-
1
-
-
0027523909
-
Molecular characterization of a thyroid tumor-specific transforming sequence formed by the fusion of ret tyrosine kinase and the regulatory subunit RIα or cyclic AMP-dependent protein kinase A
-
Bongarzone I, Monzini N, Borrello MG, Carcano C, Ferraresi G, Arighi E, Mondellini P, Della Porta G, Pierotti MA: Molecular characterization of a thyroid tumor-specific transforming sequence formed by the fusion of ret tyrosine kinase and the regulatory subunit RIα or cyclic AMP-dependent protein kinase A. Mol Cell Biol 1993, 13:358-366
-
(1993)
Mol Cell Biol
, vol.13
, pp. 358-366
-
-
Bongarzone, I.1
Monzini, N.2
Borrello, M.G.3
Carcano, C.4
Ferraresi, G.5
Arighi, E.6
Mondellini, P.7
Della Porta, G.8
Pierotti, M.A.9
-
2
-
-
0025022463
-
PTC is a novel rearranged form of the ret proto-oncogene and is frequently detected in vivo in human thryoid papillary carcinomas
-
Grieco M, Santoro M, Berlingieri MT, Melillo RM, Donghi R, Bongarzone I, Pierotti MA, Della Porta G, Fusca A, Vecchio G: PTC is a novel rearranged form of the ret proto-oncogene and is frequently detected in vivo in human thryoid papillary carcinomas. Cell 1990, 60:557-563
-
(1990)
Cell
, vol.60
, pp. 557-563
-
-
Grieco, M.1
Santoro, M.2
Berlingieri, M.T.3
Melillo, R.M.4
Donghi, R.5
Bongarzone, I.6
Pierotti, M.A.7
Della Porta, G.8
Fusca, A.9
Vecchio, G.10
-
3
-
-
0027955122
-
Molecular characterization of RET/PTC3; a novel rearranged version of the RET proto-oncogene in a human thyroid papillary carcinoma
-
Santoro M, Dathan NA, Berlingieri MT, Bongarzone I, Paulin C, Grieco M, Pierotti MA, Vecchio G, Fusco A: Molecular characterization of RET/PTC3; a novel rearranged version of the RET proto-oncogene in a human thyroid papillary carcinoma. Oncogene 1994, 9:509-516
-
(1994)
Oncogene
, vol.9
, pp. 509-516
-
-
Santoro, M.1
Dathan, N.A.2
Berlingieri, M.T.3
Bongarzone, I.4
Paulin, C.5
Grieco, M.6
Pierotti, M.A.7
Vecchio, G.8
Fusco, A.9
-
4
-
-
0027231568
-
Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A
-
Mulligan LM, Kwok JB, Healey CS, Elsdon MJ, Eng C, Gardner E, Love DR, Mole SE, Moore JK, Papi L, Ponder MA, Telenius H, Tunnacliffe A, Ponder BAJ: Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A. Nature 1993, 363:458-460
-
(1993)
Nature
, vol.363
, pp. 458-460
-
-
Mulligan, L.M.1
Kwok, J.B.2
Healey, C.S.3
Elsdon, M.J.4
Eng, C.5
Gardner, E.6
Love, D.R.7
Mole, S.E.8
Moore, J.K.9
Papi, L.10
Ponder, M.A.11
Telenius, H.12
Tunnacliffe, A.13
Ponder, B.A.J.14
-
5
-
-
0027303248
-
Mutations in the RET proto-oncogene are associated with MEN2A and FMTC
-
Donis-Keller H, Dou S, Chi D, Carlson KM, Toshima K, Lairmore TC, Howe JR, Moley JF, Goodfellow P, Wells SA: Mutations in the RET proto-oncogene are associated with MEN2A and FMTC. Hum Mol Genet 1993, 2:851-856
-
(1993)
Hum Mol Genet
, vol.2
, pp. 851-856
-
-
Donis-Keller, H.1
Dou, S.2
Chi, D.3
Carlson, K.M.4
Toshima, K.5
Lairmore, T.C.6
Howe, J.R.7
Moley, J.F.8
Goodfellow, P.9
Wells, S.A.10
-
6
-
-
0028174024
-
A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma
-
Hofstra RM, Landsvater RM, Ceccherini I, Stulp RP, Stelwagen T, Luo Y, Pasini B, Hoppener JW, van Amstel HK, Romeo G, Lips CJM, Buys CHCM: A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma. Nature 1994, 367:375-376
-
(1994)
Nature
, vol.367
, pp. 375-376
-
-
Hofstra, R.M.1
Landsvater, R.M.2
Ceccherini, I.3
Stulp, R.P.4
Stelwagen, T.5
Luo, Y.6
Pasini, B.7
Hoppener, J.W.8
Van Amstel, H.K.9
Romeo, G.10
Lips, C.J.M.11
Buys, C.12
-
7
-
-
0027977002
-
Single missense mutation in the tyrosine kinase catalytic domain of the RET protooncogene is associated with multiple endocrine neoplasia type 2B
-
Carlson KM, Dou S, Chi D, Scavarda N, Toshima K, Jackson CE, Wells SAJ, Goodfellow PJ, Donis KH: Single missense mutation in the tyrosine kinase catalytic domain of the RET protooncogene is associated with multiple endocrine neoplasia type 2B. Proc Natl Acad Sci USA 1994, 91:1579-1583
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 1579-1583
-
-
Carlson, K.M.1
Dou, S.2
Chi, D.3
Scavarda, N.4
Toshima, K.5
Jackson, C.E.6
Wells, S.A.J.7
Goodfellow, P.J.8
Donis, K.H.9
-
8
-
-
0028199074
-
Specific mutations of the RET proto-oncogene are related to disease phenotype in MEN 2A and FMTC
-
Mulligan LM, Eng C, Healey CS, Clayton D, Kwok JB, Gardner E, Ponder MA, Frilling A, Jackson CE, Lehnert H, Neumann HPH, Thibodeau SN, Ponder BAJ: Specific mutations of the RET proto-oncogene are related to disease phenotype in MEN 2A and FMTC. Nat Genet 1994, 6:70-74
-
(1994)
Nat Genet
, vol.6
, pp. 70-74
-
-
Mulligan, L.M.1
Eng, C.2
Healey, C.S.3
Clayton, D.4
Kwok, J.B.5
Gardner, E.6
Ponder, M.A.7
Frilling, A.8
Jackson, C.E.9
Lehnert, H.10
Neumann, H.P.H.11
Thibodeau, S.N.12
Ponder, B.A.J.13
-
9
-
-
0028914683
-
Activation of RET as a dominant transforming gene by germline mutations of MEN2A and MEN2B
-
Santoro M, Carlomagno R, Romano A, Bottaro DP, Dathan NA, Grieco M, Fusco A, Vecchio G, Matoskova B, Kraus MH, Di Fiore PP: Activation of RET as a dominant transforming gene by germline mutations of MEN2A and MEN2B Science 1995, 267:381-383
-
(1995)
Science
, vol.267
, pp. 381-383
-
-
Santoro, M.1
Carlomagno, R.2
Romano, A.3
Bottaro, D.P.4
Dathan, N.A.5
Grieco, M.6
Fusco, A.7
Vecchio, G.8
Matoskova, B.9
Kraus, M.H.10
Di Fiore, P.P.11
-
10
-
-
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 BA, Munnich A: Mutations of the RET proto-oncogene in Hirschsprung's disease Nature 1994, 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.9
Munnich, A.10
-
11
-
-
0028120882
-
Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirschsprung's disease
-
Romeo G, Ronchetto P, Luo Y, Barone V, Sen M, Ceccherini I, Pasin B, Bocciardi R, Lerone M, Kaariainen H, Martuciello G Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirschsprung's disease. Nature 1394, 367:377-378
-
(1394)
Nature
, vol.367
, pp. 377-378
-
-
Romeo, G.1
Ronchetto, P.2
Luo, Y.3
Barone, V.4
Sen, M.5
Ceccherini, I.6
Pasin, B.7
Bocciardi, R.8
Lerone, M.9
Kaariainen, H.10
Martuciello, G.11
-
12
-
-
0028138537
-
Heterogeneity and low detection rate of RET mutations in Hirschsprung disease
-
Yin L, Barone V, Seri M, Bolino A, Bocciardi R, Ceccherini I, Pasini B, Tocco T, Lerone M, Cywes S, Moore S, Vanderwinden JM, Abramowicz MJ, Kristofferson U, Larrson LT, Hamel BCJ, Silengo M, Martuciello G, Romeo G: Heterogeneity and low detection rate of RET mutations in Hirschsprung disease. Eur J Hum Gene: 1994, 2:272-280
-
(1994)
Eur J Hum Gene
, vol.2
, pp. 272-280
-
-
Yin, L.1
Barone, V.2
Seri, M.3
Bolino, A.4
Bocciardi, R.5
Ceccherini, I.6
Pasini, B.7
Tocco, T.8
Lerone, M.9
Cywes, S.10
Moore, S.11
Vanderwinden, J.M.12
Abramowicz, M.J.13
Kristofferson, U.14
Larrson, L.T.15
Hamel, B.C.J.16
Silengo, M.17
Martuciello, G.18
Romeo, G.19
-
13
-
-
0029119781
-
Diversity of Ret proto-oncogene mutations in familial and sporadic Hirschsprung disease
-
Attie T, Pelet A, Edery P, Eng C, Mulligan LM, Amiel J, Boutrand L, Beldjord C, Nihoui-Fekete C, Munnich A, Lyonnet S: Diversity of Ret proto-oncogene mutations in familial and sporadic Hirschsprung disease. Hum Mol Genet 1995, 4:2407-2408
-
(1995)
Hum Mol Genet
, vol.4
, pp. 2407-2408
-
-
Attie, T.1
Pelet, A.2
Edery, P.3
Eng, C.4
Mulligan, L.M.5
Amiel, J.6
Boutrand, L.7
Beldjord, C.8
Nihoui-Fekete, C.9
Munnich, A.10
Lyonnet, S.11
-
14
-
-
0029069528
-
Mutation analysis of the RET receptor tyrosine kinase Hirschsprung disease
-
Angrist M, Bolk S, Thiel B, Puffenberger EG, Hofstra RM, Buys CH, Cass DT, Chakravarti A: Mutation analysis of the RET receptor tyrosine kinase Hirschsprung disease. Hum Mol Genet 1995, 4:821-830
-
(1995)
Hum Mol Genet
, vol.4
, pp. 821-830
-
-
Angrist, M.1
Bolk, S.2
Thiel, B.3
Puffenberger, E.G.4
Hofstra, R.M.5
Buys, Ch.6
Cass, D.T.7
Chakravarti, A.8
-
15
-
-
0031981819
-
Mutations of the RET-GDNF signaling pathway in Ondine's curse
-
Amiel J. Salomon R, Attie T, Pelet A, Trang H, Mokhtari M, Gaultier C, Munnich A, Lyonnet S: Mutations of the RET-GDNF signaling pathway in Ondine's curse. Am J Hum Genet 1998, 62:715-717
-
(1998)
Am J Hum Genet
, vol.62
, pp. 715-717
-
-
Amiel, J.1
Salomon, R.2
Attie, T.3
Pelet, A.4
Trang, H.5
Mokhtari, M.6
Gaultier, C.7
Munnich, A.8
Lyonnet, S.9
-
16
-
-
0028174023
-
Defects in the kidney and enteric nervous system of mice lacking the tyrosine kinase receptor Ret
-
Schuchardt A, D'Agati V, Larsson BL, Costantini F, Pachnis V: Defects in the kidney and enteric nervous system of mice lacking the tyrosine kinase receptor Ret. Nature 1994, 367:380-383
-
(1994)
Nature
, vol.367
, pp. 380-383
-
-
Schuchardt, A.1
D'Agati, V.2
Larsson, B.L.3
Costantini, F.4
Pachnis, V.5
-
17
-
-
0032408664
-
Artemin, a novel member of the GDNF ligand family supports peripheral, and central neurons, and signals through the GFRα3-RET receptor
-
Baloh RH, Tansey MG, Lampe PA, Fahrner TJ, Enomoto H, Simburger KS, Leitner ML, Araki T, Johnson EM, Milbrandt J: Artemin, a novel member of the GDNF ligand family supports peripheral, and central neurons, and signals through the GFRα3-RET receptor Neuron 1998, 21:1291-1302
-
(1998)
Neuron
, vol.21
, pp. 1291-1302
-
-
Baloh, R.H.1
Tansey, M.G.2
Lampe, P.A.3
Fahrner, T.J.4
Enomoto, H.5
Simburger, K.S.6
Leitner, M.L.7
Araki, T.8
Johnson, E.M.9
Milbrandt, J.10
-
18
-
-
0031862916
-
Molecular biology of the MEN2 gene
-
Santoro M, Melillo RM, Carlomagno F, Visconti R, De Vita G, Salvatore G, Lupoli G, Fusco A, Vecchio G: Molecular biology of the MEN2 gene. J Intern Med 1998, 243:505-508
-
(1998)
J Intern Med
, vol.243
, pp. 505-508
-
-
Santoro, M.1
Melillo, R.M.2
Carlomagno, F.3
Visconti, R.4
De Vita, G.5
Salvatore, G.6
Lupoli, G.7
Fusco, A.8
Vecchio, G.9
-
19
-
-
0031941550
-
Molecular development of the kidney: A review of the results of gene disruption studies
-
Lipschutz JH: Molecular development of the kidney: a review of the results of gene disruption studies. Am J Kidney Dis 1998, 31:383-397
-
(1998)
Am J Kidney Dis
, vol.31
, pp. 383-397
-
-
Lipschutz, J.H.1
-
20
-
-
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 GFRα1 is an essential receptor component for GDNF in the developing nervous system, and Kidney Neuron 1998, 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
-
21
-
-
0032129239
-
GFRα1-deficient mice have deficits in the enteric nervous system, and kidneys
-
Enomoto H, Araki T, Jackman A, Heuckerotn RO, Snider WD, Jonnsor EM, Milbrandt J: GFRα1-deficient mice have deficits in the enteric nervous system, and kidneys. Neuron 1998, 21:317-324
-
(1998)
Neuron
, vol.21
, pp. 317-324
-
-
Enomoto, H.1
Araki, T.2
Jackman, A.3
Heuckerotn, R.O.4
Snider, W.D.5
Jonnsor, E.M.6
Milbrandt, J.7
-
23
-
-
0031966746
-
Cell and molecular biology of kidney development
-
Orellana SA, Avner ED: Cell and molecular biology of kidney development. Semin Nephrol 1998, 18:233-243
-
(1998)
Semin Nephrol
, vol.18
, pp. 233-243
-
-
Orellana, S.A.1
Avner, E.D.2
-
26
-
-
15844426332
-
Defects in enteric innervation and kidney development in mice lacking GDNF
-
Pichel JG, Shen L, Sheng HZ, Granholm A-C, Drago J, Grinberg A, Lee EJ, Huang SP, Saarma M, Hoffer BJ, Sariola H, Westphal H: Defects in enteric innervation and kidney development in mice lacking GDNF, Nature 1996, 382:73-76
-
(1996)
Nature
, vol.382
, pp. 73-76
-
-
Pichel, J.G.1
Shen, L.2
Sheng, H.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
-
27
-
-
15844384629
-
Renal and neuronal abnormalities in mice lacking GDNF
-
Moore MW, Klein RD, Farinas I, Sauer H, Armanini M, Phillips H, Reichardl LF, Ryan AM, Carver-Moore K, Rosenthal A: Renal and neuronal abnormalities in mice lacking GDNF. Nature 1996, 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
Reichardl, L.F.7
Ryan, A.M.8
Carver-Moore, K.9
Rosenthal, A.10
-
28
-
-
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: Renal agenesis and the absence of enteric neurons in mice lacking GDNF Nature 1996, 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
-
29
-
-
7144255519
-
Full activation of MEN2B mutant RET by an additional MEN2A mutation or by ligand GDNF stimulation
-
Bongarzone I, Vigano E, Alberti L, Borrello MG, Pasini B, Greco A, Mondellini P, Smith DP, Ponder BAJ, Romeo G, Pierotti MA: Full activation of MEN2B mutant RET by an additional MEN2A mutation or by ligand GDNF stimulation. Oncogene 1998, 16:2295-2301
-
(1998)
Oncogene
, vol.16
, pp. 2295-2301
-
-
Bongarzone, I.1
Vigano, E.2
Alberti, L.3
Borrello, M.G.4
Pasini, B.5
Greco, A.6
Mondellini, P.7
Smith, D.P.8
Ponder, B.A.J.9
Romeo, G.10
Pierotti, M.A.11
-
30
-
-
0033611579
-
Ganglioneuromas ana renal anomalies are induced by activated RetMEN2B in transgenic mice
-
Sweetser DA, Froelick GJ, Matsumoto AM, Kafer KE, Marck B, Palmiter RD, Kapur RP: Ganglioneuromas ana renal anomalies are induced by activated RetMEN2B in transgenic mice, Oncogene 1999, 18:877-886
-
(1999)
Oncogene
, vol.18
, pp. 877-886
-
-
Sweetser, D.A.1
Froelick, G.J.2
Matsumoto, A.M.3
Kafer, K.E.4
Marck, B.5
Palmiter, R.D.6
Kapur, R.P.7
-
31
-
-
0026041580
-
The dopamine β-hydroxylase gene promoter directs expression of E. Coli lacZ to sympathetic and other neurons in adult transgenic mice
-
Mercer EH, Hoyle GW, Kapur RP, Brinster RL, Palmiter RD: The dopamine β-hydroxylase gene promoter directs expression of E. coli lacZ to sympathetic and other neurons in adult transgenic mice. Neuron 1991, 7:703-716
-
(1991)
Neuron
, vol.7
, pp. 703-716
-
-
Mercer, E.H.1
Hoyle, G.W.2
Kapur, R.P.3
Brinster, R.L.4
Palmiter, R.D.5
-
32
-
-
0025937249
-
Some neuronal cell populations express human dopamine β-hydroxylase-lacZ transgenes transiently curing embryonic development
-
Kapur RP, Hoyle GW, Mercer EH, Brinster RL, Palmiter RD: Some neuronal cell populations express human dopamine β-hydroxylase-lacZ transgenes transiently curing embryonic development Neuron 1991, 7:717-727
-
(1991)
Neuron
, vol.7
, pp. 717-727
-
-
Kapur, R.P.1
Hoyle, G.W.2
Mercer, E.H.3
Brinster, R.L.4
Palmiter, R.D.5
-
33
-
-
0031984825
-
Sox10 mutation disrupts neural crest development in Dom hirschsprung mouse model
-
Southard-Smith EM, Kos L, Pavan WJ: Sox10 mutation disrupts neural crest development in Dom Hirschsprung mouse model Nat Genet 1998, 18:60-64
-
(1998)
Nat Genet
, vol.18
, pp. 60-64
-
-
Southard-Smith, E.M.1
Kos, L.2
Pavan, W.J.3
-
34
-
-
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, Lemort N, Goossens M, Wegner M: Mutation of the Sry-related Sox10 gene in Dominant megacolon, a mouse model for human Hirschsprung disease. Proc Natl Acad Sci USA 1998, 95: 5161-5165
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 5161-5165
-
-
Herbarth, B.1
Pingault, V.2
Bondurand, N.3
Kuhlbrodt, K.4
Hermans-Borgmeyer, I.5
Puliti, A.6
Lemort, N.7
Goossens, M.8
Wegner, M.9
-
35
-
-
0028158524
-
Fine structure mapping and deletion analysis of the murine piebald locus
-
Metallinos DL, Oppenheimer AJ, Rirchik EM, Russell LB, Dietrich W, Tilghman SM: Fine structure mapping and deletion analysis of the murine piebald locus. Genetics 1994, 136:217-223
-
(1994)
Genetics
, vol.136
, pp. 217-223
-
-
Metallinos, D.L.1
Oppenheimer, A.J.2
Rirchik, E.M.3
Russell, L.B.4
Dietrich, W.5
Tilghman, S.M.6
-
36
-
-
0029879543
-
Abnormal microenvironmental signals underlie intestinal aganglionosis in dominant megacolon mutant mice
-
Kapur RP, Livingston R, Doggett B, Sweetser DA, Siebert JR, Palmiter RD: Abnormal microenvironmental signals underlie intestinal aganglionosis in Dominant megacolon mutant mice Dev Biol 1996, 174:360-369
-
(1996)
Dev Biol
, vol.174
, pp. 360-369
-
-
Kapur, R.P.1
Livingston, R.2
Doggett, B.3
Sweetser, D.A.4
Siebert, J.R.5
Palmiter, R.D.6
-
37
-
-
0030733083
-
Glial-cell-line-derived neurotrophic factor is required for bud initiation from ureteric epithelium
-
Sainio K, Suvanto P, Davies J, Wartiovaara J, Wartiovaara K, Saarma M, Arumae U, Meng X, Lindahl M, Pachnis V, Sariola H: Glial-cell-line-derived neurotrophic factor is required for bud initiation from ureteric epithelium. Development 1997, 124:4077-4087
-
(1997)
Development
, vol.124
, pp. 4077-4087
-
-
Sainio, K.1
Suvanto, P.2
Davies, J.3
Wartiovaara, J.4
Wartiovaara, K.5
Saarma, M.6
Arumae, U.7
Meng, X.8
Lindahl, M.9
Pachnis, V.10
Sariola, H.11
-
38
-
-
0021747818
-
Association of megacolon with a new dominant spotting gene (Dom) in the mouse
-
Lane PW, Liu HM: Association of megacolon with a new dominant spotting gene (Dom) in the mouse. J Hered 1984, 75:435-439
-
(1984)
J Hered
, vol.75
, pp. 435-439
-
-
Lane, P.W.1
Liu, H.M.2
-
40
-
-
0031436817
-
Oncogenesis and altered differentiation induced by activated Ras in neuroblasts of transgenic mice
-
Sweetser DA, Kapur RP, Froelick GJ, Kafer KE, Palmiter RD Oncogenesis and altered differentiation induced by activated Ras in neuroblasts of transgenic mice. Oncogene 1997, 15:2783-2794
-
(1997)
Oncogene
, vol.15
, pp. 2783-2794
-
-
Sweetser, D.A.1
Kapur, R.P.2
Froelick, G.J.3
Kafer, K.E.4
Palmiter, R.D.5
-
41
-
-
0027204790
-
Expression of NGF in sympathetic neurons leads to excessive axon outgrowth from ganglia but decreased terminal innervation within tissues
-
Hoyle GW, Mercer EH, Palmiter RD, Brinster RL: Expression of NGF in sympathetic neurons leads to excessive axon outgrowth from ganglia but decreased terminal innervation within tissues. Neuron 1993, 10: 1019-1034
-
(1993)
Neuron
, vol.10
, pp. 1019-1034
-
-
Hoyle, G.W.1
Mercer, E.H.2
Palmiter, R.D.3
Brinster, R.L.4
-
42
-
-
0027423210
-
The rat renal nerves during development
-
Liu L, Barajas L: The rat renal nerves during development. Anat Embryol 1993, 188:345-361
-
(1993)
Anat Embryol
, vol.188
, pp. 345-361
-
-
Liu, L.1
Barajas, L.2
-
43
-
-
0029986382
-
Development of NOS-containing neuronal somata in the rat kidney
-
Liu G-L, Liu L, Barajas L: Development of NOS-containing neuronal somata in the rat kidney. J Auton Nerv Sys 1996, 58:81-88
-
(1996)
J Auton Nerv Sys
, vol.58
, pp. 81-88
-
-
Liu, G.-L.1
Liu, L.2
Barajas, L.3
-
44
-
-
0029873202
-
Distribution of nitric oxide synthase-containing neuronal somata and postganglionic fibers in the rat kidney
-
Liu L, Liu G-L, Barajas L: Distribution of nitric oxide synthase-containing neuronal somata and postganglionic fibers in the rat kidney. J Comp Neurol 1996, 369:16-30
-
(1996)
J Comp Neurol
, vol.369
, pp. 16-30
-
-
Liu, L.1
Liu, G.-L.2
Barajas, L.3
-
45
-
-
0032584690
-
Evidence for NOS-containmg renal neuronal somata transiently expressing a catecholaminergic phenotype during development in the rat
-
Liu L, Liu GL, Barajas L Evidence for NOS-containmg renal neuronal somata transiently expressing a catecholaminergic phenotype during development in the rat. Neurosci Lett 1998, 251:161-164
-
(1998)
Neurosci Lett
, vol.251
, pp. 161-164
-
-
Liu, L.1
Liu, G.L.2
Barajas, L.3
-
46
-
-
0023200702
-
Beta adrenergic control of macromolecule synthesis in neonatal rat heart, kidney, and lung: Relationship to sympathetic neuronal development
-
Slotkin TA, Whitmore WL, Orband-Miller L, Queen KL, Haim K: Beta adrenergic control of macromolecule synthesis in neonatal rat heart, kidney, and lung: relationship to sympathetic neuronal development. J Pharmacol Exp Ther 1987, 243:101-109
-
(1987)
J Pharmacol Exp Ther
, vol.243
, pp. 101-109
-
-
Slotkin, T.A.1
Whitmore, W.L.2
Orband-Miller, L.3
Queen, K.L.4
Haim, K.5
-
47
-
-
0028575918
-
Renal failure in the neonate with in utero exposure to non-steroidal anti-inflammatory agents
-
Kaplan BS, Restaino I, Raval DS, Gottleib RP, Berstein J: Renal failure in the neonate with in utero exposure to non-steroidal anti-inflammatory agents. Pediatr Nephrol 1994, 8:700-704
-
(1994)
Pediatr Nephrol
, vol.8
, pp. 700-704
-
-
Kaplan, B.S.1
Restaino, I.2
Raval, D.S.3
Gottleib, R.P.4
Berstein, J.5
-
48
-
-
0028023781
-
Fetal renal maldevelopment with oligohydramnios following maternal use of piroxicam
-
Voyer LE, Drut R, Mendez JH: Fetal renal maldevelopment with oligohydramnios following maternal use of piroxicam. Pediatr Nephrol 1994, 8:592-594
-
(1994)
Pediatr Nephrol
, vol.8
, pp. 592-594
-
-
Voyer, L.E.1
Drut, R.2
Mendez, J.H.3
-
49
-
-
0025897135
-
Renal dysgenesis in a monozygotic twin: Association with in utero exposure to indomethacin
-
Restaino I, Kaplan BS, Kaplan P, Rosenberg HK, Witzleben C. Roberts N: Renal dysgenesis in a monozygotic twin: association with in utero exposure to indomethacin. Am J Med Genet 1991, 39:252-257
-
(1991)
Am J Med Genet
, vol.39
, pp. 252-257
-
-
Restaino, I.1
Kaplan, B.S.2
Kaplan, P.3
Rosenberg, H.K.4
Witzleben, C.5
Roberts, N.6
-
50
-
-
0032009994
-
Nonsteroidal anti-inflammatory drug fetal nephrotoxicity
-
Bernstein J, Werner AL, Verani R: Nonsteroidal anti-inflammatory drug fetal nephrotoxicity. Pediatr Dev Pathol 1998, 1:153-156
-
(1998)
Pediatr Dev Pathol
, vol.1
, pp. 153-156
-
-
Bernstein, J.1
Werner, A.L.2
Verani, R.3
-
51
-
-
0032530761
-
Transgenic expression of the endothelin-B receptor prevents congenital intestinal aganglionosis in a rat model of hirschsprung disease
-
Gariepy CE, Williams SC, Richardson JA, Hammer RE, Yanagisawa M: Transgenic expression of the endothelin-B receptor prevents congenital intestinal aganglionosis in a rat model of Hirschsprung disease. J Clin Invest 1998, 102:1092-1101
-
(1998)
J Clin Invest
, vol.102
, pp. 1092-1101
-
-
Gariepy, C.E.1
Williams, S.C.2
Richardson, J.A.3
Hammer, R.E.4
Yanagisawa, M.5
|