-
1
-
-
0035078125
-
Histochemical and immunohistochemical study of the intrinsic innervation in colonic dysganglionosis
-
Nogueira A, Campos M, Soares-Oliveira M, Estevao-Costa J, Silva P, Carneiro F, Carvalho JL. Histochemical and immunohistochemical study of the intrinsic innervation in colonic dysganglionosis. Pediatr Surg Int 2001; 17: 144-151
-
(2001)
Pediatr. Surg. Int.
, vol.17
, pp. 144-151
-
-
Nogueira, A.1
Campos, M.2
Soares-Oliveira, M.3
Estevao-Costa, J.4
Silva, P.5
Carneiro, F.6
Carvalho, J.L.7
-
2
-
-
0035000883
-
Cell-adhesion molecules and fibroblast growth factor signalling in Hirschsprung's disease
-
Yoneda A, Wang Y, O'Briain DS, Puri P. Cell-adhesion molecules and fibroblast growth factor signalling in Hirschsprung's disease. Pediatr Surg Int 2001; 17: 299-303
-
(2001)
Pediatr. Surg. Int.
, vol.17
, pp. 299-303
-
-
Yoneda, A.1
Wang, Y.2
O'Briain, D.S.3
Puri, P.4
-
3
-
-
0035117136
-
The development of colon innervation in trisomy 16 mice and Hirschsprungs disease
-
Li JC, Mi KH, Zhou JL, Busch L, Kuhnel W. The development of colon innervation in trisomy 16 mice and Hirschsprungs disease. World J Gastroenterol 2001; 7: 16-21
-
(2001)
World J. Gastroenterol.
, vol.7
, pp. 16-21
-
-
Li, J.C.1
Mi, K.H.2
Zhou, J.L.3
Busch, L.4
Kuhnel, W.5
-
4
-
-
0036181799
-
Increased smooth muscle contractility of intestine in the genetic null of the endothelin ETB receptor: A rat model for long segment Hirschsprung's disease
-
Won KJ, Torihashi S, Mitsui-Saito M, Hori M, Sato K, Suzuki T, Ozaki H, Karaki H. Increased smooth muscle contractility of intestine in the genetic null of the endothelin ETB receptor: a rat model for long segment Hirschsprung's disease. Gut 2002; 50: 355-360
-
(2002)
Gut
, vol.50
, pp. 355-360
-
-
Won, K.J.1
Torihashi, S.2
Mitsui-Saito, M.3
Hori, M.4
Sato, K.5
Suzuki, T.6
Ozaki, H.7
Karaki, H.8
-
5
-
-
0034764984
-
Hirschsprung disease, associated syndromes, and genetics: A review
-
Amiel J, Lyonnet S. Hirschsprung disease, associated syndromes, and genetics: a review. J Med Genet 2001; 38: 729-739
-
(2001)
J. Med. Genet.
, vol.38
, pp. 729-739
-
-
Amiel, J.1
Lyonnet, S.2
-
6
-
-
0033986373
-
Transgenic rescue of aganglionosis and piebaldism in lethal spotted mice
-
Rice J, Doggett B, Sweetser DA, Yanagisawa H, Yanagisawa M, Kapur RP. Transgenic rescue of aganglionosis and piebaldism in lethal spotted mice. Dev Dyn 2000; 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
-
7
-
-
0034950648
-
Functional analysis of RET with Hirschsprung mutations affecting its kinase domain
-
Iwashita T, Kurokawa K, Qiao S, Murakami H, Asai N, Kawai K, Hashimoto M, Watanabe T, Ichihara M, Takahashi M. Functional analysis of RET with Hirschsprung mutations affecting its kinase domain. Gastroenterology 2001; 121: 24-33
-
(2001)
Gastroenterology
, vol.121
, pp. 24-33
-
-
Iwashita, T.1
Kurokawa, K.2
Qiao, S.3
Murakami, H.4
Asai, N.5
Kawai, K.6
Hashimoto, M.7
Watanabe, T.8
Ichihara, M.9
Takahashi, M.10
-
8
-
-
17944399513
-
A rare haplotype of the RET proto-oncogene is a risk-modifying allele in hirschsprung disease
-
Griseri P, Pesce B, Patrone G, Osinga J, Puppo F, Sancandi M, Hofstra R, Romeo G, Ravazzolo R, Devoto M, Ceccherini I. A rare haplotype of the RET proto-oncogene is a risk-modifying allele in hirschsprung disease. Am J Hum Genet 2002; 71: 969-974
-
(2002)
Am. J. Hum. Genet.
, vol.71
, pp. 969-974
-
-
Griseri, P.1
Pesce, B.2
Patrone, G.3
Osinga, J.4
Puppo, F.5
Sancandi, M.6
Hofstra, R.7
Romeo, G.8
Ravazzolo, R.9
Devoto, M.10
Ceccherini, I.11
-
9
-
-
0035479144
-
The RET receptor: Function in development and dysfunction in congenital malformation
-
Manie S, Santoro M, Fusco A, Billaud M. The RET receptor: function in development and dysfunction in congenital malformation. Trends Genet 2001; 17: 580-589
-
(2001)
Trends Genet.
, vol.17
, pp. 580-589
-
-
Manie, S.1
Santoro, M.2
Fusco, A.3
Billaud, M.4
-
10
-
-
0036284060
-
Glial-derived neurotropic factor and RET gene expression in normal human anterior pituitary cell types and in pituitary tumors
-
Japon MA, Urbano AG, Saez C, Segura DI, Cerro AL, Dieguez C, Alvarez CV. Glial-derived neurotropic factor and RET gene expression in normal human anterior pituitary cell types and in pituitary tumors. J Clin Endocrinol Metab 2002; 87: 1879-1884
-
(2002)
J. Clin. Endocrinol. Metab.
, vol.87
, pp. 1879-1884
-
-
Japon, M.A.1
Urbano, A.G.2
Saez, C.3
Segura, D.I.4
Cerro, A.L.5
Dieguez, C.6
Alvarez, C.V.7
-
11
-
-
0032879734
-
Lessons from genetically engineered animal models. II. Disorders of enteric neuronal development: Insights from transgenic mice
-
Gershon MD. Lessons from genetically engineered animal models. II. Disorders of enteric neuronal development: insights from transgenic mice. Am J Physiol 1999; 277(2Pt 1): G262-267
-
(1999)
Am. J. Physiol.
, vol.277
, Issue.2 PART 1
-
-
Gershon, M.D.1
-
12
-
-
0033624669
-
Characterisation of the human GFRalpha-3 locus and investigation of the gene in Hirschsprung disease
-
Onochie CI, Korngut LM, Vanhorne JB, Myers SM, Michaud D, Mulligan LM. Characterisation of the human GFRalpha-3 locus and investigation of the gene in Hirschsprung disease. J Med Genet 2000; 37: 674-679
-
(2000)
J. Med. Genet.
, vol.37
, pp. 674-679
-
-
Onochie, C.I.1
Korngut, L.M.2
Vanhorne, J.B.3
Myers, S.M.4
Michaud, D.5
Mulligan, L.M.6
-
13
-
-
0034648508
-
Mutational analysis of RET/GDNF/NTN genes in children with total colonic aganglionosis with small bowel involvement
-
Inoue K, Shimotake T, Iwai N. Mutational analysis of RET/GDNF/NTN genes in children with total colonic aganglionosis with small bowel involvement. Am J Med Genet 2000; 93: 278-284
-
(2000)
Am. J. Med. Genet.
, vol.93
, pp. 278-284
-
-
Inoue, K.1
Shimotake, T.2
Iwai, N.3
-
14
-
-
0035035064
-
Analysis of the RET, GDNF, EDN3, and EDNRB genes in patients with intestinal neuronal dysplasia and Hirschsprung disease
-
Gath R, Goessling A, Keller KM, Koletzko S, Coerdt W, Muntefering H, Wirth S, Hofstra RM, Mulligan L, Eng C, von-Deimling A. Analysis of the RET, GDNF, EDN3, and EDNRB genes in patients with intestinal neuronal dysplasia and Hirschsprung disease. Gut 2001; 48: 671-675
-
(2001)
Gut
, vol.48
, pp. 671-675
-
-
Gath, R.1
Goessling, A.2
Keller, K.M.3
Koletzko, S.4
Coerdt, W.5
Muntefering, H.6
Wirth, S.7
Hofstra, R.M.8
Mulligan, L.9
Eng, C.10
von-Deimling, A.11
-
15
-
-
0034968236
-
Novel RET mutations in Hirschsprung's disease patients from the diverse South African population
-
Julies MG, Moore SW, Kotze MJ, du Plessis L. Novel RET mutations in Hirschsprung's disease patients from the diverse South African population. Eur J Hun Genet 2001; 9: 419-423
-
(2001)
Eur. J. Hun. Genet.
, vol.9
, pp. 419-423
-
-
Julies, M.G.1
Moore, S.W.2
Kotze, M.J.3
du Plessis, L.4
-
16
-
-
0035032207
-
Mutational analysis of the RET and GDNF gene in children with hypoganglionosis
-
Inoue K, Shimotake T, Tomiyama H, Iwai N. Mutational analysis of the RET and GDNF gene in children with hypoganglionosis. Eur J Pediatr Surg 2001; 11: 120-123
-
(2001)
Eur. J. Pediatr. Surg.
, vol.11
, pp. 120-123
-
-
Inoue, K.1
Shimotake, T.2
Tomiyama, H.3
Iwai, N.4
-
17
-
-
0035049513
-
A homozygous missense mutation in the tyrosine E kinase domain of the RET proto-oncogene in an infant with total intestinal aganglionosis
-
Shimotake T, Go S, Inoue K, Tomiyama H, Iwai N. A homozygous missense mutation in the tyrosine E kinase domain of the RET proto-oncogene in an infant with total intestinal aganglionosis. Am J Gastroenterol 2001; 96: 1286-1291
-
(2001)
Am. J. Gastroenterol.
, vol.96
, pp. 1286-1291
-
-
Shimotake, T.1
Go, S.2
Inoue, K.3
Tomiyama, H.4
Iwai, N.5
-
18
-
-
0034069860
-
RET and GDNF gene scanning in Hirschsprung patients using two dual denaturing gel systems
-
Hofstra RM, Wu Y, Stulp RP, Elfferich P, Osinga J, Maas SM, Siderius L, Brooks AS, vdEnde JJ, Heydendael VM, Severijnen RS, Bax KM, Meijers C, Buys CH. RET and GDNF gene scanning in Hirschsprung patients using two dual denaturing gel systems. Hum Mutat 2000; 15: 418-429
-
(2000)
Hum. Mutat.
, vol.15
, pp. 418-429
-
-
Hofstra, R.M.1
Wu, Y.2
Stulp, R.P.3
Elfferich, P.4
Osinga, J.5
Maas, S.M.6
Siderius, L.7
Brooks, A.S.8
vdEnde, J.J.9
Heydendael, V.M.10
Severijnen, R.S.11
Bax, K.M.12
Meijers, C.13
Buys, C.H.14
-
19
-
-
0033973161
-
Incidence of RET mutation in patients with Hirschsprung's disease
-
Sancandi M, Ceccherini I, Costa M, Fava M, Chen B, Wu Y, Hofstra R, Laurie T, Griffths M, Burge D, Tam PK. Incidence of RET mutation in patients with Hirschsprung's disease. J Pediatr Surg 2000; 35: 139-142
-
(2000)
J. Pediatr. Surg.
, vol.35
, pp. 139-142
-
-
Sancandi, M.1
Ceccherini, I.2
Costa, M.3
Fava, M.4
Chen, B.5
Wu, Y.6
Hofstra, R.7
Laurie, T.8
Griffths, M.9
Burge, D.10
Tam, P.K.11
-
20
-
-
0037029395
-
Association between c135G/A genotype and RET proto-oncogene germline mutations and phenotype of Hirschsprung's disease
-
Fitze G, Cramer J, Ziegler A, Schierz M, Schreiber M, Kuhlisch E, Roesner D, Schackert HK. Association between c135G/A genotype and RET proto-oncogene germline mutations and phenotype of Hirschsprung's disease. Lancet 2002; 359: 1200-1205
-
(2002)
Lancet
, vol.359
, pp. 1200-1205
-
-
Fitze, G.1
Cramer, J.2
Ziegler, A.3
Schierz, M.4
Schreiber, M.5
Kuhlisch, E.6
Roesner, D.7
Schackert, H.K.8
-
21
-
-
0033330662
-
A novel 9-base pair duplication in RET exon 8 in familial medullary thyroid carcinoma
-
Pigny P, Bauters C, Wemeau JL, Houcke ML, Crepin M, Caron P, Giraud S, Calender A, Buisine MP, Kerckaert JP, Porchet N. A novel 9-base pair duplication in RET exon 8 in familial medullary thyroid carcinoma. J Clin Endocrinol Metab 1999; 84: 1700-1704
-
(1999)
J. Clin. Endocrinol. Metab.
, vol.84
, pp. 1700-1704
-
-
Pigny, P.1
Bauters, C.2
Wemeau, J.L.3
Houcke, M.L.4
Crepin, M.5
Caron, P.6
Giraud, S.7
Calender, A.8
Buisine, M.P.9
Kerckaert, J.P.10
Porchet, N.11
-
22
-
-
0033854456
-
RET genotypes comprising specific haplotypes of polymorphic variants predispose to isolated Hirschsprung disease
-
Borrego S, Ruiz A, Saez ME, Gimm O, Gao X, Lopez-Alonso M, Hernandez A, Wright FA, Antinolo G, Eng C. RET genotypes comprising specific haplotypes of polymorphic variants predispose to isolated Hirschsprung disease. J Med Genet 2000; 37: 572-578
-
(2000)
J. Med. Genet.
, vol.37
, pp. 572-578
-
-
Borrego, S.1
Ruiz, A.2
Saez, M.E.3
Gimm, O.4
Gao, X.5
Lopez-Alonso, M.6
Hernandez, A.7
Wright, F.A.8
Antinolo, G.9
Eng, C.10
-
24
-
-
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 RM, Angrist M, Salomon R, Croaker D, Buys CH, Lyonnet S, Chakravarti A. 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 USA 2000; 97: 268-273
-
(2000)
Proc. Natl. Acad. Sci. USA
, vol.97
, pp. 268-273
-
-
Bolk, S.1
Pelet, A.2
Hofstra, R.M.3
Angrist, M.4
Salomon, R.5
Croaker, D.6
Buys, C.H.7
Lyonnet, S.8
Chakravarti, A.9
-
25
-
-
0041336928
-
The constipated child: How likely is Hirschsprung's disease?
-
Khan AR, Vujanic GM, Huddart S. The constipated child: how likely is Hirschsprung's disease? Pediatr Surg Int 2003; 19 439-442
-
(2003)
Pediatr. Surg. Int.
, vol.19
, pp. 439-442
-
-
Khan, A.R.1
Vujanic, G.M.2
Huddart, S.3
-
26
-
-
0036985513
-
Comparison of five commercial kits for DNA extraction from human blood, saliva and muscle samples
-
Pepinski W, Soltyszewski I, Janica J, Skawronska M, Koc-Zorawska E. Comparison of five commercial kits for DNA extraction from human blood, saliva and muscle samples. Rocz Akad Med Bialymst 2002; 47: 270-275
-
(2002)
Rocz. Akad. Med. Bialymst.
, vol.47
, pp. 270-275
-
-
Pepinski, W.1
Soltyszewski, I.2
Janica, J.3
Skawronska, M.4
Koc-Zorawska, E.5
-
27
-
-
18344384747
-
Specific haplotypes of the RET proto-oncogene are over-represented in patients with sporadic papillary thyroid carcinoma
-
Lesueur F, Corbex M, McKay JD, Lima J, Soares P, Griseri P, Burgess J, Ceccherini I, Landolfi S, Papotti M, Amorim A, Goldgar DE, Romeo G. Specific haplotypes of the RET proto-oncogene are over-represented in patients with sporadic papillary thyroid carcinoma. J Med Genet 2002; 39: 260-265
-
(2002)
J. Med. Genet.
, vol.39
, pp. 260-265
-
-
Lesueur, F.1
Corbex, M.2
McKay, J.D.3
Lima, J.4
Soares, P.5
Griseri, P.6
Burgess, J.7
Ceccherini, I.8
Landolfi, S.9
Papotti, M.10
Amorim, A.11
Goldgar, D.E.12
Romeo, G.13
-
28
-
-
0034967978
-
Docking protein FRS2 links the protein tyrosine kinase RET and its oncogenic forms with the mitogen-activated protein kinase signaling cascade
-
Melillo RM, Santoro M, Ong SH, Billaud M, Fusco A, Hadari YR, Schlessinger J, Lax I. Docking protein FRS2 links the protein tyrosine kinase RET and its oncogenic forms with the mitogen-activated protein kinase signaling cascade. Mol Cell Biol 2001; 21: 4177-4187
-
(2001)
Mol. Cell Biol.
, vol.21
, pp. 4177-4187
-
-
Melillo, R.M.1
Santoro, M.2
Ong, S.H.3
Billaud, M.4
Fusco, A.5
Hadari, Y.R.6
Schlessinger, J.7
Lax, I.8
-
29
-
-
0033813240
-
A single-nucleotide polymorphic variant of the RET proto-oncogene is underrepresented in sporadic Hirschsprung disease
-
Griseri P, Sancandi M, Patrone G, Bocciardi R, Hofstra R, Ravazzolo R, Devoto M, Romeo G, Ceccherini I. A single-nucleotide polymorphic variant of the RET proto-oncogene is underrepresented in sporadic Hirschsprung disease. Eur J Hum Genet 2000; 8: 721-724
-
(2000)
Eur. J. Hum. Genet.
, vol.8
, pp. 721-724
-
-
Griseri, P.1
Sancandi, M.2
Patrone, G.3
Bocciardi, R.4
Hofstra, R.5
Ravazzolo, R.6
Devoto, M.7
Romeo, G.8
Ceccherini, I.9
-
30
-
-
0033729031
-
Multiple endocrine neoplasia type 2 and RET: From neoplasia to neurogenesis
-
Hansford JR, Mulligan LM. Multiple endocrine neoplasia type 2 and RET: from neoplasia to neurogenesis. J Med Genet 2000; 37: 817-827
-
(2000)
J. Med. Genet.
, vol.37
, pp. 817-827
-
-
Hansford, J.R.1
Mulligan, L.M.2
-
31
-
-
0032547951
-
A 5′-CG-3′-rich region in the promoter of the transcriptionally frequently silenced RET protooncogene lacks methylated cytidine residues
-
Munnes M, Patrone G, Schmitz B, Romeo G, Doerfler W. A 5′-CG-3′-rich region in the promoter of the transcriptionally frequently silenced RET protooncogene lacks methylated cytidine residues. Oncogene 1998; 17: 2573-2583
-
(1998)
Oncogene
, vol.17
, pp. 2573-2583
-
-
Munnes, M.1
Patrone, G.2
Schmitz, B.3
Romeo, G.4
Doerfler, W.5
-
32
-
-
0034605384
-
Familial form of hirschsprung disease: Nucleotide sequence studies reveal point mutations in the RET proto-oncogene in two of six families but not in other candidate genes
-
Munnes M, Fanaei S, Schmitz B, Muiznieks I, Holschneider AM, Doerfler W. Familial form of hirschsprung disease: nucleotide sequence studies reveal point mutations in the RET proto-oncogene in two of six families but not in other candidate genes. Am J Med Genet 2000; 94: 19-27
-
(2000)
Am. J. Med. Genet.
, vol.94
, pp. 19-27
-
-
Munnes, M.1
Fanaei, S.2
Schmitz, B.3
Muiznieks, I.4
Holschneider, A.M.5
Doerfler, W.6
-
34
-
-
0034577987
-
Molecular genetics of Hirschsprung disease: A model of multigenic neurocristopathy
-
Amiel J, Salomon R, Attie-Bitach T, Touraine R, Steffann J, Pelet A, Nihoul-Fekete C, Vekemans M, Munnich A, Lyonnet S. Molecular genetics of Hirschsprung disease: a model of multigenic neurocristopathy. J Soc Biol 2000; 194: 125-128
-
(2000)
J. Soc. Biol.
, vol.194
, pp. 125-128
-
-
Amiel, J.1
Salomon, R.2
Attie-Bitach, T.3
Touraine, R.4
Steffann, J.5
Pelet, A.6
Nihoul-Fekete, C.7
Vekemans, M.8
Munnich, A.9
Lyonnet, S.10
-
35
-
-
0034450101
-
cDNA sequence and genomic structure of the rat RET proto-oncogene
-
Matera I, De Miguel-Rodriguez M, Fernandez-Santos JM, Santamaria G, Puliti A, Ravazzolo R, Romeo G, Galera-Davidson H, Ceccherini I. cDNA sequence and genomic structure of the rat RET proto-oncogene. DNA Seq 2000; 11: 405-417
-
(2000)
DNA Seq.
, vol.11
, pp. 405-417
-
-
Matera, I.1
De Miguel-Rodriguez, M.2
Fernandez-Santos, J.M.3
Santamaria, G.4
Puliti, A.5
Ravazzolo, R.6
Romeo, G.7
Galera-Davidson, H.8
Ceccherini, I.9
-
36
-
-
0034092852
-
Japanese patients with sporadic Hirschsprung: Mutation analysis of the receptor tyrosine kinase proto-oncogene, endothelin-B receptor, endothelin-3, glial cell line-derived neurotrophic factor and neurturin genes: A comparison with similar studies
-
Sakai T, Nirasawa Y, Itoh Y, Wakizaka A. Japanese patients with sporadic Hirschsprung: mutation analysis of the receptor tyrosine kinase proto-oncogene, endothelin-B receptor, endothelin-3, glial cell line-derived neurotrophic factor and neurturin genes: a comparison with similar studies. Eur J Pediatr 2000; 159: 160-167
-
(2000)
Eur. J. Pediatr.
, vol.159
, pp. 160-167
-
-
Sakai, T.1
Nirasawa, Y.2
Itoh, Y.3
Wakizaka, A.4
-
37
-
-
0034660859
-
Tyrosine 1062 of RET-MEN2A mediates activation of Akt (protein kinase B) and mitogen-activated protein kinase pathways leading to PC12 cell survival
-
De Vita G, Melillo RM, Carlomagno F, Visconti R, Castellone MD, Bellacosa A, Billaud M, Fusco A, Tsichlis PN, Santoro M. Tyrosine 1062 of RET-MEN2A mediates activation of Akt (protein kinase B) and mitogen-activated protein kinase pathways leading to PC12 cell survival. Cancer Res 2000; 60: 3727-3731
-
(2000)
Cancer Res.
, vol.60
, pp. 3727-3731
-
-
De Vita, G.1
Melillo, R.M.2
Carlomagno, F.3
Visconti, R.4
Castellone, M.D.5
Bellacosa, A.6
Billaud, M.7
Fusco, A.8
Tsichlis, P.N.9
Santoro, M.10
-
38
-
-
0036156121
-
Multigenerational familial medullary thyroid cancer (FMTC): Evidence for FMTC phenocopies and association with papillary thyroid cancer
-
Fugazzola L, Cerutti N, Mannavola D, Ghilardi G, Alberti L, Romoli R, Beck-Peccoz P. Multigenerational familial medullary thyroid cancer (FMTC): evidence for FMTC phenocopies and association with papillary thyroid cancer. Clin Endocrinol 2002; 56: 53-63
-
(2002)
Clin. Endocrinol.
, vol.56
, pp. 53-63
-
-
Fugazzola, L.1
Cerutti, N.2
Mannavola, D.3
Ghilardi, G.4
Alberti, L.5
Romoli, R.6
Beck-Peccoz, P.7
-
39
-
-
0035404426
-
Germline mutations of the ret proto-oncogene in Chilean patients with hereditary and sporadic medullary thyroid carcinoma
-
Wohllk N, Becker P, Youlton R, Cote GJ, Gagel RF. Germline mutations of the ret proto-oncogene in Chilean patients with hereditary and sporadic medullary thyroid carcinoma. Rev Med Chil 2001; 129: 713-718
-
(2001)
Rev. Med. Chil.
, vol.129
, pp. 713-718
-
-
Wohllk, N.1
Becker, P.2
Youlton, R.3
Cote, G.J.4
Gagel, R.F.5
-
40
-
-
0035724172
-
Multiple endocrine neoplasia type 2 syndromes may be associated with renal malformations
-
Lore F, Talidis F, Di Cairano G, Renieri A. Multiple endocrine neoplasia type 2 syndromes may be associated with renal malformations. J Intern Med 2001; 250: 37-42
-
(2001)
J. Intern. Med.
, vol.250
, pp. 37-42
-
-
Lore, F.1
Talidis, F.2
Di Cairano, G.3
Renieri, A.4
-
41
-
-
0034935625
-
Large-scale analysis of mutations in RET exon 16 in sporadic medullary thyroid carcinomas in Japan
-
Takano T, Miyauchi A, Yoshida H, Hasegawa Y, Kuma K, Amino N. Large-scale analysis of mutations in RET exon 16 in sporadic medullary thyroid carcinomas in Japan. Jpn J Cancer Res 2001; 92 645-648
-
(2001)
Jpn. J. Cancer Res.
, vol.92
, pp. 645-648
-
-
Takano, T.1
Miyauchi, A.2
Yoshida, H.3
Hasegawa, Y.4
Kuma, K.5
Amino, N.6
-
42
-
-
0035099911
-
A large family with hereditary MTC: Role of RET genetic analysis in differential diagnosis between MEN 2A and FMTC
-
Chiefari E, Chiarella R, Crocetti U, Tardio B, Arturi F, Russo D, Trischitta V, Filetti S, Zingrillo M. A large family with hereditary MTC: role of RET genetic analysis in differential diagnosis between MEN 2A and FMTC. Horm Metab Res 2001; 33: 52-56
-
(2001)
Horm. Metab. Res.
, vol.33
, pp. 52-56
-
-
Chiefari, E.1
Chiarella, R.2
Crocetti, U.3
Tardio, B.4
Arturi, F.5
Russo, D.6
Trischitta, V.7
Filetti, S.8
Zingrillo, M.9
-
43
-
-
1642574220
-
Highly recurrent RET mutations and novel mutations in genes of the receptor tyrosine kinase and endothelin receptor B pathways in Chinese patients with sporadic Hirschsprung disease
-
Garcia-Barcelo M, Sham MH, Lee WS, Lui VC, Chen BL, Wong KK, Wong JS, Tam PK. Highly recurrent RET mutations and novel mutations in genes of the receptor tyrosine kinase and endothelin receptor B pathways in Chinese patients with sporadic Hirschsprung disease. Clin Chem 2004; 50: 93-100
-
(2004)
Clin. Chem.
, vol.50
, pp. 93-100
-
-
Garcia-Barcelo, M.1
Sham, M.H.2
Lee, W.S.3
Lui, V.C.4
Chen, B.L.5
Wong, K.K.6
Wong, J.S.7
Tam, P.K.8
-
44
-
-
0035154068
-
Congenital central hypoventilation syndrome associated with Hirschsprung's disease: Mutation analysis of the RET and endothelin-signaling pathways
-
Sakai T, Wakizaka A, Nirasawa Y. Congenital central hypoventilation syndrome associated with Hirschsprung's disease: mutation analysis of the RET and endothelin-signaling pathways. Eur J Pediatr Surg 2001; 11: 335-337
-
(2001)
Eur. J. Pediatr. Surg.
, vol.11
, pp. 335-337
-
-
Sakai, T.1
Wakizaka, A.2
Nirasawa, Y.3
-
45
-
-
0036220980
-
RET mutation profile and variable clinical manifestations in a family with multiple endocrine neoplasia type 2A and Hirschsprung's disease
-
Pasini B, Rossi R, Ambrosio MR, Zatelli MC, Gullo M, Gobbo M, Collini P, Aiello A, Pansini G, Trasforini G, degli Uberti EC. RET mutation profile and variable clinical manifestations in a family with multiple endocrine neoplasia type 2A and Hirschsprung's disease. Surgery 2002; 131: 373-381
-
(2002)
Surgery
, vol.131
, pp. 373-381
-
-
Pasini, B.1
Rossi, R.2
Ambrosio, M.R.3
Zatelli, M.C.4
Gullo, M.5
Gobbo, M.6
Collini, P.7
Aiello, A.8
Pansini, G.9
Trasforini, G.10
degli Uberti, E.C.11
-
46
-
-
0034807019
-
The sensitivity of activated Cys Ret mutants to glial cell line-derived neurotrophic factor is mandatory to rescue neuroectodermic cells from apoptosis
-
Mograbi B, Bocciardi R, Bourget I, Juhel T, Farahi-Far D, Romeo G, Ceccherini I, Rossi B. The sensitivity of activated Cys Ret mutants to glial cell line-derived neurotrophic factor is mandatory to rescue neuroectodermic cells from apoptosis. Mol Cell Biol 2001; 21: 6719-6730
-
(2001)
Mol. Cell Biol.
, vol.21
, pp. 6719-6730
-
-
Mograbi, B.1
Bocciardi, R.2
Bourget, I.3
Juhel, T.4
Farahi-Far, D.5
Romeo, G.6
Ceccherini, I.7
Rossi, B.8
|