L, Piro F, Maragliano G, et al,. (2009) Phenotypic spectrum of STRA6 mutations: from Matthew-Wood syndrome to non-lethal anophthalmia. Hum Mutat 30, E673-E681.
-
(2009)
Hum Mutat
, vol.30
-
-
Chassaing, N.1
Golzio, C.2
Odent, S.3
Lequeux, L.4
Vigouroux, A.5
Martinovic-Bouriel, J.6
Tiziano, F.D.7
Masini, L.8
Piro, F.9
Maragliano, G.10
-
64
-
-
34249886291
-
The PDAC syndrome (pulmonary hypoplasia/agenesis, diaphragmatic hernia/eventration, anophthalmia/microphthalmia, and cardiac defect) (Spear syndrome, Matthew-Wood syndrome): Report of eight cases including a living child and further evidence for autosomal recessive inheritance
-
Chitayat D, Sroka H, Keating S, Colby RS, Ryan G, Toi A, Blaser S, Viero S, Devisme L, Boute-Benejean O, et al,. (2007) The PDAC syndrome (pulmonary hypoplasia/agenesis, diaphragmatic hernia/eventration, anophthalmia/ microphthalmia, and cardiac defect) (Spear syndrome, Matthew-Wood syndrome): report of eight cases including a living child and further evidence for autosomal recessive inheritance. Am J Med Genet A 143A, 1268-1281.
-
(2007)
Am J Med Genet A
, vol.143 A
, pp. 1268-1281
-
-
Chitayat, D.1
Sroka, H.2
Keating, S.3
Colby, R.S.4
Ryan, G.5
Toi, A.6
Blaser, S.7
Viero, S.8
Devisme, L.9
Boute-Benejean, O.10
-
65
-
-
0028073019
-
Function of the retinoic acid receptors (RARs) during development (II). Multiple abnormalities at various stages of organogenesis in RAR double mutants
-
Mendelsohn C, Lohnes D, Decimo D, Lufkin T, LeMeur M, Chambon P, &, Mark M, (1994) Function of the retinoic acid receptors (RARs) during development (II). Multiple abnormalities at various stages of organogenesis in RAR double mutants. Development 120, 2749-2771.
-
(1994)
Development
, vol.120
, pp. 2749-2771
-
-
Mendelsohn, C.1
Lohnes, D.2
Decimo, D.3
Lufkin, T.4
Lemeur, M.5
Chambon, P.6
Mark, M.7
-
66
-
-
79951800368
-
Recent developments in the genetic factors underlying congenital diaphragmatic hernia
-
Brady PD, Srisupundit K, Devriendt K, Fryns JP, Deprest JA, &, Vermeesch JR, (2011) Recent developments in the genetic factors underlying congenital diaphragmatic hernia. Fetal Diagn Ther 29, 25-39.
-
(2011)
Fetal Diagn Ther
, vol.29
, pp. 25-39
-
-
Brady, P.D.1
Srisupundit, K.2
Devriendt, K.3
Fryns, J.P.4
Deprest, J.A.5
Vermeesch, J.R.6
-
67
-
-
78049422339
-
Retinoid pathway and congenital diaphragmatic hernia: Hypothesis from the analysis of chromosomal abnormalities
-
Goumy C, Gouas L, Marceau G, Coste K, Veronese L, Gallot D, Sapin V, Vago P, &, Tchirkov A, (2010) Retinoid pathway and congenital diaphragmatic hernia: hypothesis from the analysis of chromosomal abnormalities. Fetal Diagn Ther 28, 129-139.
-
(2010)
Fetal Diagn Ther
, vol.28
, pp. 129-139
-
-
Goumy, C.1
Gouas, L.2
Marceau, G.3
Coste, K.4
Veronese, L.5
Gallot, D.6
Sapin, V.7
Vago, P.8
Tchirkov, A.9
-
68
-
-
84875606307
-
Variants in GATA4 are a rare cause of familial and sporadic congenital diaphragmatic hernia
-
Yu L, Wynn J, Cheung YH, Shen Y, Mychaliska GB, Crombleholme TM, Azarow KS, Lim FY, Chung DH, Potoka D, et al,. (2013) Variants in GATA4 are a rare cause of familial and sporadic congenital diaphragmatic hernia. Hum Genet 132, 285-292.
-
(2013)
Hum Genet
, vol.132
, pp. 285-292
-
-
Yu, L.1
Wynn, J.2
Cheung, Y.H.3
Shen, Y.4
Mychaliska, G.B.5
Crombleholme, T.M.6
Azarow, K.S.7
Lim, F.Y.8
Chung, D.H.9
Potoka, D.10
-
69
-
-
84870242761
-
A family-based paradigm to identify candidate chromosomal regions for isolated congenital diaphragmatic hernia
-
Arrington CB, Bleyl SB, Matsunami N, Bowles NE, Leppert TI, Demarest BL, Osborne K, Yoder BA, Byrne JL, Schiffman JD, et al,. (2012) A family-based paradigm to identify candidate chromosomal regions for isolated congenital diaphragmatic hernia. Am J Med Genet A 158A, 3137-3147.
-
(2012)
Am J Med Genet A
, vol.158 A
, pp. 3137-3147
-
-
Arrington, C.B.1
Bleyl, S.B.2
Matsunami, N.3
Bowles, N.E.4
Leppert, T.I.5
Demarest, B.L.6
Osborne, K.7
Yoder, B.A.8
Byrne, J.L.9
Schiffman, J.D.10
-
70
-
-
84870247613
-
Congenital diaphragmatic hernia interval on chromosome 8p23.1 characterized by genetics and protein interaction networks
-
Longoni M, Lage K, Russell MK, Loscertales M, Abdul-Rahman OA, Baynam G, Bleyl SB, Brady PD, Breckpot J, Chen CP, et al,. (2012) Congenital diaphragmatic hernia interval on chromosome 8p23.1 characterized by genetics and protein interaction networks. Am J Med Genet A 158A, 3148-3158.
-
(2012)
Am J Med Genet A
, vol.158 A
, pp. 3148-3158
-
-
Longoni, M.1
Lage, K.2
Russell, M.K.3
Loscertales, M.4
Abdul-Rahman, O.A.5
Baynam, G.6
Bleyl, S.B.7
Brady, P.D.8
Breckpot, J.9
Chen, C.P.10
-
71
-
-
12344253867
-
Coregulation of GATA factors by the Friend of GATA (FOG) family of multitype zinc finger proteins
-
Cantor AB, &, Orkin SH, (2005) Coregulation of GATA factors by the Friend of GATA (FOG) family of multitype zinc finger proteins. Semin Cell Dev Biol 16, 117-128.
-
(2005)
Semin Cell Dev Biol
, vol.16
, pp. 117-128
-
-
Cantor, A.B.1
Orkin, S.H.2
-
72
-
-
20244372562
-
Congenital diaphragmatic hernia and chromosome 15q26: Determination of a candidate region by use of fluorescent in situ hybridization and array-based comparative genomic hybridization
-
Klaassens M, van Dooren M, Eussen HJ, Douben H, den Dekker AT, Lee C, Donahoe PK, Galjaard RJ, Goemaere N, de Krijger RR, et al,. (2005) Congenital diaphragmatic hernia and chromosome 15q26: determination of a candidate region by use of fluorescent in situ hybridization and array-based comparative genomic hybridization. Am J Hum Genet 76, 877-882.
-
(2005)
Am J Hum Genet
, vol.76
, pp. 877-882
-
-
Klaassens, M.1
Van Dooren, M.2
Eussen, H.J.3
Douben, H.4
Den Dekker, A.T.5
Lee, C.6
Donahoe, P.K.7
Galjaard, R.J.8
Goemaere, N.9
De Krijger, R.R.10
-
73
-
-
28044455227
-
Mouse lacking COUP-TFII as an animal model of Bochdalek-type congenital diaphragmatic hernia
-
You LR, Takamoto N, Yu CT, Tanaka T, Kodama T, Demayo FJ, Tsai SY, &, Tsai MJ, (2005) Mouse lacking COUP-TFII as an animal model of Bochdalek-type congenital diaphragmatic hernia. Proc Natl Acad Sci USA 102, 16351-16356.
-
(2005)
Proc Natl Acad Sci USA
, vol.102
, pp. 16351-16356
-
-
You, L.R.1
Takamoto, N.2
Yu, C.T.3
Tanaka, T.4
Kodama, T.5
Demayo, F.J.6
Tsai, S.Y.7
Tsai, M.J.8
-
74
-
-
84857401680
-
Congenital diaphragmatic hernia candidate genes derived from embryonic transcriptomes
-
Russell MK, Longoni M, Wells J, Maalouf FI, Tracy AA, Loscertales M, Ackerman KG, Pober BR, Lage K, Bult CJ, et al,. (2012) Congenital diaphragmatic hernia candidate genes derived from embryonic transcriptomes. Proc Natl Acad Sci USA 109, 2978-2983.
-
(2012)
Proc Natl Acad Sci USA
, vol.109
, pp. 2978-2983
-
-
Russell, M.K.1
Longoni, M.2
Wells, J.3
Maalouf, F.I.4
Tracy, A.A.5
Loscertales, M.6
Ackerman, K.G.7
Pober, B.R.8
Lage, K.9
Bult, C.J.10
-
75
-
-
0033963166
-
The role of Lbx1 in migration of muscle precursor cells
-
Brohmann H, Jagla K, &, Birchmeier C, (2000) The role of Lbx1 in migration of muscle precursor cells. Development 127, 437-445.
-
(2000)
Development
, vol.127
, pp. 437-445
-
-
Brohmann, H.1
Jagla, K.2
Birchmeier, C.3
-
76
-
-
0033973639
-
Lbx1 is required for muscle precursor migration along a lateral pathway into the limb
-
Gross MK, Moran-Rivard L, Velasquez T, Nakatsu MN, Jagla K, &, Goulding M, (2000) Lbx1 is required for muscle precursor migration along a lateral pathway into the limb. Development 127, 413-424.
-
(2000)
Development
, vol.127
, pp. 413-424
-
-
Gross, M.K.1
Moran-Rivard, L.2
Velasquez, T.3
Nakatsu, M.N.4
Jagla, K.5
Goulding, M.6
-
77
-
-
74049104037
-
Tbx4 and tbx5 acting in connective tissue are required for limb muscle and tendon patterning
-
Hasson P, DeLaurier A, Bennett M, Grigorieva E, Naiche LA, Papaioannou VE, Mohun TJ, &, Logan MP, (2010) Tbx4 and tbx5 acting in connective tissue are required for limb muscle and tendon patterning. Dev Cell 18, 148-156.
-
(2010)
Dev Cell
, vol.18
, pp. 148-156
-
-
Hasson, P.1
Delaurier, A.2
Bennett, M.3
Grigorieva, E.4
Naiche, L.A.5
Papaioannou, V.E.6
Mohun, T.J.7
Logan, M.P.8
-
78
-
-
0346783321
-
A Tcf4-positive mesodermal population provides a prepattern for vertebrate limb muscle patterning
-
Kardon G, Harfe BD, &, Tabin CJ, (2003) A Tcf4-positive mesodermal population provides a prepattern for vertebrate limb muscle patterning. Dev Cell 5, 937-944.
-
(2003)
Dev Cell
, vol.5
, pp. 937-944
-
-
Kardon, G.1
Harfe, B.D.2
Tabin, C.J.3
|