-
1
-
-
0034764984
-
Hirschsprung disease, associated syndromes, and genetics: A review
-
Amiel J, Lyonnet S. 2001. Hirschsprung disease, associated syndromes, and genetics: a review. J Med Genet 38:729-739.
-
(2001)
J Med Genet
, vol.38
, pp. 729-739
-
-
Amiel, J.1
Lyonnet, S.2
-
2
-
-
9044220230
-
Heterozygous endothelin receptor B (EDNRB) mutations in isolated Hirschsprung disease
-
Amiel J, Attie T, Jan D, Pelet A, Edery P, Bidaud C, Lacombe D, Tam P, Simeoni J, Flori E, Nihoul-Fekete C, Munnich A, Lyonnet S. 1996. Heterozygous endothelin receptor B (EDNRB) mutations in isolated Hirschsprung disease. Hum Mol Genet 5:355-357.
-
(1996)
Hum Mol Genet
, vol.5
, pp. 355-357
-
-
Amiel, J.1
Attie, T.2
Jan, D.3
Pelet, A.4
Edery, P.5
Bidaud, C.6
Lacombe, D.7
Tam, P.8
Simeoni, J.9
Flori, E.10
Nihoul-Fekete, C.11
Munnich, A.12
Lyonnet, S.13
-
3
-
-
0035213144
-
Large-scale deletions and SMADIP1 truncating mutations in syndromic Hirschsprung disease with involvement of midline structures
-
Amiel J, Espinosa-Parrilla Y, Steffann J, Gosset P, Pelet A, Prieur M, Boute O, Choiset A, Lacombe D, Philip N, Le Merrer M, Tanaka H, Till M, Touraine R, Toutain A, Vekemans M, Munnich A, Lyonnet S. 2001. Large-scale deletions and SMADIP1 truncating mutations in syndromic Hirschsprung disease with involvement of midline structures. Am J Hum Genet 69:1370-1377.
-
(2001)
Am J Hum Genet
, vol.69
, pp. 1370-1377
-
-
Amiel, J.1
Espinosa-Parrilla, Y.2
Steffann, J.3
Gosset, P.4
Pelet, A.5
Prieur, M.6
Boute, O.7
Choiset, A.8
Lacombe, D.9
Philip, N.10
Le Merrer, M.11
Tanaka, H.12
Till, M.13
Touraine, R.14
Toutain, A.15
Vekemans, M.16
Munnich, A.17
Lyonnet, S.18
-
4
-
-
33645998136
-
The cell adhesion molecule 11 is required for chain migration of neural crest cells in the developing mouse gut
-
Anderson RB, Turner KN, Nikonenko AG, Hemperly J, Schachner M, Young HM. 2006. The cell adhesion molecule 11 is required for chain migration of neural crest cells in the developing mouse gut. Gastroenterology 130:1221-1232.
-
(2006)
Gastroenterology
, vol.130
, pp. 1221-1232
-
-
Anderson, R.B.1
Turner, K.N.2
Nikonenko, A.G.3
Hemperly, J.4
Schachner, M.5
Young, H.M.6
-
5
-
-
0030292383
-
Germline mutations in glial cell line-derived neurotrophic factor (GDNF) and RET in a Hirschsprung disease patient
-
Angrist M, Bolk S, Halushka M, Lapchak PA, Chakravarti A. 1996. Germline mutations in glial cell line-derived neurotrophic factor (GDNF) and RET in a Hirschsprung disease patient. Nat Genet 14:341-344.
-
(1996)
Nat Genet
, vol.14
, pp. 341-344
-
-
Angrist, M.1
Bolk, S.2
Halushka, M.3
Lapchak, P.A.4
Chakravarti, A.5
-
7
-
-
0347194147
-
Enteric nervous system progenitors are coordinately controlled by the G protein-coupled receptor EDNRB and the receptor tyrosine kinase RET
-
Barlow A, de Graaff E, Pachnis V. 2003. Enteric nervous system progenitors are coordinately controlled by the G protein-coupled receptor EDNRB and the receptor tyrosine kinase RET. Neuron 40:905-916.
-
(2003)
Neuron
, vol.40
, pp. 905-916
-
-
Barlow, A.1
de Graaff, E.2
Pachnis, V.3
-
8
-
-
0028609612
-
Interaction of endothelin-3 with endothelin-B receptor is essential for development of epidermal melanocytes and enteric neurons
-
Baynash AG, Hosoda K, Giaid A, Richardson JA, Emoto N, Hammer RE, Yanagisawa M. 1994. Interaction of endothelin-3 with endothelin-B receptor is essential for development of epidermal melanocytes and enteric neurons. Cell 79:1277-1285.
-
(1994)
Cell
, vol.79
, pp. 1277-1285
-
-
Baynash, A.G.1
Hosoda, K.2
Giaid, A.3
Richardson, J.A.4
Emoto, N.5
Hammer, R.E.6
Yanagisawa, M.7
-
9
-
-
12644284522
-
Endothelin-3 gene mutations in isolated and syndromic Hirschsprung disease
-
Bidaud C, Salomon R, Van Camp G, Pelet A, Attie T, Eng C, Bonduelle M, Amiel J, Nihoul-Fekete C, Willems PJ, Munnich A, Lyonnet S. 1997. Endothelin-3 gene mutations in isolated and syndromic Hirschsprung disease. Eur J Hum Genet 5:247-251.
-
(1997)
Eur J Hum Genet
, vol.5
, pp. 247-251
-
-
Bidaud, C.1
Salomon, R.2
Van Camp, G.3
Pelet, A.4
Attie, T.5
Eng, C.6
Bonduelle, M.7
Amiel, J.8
Nihoul-Fekete, C.9
Willems, P.J.10
Munnich, A.11
Lyonnet, S.12
-
10
-
-
0034602646
-
A human model for multigenic inheritance: Phenotypic expression in Hirschsprung disease requires both the RET gene and a new 9q31 locus
-
Bolk S, Pelet A, Hofstra RMW, Angrist M, Salomon R, Croaker D, Buys CHCM, Lyonnet S, Chakravarti A. 2000. A human model for multigenic inheritance: phenotypic expression in Hirschsprung disease requires both the RET gene and a new 9q31 locus. Proc Natl Acad Sci U S A 97:268-273.
-
(2000)
Proc Natl Acad Sci U S A
, vol.97
, pp. 268-273
-
-
Bolk, S.1
Pelet, A.2
Hofstra, R.M.W.3
Angrist, M.4
Salomon, R.5
Croaker, D.6
Buys, C.H.C.M.7
Lyonnet, S.8
Chakravarti, A.9
-
11
-
-
33744511178
-
Lack of {beta}1 integrins in enteric neural crest cells leads to a Hirschsprung-like phenotype
-
Breau MA, Pietri T, Eder O, Blanche M, Brakebusch C, Fassler R, Thiery JP, Dufour S. 2006. Lack of {beta}1 integrins in enteric neural crest cells leads to a Hirschsprung-like phenotype. Development 133:1725-1734.
-
(2006)
Development
, vol.133
, pp. 1725-1734
-
-
Breau, M.A.1
Pietri, T.2
Eder, O.3
Blanche, M.4
Brakebusch, C.5
Fassler, R.6
Thiery, J.P.7
Dufour, S.8
-
12
-
-
0032114122
-
GFRα1 is an essential receptor component for GDNF in the developing nervous system and kidney
-
Cacalano G, Farinas I, Wang L-C, Hagler K, Forgie A, Moore M, Armanini M, Phillips H, Ryan AM, Reichardt LF, Hynes M, Davies A, Rosenthal A. 1998. GFRα1 is an essential receptor component for GDNF in the developing nervous system and kidney. Neuron 21:53-62.
-
(1998)
Neuron
, vol.21
, pp. 53-62
-
-
Cacalano, G.1
Farinas, I.2
Wang, L.-C.3
Hagler, K.4
Forgie, A.5
Moore, M.6
Armanini, M.7
Phillips, H.8
Ryan, A.M.9
Reichardt, L.F.10
Hynes, M.11
Davies, A.12
Rosenthal, A.13
-
13
-
-
0035394107
-
Loss-of-function mutations in SIP1 Smad interacting protein 1 result in a syndromic Hirschsprung disease
-
Cacheux V, Dastot-Le Moal F, Kaariainen H, Bondurand N, Rintala R, Boissier B, Wilson M, Mowat D, Goossens M. 2001. Loss-of-function mutations in SIP1 Smad interacting protein 1 result in a syndromic Hirschsprung disease. Hum Mol Genet 10:1503-1510.
-
(2001)
Hum Mol Genet
, vol.10
, pp. 1503-1510
-
-
Cacheux, V.1
Dastot-Le Moal, F.2
Kaariainen, H.3
Bondurand, N.4
Rintala, R.5
Boissier, B.6
Wilson, M.7
Mowat, D.8
Goossens, M.9
-
14
-
-
5544326532
-
Interactions between Sox10 and EdnrB modulate penetrance and severity of aganglionosis in the Sox10Dom mouse model of Hirschsprung disease
-
Cantrell VA, Owens SE, Chandler RL, Airey DC, Bradley KM, Smith JR, Southard-Smith EM. 2004. Interactions between Sox10 and EdnrB modulate penetrance and severity of aganglionosis in the Sox10Dom mouse model of Hirschsprung disease. Hum Mol Genet 13:2289-2301.
-
(2004)
Hum Mol Genet
, vol.13
, pp. 2289-2301
-
-
Cantrell, V.A.1
Owens, S.E.2
Chandler, R.L.3
Airey, D.C.4
Bradley, K.M.5
Smith, J.R.6
Southard-Smith, E.M.7
-
15
-
-
0036788576
-
Genome-wide association study and mouse model identify interaction between RET and EDNRB pathways in Hirschsprung disease
-
Carrasquillo MM, McCallion AS, Puffenberger EG, Kashuk CS, Nouri N, Chakravarti A. 2002. Genome-wide association study and mouse model identify interaction between RET and EDNRB pathways in Hirschsprung disease. Nat Genet 32:237-244.
-
(2002)
Nat Genet
, vol.32
, pp. 237-244
-
-
Carrasquillo, M.M.1
McCallion, A.S.2
Puffenberger, E.G.3
Kashuk, C.S.4
Nouri, N.5
Chakravarti, A.6
-
16
-
-
0027972513
-
Mutations of the RET proto-oncogene in Hirschsprung's disease
-
Edery P, Lyonnet S, Mulligan LM, Pelet A, Dow E, Abel L, Holder S, Nihoul-Fekete C, Ponder BAJ, Munnich A. 1994. Mutations of the RET proto-oncogene in Hirschsprung's disease. Nature 367:378-380.
-
(1994)
Nature
, vol.367
, pp. 378-380
-
-
Edery, P.1
Lyonnet, S.2
Mulligan, L.M.3
Pelet, A.4
Dow, E.5
Abel, L.6
Holder, S.7
Nihoul-Fekete, C.8
Ponder, B.A.J.9
Munnich, A.10
-
17
-
-
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 RM, Martelli H, Bidaud C, Munnich A, Lyonnet S. 1996. Mutation of the endothelin-3 gene in the Waardenburg-Hirschsprung disease (Shah-Waardenburg syndrome). Nat Genet 12:442-444.
-
(1996)
Nat Genet
, vol.12
, pp. 442-444
-
-
Edery, P.1
Attie, T.2
Amiel, J.3
Pelet, A.4
Eng, C.5
Hofstra, R.M.6
Martelli, H.7
Bidaud, C.8
Munnich, A.9
Lyonnet, S.10
-
18
-
-
17244383525
-
A common sex-dependent mutation in a RET enhancer underlies Hirschsprung disease risk
-
Emison ES, McCallion AS, Kashuk CS, Bush RT, Grice E, Lin S, Portnoy ME, Cutler DJ, Green ED, Chakravarti A. 2005. A common sex-dependent mutation in a RET enhancer underlies Hirschsprung disease risk. Nature 434:857-863.
-
(2005)
Nature
, vol.434
, pp. 857-863
-
-
Emison, E.S.1
McCallion, A.S.2
Kashuk, C.S.3
Bush, R.T.4
Grice, E.5
Lin, S.6
Portnoy, M.E.7
Cutler, D.J.8
Green, E.D.9
Chakravarti, A.10
-
19
-
-
0032129239
-
GFRα1 deficient mice have deficits in the enteric nervous system and kidneys
-
Enomoto H, Araki T, Jackman A, Heuckeroth RO, Snider WD, Johnson EMJ, Milbrandt J. 1998. GFRα1 deficient mice have deficits in the enteric nervous system and kidneys. Neuron 21:317-324.
-
(1998)
Neuron
, vol.21
, pp. 317-324
-
-
Enomoto, H.1
Araki, T.2
Jackman, A.3
Heuckeroth, R.O.4
Snider, W.D.5
Johnson, E.M.J.6
Milbrandt, J.7
-
20
-
-
0242637173
-
Newly proliferated cells in the adult male amygdala are affected by gonadal steroid hormones
-
Fowler CD, Freeman ME, Wang Z. 2003. Newly proliferated cells in the adult male amygdala are affected by gonadal steroid hormones. J Neurobiol 57:257-269.
-
(2003)
J Neurobiol
, vol.57
, pp. 257-269
-
-
Fowler, C.D.1
Freeman, M.E.2
Wang, Z.3
-
21
-
-
2142750165
-
Embryonic development of the ganglion plexuses and the concentric layer structure of human gut: A topographical study
-
Fu M, Tam PK, Sham MH, Lui VC. 2004. Embryonic development of the ganglion plexuses and the concentric layer structure of human gut: a topographical study. Anat Embryol (Berl) 208:33-41.
-
(2004)
Anat Embryol (Berl)
, vol.208
, pp. 33-41
-
-
Fu, M.1
Tam, P.K.2
Sham, M.H.3
Lui, V.C.4
-
22
-
-
0041703018
-
Endothelin- converting enzyme-1 (ECE-1) is a downstream target of the homeobox transcription factor Nkx2-5
-
Funke-Kaiser H, Lemmer J, Langsdorff CV, Thomas A, Kovacevic SD, Strasdat M, Behrouzi T, Zollmann FS, Paul M, Orzechowski HD. 2003a. Endothelin- converting enzyme-1 (ECE-1) is a downstream target of the homeobox transcription factor Nkx2-5. FASEB J 17:1487-1489.
-
(2003)
FASEB J
, vol.17
, pp. 1487-1489
-
-
Funke-Kaiser, H.1
Lemmer, J.2
Langsdorff, C.V.3
Thomas, A.4
Kovacevic, S.D.5
Strasdat, M.6
Behrouzi, T.7
Zollmann, F.S.8
Paul, M.9
Orzechowski, H.D.10
-
23
-
-
0037440673
-
Differential binding of transcription factor E2F-2 to the endothelin-converting enzyme-1b promoter affects blood pressure regulation
-
Funke-Kaiser H, Reichenberger F, Kopke K, Herrmann SM, Pfeifer J, Orzechowski HD, Zidek W, Paul M, Brand E. 2003b. Differential binding of transcription factor E2F-2 to the endothelin-converting enzyme-1b promoter affects blood pressure regulation. Hum Mol Genet 12:423-433.
-
(2003)
Hum Mol Genet
, vol.12
, pp. 423-433
-
-
Funke-Kaiser, H.1
Reichenberger, F.2
Kopke, K.3
Herrmann, S.M.4
Pfeifer, J.5
Orzechowski, H.D.6
Zidek, W.7
Paul, M.8
Brand, E.9
-
24
-
-
10744220261
-
Regulation of the major isoform of human endothelin-converting enzyme-1 by a strong housekeeping promoter modulated by polymorphic microsatellites
-
Funke-Kaiser H, Thomas A, Bremer J, Kovacevic SD, Scheuch K, Bolbrinker J, Theis S, Lemmer J, Zimmermann A, Zollmann FS, Herrmann SM, Paul M, Orzechowski HD. 2003c. Regulation of the major isoform of human endothelin-converting enzyme-1 by a strong housekeeping promoter modulated by polymorphic microsatellites. J Hypertens 21:2111-2124.
-
(2003)
J Hypertens
, vol.21
, pp. 2111-2124
-
-
Funke-Kaiser, H.1
Thomas, A.2
Bremer, J.3
Kovacevic, S.D.4
Scheuch, K.5
Bolbrinker, J.6
Theis, S.7
Lemmer, J.8
Zimmermann, A.9
Zollmann, F.S.10
Herrmann, S.M.11
Paul, M.12
Orzechowski, H.D.13
-
25
-
-
18544365991
-
Segregation at three loci explains familial and population risk in Hirschsprung disease
-
Gabriel SB, Salomon R, Pelet A, Angrist M, Amiel J, Fornage M, Attie-Bitach T, Olson JM, Hofstra R, Buys C, Steffann J, Munnich A, Lyonnet S, Chakravarti A. 2002. Segregation at three loci explains familial and population risk in Hirschsprung disease. Nat Genet 31:89-93.
-
(2002)
Nat Genet
, vol.31
, pp. 89-93
-
-
Gabriel, S.B.1
Salomon, R.2
Pelet, A.3
Angrist, M.4
Amiel, J.5
Fornage, M.6
Attie-Bitach, T.7
Olson, J.M.8
Hofstra, R.9
Buys, C.10
Steffann, J.11
Munnich, A.12
Lyonnet, S.13
Chakravarti, A.14
-
26
-
-
0345385015
-
Association study of PHOX2B as a candidate gene for Hirschsprung's disease
-
Garcia-Barcelo M, Sham MH, Lui VC, Chen BL, Ott J, Tam PK. 2003. Association study of PHOX2B as a candidate gene for Hirschsprung's disease. Gut 52:563-567.
-
(2003)
Gut
, vol.52
, pp. 563-567
-
-
Garcia-Barcelo, M.1
Sham, M.H.2
Lui, V.C.3
Chen, B.L.4
Ott, J.5
Tam, P.K.6
-
27
-
-
0038074091
-
GDNF availability determines enteric neuron number by controlling precursor proliferation
-
Gianino S, Grider JR, Cresswell J, Enomoto H, Heuckeroth RO. 2003. GDNF availability determines enteric neuron number by controlling precursor proliferation. Development 130:2187-2198.
-
(2003)
Development
, vol.130
, pp. 2187-2198
-
-
Gianino, S.1
Grider, J.R.2
Cresswell, J.3
Enomoto, H.4
Heuckeroth, R.O.5
-
28
-
-
0024550983
-
Androgen increases the number of cells in fetal mouse spinal cord cultures: Implications for motoneuron survival
-
Hauser KF, Toran-Allerand CD. 1989. Androgen increases the number of cells in fetal mouse spinal cord cultures: implications for motoneuron survival. Brain Res 485:157-164.
-
(1989)
Brain Res
, vol.485
, pp. 157-164
-
-
Hauser, K.F.1
Toran-Allerand, C.D.2
-
29
-
-
0033366516
-
A loss-of-function mutation in the endothelin-converting enzyme 1 (ECE-1) associated with Hirschsprung disease, cardiac defects, and autonomic dysfunction
-
Hofstra RM, Valdenaire O, Arch E, Osinga J, Kroes H, Loffler BM, Hamosh A, Meijers C, Buys CH. 1999. A loss-of-function mutation in the endothelin-converting enzyme 1 (ECE-1) associated with Hirschsprung disease, cardiac defects, and autonomic dysfunction. Am J Hum Genet 64:304-308.
-
(1999)
Am J Hum Genet
, vol.64
, pp. 304-308
-
-
Hofstra, R.M.1
Valdenaire, O.2
Arch, E.3
Osinga, J.4
Kroes, H.5
Loffler, B.M.6
Hamosh, A.7
Meijers, C.8
Buys, C.H.9
-
30
-
-
17944401148
-
Hirschsprung disease and L1CAM: Is the disturbed sex ratio caused by L1CAM mutations?
-
Hofstra RM, Elfferich P, Osinga J, Verlind E, Fransen E, Lopez Pison J, de DieSmulders CE, Stolte-Dijkstra I, Buys CH. 2002. Hirschsprung disease and L1CAM: is the disturbed sex ratio caused by L1CAM mutations? J Med Genet 39:E11.
-
(2002)
J Med Genet
, vol.39
-
-
Hofstra, R.M.1
Elfferich, P.2
Osinga, J.3
Verlind, E.4
Fransen, E.5
Lopez Pison, J.6
de DieSmulders, C.E.7
Stolte-Dijkstra, I.8
Buys, C.H.9
-
31
-
-
0028639196
-
Targeted and natural (piebald-lethal) mutations of endothelin-B receptor gene produce megacolon associated with spotted coat color in mice
-
Hosoda K, Hammer RE, Richardson JA, Baynash AG, Cheung JC, Giaid A, Yanagisawa M. 1994. Targeted and natural (piebald-lethal) mutations of endothelin-B receptor gene produce megacolon associated with spotted coat color in mice. Cell 79:1267-1276.
-
(1994)
Cell
, vol.79
, 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
Yanagisawa, M.7
-
32
-
-
0028984958
-
Mesenchymal and neuronal cell expression of the p75 neurotrophin receptor gene occur by different mechanisms
-
Huber LJ, Chao MV. 1995. Mesenchymal and neuronal cell expression of the p75 neurotrophin receptor gene occur by different mechanisms. Dev Biol 167:227-238.
-
(1995)
Dev Biol
, vol.167
, pp. 227-238
-
-
Huber, L.J.1
Chao, M.V.2
-
33
-
-
0029822720
-
De novo mutation of GDNF, ligand for the RET/GDNFR-alpha receptor complex, in Hirschsprung disease
-
Ivanchuk SM, Meyers SM, Eng C, Mulligan LM. 1996. De novo mutation of GDNF, ligand for the RET/GDNFR-alpha receptor complex, in Hirschsprung disease. Hum Mol Genet 5:2023-2026.
-
(1996)
Hum Mol Genet
, vol.5
, pp. 2023-2026
-
-
Ivanchuk, S.M.1
Meyers, S.M.2
Eng, C.3
Mulligan, L.M.4
-
34
-
-
9444225531
-
Mice expressing a dominant-negative Ret mutation phenocopy human Hirschsprung disease and delineate a direct role of Ret in spermatogenesis
-
Jain S, Naughton CK, Yang M, Strickland A, Vij K, Encinas M, Golden J, Gupta A, Heuckeroth R, Johnson EM Jr, Milbrandt J. 2004. Mice expressing a dominant-negative Ret mutation phenocopy human Hirschsprung disease and delineate a direct role of Ret in spermatogenesis. Development 131:5503-5513.
-
(2004)
Development
, vol.131
, pp. 5503-5513
-
-
Jain, S.1
Naughton, C.K.2
Yang, M.3
Strickland, A.4
Vij, K.5
Encinas, M.6
Golden, J.7
Gupta, A.8
Heuckeroth, R.9
Johnson Jr, E.M.10
Milbrandt, J.11
-
35
-
-
0026673148
-
A transgenic model for studying development of the enteric nervous system in normal and aganglionic mice
-
Kapur RP, Yost C, Palmiter RD. 1992. A transgenic model for studying development of the enteric nervous system in normal and aganglionic mice. Development 116:167-175.
-
(1992)
Development
, vol.116
, pp. 167-175
-
-
Kapur, R.P.1
Yost, C.2
Palmiter, R.D.3
-
36
-
-
0028784063
-
Intercellular signals downstream of endothelin receptor-B mediate colonization of the large intestine by enteric neuroblasts
-
Kapur RP, Sweetser DA, Doggett B, Siebert JR, Palmiter RD. 1995. Intercellular signals downstream of endothelin receptor-B mediate colonization of the large intestine by enteric neuroblasts. Development 121:3787-3795.
-
(1995)
Development
, vol.121
, pp. 3787-3795
-
-
Kapur, R.P.1
Sweetser, D.A.2
Doggett, B.3
Siebert, J.R.4
Palmiter, R.D.5
-
37
-
-
0037293487
-
Aggressive behavior and serum testosterone concentration during the maturation process of male mice: The effects of fetal exposure to bisphenol A
-
Kawai K, Nozaki T, Nishikata H, Aou S, Takii M, Kubo C. 2003. Aggressive behavior and serum testosterone concentration during the maturation process of male mice: the effects of fetal exposure to bisphenol A. Environ Health Perspect 111:175-178.
-
(2003)
Environ Health Perspect
, vol.111
, pp. 175-178
-
-
Kawai, K.1
Nozaki, T.2
Nishikata, H.3
Aou, S.4
Takii, M.5
Kubo, C.6
-
38
-
-
0034061353
-
Reduced endothelin-3 expression in sporadic Hirschsprung disease
-
Kenny SE, Hofstra RM, Buys CH, Vaillant CR, Lloyd DA, Edgar DH. 2000. Reduced endothelin-3 expression in sporadic Hirschsprung disease. Br J Surg 87:580-585.
-
(2000)
Br J Surg
, vol.87
, pp. 580-585
-
-
Kenny, S.E.1
Hofstra, R.M.2
Buys, C.H.3
Vaillant, C.R.4
Lloyd, D.A.5
Edgar, D.H.6
-
39
-
-
0018676390
-
Hirschsprung's disease - a survey of the members of the surgical section of the American Academy of Pediatrics
-
Kleinhaus S, Boley SJ, Sheran M, Sieber WK. 1979. Hirschsprung's disease - a survey of the members of the surgical section of the American Academy of Pediatrics. J Pediatr Surg 14:588-597.
-
(1979)
J Pediatr Surg
, vol.14
, pp. 588-597
-
-
Kleinhaus, S.1
Boley, S.J.2
Sheran, M.3
Sieber, W.K.4
-
40
-
-
0346599161
-
Temporally distinct requirements for endothelin receptor B in the generation and migration of gut neural crest stem cells
-
Kruger GM, Mosher JT, Tsai YH, Yeager KJ, Iwashita T, Gariepy CE, Morrison SJ. 2003. Temporally distinct requirements for endothelin receptor B in the generation and migration of gut neural crest stem cells. Neuron 40:917-928.
-
(2003)
Neuron
, vol.40
, pp. 917-928
-
-
Kruger, G.M.1
Mosher, J.T.2
Tsai, Y.H.3
Yeager, K.J.4
Iwashita, T.5
Gariepy, C.E.6
Morrison, S.J.7
-
41
-
-
8044257726
-
Mutations of the endothelin-B receptor and endothelin-3 genes in Hirschsprung's disease
-
Kusafuka T, Puri P. 1997. Mutations of the endothelin-B receptor and endothelin-3 genes in Hirschsprung's disease. Pediatr Surg Int 12:19-23.
-
(1997)
Pediatr Surg Int
, vol.12
, pp. 19-23
-
-
Kusafuka, T.1
Puri, P.2
-
42
-
-
0033791525
-
Pax3 is-required for enteric ganglia formation and functions with Sox10 to modulate expression of c-Ret
-
Lang D, Chen F, Milewski R, Li J, Lu MM, Epstein JA. 2000. Pax3 is-required for enteric ganglia formation and functions with Sox10 to modulate expression of c-Ret. J Clin Invest 106:963-971.
-
(2000)
J Clin Invest
, vol.106
, pp. 963-971
-
-
Lang, D.1
Chen, F.2
Milewski, R.3
Li, J.4
Lu, M.M.5
Epstein, J.A.6
-
43
-
-
31744442077
-
Molecular mechanisms of RET-induced Hirschsprung pathogenesis
-
Lantieri F, Griseri P, Ceccherini I. 2006. Molecular mechanisms of RET-induced Hirschsprung pathogenesis. Ann Med 38:11-19.
-
(2006)
Ann Med
, vol.38
, pp. 11-19
-
-
Lantieri, F.1
Griseri, P.2
Ceccherini, I.3
-
44
-
-
0036489187
-
Hydrogen peroxide regulation of bovine endothelin-converting enzyme-1
-
Lopez-Ongil S, Saura M, Zaragoza C, Gonzalez-Santiago L, Rodriguez-Puyol M, Lowenstein CJ, Rodriguez-Puyol D. 2002. Hydrogen peroxide regulation of bovine endothelin-converting enzyme-1. Free Radic Biol Med 32:406-413.
-
(2002)
Free Radic Biol Med
, vol.32
, pp. 406-413
-
-
Lopez-Ongil, S.1
Saura, M.2
Zaragoza, C.3
Gonzalez-Santiago, L.4
Rodriguez-Puyol, M.5
Lowenstein, C.J.6
Rodriguez-Puyol, D.7
-
45
-
-
0028199116
-
Mutations of RET proto-oncogene in Hirschsprung disease]
-
Lyonnet S, Edery P, Mulligan LM, Pelet A, Dow E, Abel L, Holder S, Nihoul-Fekete C, Ponder BA, Munnich A. 1994. [Mutations of RET proto-oncogene in Hirschsprung disease]. C R Acad Sci III 317:358-362.
-
(1994)
C R Acad Sci III
, vol.317
, pp. 358-362
-
-
Lyonnet, S.1
Edery, P.2
Mulligan, L.M.3
Pelet, A.4
Dow, E.5
Abel, L.6
Holder, S.7
Nihoul-Fekete, C.8
Ponder, B.A.9
Munnich, A.10
-
46
-
-
0037452581
-
Phenotype variation in two-locus mouse models of Hirschsprung disease: Tissue-specific interaction between Ret and Ednrb
-
McCallion AS, Stames E, Conlon RA, Chakravarti A. 2003. Phenotype variation in two-locus mouse models of Hirschsprung disease: tissue-specific interaction between Ret and Ednrb. Proc Natl Acad Sci U S A 100:1826-1831.
-
(2003)
Proc Natl Acad Sci U S A
, vol.100
, pp. 1826-1831
-
-
McCallion, A.S.1
Stames, E.2
Conlon, R.A.3
Chakravarti, A.4
-
47
-
-
15844384629
-
Renal and neuronal abnormalities in mice lacking GDNF
-
Moore MW, Klein RD, Farinas I, Sauer H, Armanini M, Phillips H, Reichart LF, Ryan AM, Carver-Moore K, Rosenthal A. 1996. Renal and neuronal abnormalities in mice lacking GDNF. Nature 382:76-79.
-
(1996)
Nature
, vol.382
, pp. 76-79
-
-
Moore, M.W.1
Klein, R.D.2
Farinas, I.3
Sauer, H.4
Armanini, M.5
Phillips, H.6
Reichart, L.F.7
Ryan, A.M.8
Carver-Moore, K.9
Rosenthal, A.10
-
48
-
-
0025950803
-
Expression of the mouse anti-mullerian hormone gene suggests a role in both male and female sexual differentiation
-
Munsterberg A, Lovell-Badge R. 1991. Expression of the mouse anti-mullerian hormone gene suggests a role in both male and female sexual differentiation. Development 113:613-624.
-
(1991)
Development
, vol.113
, pp. 613-624
-
-
Munsterberg, A.1
Lovell-Badge, R.2
-
49
-
-
24944500376
-
Androgens activate mitogen-activated protein kinase signaling: Role in neuroprotection
-
Nguyen TV, Yao M, Pike CJ. 2005. Androgens activate mitogen-activated protein kinase signaling: role in neuroprotection. J Neurochem 94:1639-1651.
-
(2005)
J Neurochem
, vol.94
, pp. 1639-1651
-
-
Nguyen, T.V.1
Yao, M.2
Pike, C.J.3
-
50
-
-
0038686798
-
The regional pattern of retinoic acid synthesis by RALDH2 is essential for the development of posterior pharyngeal arches and the enteric nervous system
-
Niederreither K, Vermot J, Roux IL, Schuhbaur B, Chambon P, Dolle P. 2003. The regional pattern of retinoic acid synthesis by RALDH2 is essential for the development of posterior pharyngeal arches and the enteric nervous system. Development 130:2525-2534.
-
(2003)
Development
, vol.130
, pp. 2525-2534
-
-
Niederreither, K.1
Vermot, J.2
Roux, I.L.3
Schuhbaur, B.4
Chambon, P.5
Dolle, P.6
-
51
-
-
3042846766
-
Hydrocephalus and Hirschsprung's disease with a mutation of L1CAM
-
Okamoto N, Del Maestro R, Valero R, Monros E, Poo P, Kanemura Y, Yamasaki M. 2004. Hydrocephalus and Hirschsprung's disease with a mutation of L1CAM. J Hum Genet 49:334-337.
-
(2004)
J Hum Genet
, vol.49
, pp. 334-337
-
-
Okamoto, N.1
Del Maestro, R.2
Valero, R.3
Monros, E.4
Poo, P.5
Kanemura, Y.6
Yamasaki, M.7
-
52
-
-
0030738352
-
Hydrocephalus and Hirschsprung's disease in a patient with a mutation of L1CAM
-
Okamoto N, Wada Y, Goto M. 1997. Hydrocephalus and Hirschsprung's disease in a patient with a mutation of L1CAM. J Med Genet 34:670-671.
-
(1997)
J Med Genet
, vol.34
, pp. 670-671
-
-
Okamoto, N.1
Wada, Y.2
Goto, M.3
-
53
-
-
0031627570
-
Endothelial expression of endothelin-converting enzyme-1 beta mRNA is regulated by the transcription factor Ets-1
-
Orzechowski HD, Gunther A, Menzel S, Funke-Kaiser H, Richter M, Bohnemeier H, Paul M. 1998. Endothelial expression of endothelin-converting enzyme-1 beta mRNA is regulated by the transcription factor Ets-1. J Cardiovasc Pharmacol 31 Suppl 1:S55-S57.
-
(1998)
J Cardiovasc Pharmacol
, vol.31
, Issue.SUPPL. 1
-
-
Orzechowski, H.D.1
Gunther, A.2
Menzel, S.3
Funke-Kaiser, H.4
Richter, M.5
Bohnemeier, H.6
Paul, M.7
-
54
-
-
0035206913
-
Transcriptional mechanism of protein kinase C-induced isoform-specific expression of the gene for endothelin-converting enzyme-1 in human endothelial cells
-
Orzechowski HD, Gunther A, Menzel S, Zimmermann A, Funke-Kaiser H, Real R, Subkowski T, Zollmann FS, Paul M. 2001. Transcriptional mechanism of protein kinase C-induced isoform-specific expression of the gene for endothelin-converting enzyme-1 in human endothelial cells. Mol Pharmacol 60:1332-1342.
-
(2001)
Mol Pharmacol
, vol.60
, pp. 1332-1342
-
-
Orzechowski, H.D.1
Gunther, A.2
Menzel, S.3
Zimmermann, A.4
Funke-Kaiser, H.5
Real, R.6
Subkowski, T.7
Zollmann, F.S.8
Paul, M.9
-
55
-
-
0032817690
-
Altered endothelin-3 and endothelin-B receptor mRNA expression in Hirschsprung's disease
-
Oue T, Puri P. 1999. Altered endothelin-3 and endothelin-B receptor mRNA expression in Hirschsprung's disease: J Pediatr Surg 34:1257-1260.
-
(1999)
J Pediatr Surg
, vol.34
, pp. 1257-1260
-
-
Oue, T.1
Puri, P.2
-
56
-
-
20644436686
-
Genomewide linkage identifies novel modifier loci of aganglionosis in the Sox10Dom model of Hirschsprung disease
-
Owens SE, Broman KW, Wiltshire T, Elmore JB, Bradley KM, Smith JR, Southard-Smith EM. 2005. Genomewide linkage identifies novel modifier loci of aganglionosis in the Sox10Dom model of Hirschsprung disease. Hum Mol Genet 14:1549-1558.
-
(2005)
Hum Mol Genet
, vol.14
, pp. 1549-1558
-
-
Owens, S.E.1
Broman, K.W.2
Wiltshire, T.3
Elmore, J.B.4
Bradley, K.M.5
Smith, J.R.6
Southard-Smith, E.M.7
-
58
-
-
0037083016
-
Hydrocephalus and intestinal aganglionosis: Is L1CAM a modifier gene in Hirschsprung disease?
-
Parisi MA, Kapur RP, Neilson I, Hofstra RM, Holloway LW, Michaelis RC, Leppig KA. 2002. Hydrocephalus and intestinal aganglionosis: is L1CAM a modifier gene in Hirschsprung disease? Am J Med Genet 108:51-56.
-
(2002)
Am J Med Genet
, vol.108
, pp. 51-56
-
-
Parisi, M.A.1
Kapur, R.P.2
Neilson, I.3
Hofstra, R.M.4
Holloway, L.W.5
Michaelis, R.C.6
Leppig, K.A.7
-
59
-
-
0242490258
-
Genetic background modifies intestinal pseudo-obstruction and the expression of a reporter gene in Hox11L1-/- mice
-
Parisi MA, Baldessari AE, Iida MH, Clarke CM, Doggett B, Shirasawa S, Kapur RP. 2003. Genetic background modifies intestinal pseudo-obstruction and the expression of a reporter gene in Hox11L1-/- mice. Gastroenterology 125:1428-1440.
-
(2003)
Gastroenterology
, vol.125
, pp. 1428-1440
-
-
Parisi, M.A.1
Baldessari, A.E.2
Iida, M.H.3
Clarke, C.M.4
Doggett, B.5
Shirasawa, S.6
Kapur, R.P.7
-
60
-
-
0036578787
-
Dissecting Hirschsprung disease
-
Passarge E. 2002. Dissecting Hirschsprung disease. Nat Genet 31:11-12.
-
(2002)
Nat Genet
, vol.31
, pp. 11-12
-
-
Passarge, E.1
-
61
-
-
0033609337
-
The homeobox gene Phox2b is essential for the development of autonomic neural crest derivatives
-
Pattyn A, Morin X, Cremer H, Goridis C, Brunet J-F. 1999. The homeobox gene Phox2b is essential for the development of autonomic neural crest derivatives. Nature 399:366-370.
-
(1999)
Nature
, vol.399
, pp. 366-370
-
-
Pattyn, A.1
Morin, X.2
Cremer, H.3
Goridis, C.4
Brunet, J.-F.5
-
62
-
-
15844426332
-
Defects in enteric innervation and kidney development in mice lacking GDNF
-
Pichel JG, Shen L, Hui SZ, Granholm A-C, Drago J, Grinberg A, Lee EJ, Huang SP, Saarma M, Hoffer BJ, Sariola H, Westphal H. 1996. Defects in enteric innervation and kidney development in mice lacking GDNF. Nature 382:73-76.
-
(1996)
Nature
, vol.382
, pp. 73-76
-
-
Pichel, J.G.1
Shen, L.2
Hui, S.Z.3
Granholm, A.-C.4
Drago, J.5
Grinberg, A.6
Lee, E.J.7
Huang, S.P.8
Saarma, M.9
Hoffer, B.J.10
Sariola, H.11
Westphal, H.12
-
63
-
-
17344366171
-
Sox 10 mutations in patients with Waardenburg-Hirschsprung disease
-
Pingault V, Bondurand N, Kuhlbrodt K, Goerich DE, Prehu M-O, Puliti A, Herbarth B, Hermans-Borgmeyer I, Legius E, Matthijs G, Amiel J, Lyonnet S, Ceccherini I, Romeo G, Smith JC, Read AP, Wegner M, Goossens M. 1998. Sox 10 mutations in patients with Waardenburg-Hirschsprung disease. Nat Genet 18:171-173.
-
(1998)
Nat Genet
, vol.18
, pp. 171-173
-
-
Pingault, V.1
Bondurand, N.2
Kuhlbrodt, K.3
Goerich, D.E.4
Prehu, M.-O.5
Puliti, A.6
Herbarth, B.7
Hermans-Borgmeyer, I.8
Legius, E.9
Matthijs, G.10
Amiel, J.11
Lyonnet, S.12
Ceccherini, I.13
Romeo, G.14
Smith, J.C.15
Read, A.P.16
Wegner, M.17
Goossens, M.18
-
64
-
-
0028618372
-
A missense mutation of the endothelin-B receptor gene in multigenic Hirschsprung's disease
-
Puffenberger IG, Hosoda K, Washington SS, Nakao K, deWit D, Yanagisawa M, Chakravarti A. 1994. A missense mutation of the endothelin-B receptor gene in multigenic Hirschsprung's disease. Cell 79:1257-1266.
-
(1994)
Cell
, vol.79
, pp. 1257-1266
-
-
Puffenberger, I.G.1
Hosoda, K.2
Washington, S.S.3
Nakao, K.4
deWit, D.5
Yanagisawa, M.6
Chakravarti, A.7
-
65
-
-
0033916281
-
Hedgehog signals regulate multiple aspects of gastrointestinal development
-
Ramalho-Santos M, Melton DA, McMahon AP. 2000. Hedgehog signals regulate multiple aspects of gastrointestinal development. Development 127:2763-2772.
-
(2000)
Development
, vol.127
, pp. 2763-2772
-
-
Ramalho-Santos, M.1
Melton, D.A.2
McMahon, A.P.3
-
66
-
-
0026756410
-
Hirschsprung's disease. Evaluation of mortality and long-term function in 260 cases
-
discussion 941-942
-
Rescorla FJ, Morrison AM, Engles D, West KW, Grosfeld JL. 1992. Hirschsprung's disease. Evaluation of mortality and long-term function in 260 cases. Arch Surg 127:934-941; discussion 941-942.
-
(1992)
Arch Surg
, vol.127
, pp. 934-941
-
-
Rescorla, F.J.1
Morrison, A.M.2
Engles, D.3
West, K.W.4
Grosfeld, J.L.5
-
67
-
-
0031762643
-
Embryology and endocrinology of genital development
-
Rey R, Picard JY. 1998. Embryology and endocrinology of genital development. Baillieres Clin Endocrinol Metab 12:17-33.
-
(1998)
Baillieres Clin Endocrinol Metab
, vol.12
, pp. 17-33
-
-
Rey, R.1
Picard, J.Y.2
-
68
-
-
0033986373
-
Transgenic rescue of aganglionosis and piebaldism in lethal spotted mice
-
Rice J, Doggett B, Sweetser DA, Yanagisawa H, Yanagisawa M, Kapur RP. 2000. Transgenic rescue of aganglionosis and piebaldism in lethal spotted mice. Dev Dyn 217:120-132.
-
(2000)
Dev Dyn
, vol.217
, pp. 120-132
-
-
Rice, J.1
Doggett, B.2
Sweetser, D.A.3
Yanagisawa, H.4
Yanagisawa, M.5
Kapur, R.P.6
-
69
-
-
0028203639
-
An epidemiological study of Hirschsprung's disease and additional anomalies
-
Russell MB, Russell CA, Niebuhr E. 1994. An epidemiological study of Hirschsprung's disease and additional anomalies. Acta Paediatr 83:68-71.
-
(1994)
Acta Paediatr
, vol.83
, pp. 68-71
-
-
Russell, M.B.1
Russell, C.A.2
Niebuhr, E.3
-
71
-
-
0029901727
-
Renal agenesis and the absence of enteric neurons in mice lacking GDNF
-
Sanchez MP, Silos-Santiago I, Frisen J, He B, Lira SA, Barbacid M. 1996. Renal agenesis and the absence of enteric neurons in mice lacking GDNF. Nature 382:70-73.
-
(1996)
Nature
, vol.382
, pp. 70-73
-
-
Sanchez, M.P.1
Silos-Santiago, I.2
Frisen, J.3
He, B.4
Lira, S.A.5
Barbacid, M.6
-
72
-
-
0028174023
-
-
Schuchardt A, D'Agati V, Larsson-Blomberg L, Constantini F, Pachnis V. 1994. Defects in the kidney and enteric nervous system of mice lacking the tyrosine kinase receptor Ret. Nature 367:380-383.
-
Schuchardt A, D'Agati V, Larsson-Blomberg L, Constantini F, Pachnis V. 1994. Defects in the kidney and enteric nervous system of mice lacking the tyrosine kinase receptor Ret. Nature 367:380-383.
-
-
-
-
73
-
-
0036157933
-
Gdnf haploinsufficiency causes Hirschsprung-like intestinal obstruction and early-onset lethality in mice
-
Shen L, Pichel JG, Mayeli T, Sariola H, Lu B, Westphal H. 2002. Gdnf haploinsufficiency causes Hirschsprung-like intestinal obstruction and early-onset lethality in mice. Am J Hum Genet 70:435-447.
-
(2002)
Am J Hum Genet
, vol.70
, pp. 435-447
-
-
Shen, L.1
Pichel, J.G.2
Mayeli, T.3
Sariola, H.4
Lu, B.5
Westphal, H.6
-
75
-
-
0030139478
-
Hirschsprung's disease
-
Skinner M. 1996. Hirschsprung's disease. Curr Probl Surg 33:391-461.
-
(1996)
Curr Probl Surg
, vol.33
, pp. 391-461
-
-
Skinner, M.1
-
76
-
-
0031984825
-
Sox 10 mutation disrupts neural crest development in Dom Hirshsprung mouse model
-
Southard-Smith EM, Kos L, Pavan WJ. 1998. Sox 10 mutation disrupts neural crest development in Dom Hirshsprung mouse model. Nat Genet 18:60-64.
-
(1998)
Nat Genet
, vol.18
, pp. 60-64
-
-
Southard-Smith, E.M.1
Kos, L.2
Pavan, W.J.3
-
77
-
-
0032898565
-
The Sox10(Dom) mouse: Modeling the genetic variation of Waardenburg-Shah (WS4) syndrome
-
Southard-Smith EM, Angrist M, Ellison JS, Agarwala R, Baxevanis AD, Chakravarti A, Pavan WJ. 1999. The Sox10(Dom) mouse: modeling the genetic variation of Waardenburg-Shah (WS4) syndrome. Genome Res 9:215-225.
-
(1999)
Genome Res
, vol.9
, pp. 215-225
-
-
Southard-Smith, E.M.1
Angrist, M.2
Ellison, J.S.3
Agarwala, R.4
Baxevanis, A.D.5
Chakravarti, A.6
Pavan, W.J.7
-
78
-
-
33746027408
-
Interactions between Sox10, Edn3 and Ednrb during enteric nervous system and melanocyte development
-
Stanchina L, Baral V, Robert F, Pingault V, Lemort N, Pachnis V, Goossens M, Bondurand N. 2006. Interactions between Sox10, Edn3 and Ednrb during enteric nervous system and melanocyte development. Dev Biol 295:232-249.
-
(2006)
Dev Biol
, vol.295
, pp. 232-249
-
-
Stanchina, L.1
Baral, V.2
Robert, F.3
Pingault, V.4
Lemort, N.5
Pachnis, V.6
Goossens, M.7
Bondurand, N.8
-
79
-
-
0035992674
-
The effect of castration on endothelins, their receptors and endothelin converting enzyme in rat prostate
-
Takahashi W, Afiatpour P, Jr Foster HE, Ikeda K, Wada Y, Weiss RM, Latifpour J. 2002. The effect of castration on endothelins, their receptors and endothelin converting enzyme in rat prostate. Naunyn Schmiedebergs Arch Pharmacol 366:166-176.
-
(2002)
Naunyn Schmiedebergs Arch Pharmacol
, vol.366
, pp. 166-176
-
-
Takahashi, W.1
Afiatpour Jr, P.2
Foster, H.E.3
Ikeda, K.4
Wada, Y.5
Weiss, R.M.6
Latifpour, J.7
-
80
-
-
20444480612
-
New insights into the regulation of mammalian sex determination and male sex differentiation
-
Viger RS, Silversides DW, Tremblay JJ. 2005. New insights into the regulation of mammalian sex determination and male sex differentiation. Vitam Horm 70:387-413.
-
(2005)
Vitam Horm
, vol.70
, pp. 387-413
-
-
Viger, R.S.1
Silversides, D.W.2
Tremblay, J.J.3
-
81
-
-
0141987907
-
Insulin-like growth factor I (IGF-I) regulates endocrine activity of the embryonic testis in the mouse
-
Villalpando I, Lopez-Olmos V. 2003. Insulin-like growth factor I (IGF-I) regulates endocrine activity of the embryonic testis in the mouse. J Steroid Biochem Mol Biol 86:151-158.
-
(2003)
J Steroid Biochem Mol Biol
, vol.86
, pp. 151-158
-
-
Villalpando, I.1
Lopez-Olmos, V.2
-
82
-
-
33748767136
-
Differential gene expression and functional analysis implicate novel mechanisms in enteric nervous system precursor migration and neuritogenesis
-
Vohra BP, Tsuji K, Nagashimada M, Uesaka T, Wind D, Fu M, Armon J, Enomoto H, Heuckeroth RO. 2006. Differential gene expression and functional analysis implicate novel mechanisms in enteric nervous system precursor migration and neuritogenesis. Dev Biol 298:259-271.
-
(2006)
Dev Biol
, vol.298
, pp. 259-271
-
-
Vohra, B.P.1
Tsuji, K.2
Nagashimada, M.3
Uesaka, T.4
Wind, D.5
Fu, M.6
Armon, J.7
Enomoto, H.8
Heuckeroth, R.O.9
-
83
-
-
0035065576
-
Mutations in SIP1, encoding Smad interacting protein-1, cause a form of Hirschsprung disease
-
Wakamatsu N, Yamada Y, Yamada K, Ono T, Nomura N, Taniguchi H, Kitoh H, Mutoh N, Yamanaka T, Mushiake K, Kato K, Sonta S, Nagaya M. 2001. Mutations in SIP1, encoding Smad interacting protein-1, cause a form of Hirschsprung disease. Nat Genet 27:369-370.
-
(2001)
Nat Genet
, vol.27
, pp. 369-370
-
-
Wakamatsu, N.1
Yamada, Y.2
Yamada, K.3
Ono, T.4
Nomura, N.5
Taniguchi, H.6
Kitoh, H.7
Mutoh, N.8
Yamanaka, T.9
Mushiake, K.10
Kato, K.11
Sonta, S.12
Nagaya, M.13
-
84
-
-
28044448978
-
Mullerian Inhibiting Substance acts as a motor neuron survival factor in vitro
-
Wang PY, Koishi K, McGeachie AB, Kimber M, Maclaughlin DT, Donahoe PK, McLennan IS. 2005. Mullerian Inhibiting Substance acts as a motor neuron survival factor in vitro. Proc Natl Acad Sci U S A 102:16421-16425.
-
(2005)
Proc Natl Acad Sci U S A
, vol.102
, pp. 16421-16425
-
-
Wang, P.Y.1
Koishi, K.2
McGeachie, A.B.3
Kimber, M.4
Maclaughlin, D.T.5
Donahoe, P.K.6
McLennan, I.S.7
-
85
-
-
0032938812
-
Inhibition of in vitro enteric neuronal development by endothelin-3: Mediation by endothelin B receptors
-
Wu JJ, Chen J-X, Rothman TP, Gershon MD. 1999. Inhibition of in vitro enteric neuronal development by endothelin-3: mediation by endothelin B receptors. Development 126:1161-1173.
-
(1999)
Development
, vol.126
, pp. 1161-1173
-
-
Wu, J.J.1
Chen, J.-X.2
Rothman, T.P.3
Gershon, M.D.4
-
86
-
-
17744417682
-
A single rostrocaudal colonization of the rodent intestine by enteric neuron precursors is revealed by the expression of Pho2b, Ret, and p75 and by explants grown under the kidney capsule or in organ tissue
-
Young HM, Hearn CJ, Ciampoli D, Southwell BR, Brunet J-F, Newgreen DF. 1998. A single rostrocaudal colonization of the rodent intestine by enteric neuron precursors is revealed by the expression of Pho2b, Ret, and p75 and by explants grown under the kidney capsule or in organ tissue. Dev Biol 202:67-84.
-
(1998)
Dev Biol
, vol.202
, pp. 67-84
-
-
Young, H.M.1
Hearn, C.J.2
Ciampoli, D.3
Southwell, B.R.4
Brunet, J.-F.5
Newgreen, D.F.6
|