-
1
-
-
0010312457
-
Ueber die Visceralbogen der Wirbelthiere im Allgemeinen und deren Metamorphose bei den Säugethieren und Vögeln
-
Sittenfeld
-
Reichert K.B. Ueber die Visceralbogen der Wirbelthiere im Allgemeinen und deren Metamorphose bei den Säugethieren und Vögeln. Archiv für Anatomie, Physiologie und wissenschaftliche Medicin 1837, Sittenfeld.
-
(1837)
Archiv für Anatomie, Physiologie und wissenschaftliche Medicin
-
-
Reichert, K.B.1
-
3
-
-
0006636226
-
Development of the auricle in the human embryo
-
Streeter G.L. Development of the auricle in the human embryo. Contrib Embryol 1922, 69:111.
-
(1922)
Contrib Embryol
, vol.69
, pp. 111
-
-
Streeter, G.L.1
-
4
-
-
0029828103
-
Rhombencephalic neural crest segmentation is preserved throughout craniofacial ontogeny
-
Kontges G., Lumsden A. Rhombencephalic neural crest segmentation is preserved throughout craniofacial ontogeny. Development 1996, 122(10):3229-3242.
-
(1996)
Development
, vol.122
, Issue.10
, pp. 3229-3242
-
-
Kontges, G.1
Lumsden, A.2
-
5
-
-
0026487321
-
Vital dye analysis of cranial neural crest cell migration in the mouse embryo
-
Serbedzija G.N., Bronner-Fraser M., Fraser S.E. Vital dye analysis of cranial neural crest cell migration in the mouse embryo. Development 1992, 116:297-307.
-
(1992)
Development
, vol.116
, pp. 297-307
-
-
Serbedzija, G.N.1
Bronner-Fraser, M.2
Fraser, S.E.3
-
6
-
-
0002578601
-
Further experiments on the extirpation and transplantation of mesectoderm in Amblystoma punctatum
-
Stone L.S. Further experiments on the extirpation and transplantation of mesectoderm in Amblystoma punctatum. J Exp Zool 1926, 44(1):95-131.
-
(1926)
J Exp Zool
, vol.44
, Issue.1
, pp. 95-131
-
-
Stone, L.S.1
-
7
-
-
0016746976
-
Mesenchymal derivatives of the neural crest: analysis of chimaeric quail and chick embryos
-
Le Lievre C.S., Le Douarin N.M. Mesenchymal derivatives of the neural crest: analysis of chimaeric quail and chick embryos. J Embryol Exp Morphol 1975, 34:125-154.
-
(1975)
J Embryol Exp Morphol
, vol.34
, pp. 125-154
-
-
Le Lievre, C.S.1
Le Douarin, N.M.2
-
8
-
-
0026354336
-
Segmental origin and migration of neural crest cells in the hindbrain region of the chick embryo
-
Lumsden A., Sprawson N., Graham A. Segmental origin and migration of neural crest cells in the hindbrain region of the chick embryo. Development 1991, 113(4):1281-1291.
-
(1991)
Development
, vol.113
, Issue.4
, pp. 1281-1291
-
-
Lumsden, A.1
Sprawson, N.2
Graham, A.3
-
9
-
-
0027415509
-
The triple origin of skull in higher vertebrates: a study in quail-chick chimeras
-
Couly G.F., Coltey P.M., Le Douarin N.M. The triple origin of skull in higher vertebrates: a study in quail-chick chimeras. Development 1993, 117(2):409-429.
-
(1993)
Development
, vol.117
, Issue.2
, pp. 409-429
-
-
Couly, G.F.1
Coltey, P.M.2
Le Douarin, N.M.3
-
10
-
-
0020522839
-
Contributions of placodal and neural crest cells to avian cranial peripheral ganglia
-
D'Amico-Martel A., Noden D. Contributions of placodal and neural crest cells to avian cranial peripheral ganglia. Am J Anat 1983, 166:445-468.
-
(1983)
Am J Anat
, vol.166
, pp. 445-468
-
-
D'Amico-Martel, A.1
Noden, D.2
-
11
-
-
23944503750
-
Second branchial arch lineages of the middle ear of wild-type and Hoxa2 mutant mice
-
O'Gorman S. Second branchial arch lineages of the middle ear of wild-type and Hoxa2 mutant mice. Dev Dyn 2005, 234(1):124-131.
-
(2005)
Dev Dyn
, vol.234
, Issue.1
, pp. 124-131
-
-
O'Gorman, S.1
-
12
-
-
0020080113
-
The segregation and early migration of cranial neural crest cells in the avian embryo
-
Tosney K. The segregation and early migration of cranial neural crest cells in the avian embryo. Dev Biol 1982, 89:13-24.
-
(1982)
Dev Biol
, vol.89
, pp. 13-24
-
-
Tosney, K.1
-
13
-
-
0023832833
-
A morphological and experimental study of the mesencephalic neural crest cells in the mouse embryo using wheat-germ agglutinin gold conjugate as the cell marker
-
Chan W.Y., Tam P.P.L. A morphological and experimental study of the mesencephalic neural crest cells in the mouse embryo using wheat-germ agglutinin gold conjugate as the cell marker. Development 1988, 102(2):427-442.
-
(1988)
Development
, vol.102
, Issue.2
, pp. 427-442
-
-
Chan, W.Y.1
Tam, P.P.L.2
-
14
-
-
50549180994
-
A radioautographic analysis of the migration and localization of trunk neural crest cells in the chick
-
Weston J.A. A radioautographic analysis of the migration and localization of trunk neural crest cells in the chick. Dev Biol 1963, 6(3):279-310.
-
(1963)
Dev Biol
, vol.6
, Issue.3
, pp. 279-310
-
-
Weston, J.A.1
-
15
-
-
70349840622
-
Schwann cell precursors from nerve innervation are a cellular origin of melanocytes in skin
-
Adameyko I., Lallemend F., Aquino J.B., Pereira J.A., Topilko P., Müller T., et al. Schwann cell precursors from nerve innervation are a cellular origin of melanocytes in skin. Cell 2009, 139(2):366-379.
-
(2009)
Cell
, vol.139
, Issue.2
, pp. 366-379
-
-
Adameyko, I.1
Lallemend, F.2
Aquino, J.B.3
Pereira, J.A.4
Topilko, P.5
Müller, T.6
-
16
-
-
0027674655
-
From the crest to the periphery: control of pigment cell migration and lineage segregation
-
Erickson C.A. From the crest to the periphery: control of pigment cell migration and lineage segregation. Pigment Cell Res 1993, 6(5):336-347.
-
(1993)
Pigment Cell Res
, vol.6
, Issue.5
, pp. 336-347
-
-
Erickson, C.A.1
-
17
-
-
0031931010
-
Mutations in microphthalmia, the mouse homolog of the human deafness gene MITF, affect neuroepithelial and neural crest-derived melanocytes differently
-
Nakayama A., Nguyen M.-T.T., Chen C.C., Opdecamp K., Hodgkinson C.A., Arnheiter H. Mutations in microphthalmia, the mouse homolog of the human deafness gene MITF, affect neuroepithelial and neural crest-derived melanocytes differently. Mech Dev 1998, 70(1-2):155-166.
-
(1998)
Mech Dev
, vol.70
, Issue.1-2
, pp. 155-166
-
-
Nakayama, A.1
Nguyen, M.-T.T.2
Chen, C.C.3
Opdecamp, K.4
Hodgkinson, C.A.5
Arnheiter, H.6
-
18
-
-
0031128057
-
Retinoic acid disturbs mouse middle ear development in a stage-dependent fashion
-
Mallo M. Retinoic acid disturbs mouse middle ear development in a stage-dependent fashion. Dev Biol 1997, 184(1):175-186.
-
(1997)
Dev Biol
, vol.184
, Issue.1
, pp. 175-186
-
-
Mallo, M.1
-
19
-
-
0032807177
-
Pathogenesis of retinoic acid-induced ear malformations in a primate model
-
Wei X., Makori N., Peterson P.E., Hummler H., Hendrickx A.G. Pathogenesis of retinoic acid-induced ear malformations in a primate model. Teratology 1999, 60(2):83-92.
-
(1999)
Teratology
, vol.60
, Issue.2
, pp. 83-92
-
-
Wei, X.1
Makori, N.2
Peterson, P.E.3
Hummler, H.4
Hendrickx, A.G.5
-
20
-
-
48249120908
-
Molecular dynamics of retinoic acid-induced craniofacial malformations: implications for the origin of Gnathostome Jaws
-
Vieux-Rochas M., Coen L., Sato T., Kurihara Y., Gitton Y., Barbieri O., et al. Molecular dynamics of retinoic acid-induced craniofacial malformations: implications for the origin of Gnathostome Jaws. PLoS ONE 2007, 2(6):e510.
-
(2007)
PLoS ONE
, vol.2
, Issue.6
-
-
Vieux-Rochas, M.1
Coen, L.2
Sato, T.3
Kurihara, Y.4
Gitton, Y.5
Barbieri, O.6
-
22
-
-
4644342396
-
From placode to polarization: new tunes in inner ear development
-
Barald K.F., Kelley M.W. From placode to polarization: new tunes in inner ear development. Development 2004, 131(17):4119-4130.
-
(2004)
Development
, vol.131
, Issue.17
, pp. 4119-4130
-
-
Barald, K.F.1
Kelley, M.W.2
-
23
-
-
36049010017
-
The molecular biology of ear development -"Twenty years are nothing"
-
Giraldez F., Fritzsch B. The molecular biology of ear development -"Twenty years are nothing". Int J Dev Biol 2007, 51(6/7):429.
-
(2007)
Int J Dev Biol
, vol.51
, Issue.6-7
, pp. 429
-
-
Giraldez, F.1
Fritzsch, B.2
-
24
-
-
2342510998
-
Generation of Pax2-Cre mice by modification of a Pax2 bacterial artificial chromosome
-
Ohyama T., Groves A.K. Generation of Pax2-Cre mice by modification of a Pax2 bacterial artificial chromosome. Genesis 2004, 38(4):195-199.
-
(2004)
Genesis
, vol.38
, Issue.4
, pp. 195-199
-
-
Ohyama, T.1
Groves, A.K.2
-
25
-
-
81755162275
-
Dual embryonic origin of the mammalian otic vesicle forming the inner ear
-
Freyer L., Aggarwal V., Morrow B.E. Dual embryonic origin of the mammalian otic vesicle forming the inner ear. Development 2011, 138(24):5403-5414.
-
(2011)
Development
, vol.138
, Issue.24
, pp. 5403-5414
-
-
Freyer, L.1
Aggarwal, V.2
Morrow, B.E.3
-
26
-
-
77956329426
-
Glial but not neuronal development in the cochleo-vestibular ganglion requires Sox10
-
Breuskin I., Bodson M., Thelen N., Thiry M., Borgs L., Nguyen L., et al. Glial but not neuronal development in the cochleo-vestibular ganglion requires Sox10. J Neurochem 2010, 114(6):1827-1839.
-
(2010)
J Neurochem
, vol.114
, Issue.6
, pp. 1827-1839
-
-
Breuskin, I.1
Bodson, M.2
Thelen, N.3
Thiry, M.4
Borgs, L.5
Nguyen, L.6
-
27
-
-
0018196336
-
Participation of neural crest-derived cells in the genesis of the skull in birds
-
Le Lievre C.S. Participation of neural crest-derived cells in the genesis of the skull in birds. J Embryol Exp Morphol 1978, 47:17-37.
-
(1978)
J Embryol Exp Morphol
, vol.47
, pp. 17-37
-
-
Le Lievre, C.S.1
-
28
-
-
0022930851
-
Epithelial-mesenchymal tissue interactions guiding otic capsule formation: the role of the otocyst
-
McPhee J.R., Van De Water T.R. Epithelial-mesenchymal tissue interactions guiding otic capsule formation: the role of the otocyst. J Embryol Exp Morphol 1986, 97(1):1-24.
-
(1986)
J Embryol Exp Morphol
, vol.97
, Issue.1
, pp. 1-24
-
-
McPhee, J.R.1
Van De Water, T.R.2
-
29
-
-
84865350251
-
The origin of the stapes and relationship to the otic capsule and oval window
-
Thompson H., Ohazama A., Sharpe P.T., Tucker A.S. The origin of the stapes and relationship to the otic capsule and oval window. Dev Dyn 2012, 241(9):1396-1404.
-
(2012)
Dev Dyn
, vol.241
, Issue.9
, pp. 1396-1404
-
-
Thompson, H.1
Ohazama, A.2
Sharpe, P.T.3
Tucker, A.S.4
-
32
-
-
34347150259
-
The production of pigment in vitro by chick neural crest
-
Dorris F. The production of pigment in vitro by chick neural crest. Wilhelm Roux' Arch Entwickl 1938, 138(3-4):323-334.
-
(1938)
Wilhelm Roux' Arch Entwickl
, vol.138
, Issue.3-4
, pp. 323-334
-
-
Dorris, F.1
-
33
-
-
84982062906
-
An experimental study of the origin of pigment cells in amphibia
-
DuShane G.P. An experimental study of the origin of pigment cells in amphibia. J Exp Zool 1935, 72(1):1-31.
-
(1935)
J Exp Zool
, vol.72
, Issue.1
, pp. 1-31
-
-
DuShane, G.P.1
-
34
-
-
0001047092
-
Origin of pigment cells from the neural crest in the mouse embryo
-
Rawles M.E. Origin of pigment cells from the neural crest in the mouse embryo. Physiol Zool 1947, 248-266.
-
(1947)
Physiol Zool
, pp. 248-266
-
-
Rawles, M.E.1
-
35
-
-
0017644138
-
Pigmentation of the stria vascularis the contribution of neural crest melanocytes
-
Hilding D., Ginzberg R.D. Pigmentation of the stria vascularis the contribution of neural crest melanocytes. Acta Otolaryngol 1977, 84(1-6):24-37.
-
(1977)
Acta Otolaryngol
, vol.84
, Issue.1-6
, pp. 24-37
-
-
Hilding, D.1
Ginzberg, R.D.2
-
36
-
-
0025940323
-
Mutation of the KIT (mast/stem cell growth factor receptor) protooncogene in human piebaldism
-
Giebel L.B., Spritz R.A. Mutation of the KIT (mast/stem cell growth factor receptor) protooncogene in human piebaldism. Proc Natl Acad Sci USA 1991, 88(19):8696-8699.
-
(1991)
Proc Natl Acad Sci USA
, vol.88
, Issue.19
, pp. 8696-8699
-
-
Giebel, L.B.1
Spritz, R.A.2
-
37
-
-
0027470985
-
Characteristics of stria vascularis melanocytes of viable dominant spotting (WvWv) mouse mutants
-
Cable J., Barkway C., Steel K.P. Characteristics of stria vascularis melanocytes of viable dominant spotting (WvWv) mouse mutants. Hear Res 1992, 64(1):6-20.
-
(1992)
Hear Res
, vol.64
, Issue.1
, pp. 6-20
-
-
Cable, J.1
Barkway, C.2
Steel, K.P.3
-
38
-
-
0024280901
-
The dominant-white spotting (W) locus of the mouse encodes the c-kit proto-oncogene
-
Geissler E.N., Ryan M.A., Housman D.E. The dominant-white spotting (W) locus of the mouse encodes the c-kit proto-oncogene. Cell 1988, 55(1):185-192.
-
(1988)
Cell
, vol.55
, Issue.1
, pp. 185-192
-
-
Geissler, E.N.1
Ryan, M.A.2
Housman, D.E.3
-
39
-
-
15544370702
-
Identification of a novel point mutation of mouse proto-oncogene c-kit through N-ethyl-N-nitrosourea mutagenesis
-
Ruan H.-B., Zhang N., Gao X. Identification of a novel point mutation of mouse proto-oncogene c-kit through N-ethyl-N-nitrosourea mutagenesis. Genetics 2005, 169(2):819-831.
-
(2005)
Genetics
, vol.169
, Issue.2
, pp. 819-831
-
-
Ruan, H.-B.1
Zhang, N.2
Gao, X.3
-
40
-
-
0016169528
-
The neurocristopathies: a unifying concept of disease arising in neural crest maldevelopment
-
Bolande R.P. The neurocristopathies: a unifying concept of disease arising in neural crest maldevelopment. Hum Pathol 1974, 5(4):409-429.
-
(1974)
Hum Pathol
, vol.5
, Issue.4
, pp. 409-429
-
-
Bolande, R.P.1
-
41
-
-
0025218051
-
The neurocristopathies: reinterpretation based upon the mechanism of abnormal morphogenesis
-
Jones M.C. The neurocristopathies: reinterpretation based upon the mechanism of abnormal morphogenesis. Cleft Palate Craniofac J 1990, 27(2):136-140.
-
(1990)
Cleft Palate Craniofac J
, vol.27
, Issue.2
, pp. 136-140
-
-
Jones, M.C.1
-
42
-
-
77950389859
-
Review and update of mutations causing Waardenburg syndrome
-
Pingault V., Ente D., Dastot-Le Moal F., Goossens M., Marlin S., Bondurand N. Review and update of mutations causing Waardenburg syndrome. Hum Mutat 2010, 31(4):391-406.
-
(2010)
Hum Mutat
, vol.31
, Issue.4
, pp. 391-406
-
-
Pingault, V.1
Ente, D.2
Dastot-Le Moal, F.3
Goossens, M.4
Marlin, S.5
Bondurand, N.6
-
43
-
-
0030739603
-
Waardenburg syndrome
-
Read A.P., Newton V.E. Waardenburg syndrome. J Med Genet 1997, 34(8):656-665.
-
(1997)
J Med Genet
, vol.34
, Issue.8
, pp. 656-665
-
-
Read, A.P.1
Newton, V.E.2
-
44
-
-
0035086454
-
Vestibular phenotype for Waardenburg syndrome?
-
Black F.O., Pesznecker S.C., Allen K., Gianna C.A. Vestibular phenotype for Waardenburg syndrome?. Otol Neurotol 2001, 22(2):188-194.
-
(2001)
Otol Neurotol
, vol.22
, Issue.2
, pp. 188-194
-
-
Black, F.O.1
Pesznecker, S.C.2
Allen, K.3
Gianna, C.A.4
-
45
-
-
84902418140
-
Congenital vestibular disorders
-
Thieme Medical Publishers, New York, NY, P.C. Weber (Ed.)
-
Kaneaster S.K., Saunders J.E. Congenital vestibular disorders. Vertigo and disequilibrium a practical guide to diagnosis and management 2008, 119-124. Thieme Medical Publishers, New York, NY. P.C. Weber (Ed.).
-
(2008)
Vertigo and disequilibrium a practical guide to diagnosis and management
, pp. 119-124
-
-
Kaneaster, S.K.1
Saunders, J.E.2
-
46
-
-
0024314157
-
Another role for melanocytes: their importance for normal stria vascularis development in the mammalian inner ear
-
Steel K.P., Barkway C. Another role for melanocytes: their importance for normal stria vascularis development in the mammalian inner ear. Development 1989, 107(3):453-463.
-
(1989)
Development
, vol.107
, Issue.3
, pp. 453-463
-
-
Steel, K.P.1
Barkway, C.2
-
47
-
-
0026602124
-
Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene
-
Tassabehji M., Read A.P., Newton V.E., Harris R., Balling R., Gruss P., et al. Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene. Nature 1992, 355(6361):635-636.
-
(1992)
Nature
, vol.355
, Issue.6361
, pp. 635-636
-
-
Tassabehji, M.1
Read, A.P.2
Newton, V.E.3
Harris, R.4
Balling, R.5
Gruss, P.6
-
48
-
-
0141954262
-
Postnatal maturation of the dog stria vascularis-an immunohistochemical study
-
Coppens A.G., Salmon I., Heizmann C.W., Kiss R., Poncelet L. Postnatal maturation of the dog stria vascularis-an immunohistochemical study. Anat Rec A Discov Mol Cell Evol Biol 2003, 270A(1):82-92.
-
(2003)
Anat Rec A Discov Mol Cell Evol Biol
, vol.270 A
, Issue.1
, pp. 82-92
-
-
Coppens, A.G.1
Salmon, I.2
Heizmann, C.W.3
Kiss, R.4
Poncelet, L.5
-
49
-
-
0020594546
-
Hereditary inner-ear abnormalities in animals: relationships with human abnormalities
-
Steel K.P., Bock G.R. Hereditary inner-ear abnormalities in animals: relationships with human abnormalities. Arch Otolaryngol Head Neck Surg 1983, 109(1):22.
-
(1983)
Arch Otolaryngol Head Neck Surg
, vol.109
, Issue.1
, pp. 22
-
-
Steel, K.P.1
Bock, G.R.2
-
50
-
-
0035914234
-
Histopathology and molecular genetics of hearing loss in the human
-
Nadol J.B., Merchant S.N. Histopathology and molecular genetics of hearing loss in the human. Int J Pediatr Otorhinolaryngol 2001, 61(1):1-15.
-
(2001)
Int J Pediatr Otorhinolaryngol
, vol.61
, Issue.1
, pp. 1-15
-
-
Nadol, J.B.1
Merchant, S.N.2
-
51
-
-
0034841797
-
Otopathology in a case of type I Waardenburg's syndrome
-
Merchant S.N., McKenna M.J., Baldwin C.T., Milunsky A., Nadol J.B. Otopathology in a case of type I Waardenburg's syndrome. Ann Otol Rhinol Laryngol 2001, 110(9):875-882.
-
(2001)
Ann Otol Rhinol Laryngol
, vol.110
, Issue.9
, pp. 875-882
-
-
Merchant, S.N.1
McKenna, M.J.2
Baldwin, C.T.3
Milunsky, A.4
Nadol, J.B.5
-
52
-
-
74349097441
-
Melanin precursors prevent premature age-related and noise-induced hearing loss in albino mice
-
Murillo-Cuesta S., Contreras J., Zurita E., Cediel R., Cantero M., Varela-Nieto I., et al. Melanin precursors prevent premature age-related and noise-induced hearing loss in albino mice. Pigment Cell Melanoma Res 2010, 23(1):72-83.
-
(2010)
Pigment Cell Melanoma Res
, vol.23
, Issue.1
, pp. 72-83
-
-
Murillo-Cuesta, S.1
Contreras, J.2
Zurita, E.3
Cediel, R.4
Cantero, M.5
Varela-Nieto, I.6
-
53
-
-
60849123899
-
Absence of strial melanin coincides with age-associated marginal cell loss and endocochlear potential decline
-
Ohlemiller K.K., Rybak Rice M.E., Lett J.M., Gagnon P.M. Absence of strial melanin coincides with age-associated marginal cell loss and endocochlear potential decline. Hear Res 2009, 249(1-2):1-14.
-
(2009)
Hear Res
, vol.249
, Issue.1-2
, pp. 1-14
-
-
Ohlemiller, K.K.1
Rybak Rice, M.E.2
Lett, J.M.3
Gagnon, P.M.4
-
54
-
-
0035038927
-
Sensorineural deafness and pigmentation genes: melanocytes and the Mitf transcriptional network
-
Price E.R., Fisher D.E. Sensorineural deafness and pigmentation genes: melanocytes and the Mitf transcriptional network. Neuron 2001, 30(1):15-18.
-
(2001)
Neuron
, vol.30
, Issue.1
, pp. 15-18
-
-
Price, E.R.1
Fisher, D.E.2
-
55
-
-
0025188791
-
Mouse and hamster mutants as models for Waardenburg syndromes in humans
-
Asher J.H., Friedman T.B. Mouse and hamster mutants as models for Waardenburg syndromes in humans. J Med Genet 1990, 27(10):618-626.
-
(1990)
J Med Genet
, vol.27
, Issue.10
, pp. 618-626
-
-
Asher, J.H.1
Friedman, T.B.2
-
56
-
-
0042337138
-
Mouse models for four types of Waardenburg syndrome
-
Tachibana M., Kobayashi Y., Matsushima Y. Mouse models for four types of Waardenburg syndrome. Pigment Cell Res 2003, 16(5):448-454.
-
(2003)
Pigment Cell Res
, vol.16
, Issue.5
, pp. 448-454
-
-
Tachibana, M.1
Kobayashi, Y.2
Matsushima, Y.3
-
57
-
-
0028051530
-
Microphthalmia-associated transcription factor as a regulator for melanocyte-specific transcription of the human tyrosinase gene
-
Yasumoto K., Yokoyama K., Shibata K., Tomita Y., Shibahara S. Microphthalmia-associated transcription factor as a regulator for melanocyte-specific transcription of the human tyrosinase gene. Mol Cell Biol 1994, 14(12):8058-8070.
-
(1994)
Mol Cell Biol
, vol.14
, Issue.12
, pp. 8058-8070
-
-
Yasumoto, K.1
Yokoyama, K.2
Shibata, K.3
Tomita, Y.4
Shibahara, S.5
-
58
-
-
33745177750
-
Interspecies difference in the regulation of melanocyte development by SOX10 and MITF
-
Hou L., Arnheiter H., Pavan W.J. Interspecies difference in the regulation of melanocyte development by SOX10 and MITF. Proc Natl Acad Sci USA 2006, 103(24):9081-9085.
-
(2006)
Proc Natl Acad Sci USA
, vol.103
, Issue.24
, pp. 9081-9085
-
-
Hou, L.1
Arnheiter, H.2
Pavan, W.J.3
-
59
-
-
0030746395
-
Melanocyte development in vivo and in neural crest cell cultures: crucial dependence on the Mitf basic-helix-loop-helix-zipper transcription factor
-
Opdecamp K., Nakayama A., Nguyen M.T., Hodgkinson C.A., Pavan W.J., Arnheiter H. Melanocyte development in vivo and in neural crest cell cultures: crucial dependence on the Mitf basic-helix-loop-helix-zipper transcription factor. Development 1997, 124(12):2377-2386.
-
(1997)
Development
, vol.124
, Issue.12
, pp. 2377-2386
-
-
Opdecamp, K.1
Nakayama, A.2
Nguyen, M.T.3
Hodgkinson, C.A.4
Pavan, W.J.5
Arnheiter, H.6
-
60
-
-
0035110947
-
Transcription factors in melanocyte development: distinct roles for Pax-3 and Mitf
-
Hornyak T.J., Hayes D.J., Chiu L.-Y., Ziff E.B. Transcription factors in melanocyte development: distinct roles for Pax-3 and Mitf. Mech Dev 2001, 101(1-2):47-59.
-
(2001)
Mech Dev
, vol.101
, Issue.1-2
, pp. 47-59
-
-
Hornyak, T.J.1
Hayes, D.J.2
Chiu, L.-Y.3
Ziff, E.B.4
-
61
-
-
21044439392
-
Neural crest determination by co-activation of Pax3 and Zic1 genes in Xenopus ectoderm
-
Sato T., Sasai N., Sasai Y. Neural crest determination by co-activation of Pax3 and Zic1 genes in Xenopus ectoderm. Development 2005, 132(10):2355-2363.
-
(2005)
Development
, vol.132
, Issue.10
, pp. 2355-2363
-
-
Sato, T.1
Sasai, N.2
Sasai, Y.3
-
62
-
-
77949389034
-
Roles of endothelin signaling in melanocyte development and melanoma
-
Saldana-Caboverde A., Kos L. Roles of endothelin signaling in melanocyte development and melanoma. Pigment Cell Melanoma Res 2010, 23(2):160-170.
-
(2010)
Pigment Cell Melanoma Res
, vol.23
, Issue.2
, pp. 160-170
-
-
Saldana-Caboverde, A.1
Kos, L.2
-
63
-
-
0027943189
-
Waardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) gene
-
Tassabehji M., Newton V.E., Read A.P. Waardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) gene. Nat Genet 1994, 8(3):251-255.
-
(1994)
Nat Genet
, vol.8
, Issue.3
, pp. 251-255
-
-
Tassabehji, M.1
Newton, V.E.2
Read, A.P.3
-
64
-
-
0030979154
-
Apparent digenic inheritance of Waardenburg syndrome type 2 (WS2) and Autosomal Recessive Ocular Albinism (AROA)
-
Morell R., Spritz R.A., Ho L., Pierpont J., Guo W., Friedman T.B., et al. Apparent digenic inheritance of Waardenburg syndrome type 2 (WS2) and Autosomal Recessive Ocular Albinism (AROA). Hum Mol Genet 1997, 6(5):659-664.
-
(1997)
Hum Mol Genet
, vol.6
, Issue.5
, pp. 659-664
-
-
Morell, R.1
Spritz, R.A.2
Ho, L.3
Pierpont, J.4
Guo, W.5
Friedman, T.B.6
-
65
-
-
0031964911
-
Mutation of the MITF gene in albinism-deafness syndrome (Tietz syndrome)
-
Amiel J., Watkin P.M., Tassabehji M., Read A.P., Winter R.M. Mutation of the MITF gene in albinism-deafness syndrome (Tietz syndrome). Clin Dysmorphol 1998, 7(1):17.
-
(1998)
Clin Dysmorphol
, vol.7
, Issue.1
, pp. 17
-
-
Amiel, J.1
Watkin, P.M.2
Tassabehji, M.3
Read, A.P.4
Winter, R.M.5
-
66
-
-
0027204149
-
Mutations at the mouse microphthalmia locus are associated with defects in a gene encoding a novel basic-helix-loop-helix-zipper protein
-
Hodgkinson C.A., Moore K.J., Nakayama A., Steingrímsson E., Copeland N.G., Jenkins N.A., et al. Mutations at the mouse microphthalmia locus are associated with defects in a gene encoding a novel basic-helix-loop-helix-zipper protein. Cell 1993, 74(2):395-404.
-
(1993)
Cell
, vol.74
, Issue.2
, pp. 395-404
-
-
Hodgkinson, C.A.1
Moore, K.J.2
Nakayama, A.3
Steingrímsson, E.4
Copeland, N.G.5
Jenkins, N.A.6
-
67
-
-
0027386022
-
A helix-loop-helix transcription factor-like gene is located at the mi locus
-
Hughes M.J., Lingrel J.B., Krakowsky J.M., Anderson K.P. A helix-loop-helix transcription factor-like gene is located at the mi locus. J Biol Chem 1993, 268(28):20687-20690.
-
(1993)
J Biol Chem
, vol.268
, Issue.28
, pp. 20687-20690
-
-
Hughes, M.J.1
Lingrel, J.B.2
Krakowsky, J.M.3
Anderson, K.P.4
-
68
-
-
0014935865
-
The relationship between abnormalities of pigmentation and of the inner ear
-
Deol M.S. The relationship between abnormalities of pigmentation and of the inner ear. Proc R Soc Lond B Biol Sci 1970, 175(1039):201-217.
-
(1970)
Proc R Soc Lond B Biol Sci
, vol.175
, Issue.1039
, pp. 201-217
-
-
Deol, M.S.1
-
69
-
-
0026584439
-
An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome
-
Baldwin C.T., Hoth C.F., Amos J.A., da-Silva E.O., Milunsky A. An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome. Nature 1992, 355(6361):637-638.
-
(1992)
Nature
, vol.355
, Issue.6361
, pp. 637-638
-
-
Baldwin, C.T.1
Hoth, C.F.2
Amos, J.A.3
da-Silva, E.O.4
Milunsky, A.5
-
70
-
-
0026893878
-
A frameshift mutation in the HuP2 paired domain of the probable human homolog of murine Pax-3 is responsible for Waardenburg syndrome type 1 in an Indonesian family
-
Morell R., Friedman T.B., Moeljopawiro S., Hartono S., Asher J.H. A frameshift mutation in the HuP2 paired domain of the probable human homolog of murine Pax-3 is responsible for Waardenburg syndrome type 1 in an Indonesian family. Hum Mol Genet 1992, 1(4):243-247.
-
(1992)
Hum Mol Genet
, vol.1
, Issue.4
, pp. 243-247
-
-
Morell, R.1
Friedman, T.B.2
Moeljopawiro, S.3
Hartono, S.4
Asher, J.H.5
-
71
-
-
0027439075
-
Mutations in the paired domain of the human PAX3 gene cause Klein-Waardenburg syndrome (WS-III) as well as Waardenburg syndrome type I (WS-I)
-
Hoth C., Milunsky A., Lipsky N., Sheffer R., Clarren S., Baldwin C. Mutations in the paired domain of the human PAX3 gene cause Klein-Waardenburg syndrome (WS-III) as well as Waardenburg syndrome type I (WS-I). Am J Hum Genet 1993, 52(3):455.
-
(1993)
Am J Hum Genet
, vol.52
, Issue.3
, pp. 455
-
-
Hoth, C.1
Milunsky, A.2
Lipsky, N.3
Sheffer, R.4
Clarren, S.5
Baldwin, C.6
-
72
-
-
0030030303
-
Missense mutation in the paired domain of PAX3 causes craniofacial-deafness-hand syndrome
-
Asher J.H., Sommer A., Morell R., Friedman T.B. Missense mutation in the paired domain of PAX3 causes craniofacial-deafness-hand syndrome. Hum Mutat 1996, 7(1):30-35.
-
(1996)
Hum Mutat
, vol.7
, Issue.1
, pp. 30-35
-
-
Asher, J.H.1
Sommer, A.2
Morell, R.3
Friedman, T.B.4
-
73
-
-
0026921154
-
Normal hearing in Splotch (Sp/+), the mouse homologue of Waardenburg syndrome type 1
-
Steel K.P., Smith R.J.H. Normal hearing in Splotch (Sp/+), the mouse homologue of Waardenburg syndrome type 1. Nat Genet 1992, 2(1):75-79.
-
(1992)
Nat Genet
, vol.2
, Issue.1
, pp. 75-79
-
-
Steel, K.P.1
Smith, R.J.H.2
-
74
-
-
0025925068
-
Splotch (Sp2H), a mutation affecting development of the mouse neural tube, shows a deletion within the paired homeodomain of Pax-3
-
Epstein D.J., Vekemans M., Gros P. Splotch (Sp2H), a mutation affecting development of the mouse neural tube, shows a deletion within the paired homeodomain of Pax-3. Cell 1991, 67(4):767-774.
-
(1991)
Cell
, vol.67
, Issue.4
, pp. 767-774
-
-
Epstein, D.J.1
Vekemans, M.2
Gros, P.3
-
75
-
-
0036898925
-
SLUG (SNAI2) deletions in patients with Waardenburg disease
-
Sánchez-Martín M., Rodríguez-García A., Pérez-Losada J., Sagrera A., Read A.P., Sánchez-García I. SLUG (SNAI2) deletions in patients with Waardenburg disease. Hum Mol Genet 2002, 11(25):3231-3236.
-
(2002)
Hum Mol Genet
, vol.11
, Issue.25
, pp. 3231-3236
-
-
Sánchez-Martín, M.1
Rodríguez-García, A.2
Pérez-Losada, J.3
Sagrera, A.4
Read, A.P.5
Sánchez-García, I.6
-
76
-
-
0037103359
-
Zinc-finger transcription factor Slug contributes to the function of the stem cell factor c-kit signaling pathway
-
Pérez-Losada J., Sánchez-Martín M., Rodríguez-García A., Sánchez M.L., Orfao A., Flores T., et al. Zinc-finger transcription factor Slug contributes to the function of the stem cell factor c-kit signaling pathway. Blood 2002, 100(4):1274-1286.
-
(2002)
Blood
, vol.100
, Issue.4
, pp. 1274-1286
-
-
Pérez-Losada, J.1
Sánchez-Martín, M.2
Rodríguez-García, A.3
Sánchez, M.L.4
Orfao, A.5
Flores, T.6
-
77
-
-
17344366171
-
SOX10 mutations in patients with Waardenburg-Hirschsprung disease
-
Pingault V., Bondurand N., Kuhlbrodt K., Goerich D.E., Prehu M.O., Puliti A., et al. SOX10 mutations in patients with Waardenburg-Hirschsprung disease. Nat Genet 1998, 18(2):171-173.
-
(1998)
Nat Genet
, vol.18
, Issue.2
, pp. 171-173
-
-
Pingault, V.1
Bondurand, N.2
Kuhlbrodt, K.3
Goerich, D.E.4
Prehu, M.O.5
Puliti, A.6
-
78
-
-
0032574721
-
Mutation of the Sry-related Sox10 gene in dominant megacolon, a mouse model for human Hirschsprung disease
-
Herbarth B., Pingault V., Bondurand N., Kuhlbrodt K., Hermans-Borgmeyer I., Puliti A., et al. Mutation of the Sry-related Sox10 gene in dominant megacolon, a mouse model for human Hirschsprung disease. Proc Natl Acad Sci USA 1998, 95(9):5161-5165.
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, Issue.9
, pp. 5161-5165
-
-
Herbarth, B.1
Pingault, V.2
Bondurand, N.3
Kuhlbrodt, K.4
Hermans-Borgmeyer, I.5
Puliti, A.6
-
79
-
-
0031984825
-
SOX10 mutation disrupts neural crest development in Dom Hirschsprung mouse model
-
Southard-Smith E.M., Kos L., Pavan W.J. SOX10 mutation disrupts neural crest development in Dom Hirschsprung mouse model. Nat Genet 1998, 18(1):60-64.
-
(1998)
Nat Genet
, vol.18
, Issue.1
, pp. 60-64
-
-
Southard-Smith, E.M.1
Kos, L.2
Pavan, W.J.3
-
80
-
-
0006457459
-
Mutation of the endothelin-3 gene in the Waardenburg-Hirschsprung disease (Shah-Waardenburg syndrome)
-
Edery P., Attie T., Amiel J., Pelet A., Eng C., Hofstra R.M., et al. Mutation of the endothelin-3 gene in the Waardenburg-Hirschsprung disease (Shah-Waardenburg syndrome). Nat Genet 1996, 12(4):442-444.
-
(1996)
Nat Genet
, vol.12
, Issue.4
, pp. 442-444
-
-
Edery, P.1
Attie, T.2
Amiel, J.3
Pelet, A.4
Eng, C.5
Hofstra, R.M.6
-
81
-
-
0028609612
-
Interaction of endothelin-3 with endothelin-B receptor is essential for development of epidermal melanocytes and enteric neurons
-
Baynash A.G., Hosoda K., Giaid A., Richardson J.A., Emoto N., Hammer R.E., et al. Interaction of endothelin-3 with endothelin-B receptor is essential for development of epidermal melanocytes and enteric neurons. Cell 1994, 79(7):1277-1285.
-
(1994)
Cell
, vol.79
, Issue.7
, pp. 1277-1285
-
-
Baynash, A.G.1
Hosoda, K.2
Giaid, A.3
Richardson, J.A.4
Emoto, N.5
Hammer, R.E.6
-
82
-
-
0028862473
-
Mutation of the endothelin-receptor B gene in Waardenburg-Hirschsprung disease
-
Attié T., Till M., Pelet A., Amiel J., Edery P., Boutrand L., et al. Mutation of the endothelin-receptor B gene in Waardenburg-Hirschsprung disease. Hum Mol Genet 1995, 4(12):2407-2409.
-
(1995)
Hum Mol Genet
, vol.4
, Issue.12
, pp. 2407-2409
-
-
Attié, T.1
Till, M.2
Pelet, A.3
Amiel, J.4
Edery, P.5
Boutrand, L.6
-
83
-
-
0036134088
-
A mouse model of Waardenburg syndrome type 4 with a new spontaneous mutation of the endothelin-B receptor gene
-
Matsushima Y., Shinkai Y., Kobayashi Y., Sakamoto M., Kunieda T., Tachibana M. A mouse model of Waardenburg syndrome type 4 with a new spontaneous mutation of the endothelin-B receptor gene. Mamm Genome 2002, 13(1):30-35.
-
(2002)
Mamm Genome
, vol.13
, Issue.1
, pp. 30-35
-
-
Matsushima, Y.1
Shinkai, Y.2
Kobayashi, Y.3
Sakamoto, M.4
Kunieda, T.5
Tachibana, M.6
-
84
-
-
0028639196
-
Targeted and natural (piebald-lethal) mutations of endothelin-B receptor gene produce megacolon associated with spotted coat color in mice
-
Hosoda K., Hammer R.E., Richardson J.A., Baynash A.G., Cheung J.C., Giaid A., et al. Targeted and natural (piebald-lethal) mutations of endothelin-B receptor gene produce megacolon associated with spotted coat color in mice. Cell 1994, 79(7):1267-1276.
-
(1994)
Cell
, vol.79
, Issue.7
, pp. 1267-1276
-
-
Hosoda, K.1
Hammer, R.E.2
Richardson, J.A.3
Baynash, A.G.4
Cheung, J.C.5
Giaid, A.6
-
85
-
-
0642349268
-
Formation of the outer and middle ear, molecular mechanisms
-
Mallo M. Formation of the outer and middle ear, molecular mechanisms. Curr Top Dev Biol 2003, 85-113.
-
(2003)
Curr Top Dev Biol
, pp. 85-113
-
-
Mallo, M.1
-
86
-
-
0001880484
-
Experimentelle untersuchungen uber die determination des knorpeligen Kopfskelettes bei Urodelen
-
Horstadius S., Sellman S. Experimentelle untersuchungen uber die determination des knorpeligen Kopfskelettes bei Urodelen. Nov Act Reg Soc Scient Ups Ser 1946, 13:1-170.
-
(1946)
Nov Act Reg Soc Scient Ups Ser
, vol.13
, pp. 1-170
-
-
Horstadius, S.1
Sellman, S.2
-
87
-
-
0342959301
-
Ectodermal origin of the cartilages of the head
-
Platt J.B. Ectodermal origin of the cartilages of the head. Anat Anz 1893, 8:506-509.
-
(1893)
Anat Anz
, vol.8
, pp. 506-509
-
-
Platt, J.B.1
-
88
-
-
0345502613
-
The development of the cartilaginous skull and of the branchial and hypoglossal musculature in Necturus
-
Platt J.B. The development of the cartilaginous skull and of the branchial and hypoglossal musculature in Necturus. Morphol Jb 1897, 25:377-464.
-
(1897)
Morphol Jb
, vol.25
, pp. 377-464
-
-
Platt, J.B.1
-
89
-
-
0020435645
-
Patterns and organization of craniofacial skeletogenic and myogenic mesenchyme: a perspective
-
Noden D.M. Patterns and organization of craniofacial skeletogenic and myogenic mesenchyme: a perspective. Prog Clin Biol Res 1982, 101:167-203.
-
(1982)
Prog Clin Biol Res
, vol.101
, pp. 167-203
-
-
Noden, D.M.1
-
90
-
-
0021320185
-
Craniofacial development; new views on old problems
-
Noden D. Craniofacial development; new views on old problems. Anat Rec 1984, 208:1-13.
-
(1984)
Anat Rec
, vol.208
, pp. 1-13
-
-
Noden, D.1
-
91
-
-
79955027297
-
Can you hear me now? Understanding vertebrate middle ear development
-
Chapman S.C. Can you hear me now? Understanding vertebrate middle ear development. Front Biosci 2011, 16:1675.
-
(2011)
Front Biosci
, vol.16
, pp. 1675
-
-
Chapman, S.C.1
-
92
-
-
34047217099
-
Fate of cranial neural crest cells during craniofacial development in endothelin-A receptor-deficient mice
-
Abe M., Ruest L.B., Clouthier D.E. Fate of cranial neural crest cells during craniofacial development in endothelin-A receptor-deficient mice. Int J Dev Biol 2007, 51(2):97.
-
(2007)
Int J Dev Biol
, vol.51
, Issue.2
, pp. 97
-
-
Abe, M.1
Ruest, L.B.2
Clouthier, D.E.3
-
93
-
-
57349122369
-
Segmentation of the vertebrate skull: neural-crest derivation of adult cartilages in the clawed frog, Xenopus laevis
-
Gross J.B., Hanken J. Segmentation of the vertebrate skull: neural-crest derivation of adult cartilages in the clawed frog, Xenopus laevis. Integr Comp Biol 2008, 48(5):681-696.
-
(2008)
Integr Comp Biol
, vol.48
, Issue.5
, pp. 681-696
-
-
Gross, J.B.1
Hanken, J.2
-
94
-
-
0033973655
-
All for one and one for all: condensations and the initiation of skeletal development
-
Hall B.K., Miyake T. All for one and one for all: condensations and the initiation of skeletal development. BioEssays 2000, 22(2):138-147.
-
(2000)
BioEssays
, vol.22
, Issue.2
, pp. 138-147
-
-
Hall, B.K.1
Miyake, T.2
-
95
-
-
0017838518
-
A histological study of the development of the avian middle ear and tympanum
-
Jaskoll T.F., Maderson P.F.A. A histological study of the development of the avian middle ear and tympanum. Anat Rec 1978, 190(2):177-199.
-
(1978)
Anat Rec
, vol.190
, Issue.2
, pp. 177-199
-
-
Jaskoll, T.F.1
Maderson, P.F.A.2
-
96
-
-
0036194556
-
Fate of the mesenchyme in the process of pneumatization
-
Palva T., Ramsay H. Fate of the mesenchyme in the process of pneumatization. Otol Neurotol 2002, 23(2):192-199.
-
(2002)
Otol Neurotol
, vol.23
, Issue.2
, pp. 192-199
-
-
Palva, T.1
Ramsay, H.2
-
97
-
-
12244254480
-
Apoptosis and regression of embryonic mesenchyme in the development of the middle ear spaces
-
Palva T., Pääkkö P., Ramsay H., Chrobok V., Simáková E. Apoptosis and regression of embryonic mesenchyme in the development of the middle ear spaces. Acta Otolaryngol 2003, 123(2):209.
-
(2003)
Acta Otolaryngol
, vol.123
, Issue.2
, pp. 209
-
-
Palva, T.1
Pääkkö, P.2
Ramsay, H.3
Chrobok, V.4
Simáková, E.5
-
98
-
-
77952298971
-
Defects in middle ear cavitation cause conductive hearing loss in the Tcof1 mutant mouse
-
Richter C.A., Amin S., Linden J., Dixon J., Dixon M.J., Tucker A.S. Defects in middle ear cavitation cause conductive hearing loss in the Tcof1 mutant mouse. Hum Mol Genet 2010, 19(8):1551-1560.
-
(2010)
Hum Mol Genet
, vol.19
, Issue.8
, pp. 1551-1560
-
-
Richter, C.A.1
Amin, S.2
Linden, J.3
Dixon, J.4
Dixon, M.J.5
Tucker, A.S.6
-
99
-
-
33748614339
-
Tcof1/Treacle is required for neural crest cell formation and proliferation deficiencies that cause craniofacial abnormalities
-
Dixon J., Jones N.C., Sandell L.L., Jayasinghe S.M., Crane J., Rey J.P., et al. Tcof1/Treacle is required for neural crest cell formation and proliferation deficiencies that cause craniofacial abnormalities. Proc Natl Acad Sci USA 2006, 103:13403-13408.
-
(2006)
Proc Natl Acad Sci USA
, vol.103
, pp. 13403-13408
-
-
Dixon, J.1
Jones, N.C.2
Sandell, L.L.3
Jayasinghe, S.M.4
Crane, J.5
Rey, J.P.6
-
100
-
-
0030044346
-
Development of the mammalian ear: coordinate regulation of formation of the tympanic ring and the external acoustic meatus
-
Mallo M., Gridley T. Development of the mammalian ear: coordinate regulation of formation of the tympanic ring and the external acoustic meatus. Development 1996, 122(1):173-179.
-
(1996)
Development
, vol.122
, Issue.1
, pp. 173-179
-
-
Mallo, M.1
Gridley, T.2
-
101
-
-
0027759447
-
Hoxa-2 mutant mice exhibit homeotic transformation of skeletal elements derived from cranial neural crest
-
Gendron-Maguire M., Mallo M., Zhang M., Gridley T. Hoxa-2 mutant mice exhibit homeotic transformation of skeletal elements derived from cranial neural crest. Cell 1993, 75:1317-1331.
-
(1993)
Cell
, vol.75
, pp. 1317-1331
-
-
Gendron-Maguire, M.1
Mallo, M.2
Zhang, M.3
Gridley, T.4
-
102
-
-
0027739813
-
A homeotic transformation is generated in the rostral branchial region of the head by disruption of Hoxa-2, which acts as a selector gene
-
Rijli F.M., Mark M., Lakkaraju S., Dierich A., Dolle P., Chambon P. A homeotic transformation is generated in the rostral branchial region of the head by disruption of Hoxa-2, which acts as a selector gene. Cell 1993, 75:1333-1349.
-
(1993)
Cell
, vol.75
, pp. 1333-1349
-
-
Rijli, F.M.1
Mark, M.2
Lakkaraju, S.3
Dierich, A.4
Dolle, P.5
Chambon, P.6
-
103
-
-
0034057170
-
Fate of the mammalian cranial neural crest during tooth and mandibular morphogenesis
-
Chai Y., Jiang X., Ito Y., Bringas P., Han J., Rowitch D.H., et al. Fate of the mammalian cranial neural crest during tooth and mandibular morphogenesis. Development 2000, 127(8):1671-1679.
-
(2000)
Development
, vol.127
, Issue.8
, pp. 1671-1679
-
-
Chai, Y.1
Jiang, X.2
Ito, Y.3
Bringas, P.4
Han, J.5
Rowitch, D.H.6
-
104
-
-
0031916129
-
Cranial and cardiac neural crest defects in endothelin-A receptor-deficient mice
-
Clouthier D.E., Hosoda K., Richardson J.A., Williams S.C., Yanagisawa H., Kuwaki T., et al. Cranial and cardiac neural crest defects in endothelin-A receptor-deficient mice. Development 1998, 125(5):813-824.
-
(1998)
Development
, vol.125
, Issue.5
, pp. 813-824
-
-
Clouthier, D.E.1
Hosoda, K.2
Richardson, J.A.3
Williams, S.C.4
Yanagisawa, H.5
Kuwaki, T.6
-
105
-
-
84876734803
-
Fetal development and variations in the cartilages surrounding the human external acoustic meatus
-
Ikari Y, Katori Y, Ohtsuka A, Rodríguez-Vázquez JF, Abe H, Kawase T, Murakami G, Abe S-i. Fetal development and variations in the cartilages surrounding the human external acoustic meatus. Annals of Anatomy - Anatomischer Anzeiger 2013;195(2): 128-136.
-
(2013)
Annals of Anatomy - Anatomischer Anzeiger
, vol.195
, Issue.2
, pp. 128-136
-
-
Ikari, Y.1
Katori, Y.2
Ohtsuka, A.3
Rodríguez-Vázquez, J.F.4
Abe, H.5
Kawase, T.6
Murakami, G.7
Abe, S.-I.8
-
106
-
-
0032716324
-
Residual mesenchyme persisting into adulthood
-
Jaisinghani V.J., Paparella M.M., Schachern P.A., Schneider D.S., Le C.T. Residual mesenchyme persisting into adulthood. Am J Otolaryngol 1999, 20(6):363-370.
-
(1999)
Am J Otolaryngol
, vol.20
, Issue.6
, pp. 363-370
-
-
Jaisinghani, V.J.1
Paparella, M.M.2
Schachern, P.A.3
Schneider, D.S.4
Le, C.T.5
-
107
-
-
84860486816
-
Burden of disease caused by otitis media: systematic review and global estimates
-
Monasta L., Ronfani L., Marchetti F., Montico M., Vecchi Brumatti L., Bavcar A., et al. Burden of disease caused by otitis media: systematic review and global estimates. PLoS ONE 2012, 7(4):e36226.
-
(2012)
PLoS ONE
, vol.7
, Issue.4
-
-
Monasta, L.1
Ronfani, L.2
Marchetti, F.3
Montico, M.4
Vecchi Brumatti, L.5
Bavcar, A.6
-
109
-
-
68049112436
-
Syndromes of the first and second pharyngeal arches: a review
-
Passos-Bueno M.R., Ornelas C.C., Fanganiello R.D. Syndromes of the first and second pharyngeal arches: a review. Am J Med Genet A 2009, 149A(8):1853-1859.
-
(2009)
Am J Med Genet A
, vol.149 A
, Issue.8
, pp. 1853-1859
-
-
Passos-Bueno, M.R.1
Ornelas, C.C.2
Fanganiello, R.D.3
-
110
-
-
79951662034
-
Syndromes of the first and second branchial arches, part 2: syndromes
-
Johnson J.M., Moonis G., Green G.E., Carmody R., Burbank H.N. Syndromes of the first and second branchial arches, part 2: syndromes. Am J Neuroradiol 2011, 32(2):230-237.
-
(2011)
Am J Neuroradiol
, vol.32
, Issue.2
, pp. 230-237
-
-
Johnson, J.M.1
Moonis, G.2
Green, G.E.3
Carmody, R.4
Burbank, H.N.5
-
111
-
-
78651507778
-
Syndromes of the first and second branchial arches, part 1: embryology and characteristic defects
-
Johnson J.M., Moonis G., Green G.E., Carmody R., Burbank H.N. Syndromes of the first and second branchial arches, part 1: embryology and characteristic defects. Am J Neuroradiol 2011, 32(1):14-19.
-
(2011)
Am J Neuroradiol
, vol.32
, Issue.1
, pp. 14-19
-
-
Johnson, J.M.1
Moonis, G.2
Green, G.E.3
Carmody, R.4
Burbank, H.N.5
-
112
-
-
59649121558
-
Congenital malformations of the external and middle ear
-
Kösling S., Omenzetter M., Bartel-Friedrich S. Congenital malformations of the external and middle ear. Eur J Radiol 2009, 69(2):269-279.
-
(2009)
Eur J Radiol
, vol.69
, Issue.2
, pp. 269-279
-
-
Kösling, S.1
Omenzetter, M.2
Bartel-Friedrich, S.3
-
113
-
-
0031032028
-
High-resolution CT of the temporal bone in dysplasia of the auricle and external auditory canal
-
Mayer T.E., Brueckmann H., Siegert R., Witt A., Weerda H. High-resolution CT of the temporal bone in dysplasia of the auricle and external auditory canal. Am J Neuroradiol 1997, 18(1):53-65.
-
(1997)
Am J Neuroradiol
, vol.18
, Issue.1
, pp. 53-65
-
-
Mayer, T.E.1
Brueckmann, H.2
Siegert, R.3
Witt, A.4
Weerda, H.5
-
114
-
-
78649527789
-
Inner ear anomalies in congenital aural atresia
-
Vrabec J.T., Lin J.W. Inner ear anomalies in congenital aural atresia. Otol Neurotol 2010, 31(9):1421.
-
(2010)
Otol Neurotol
, vol.31
, Issue.9
, pp. 1421
-
-
Vrabec, J.T.1
Lin, J.W.2
-
116
-
-
0033049426
-
Development of the vertebrate ear: insights from knockouts and mutants
-
Fekete D.M. Development of the vertebrate ear: insights from knockouts and mutants. Trends Neurosci 1999, 22(6):263-269.
-
(1999)
Trends Neurosci
, vol.22
, Issue.6
, pp. 263-269
-
-
Fekete, D.M.1
-
117
-
-
0242590840
-
Lockjaw encodes a zebrafish tfap2a required for early neural crest development
-
Knight R.D., Nair S., Nelson S.S., Afshar A., Javidan Y., Geisler R., et al. Lockjaw encodes a zebrafish tfap2a required for early neural crest development. Development 2003, 130(23):5755-5768.
-
(2003)
Development
, vol.130
, Issue.23
, pp. 5755-5768
-
-
Knight, R.D.1
Nair, S.2
Nelson, S.S.3
Afshar, A.4
Javidan, Y.5
Geisler, R.6
-
118
-
-
33947140197
-
Redundant activities of Tfap2a and Tfap2c are required for neural crest induction and development of other non-neural ectoderm derivatives in zebrafish embryos
-
Li W., Cornell R.A. Redundant activities of Tfap2a and Tfap2c are required for neural crest induction and development of other non-neural ectoderm derivatives in zebrafish embryos. Dev Biol 2007, 304(1):338-354.
-
(2007)
Dev Biol
, vol.304
, Issue.1
, pp. 338-354
-
-
Li, W.1
Cornell, R.A.2
-
119
-
-
2342434215
-
Neural crest survival and differentiation in zebrafish depends on mont blanc/tfap2a gene function
-
Barrallo-Gimeno A., Holzschuh J., Driever W., Knapik E.W. Neural crest survival and differentiation in zebrafish depends on mont blanc/tfap2a gene function. Development 2004, 131:1463-1477.
-
(2004)
Development
, vol.131
, pp. 1463-1477
-
-
Barrallo-Gimeno, A.1
Holzschuh, J.2
Driever, W.3
Knapik, E.W.4
-
120
-
-
2542496696
-
An ENU-induced mutation in AP-2α leads to middle ear and ocular defects in Doarad mice
-
Ahituv N., Erven A., Fuchs H., Guy K., Ashery-Padan R., Williams T., et al. An ENU-induced mutation in AP-2α leads to middle ear and ocular defects in Doarad mice. Mamm Genome 2004, 15(6):424-432.
-
(2004)
Mamm Genome
, vol.15
, Issue.6
, pp. 424-432
-
-
Ahituv, N.1
Erven, A.2
Fuchs, H.3
Guy, K.4
Ashery-Padan, R.5
Williams, T.6
-
121
-
-
0029932525
-
Neural tube, skeletal and body wall defects in mice lacking transcription factor AP-2
-
Zhang J., Hagopian-Donaldson S., Serbedzija G., Elsemore J., Plehn-Dujowich D., McMahon A.P., et al. Neural tube, skeletal and body wall defects in mice lacking transcription factor AP-2. Nature 1996, 381(6579):238-241.
-
(1996)
Nature
, vol.381
, Issue.6579
, pp. 238-241
-
-
Zhang, J.1
Hagopian-Donaldson, S.2
Serbedzija, G.3
Elsemore, J.4
Plehn-Dujowich, D.5
McMahon, A.P.6
-
122
-
-
1242295315
-
Wnt1-Cre-mediated deletion of AP-2alpha causes multiple neural crest-related defects
-
Brewer S., Feng W., Huang J., Sullivan S., Williams T. Wnt1-Cre-mediated deletion of AP-2alpha causes multiple neural crest-related defects. Dev Biol 2004, 267:135-152.
-
(2004)
Dev Biol
, vol.267
, pp. 135-152
-
-
Brewer, S.1
Feng, W.2
Huang, J.3
Sullivan, S.4
Williams, T.5
-
123
-
-
0032506118
-
AP-2-null cells disrupt morphogenesis of the eye, face, and limbs in chimeric mice
-
Nottoli T., Hagopian-Donaldson S., Zhang J., Perkins A., Williams T. AP-2-null cells disrupt morphogenesis of the eye, face, and limbs in chimeric mice. Proc Natl Acad Sci USA 1998, 95:13714-13719.
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 13714-13719
-
-
Nottoli, T.1
Hagopian-Donaldson, S.2
Zhang, J.3
Perkins, A.4
Williams, T.5
-
124
-
-
42749083170
-
TFAP2A mutations result in branchio-oculo-facial syndrome
-
Milunsky J.M., Maher T.A., Zhao G., Roberts A.E., Stalker H.J., Zori R.T., et al. TFAP2A mutations result in branchio-oculo-facial syndrome. Am J Hum Genet 2008, 82(5):1171-1177.
-
(2008)
Am J Hum Genet
, vol.82
, Issue.5
, pp. 1171-1177
-
-
Milunsky, J.M.1
Maher, T.A.2
Zhao, G.3
Roberts, A.E.4
Stalker, H.J.5
Zori, R.T.6
-
125
-
-
3242671307
-
The Treacher Collins syndrome (TCOF1) gene product is involved in ribosomal DNA gene transcription by interacting with upstream binding factor
-
Valdez B.C., Henning D., So R.B., Dixon J., Dixon M.J. The Treacher Collins syndrome (TCOF1) gene product is involved in ribosomal DNA gene transcription by interacting with upstream binding factor. Proc Natl Acad Sci USA 2004, 101(29):10709-10714.
-
(2004)
Proc Natl Acad Sci USA
, vol.101
, Issue.29
, pp. 10709-10714
-
-
Valdez, B.C.1
Henning, D.2
So, R.B.3
Dixon, J.4
Dixon, M.J.5
-
126
-
-
84859219780
-
Mammalian neurogenesis requires Treacle-Plk1 for precise control of spindle orientation, mitotic progression, and maintenance of neural progenitor cells
-
Sakai D., Dixon J., Dixon M.J., Trainor P.A. Mammalian neurogenesis requires Treacle-Plk1 for precise control of spindle orientation, mitotic progression, and maintenance of neural progenitor cells. PLoS Genet 2012, 8(3):e1002566.
-
(2012)
PLoS Genet
, vol.8
, Issue.3
-
-
Sakai, D.1
Dixon, J.2
Dixon, M.J.3
Trainor, P.A.4
-
127
-
-
0029794933
-
Treacher Collins syndrome may result from insertions, deletions or splicing mutations, which introduce a termination codon into the gene
-
Gladwin A.J., Dixon J., Loftus S.K., Edwards S., Wasmuth J.J., Hennekam R.C., et al. Treacher Collins syndrome may result from insertions, deletions or splicing mutations, which introduce a termination codon into the gene. Hum Mol Genet 1996, 5(10):1533-1538.
-
(1996)
Hum Mol Genet
, vol.5
, Issue.10
, pp. 1533-1538
-
-
Gladwin, A.J.1
Dixon, J.2
Loftus, S.K.3
Edwards, S.4
Wasmuth, J.J.5
Hennekam, R.C.6
-
128
-
-
0030070052
-
Positional cloning of a gene involved in the pathogenesis of Treacher Collins syndrome
-
The Treacher Collins Syndrome Collaborative G., Dixon J., Edwards S.J., Gladwin A.J., Dixon M.J., Loftus S.K., et al. Positional cloning of a gene involved in the pathogenesis of Treacher Collins syndrome. Nat Genet 1996, 12(2):130-136.
-
(1996)
Nat Genet
, vol.12
, Issue.2
, pp. 130-136
-
-
The Treacher Collins Syndrome Collaborative, G.1
Dixon, J.2
Edwards, S.J.3
Gladwin, A.J.4
Dixon, M.J.5
Loftus, S.K.6
-
129
-
-
28844479695
-
Temporal requirement of Hoxa2 in cranial neural crest skeletal morphogenesis
-
Santagati F., Minoux M., Ren S.Y., Rijli F.M. Temporal requirement of Hoxa2 in cranial neural crest skeletal morphogenesis. Development 2005, 132(22):4927-4936.
-
(2005)
Development
, vol.132
, Issue.22
, pp. 4927-4936
-
-
Santagati, F.1
Minoux, M.2
Ren, S.Y.3
Rijli, F.M.4
-
130
-
-
41549169516
-
A Mutation in HOXA2 is responsible for autosomal-recessive microtia in an Iranian family
-
Alasti F., Sadeghi A., Sanati M.H., Farhadi M., Stollar E., Somers T., et al. A Mutation in HOXA2 is responsible for autosomal-recessive microtia in an Iranian family. Am J Hum Genet 2008, 82(4):982-991.
-
(2008)
Am J Hum Genet
, vol.82
, Issue.4
, pp. 982-991
-
-
Alasti, F.1
Sadeghi, A.2
Sanati, M.H.3
Farhadi, M.4
Stollar, E.5
Somers, T.6
-
131
-
-
0031894362
-
Hoxa1 and Hoxb1 synergize in patterning the hindbrain, cranial nerves and second pharyngeal arch
-
Gavalas A., Studer M., Lumsden A., Rijli F.M., Krumlauf R., Chambon P. Hoxa1 and Hoxb1 synergize in patterning the hindbrain, cranial nerves and second pharyngeal arch. Development 1998, 125(6):1123-1136.
-
(1998)
Development
, vol.125
, Issue.6
, pp. 1123-1136
-
-
Gavalas, A.1
Studer, M.2
Lumsden, A.3
Rijli, F.M.4
Krumlauf, R.5
Chambon, P.6
-
132
-
-
78649684423
-
Regulation of facial morphogenesis by endothelin signaling: insights from mice and fish
-
Clouthier D.E., Garcia E., Schilling T.F. Regulation of facial morphogenesis by endothelin signaling: insights from mice and fish. Am J Med Genet A 2010, 152A(12):2962-2973.
-
(2010)
Am J Med Genet A
, vol.152 A
, Issue.12
, pp. 2962-2973
-
-
Clouthier, D.E.1
Garcia, E.2
Schilling, T.F.3
-
133
-
-
40949143520
-
Recombinase-mediated cassette exchange reveals the selective use of Gq/G11-dependent and -independent endothelin 1/endothelin type A receptor signaling in pharyngeal arch development
-
Sato T., Kawamura Y., Asai R., Amano T., Uchijima Y., Dettlaff-Swiercz D.A., et al. Recombinase-mediated cassette exchange reveals the selective use of Gq/G11-dependent and -independent endothelin 1/endothelin type A receptor signaling in pharyngeal arch development. Development 2008, 135(4):755-765.
-
(2008)
Development
, vol.135
, Issue.4
, pp. 755-765
-
-
Sato, T.1
Kawamura, Y.2
Asai, R.3
Amano, T.4
Uchijima, Y.5
Dettlaff-Swiercz, D.A.6
-
134
-
-
0031940499
-
Dual genetic pathways of endothelin-mediated intercellular signaling revealed by targeted disruption of endothelin converting enzyme-1 gene
-
Yanagisawa H., Yanagisawa M., Kapur R.P., Richardson J.A., Williams S.C., Clouthier D.E., et al. Dual genetic pathways of endothelin-mediated intercellular signaling revealed by targeted disruption of endothelin converting enzyme-1 gene. Development 1998, 125(5):825-836.
-
(1998)
Development
, vol.125
, Issue.5
, pp. 825-836
-
-
Yanagisawa, H.1
Yanagisawa, M.2
Kapur, R.P.3
Richardson, J.A.4
Williams, S.C.5
Clouthier, D.E.6
-
135
-
-
0028360062
-
Elevated blood pressure and craniofaclal abnormalities in mice deficient in endothelin-1
-
Kurihara Y., Kurihara H., Suzuki H., Kodama T., Maemura K., Nagai R., et al. Elevated blood pressure and craniofaclal abnormalities in mice deficient in endothelin-1. Nature 1994, 368(6473):703-710.
-
(1994)
Nature
, vol.368
, Issue.6473
, pp. 703-710
-
-
Kurihara, Y.1
Kurihara, H.2
Suzuki, H.3
Kodama, T.4
Maemura, K.5
Nagai, R.6
-
136
-
-
61349114851
-
Elucidating timing and function of endothelin-A receptor signaling during craniofacial development using neural crest cell-specific gene deletion and receptor antagonism
-
Ruest L.-B., Clouthier D.E. Elucidating timing and function of endothelin-A receptor signaling during craniofacial development using neural crest cell-specific gene deletion and receptor antagonism. Dev Biol 2009, 328(1):94-108.
-
(2009)
Dev Biol
, vol.328
, Issue.1
, pp. 94-108
-
-
Ruest, L.-B.1
Clouthier, D.E.2
-
137
-
-
21344433063
-
BMP signaling and early embryonic patterning
-
Kishigami S., Mishina Y. BMP signaling and early embryonic patterning. Cytokine Growth Factor Rev 2005, 16(3):265-278.
-
(2005)
Cytokine Growth Factor Rev
, vol.16
, Issue.3
, pp. 265-278
-
-
Kishigami, S.1
Mishina, Y.2
-
138
-
-
0026440993
-
The mouse short ear skeletal morphogenesis locus is associated with defects in a bone morphogenetic member of the TGFβ superfamily
-
Kingsley D.M., Bland A.E., Grubber J.M., Marker P.C., Russell L.B., Copeland N.G., et al. The mouse short ear skeletal morphogenesis locus is associated with defects in a bone morphogenetic member of the TGFβ superfamily. Cell 1992, 71(3):399-410.
-
(1992)
Cell
, vol.71
, Issue.3
, pp. 399-410
-
-
Kingsley, D.M.1
Bland, A.E.2
Grubber, J.M.3
Marker, P.C.4
Russell, L.B.5
Copeland, N.G.6
-
139
-
-
1642392579
-
Craniofacial defects in mice lacking BMP type I receptor Alk2 in neural crest cells
-
Dudas M., Sridurongrit S., Nagy A., Okazaki K., Kaartinen V. Craniofacial defects in mice lacking BMP type I receptor Alk2 in neural crest cells. Mech Dev 2004, 121:173-182.
-
(2004)
Mech Dev
, vol.121
, pp. 173-182
-
-
Dudas, M.1
Sridurongrit, S.2
Nagy, A.3
Okazaki, K.4
Kaartinen, V.5
-
140
-
-
84874772539
-
Heterogeneity of mutational mechanisms and modes of inheritance in auriculocondylar syndrome
-
Gordon C.T., Vuillot A., Marlin S., Gerkes E., Henderson A., AlKindy A., et al. Heterogeneity of mutational mechanisms and modes of inheritance in auriculocondylar syndrome. J Med Genet 2013, 50(3):174-186.
-
(2013)
J Med Genet
, vol.50
, Issue.3
, pp. 174-186
-
-
Gordon, C.T.1
Vuillot, A.2
Marlin, S.3
Gerkes, E.4
Henderson, A.5
AlKindy, A.6
-
141
-
-
84860748491
-
A human homeotic transformation resulting from mutations in PLCB4 and GNAI3 causes auriculocondylar syndrome
-
Rieder MJ., Green GE., Park SS., Stamper BD., Gordon CT., Johnson JM., et al. A human homeotic transformation resulting from mutations in PLCB4 and GNAI3 causes auriculocondylar syndrome. Am J Hum Genet 2012, 90(5):907-914.
-
(2012)
Am J Hum Genet
, vol.90
, Issue.5
, pp. 907-914
-
-
Rieder, M.J.1
Green, G.E.2
Park, S.S.3
Stamper, B.D.4
Gordon, C.T.5
Johnson, J.M.6
-
142
-
-
33947159616
-
Phospholipase C, beta 3 is required for Endothelin1 regulation of pharyngeal arch patterning in zebrafish
-
Walker M.B., Miller C.T., Swartz M.E., Eberhart J.K., Kimmel C.B. Phospholipase C, beta 3 is required for Endothelin1 regulation of pharyngeal arch patterning in zebrafish. Dev Biol 2007, 304(1):194-207.
-
(2007)
Dev Biol
, vol.304
, Issue.1
, pp. 194-207
-
-
Walker, M.B.1
Miller, C.T.2
Swartz, M.E.3
Eberhart, J.K.4
Kimmel, C.B.5
-
143
-
-
0032524284
-
Cloning, characterization, and mapping of the mouse homeobox GeneHmx1
-
Yoshiura K.-I., Leysens N.J., Reiter R.S., Murray J.C. Cloning, characterization, and mapping of the mouse homeobox GeneHmx1. Genomics 1998, 50(1):61-68.
-
(1998)
Genomics
, vol.50
, Issue.1
, pp. 61-68
-
-
Yoshiura, K.-I.1
Leysens, N.J.2
Reiter, R.S.3
Murray, J.C.4
-
144
-
-
65449185484
-
Mouse H6 Homeobox 1 (Hmx1) mutations cause cranial abnormalities and reduced body mass
-
Munroe R., Prabhu V., Acland G., Johnson K., Harris B., O'Brien T., et al. Mouse H6 Homeobox 1 (Hmx1) mutations cause cranial abnormalities and reduced body mass. BMC Dev Biol 2009, 9(1):27.
-
(2009)
BMC Dev Biol
, vol.9
, Issue.1
, pp. 27
-
-
Munroe, R.1
Prabhu, V.2
Acland, G.3
Johnson, K.4
Harris, B.5
O'Brien, T.6
-
145
-
-
84870016764
-
Deletion of a conserved regulatory element required for Hmx1 expression in craniofacial mesenchyme in the dumbo rat: a newly identified cause of congenital ear malformation
-
Quina L.A., Kuramoto T., Luquetti D.V., Cox T.C., Serikawa T., Turner E.E. Deletion of a conserved regulatory element required for Hmx1 expression in craniofacial mesenchyme in the dumbo rat: a newly identified cause of congenital ear malformation. Dis Model Mech 2012, 5(6):812-822.
-
(2012)
Dis Model Mech
, vol.5
, Issue.6
, pp. 812-822
-
-
Quina, L.A.1
Kuramoto, T.2
Luquetti, D.V.3
Cox, T.C.4
Serikawa, T.5
Turner, E.E.6
-
146
-
-
42749084464
-
Mutation in the human homeobox gene NKX5-3 causes an oculo-auricular syndrome
-
Schorderet D.F., Nichini O., Boisset G., Polok B., Tiab L., Mayeur H., et al. Mutation in the human homeobox gene NKX5-3 causes an oculo-auricular syndrome. Am J Hum Genet 2008, 82(5):1178-1184.
-
(2008)
Am J Hum Genet
, vol.82
, Issue.5
, pp. 1178-1184
-
-
Schorderet, D.F.1
Nichini, O.2
Boisset, G.3
Polok, B.4
Tiab, L.5
Mayeur, H.6
-
147
-
-
0041923688
-
Sox9 is required for determination of the chondrogenic cell lineage in the cranial neural crest
-
Mori-Akiyama Y., Akiyama H., Rowitch D.H., de Crombrugghe B. Sox9 is required for determination of the chondrogenic cell lineage in the cranial neural crest. Proc Natl Acad Sci USA 2003, 100(16):9360-9365.
-
(2003)
Proc Natl Acad Sci USA
, vol.100
, Issue.16
, pp. 9360-9365
-
-
Mori-Akiyama, Y.1
Akiyama, H.2
Rowitch, D.H.3
de Crombrugghe, B.4
-
148
-
-
34347337494
-
Neural crest cell deficiency of c-myc causes skull and hearing defects
-
Wei K., Chen J., Akrami K., Galbraith G.C., Lopez I.A., Chen F. Neural crest cell deficiency of c-myc causes skull and hearing defects. Genesis 2007, 45(6):382-390.
-
(2007)
Genesis
, vol.45
, Issue.6
, pp. 382-390
-
-
Wei, K.1
Chen, J.2
Akrami, K.3
Galbraith, G.C.4
Lopez, I.A.5
Chen, F.6
-
149
-
-
0037227318
-
Fgfr1 regulates patterning of the pharyngeal region
-
Trokovic N., Trokovic R., Mai P., Partanen J. Fgfr1 regulates patterning of the pharyngeal region. Genes Dev 2003, 17(1):141-153.
-
(2003)
Genes Dev
, vol.17
, Issue.1
, pp. 141-153
-
-
Trokovic, N.1
Trokovic, R.2
Mai, P.3
Partanen, J.4
-
150
-
-
68849125563
-
Heparan sulfate deficiency leads to Peters anomaly in mice by disturbing neural crest TGF-β2 signaling
-
Iwao K., Inatani M., Matsumoto Y., Ogata-Iwao M., Takihara Y., Irie F., et al. Heparan sulfate deficiency leads to Peters anomaly in mice by disturbing neural crest TGF-β2 signaling. J Clin Invest 2009, 119(7):1997-2008.
-
(2009)
J Clin Invest
, vol.119
, Issue.7
, pp. 1997-2008
-
-
Iwao, K.1
Inatani, M.2
Matsumoto, Y.3
Ogata-Iwao, M.4
Takihara, Y.5
Irie, F.6
-
151
-
-
67650495042
-
Protein tyrosine phosphatase activity in the neural crest is essential for normal heart and skull development
-
Nakamura T., Gulick J., Colbert M.C., Robbins J. Protein tyrosine phosphatase activity in the neural crest is essential for normal heart and skull development. Proc Natl Acad Sci USA 2009, 106(27):11270-11275.
-
(2009)
Proc Natl Acad Sci USA
, vol.106
, Issue.27
, pp. 11270-11275
-
-
Nakamura, T.1
Gulick, J.2
Colbert, M.C.3
Robbins, J.4
-
152
-
-
1642273208
-
Ephrin-B1 forward and reverse signaling are required during mouse development
-
Davy A., Aubin J., Soriano P. Ephrin-B1 forward and reverse signaling are required during mouse development. Genes Dev 2004, 18:572-583.
-
(2004)
Genes Dev
, vol.18
, pp. 572-583
-
-
Davy, A.1
Aubin, J.2
Soriano, P.3
-
153
-
-
1942466507
-
Hedgehog signaling in the neural crest cells regulates the patterning and growth of facial primordia
-
Jeong J., Mao J., Tenzen T., Kottmann A.H., McMahon A.P. Hedgehog signaling in the neural crest cells regulates the patterning and growth of facial primordia. Genes Dev 2004, 18(8):937-951.
-
(2004)
Genes Dev
, vol.18
, Issue.8
, pp. 937-951
-
-
Jeong, J.1
Mao, J.2
Tenzen, T.3
Kottmann, A.H.4
McMahon, A.P.5
-
154
-
-
0020725070
-
The genesis of neural crest and epidermal placodes: a reinterpretation of vertebrate origins
-
Northcutt R.G., Gans C. The genesis of neural crest and epidermal placodes: a reinterpretation of vertebrate origins. Q Rev Biol 1983, 58(1):1-28.
-
(1983)
Q Rev Biol
, vol.58
, Issue.1
, pp. 1-28
-
-
Northcutt, R.G.1
Gans, C.2
-
155
-
-
0001119210
-
Neural crest and the origin of vertebrates: a new head
-
Gans C., Northcutt R. Neural crest and the origin of vertebrates: a new head. Science 1983, 220:268-274.
-
(1983)
Science
, vol.220
, pp. 268-274
-
-
Gans, C.1
Northcutt, R.2
-
156
-
-
84870479629
-
Identification of a rudimentary neural crest in a non-vertebrate chordate
-
Abitua P.B., Wagner E., Navarrete I.A., Levine M. Identification of a rudimentary neural crest in a non-vertebrate chordate. Nature 2012, 492(7427):104-107.
-
(2012)
Nature
, vol.492
, Issue.7427
, pp. 104-107
-
-
Abitua, P.B.1
Wagner, E.2
Navarrete, I.A.3
Levine, M.4
-
157
-
-
0021087096
-
Cell lineage analysis in ascidian embryos by intracellular injection of a tracer enzyme: I. Up to the eight-cell stage
-
Nishida H., Satoh N. Cell lineage analysis in ascidian embryos by intracellular injection of a tracer enzyme: I. Up to the eight-cell stage. Dev Biol 1983, 99(2):382-394.
-
(1983)
Dev Biol
, vol.99
, Issue.2
, pp. 382-394
-
-
Nishida, H.1
Satoh, N.2
-
158
-
-
0020068468
-
Auditory centers in the elasmobranch brain stem: deoxyglucose autoradiography and evoked potential recording
-
Corwin J.T., Northcutt R.G. Auditory centers in the elasmobranch brain stem: deoxyglucose autoradiography and evoked potential recording. Brain Res 1982, 236(2):261-273.
-
(1982)
Brain Res
, vol.236
, Issue.2
, pp. 261-273
-
-
Corwin, J.T.1
Northcutt, R.G.2
-
159
-
-
0002415463
-
Functional evolution of lateral line and inner ear sensory systems
-
Springer, New York, NY, S. Coombs, P. Görner, H. Münz (Eds.)
-
Kalmijn A.J. Functional evolution of lateral line and inner ear sensory systems. The mechanosensory lateral line 1989, 187-215. Springer, New York, NY. S. Coombs, P. Görner, H. Münz (Eds.).
-
(1989)
The mechanosensory lateral line
, pp. 187-215
-
-
Kalmijn, A.J.1
-
160
-
-
48549091583
-
Lateral line, otic and epibranchial placodes: developmental and evolutionary links?
-
Baker C.V.H., O'Neill P., McCole R.B. Lateral line, otic and epibranchial placodes: developmental and evolutionary links?. J Exp Zool B Mol Dev Evol 2008, 310B(4):370-383.
-
(2008)
J Exp Zool B Mol Dev Evol
, vol.310 B
, Issue.4
, pp. 370-383
-
-
Baker, C.V.H.1
O'Neill, P.2
McCole, R.B.3
-
161
-
-
0034857489
-
Origin of the vertebrate inner ear: evolution and induction of the otic placode
-
Streit A. Origin of the vertebrate inner ear: evolution and induction of the otic placode. J Anat 2001, 199(1-2):99-103.
-
(2001)
J Anat
, vol.199
, Issue.1-2
, pp. 99-103
-
-
Streit, A.1
-
162
-
-
84871238760
-
Evolution of the mammalian middle ear and jaw: adaptations and novel structures
-
Anthwal N., Joshi L., Tucker A.S. Evolution of the mammalian middle ear and jaw: adaptations and novel structures. J Anat 2013, 222(1):147-160.
-
(2013)
J Anat
, vol.222
, Issue.1
, pp. 147-160
-
-
Anthwal, N.1
Joshi, L.2
Tucker, A.S.3
-
163
-
-
0037383450
-
Two endothelin 1 effectors, hand2 and bapx1, pattern ventral pharyngeal cartilage and the jaw joint
-
Miller C.T., Yelon D., Stainier D.Y.R., Kimmel C.B. Two endothelin 1 effectors, hand2 and bapx1, pattern ventral pharyngeal cartilage and the jaw joint. Development 2003, 130(7):1353-1365.
-
(2003)
Development
, vol.130
, Issue.7
, pp. 1353-1365
-
-
Miller, C.T.1
Yelon, D.2
Stainier, D.Y.R.3
Kimmel, C.B.4
-
164
-
-
1842454975
-
Bapx1 regulates patterning in the middle ear: altered regulatory role in the transition from the proximal jaw during vertebrate evolution
-
Tucker A.S., Watson R.P., Lettice L.A., Yamada G., Hill R.E. Bapx1 regulates patterning in the middle ear: altered regulatory role in the transition from the proximal jaw during vertebrate evolution. Development 2004, 131(6):1235-1245.
-
(2004)
Development
, vol.131
, Issue.6
, pp. 1235-1245
-
-
Tucker, A.S.1
Watson, R.P.2
Lettice, L.A.3
Yamada, G.4
Hill, R.E.5
-
165
-
-
34250679840
-
Sound transmission in archaic and modern whales: anatomical adaptations for underwater hearing
-
Nummela S., Thewissen J.G.M., Bajpai S., Hussain T., Kumar K. Sound transmission in archaic and modern whales: anatomical adaptations for underwater hearing. Anat Rec 2007, 290(6):716-733.
-
(2007)
Anat Rec
, vol.290
, Issue.6
, pp. 716-733
-
-
Nummela, S.1
Thewissen, J.G.M.2
Bajpai, S.3
Hussain, T.4
Kumar, K.5
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