-
1
-
-
0004776697
-
Hirschsprung's Disease
-
P Puri Hirschsprung's Disease TO Oldham PM Colombani RP Foglia Surgery of Infants and Children: Scientific Principles and Practice 1997 Lippincott-Raven New York, NY 1277 1299 chap 80
-
(1997)
, pp. 1277-1299
-
-
Puri, P1
-
2
-
-
0024474299
-
A 40-year multinational retrospective study of 880 procedures
-
J Sherman M Snyder J Weitzman A 40-year multinational retrospective study of 880 procedures J Pediatr Surg 24 1989 833 838
-
(1989)
J Pediatr Surg
, vol.24
, pp. 833-838
-
-
Sherman, J1
Snyder, M2
Weitzman, J3
-
3
-
-
0025268652
-
A genetic study of Hirschsprung disease
-
J Badner W Sieber K Garver A genetic study of Hirschsprung disease Am J Genet 46 1990 568 580
-
(1990)
Am J Genet
, vol.46
, pp. 568-580
-
-
Badner, J1
Sieber, W2
Garver, K3
-
4
-
-
0018676390
-
A survey of the members of the American Association of Pediatrics
-
S Kleinhaus S Boley M Sheran A survey of the members of the American Association of Pediatrics J Pediatr Surg 14 1979 588 597
-
(1979)
J Pediatr Surg
, vol.14
, pp. 588-597
-
-
Kleinhaus, S1
Boley, S2
Sheran, M3
-
5
-
-
0021344732
-
Diagnosis and treatment of Hirschsprung's disease in Japan: An analysis of 1,628 patients
-
K Ikeda S Goto Diagnosis and treatment of Hirschsprung's disease in Japan: An analysis of 1,628 patients Ann Surg 199 1984 400 405
-
(1984)
Ann Surg
, vol.199
, pp. 400-405
-
-
Ikeda, K1
Goto, S2
-
6
-
-
0025730176
-
Familial Hirschsprung's disease: Report of autosomal dominant and probable autosomal recessive X-linked kindreds
-
V Stannard C Fowler L Roginson Familial Hirschsprung's disease: Report of autosomal dominant and probable autosomal recessive X-linked kindreds J Pediatr Surg 26 1990 591 594
-
(1990)
J Pediatr Surg
, vol.26
, pp. 591-594
-
-
Stannard, V1
Fowler, C2
Roginson, L3
-
7
-
-
0028103927
-
Familial Hirschsprung's disease: Study of a Texas cohort
-
C Renya Familial Hirschsprung's disease: Study of a Texas cohort Pediatrics 94 1994 347 349
-
(1994)
Pediatrics
, vol.94
, pp. 347-349
-
-
Renya, C1
-
8
-
-
84981776731
-
A family study of Hirschsprung's disease
-
M Bodian C Carter A family study of Hirschsprung's disease Ann Hum Genet 26 1963 261 277
-
(1963)
Ann Hum Genet
, vol.26
, pp. 261-277
-
-
Bodian, M1
Carter, C2
-
9
-
-
84968686453
-
Identity-by-descent mapping of Hirschsprung's disease and a large Mennonite kindred
-
E Puffenberger E Kauffman S Bolk Identity-by-descent mapping of Hirschsprung's disease and a large Mennonite kindred Am J Hum Genet 53 1993 1062
-
(1993)
Am J Hum Genet
, vol.53
, pp. 1062
-
-
Puffenberger, E1
Kauffman, E2
Bolk, S3
-
10
-
-
0027232235
-
Hirschsprung's disease: Clinical and experimental observations
-
P Puri Hirschsprung's disease: Clinical and experimental observations World J Surg 17 1993 374 384
-
(1993)
World J Surg
, vol.17
, pp. 374-384
-
-
Puri, P1
-
11
-
-
0023036805
-
Hirschsprung's disease in the newborn
-
T Polly A Coran Hirschsprung's disease in the newborn Pediatr Surg Int 1 1993 80 83
-
(1993)
Pediatr Surg Int
, vol.1
, pp. 80-83
-
-
Polly, T1
Coran, A2
-
12
-
-
0022448783
-
Partial trisomy 22 and 11 due to a paternal 11;22 translocation associated with Hirschsprung's disease
-
B Beedgen U Nutzenadel W Querfeld Partial trisomy 22 and 11 due to a paternal 11;22 translocation associated with Hirschsprung's disease Eur J Pediatr 145 1986 229 232
-
(1986)
Eur J Pediatr
, vol.145
, pp. 229-232
-
-
Beedgen, B1
Nutzenadel W Querfeld, U2
-
13
-
-
0023873321
-
Concurrent de novo interstitial deletion of band 2p22 and reciprocal translocation (3;7)(p21;g22)
-
G Webb C Keith N Campbell Concurrent de novo interstitial deletion of band 2p22 and reciprocal translocation (3;7)(p21;g22) J Med Genet 25 1988 125 127
-
(1988)
J Med Genet
, vol.25
, pp. 125-127
-
-
Webb, G1
Keith, C2
Campbell, N3
-
14
-
-
0015700640
-
Genetics of Hirschsprung's disease
-
E Passarge Genetics of Hirschsprung's disease Clin Gastroenterol 2 1973 507 513
-
(1973)
Clin Gastroenterol
, vol.2
, pp. 507-513
-
-
Passarge, E1
-
15
-
-
0024358095
-
Association of 13q deletion and Hirschsprung's disease
-
P Kiss M Osztovics Association of 13q deletion and Hirschsprung's disease J Med Genet 26 1989 793 794
-
(1989)
J Med Genet
, vol.26
, pp. 793-794
-
-
Kiss, P1
Osztovics, M2
-
16
-
-
0025944896
-
A case of Hirschsprung's disease with a chromosome 13 microdeletion, del (13)(Q32.3g33.2): Potential mapping of one disease locus
-
A Bottani Y Xie F Binkert A case of Hirschsprung's disease with a chromosome 13 microdeletion, del (13)(Q32.3g33.2): Potential mapping of one disease locus Hum Genet 87 1991 748 750
-
(1991)
Hum Genet
, vol.87
, pp. 748-750
-
-
Bottani, A1
Xie, Y2
Binkert, F3
-
17
-
-
0021722228
-
Separation of retinoblastoma and esterase D locus in a patient with sporadic retinoblastoma and del (I3)(g14.1g22.3)
-
R Sparkes M Sperkes R Kalina Separation of retinoblastoma and esterase D locus in a patient with sporadic retinoblastoma and del (I3)(g14.1g22.3) Hum Genet 68 1984 258 259
-
(1984)
Hum Genet
, vol.68
, pp. 258-259
-
-
Sparkes, R1
Sperkes, M2
Kalina, R3
-
18
-
-
0024576097
-
Interstitial deletion of distal 13q associated with Hirschsprung's disease
-
MA Lamont M Fitchett NR Dennis Interstitial deletion of distal 13q associated with Hirschsprung's disease J Med Genet 26 1989 100 104
-
(1989)
J Med Genet
, vol.26
, pp. 100-104
-
-
Lamont, MA1
Fitchett, M2
Dennis, NR3
-
19
-
-
0026724137
-
Total colonic aganglionosis associated with interstitial deletion of the long arm of chromosome 10
-
G Martucciello M Bicocchi P Dodero Total colonic aganglionosis associated with interstitial deletion of the long arm of chromosome 10 Pediatr Surg Int 7 1992 308 310
-
(1992)
Pediatr Surg Int
, vol.7
, pp. 308-310
-
-
Martucciello, G1
Bicocchi, M2
Dodero, P3
-
20
-
-
0027378022
-
Close linkage with the RET protooncogene and boundaries of deletion mutations in autosomal dominant Hirschsprung's disease
-
Y Luo I Cecchernin B Pasini Close linkage with the RET protooncogene and boundaries of deletion mutations in autosomal dominant Hirschsprung's disease Hum Mol Genet 2 1993 1803 1808
-
(1993)
Hum Mol Genet
, vol.2
, pp. 1803-1808
-
-
Luo, Y1
Cecchernin, I2
Pasini, B3
-
21
-
-
0028329089
-
Hirschsprung's disease associated with deletion of chromosome 10 (g11.2q21.2): A further link with the neurocristopathies?
-
M Fewtrell P Tam A Thomson Hirschsprung's disease associated with deletion of chromosome 10 (g11.2q21.2): A further link with the neurocristopathies? J Med Genet 31 1994 325 327
-
(1994)
J Med Genet
, vol.31
, pp. 325-327
-
-
Fewtrell, M1
Tam, P2
Thomson, A3
-
22
-
-
0018580605
-
The association of Waardenburg syndrome and Hirschsprung's megacolon
-
G Omenn V McKusick The association of Waardenburg syndrome and Hirschsprung's megacolon Am J Med Genet 3 1979 217 233
-
(1979)
Am J Med Genet
, vol.3
, pp. 217-233
-
-
Omenn, G1
McKusick, V2
-
23
-
-
0025037703
-
Waardenburg syndrome and Hirschsprung's disease: Evidence for pleiotropic effects of a single dominant gene
-
J Badner A Chakravarti Waardenburg syndrome and Hirschsprung's disease: Evidence for pleiotropic effects of a single dominant gene Am J Med Genet 35 1990 100 104
-
(1990)
Am J Med Genet
, vol.35
, pp. 100-104
-
-
Badner, J1
Chakravarti, A2
-
24
-
-
0028347048
-
Hirschsprung's disease associated with Ondine's curse: Report of three cases and review of the literature
-
E El-Halaby A Coran Hirschsprung's disease associated with Ondine's curse: Report of three cases and review of the literature J Pediatr Surg 29 1994 530 535
-
(1994)
J Pediatr Surg
, vol.29
, pp. 530-535
-
-
El-Halaby, E1
Coran, A2
-
25
-
-
0013870398
-
Association of megacolon with two recessive spotting genes in the mouse
-
P Lane Association of megacolon with two recessive spotting genes in the mouse J Hered 57 1966 29 31
-
(1966)
J Hered
, vol.57
, pp. 29-31
-
-
Lane, P1
-
26
-
-
0018733219
-
Observation of congenital aganglionosis rat (Hirschsprung's disease rat) and its genetical analyses
-
H Ikadai H Fujita Y Agematsu Observation of congenital aganglionosis rat (Hirschsprung's disease rat) and its genetical analyses Cong Anom 19 1979 31 36
-
(1979)
Cong Anom
, vol.19
, pp. 31-36
-
-
Ikadai, H1
Fujita, H2
Agematsu, Y3
-
27
-
-
0021747818
-
Association of megacolon with a new dominant spotting gene (Dom) in the mouse
-
P Lane H Liu Association of megacolon with a new dominant spotting gene (Dom) in the mouse J Hered 75 1984 435 439
-
(1984)
J Hered
, vol.75
, pp. 435-439
-
-
Lane, P1
Liu, H2
-
28
-
-
0027185569
-
A gene for Hirschsprung disease maps to the proximal long arm of chromosome 10
-
S Lyonnet A Bolino A Pelet A gene for Hirschsprung disease maps to the proximal long arm of chromosome 10 Nature Genet 4 1993 346 350
-
(1993)
Nature Genet
, vol.4
, pp. 346-350
-
-
Lyonnet, S1
Bolino, A2
Pelet, A3
-
29
-
-
0027219581
-
A gene for Hirschsprung disease (megacolon) in the mericentrometric region of human chromosome 10
-
M Angrist E Kauffman S Slaugenhaupt A gene for Hirschsprung disease (megacolon) in the mericentrometric region of human chromosome 10 Nature Genet 4 1993 351 356
-
(1993)
Nature Genet
, vol.4
, pp. 351-356
-
-
Angrist, M1
Kauffman, E2
Slaugenhaupt, S3
-
30
-
-
0024351090
-
Human ret proto-oncogene mapped to chromosome 1Og11.2
-
Y Ishizaka F Itoh T Tahira Human ret proto-oncogene mapped to chromosome 1Og11.2 Oncogene 4 1989 1519 1521
-
(1989)
Oncogene
, vol.4
, pp. 1519-1521
-
-
Ishizaka, Y1
Itoh, F2
Tahira, T3
-
31
-
-
0028120882
-
Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirschsprung's disease
-
G Romeo P Ronchetto Y Luo Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirschsprung's disease Nature 367 1994 377 378
-
(1994)
Nature
, vol.367
, pp. 377-378
-
-
Romeo, G1
Ronchetto, P2
Luo, Y3
-
32
-
-
0027972513
-
Mutations of the RET proto-oncogene in Hirschsprung's disease
-
P Edery S Lyonnet LM Mulligan Mutations of the RET proto-oncogene in Hirschsprung's disease Nature 367 1994 378 380
-
(1994)
Nature
, vol.367
, pp. 378-380
-
-
Edery, P1
Lyonnet, S2
Mulligan, LM3
-
33
-
-
0028174023
-
Defects in the kidney and enteric nervous system of mice lacking the tyrosine kinase receptor RET
-
A Schuchardt L D'Agati V Larsson-Blomberg Defects in the kidney and enteric nervous system of mice lacking the tyrosine kinase receptor RET Nature 367 1994 380 383
-
(1994)
Nature
, vol.367
, pp. 380-383
-
-
Schuchardt, A1
D'Agati V Larsson-Blomberg, L2
-
34
-
-
0028069130
-
Identity-bydescent and association mapping of a recessive gene for Hirschsprung's disease on human chromosome 13822
-
EG Puffenberger ER Kauffman S Bolk Identity-bydescent and association mapping of a recessive gene for Hirschsprung's disease on human chromosome 13822 Hum Mol Genet 3 1994 1217 1225
-
(1994)
Hum Mol Genet
, vol.3
, pp. 1217-1225
-
-
Puffenberger, EG1
Kauffman, ER2
Bolk, S3
-
35
-
-
0028639196
-
Targeted and natural (Piebald-Lethal) mutations of endothelia-B receptor gene produce megacolon associated with spotted coat color in mice
-
K Hosoda RE Hammer JA Richardson Targeted and natural (Piebald-Lethal) mutations of endothelia-B receptor gene produce megacolon associated with spotted coat color in mice Cell 79 1994 1267 1276
-
(1994)
Cell
, vol.79
, pp. 1267-1276
-
-
Hosoda, K1
Hammer, RE2
Richardson, JA3
-
36
-
-
0027499701
-
The human endothelia-B receptor gene: Structural organization and chromosomal assignment
-
H Arai K Nakao K Takaya The human endothelia-B receptor gene: Structural organization and chromosomal assignment J Biol Chem 268 1993 3463 3470
-
(1993)
J Biol Chem
, vol.268
, pp. 3463-3470
-
-
Arai, H1
Nakao, K2
Takaya, K3
-
37
-
-
0028618372
-
A missense mutation of the endothelia-B receptor gene in multigenic Hirschsprung's disease
-
EG Puffenberger K Hosoda SS Washington A missense mutation of the endothelia-B receptor gene in multigenic Hirschsprung's disease Cell 79 1994 1257 1266
-
(1994)
Cell
, vol.79
, pp. 1257-1266
-
-
Puffenberger, EG1
Hosoda, K2
Washington, SS3
-
38
-
-
15844365303
-
GDNF-induced activation of the RET protein tyrosine kinase is mediated by GDNFR-a, a novel receptor for GDNF
-
S Jing D Wen Y Yu GDNF-induced activation of the RET protein tyrosine kinase is mediated by GDNFR-a, a novel receptor for GDNF Cell 85 1996 1113 1124
-
(1996)
Cell
, vol.85
, pp. 1113-1124
-
-
Jing, S1
Wen, D2
Yu, Y3
-
39
-
-
15844406351
-
Functional receptor for GDNI encoded by the c-ret proto-oncogene
-
M Trupp E Arenas M Fainzilber Functional receptor for GDNI encoded by the c-ret proto-oncogene Nature 381 1996 785 789
-
(1996)
Nature
, vol.381
, pp. 785-789
-
-
Trupp, M1
Arenas, E2
Fainzilber, M3
-
40
-
-
15844422453
-
GDNF signalling through the RET receptor tyrosine kinase
-
P Durbec C Marcos-Gutierrez C Kilkenny GDNF signalling through the RET receptor tyrosine kinase Nature 381 1996 789793
-
(1996)
Nature
, vol.381
, pp. 789793
-
-
Durbec, P1
Marcos-Gutierrez, C2
Kilkenny, C3
-
41
-
-
15844418441
-
Characterization of a multicomponent receptor for GDNF
-
J Treanor L Goodman F de Sauvage Characterization of a multicomponent receptor for GDNF Nature 382 1996 80 83
-
(1996)
Nature
, vol.382
, pp. 80-83
-
-
Treanor, J1
Goodman, L2
de Sauvage, F3
-
42
-
-
0013543367
-
The human endothelin family: Three structurally and pharmacologically distinct isopeptides predicted by three separate genes
-
A Inoue M Yanagisawa S Kimura The human endothelin family: Three structurally and pharmacologically distinct isopeptides predicted by three separate genes Proc Natl Acad Sci USA 86 1989 2863 2867
-
(1989)
Proc Natl Acad Sci USA
, vol.86
, pp. 2863-2867
-
-
Inoue, A1
Yanagisawa, M2
Kimura, S3
-
43
-
-
0030292383
-
Germline mutations in glial cell line-derived neurotrophic factor (GDNF) and RET in a Hirschsprung disease patient
-
M Angrist S Bolk M Halushka Germline mutations in glial cell line-derived neurotrophic factor (GDNF) and RET in a Hirschsprung disease patient Nature Genet 14 1996 341 344
-
(1996)
Nature Genet
, vol.14
, pp. 341-344
-
-
Angrist, M1
Bolk, S2
Halushka, M3
-
44
-
-
16144368214
-
Germline mutations of the RET ligand GDNF are not sufficient to cause Hirschsprung's disease
-
R Salomon T Attie A Pelet Germline mutations of the RET ligand GDNF are not sufficient to cause Hirschsprung's disease Nature Genet 14 1996 345 347
-
(1996)
Nature Genet
, vol.14
, pp. 345-347
-
-
Salomon, R1
Attie, T2
Pelet, A3
-
45
-
-
0029822720
-
De novo mutation of GDNF, ligand or the RET/GDNFR-a receptor complex, in Hirschsprung disease
-
S Ivanchuk S Myers C Eng De novo mutation of GDNF, ligand or the RET/GDNFR-a receptor complex, in Hirschsprung disease Hum Mol Genet 5 1996 2023 2026
-
(1996)
Hum Mol Genet
, vol.5
, pp. 2023-2026
-
-
Ivanchuk, S1
Myers, S2
Eng, C3
-
46
-
-
0009675716
-
A homozygous mutation in the endothelia-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome)
-
J Hofstra RMW Osinga G Tan-Sindhunata A homozygous mutation in the endothelia-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome) Nature Genet 12 1996 445 447
-
(1996)
Nature Genet
, vol.12
, pp. 445-447
-
-
Hofstra RMW Osinga, J1
Tan-Sindhunata, G2
-
47
-
-
0006457459
-
Mutation of the endothelia-3 gene in the Waardenburg-Hirschsprung disease (Shah-Waardenburg syndrome)
-
P Edery T Attie J Amiel Mutation of the endothelia-3 gene in the Waardenburg-Hirschsprung disease (Shah-Waardenburg syndrome) Nature Genet 12 1996 442 444
-
(1996)
Nature Genet
, vol.12
, pp. 442-444
-
-
Edery, P1
Attie, T2
Amiel, J3
-
48
-
-
0022330363
-
Activation of a novel human transforming gene, ret, by DNA rearrangement
-
M Takahashi J Ritz G Cooper Activation of a novel human transforming gene, ret, by DNA rearrangement Cell 42 1985 581 588
-
(1985)
Cell
, vol.42
, pp. 581-588
-
-
Takahashi, M1
Ritz, J2
Cooper, G3
-
49
-
-
0024208663
-
Cloning and expression of the RET proto-oncogene encoding a tyrosine kinase with two potential transmembrane domains
-
M Takahashi Y Buma T Iwamoto Cloning and expression of the RET proto-oncogene encoding a tyrosine kinase with two potential transmembrane domains Oncogene 3 1988 571 578
-
(1988)
Oncogene
, vol.3
, pp. 571-578
-
-
Takahashi, M1
Buma, Y2
Iwamoto, T3
-
50
-
-
0024323273
-
Isolation of ret proto-oncogene cDNA with an amino-terminal signal sequence
-
M Takahashi Y Buma H Hiai Isolation of ret proto-oncogene cDNA with an amino-terminal signal sequence Oncogene 4 1989 805 806
-
(1989)
Oncogene
, vol.4
, pp. 805-806
-
-
Takahashi, M1
Buma, Y2
Hiai, H3
-
51
-
-
0025164766
-
Characterization of ret proto-oncogene mRNAs encoding two isoforms of the protein product in a human neuroblastoma cell line
-
T Tahira Y Ishizaka F Itoh Characterization of ret proto-oncogene mRNAs encoding two isoforms of the protein product in a human neuroblastoma cell line Oncogene 5 1990 97 102
-
(1990)
Oncogene
, vol.5
, pp. 97-102
-
-
Tahira, T1
Ishizaka, Y2
Itoh, F3
-
52
-
-
0027371670
-
Exon structure and flanking intronic sequences of the human RET proto-oncogene
-
I Ceccherini R Bocciardi Y Luo Exon structure and flanking intronic sequences of the human RET proto-oncogene Biochem Biophys Res Commun 196 1993 1288 1295
-
(1993)
Biochem Biophys Res Commun
, vol.196
, pp. 1288-1295
-
-
Ceccherini, I1
Bocciardi, R2
Luo, Y3
-
53
-
-
12044258692
-
Structural analysis of the human RET proto-oncogene using exon trapping
-
J Kwok E Gardner J Warner Structural analysis of the human RET proto-oncogene using exon trapping Oncogene 8 1993 2575 2582
-
(1993)
Oncogene
, vol.8
, pp. 2575-2582
-
-
Kwok, J1
Gardner, E2
Warner, J3
-
54
-
-
0026475085
-
The human protooncogene ret: A communicative cadherin?
-
R Schneider The human protooncogene ret: A communicative cadherin? TIBS 17 1992 468 469
-
(1992)
TIBS
, vol.17
, pp. 468-469
-
-
Schneider, R1
-
55
-
-
0027285510
-
GDNF: A glial cell line-derived neurotrophic factor for midbrain dopaminergic neurons
-
L Lin D Doherty J Lile GDNF: A glial cell line-derived neurotrophic factor for midbrain dopaminergic neurons Science 260 1993 1130 1132
-
(1993)
Science
, vol.260
, pp. 1130-1132
-
-
Lin, L1
Doherty, D2
Lile, J3
-
56
-
-
0028109717
-
GDNF: A potent survival factor for motoneurons present in peripheral nerve and muscle
-
C Henderson H Phillips R Pollock GDNF: A potent survival factor for motoneurons present in peripheral nerve and muscle Science 266 1994 1062 1064
-
(1994)
Science
, vol.266
, pp. 1062-1064
-
-
Henderson, C1
Phillips, H2
Pollock, R3
-
57
-
-
0028854836
-
In vivo neurotrophic effects of GDNF on neonatal and adult facial motor neurons
-
Q Yan C Matheson O Lopez In vivo neurotrophic effects of GDNF on neonatal and adult facial motor neurons Nature 373 1995 341 344
-
(1995)
Nature
, vol.373
, pp. 341-344
-
-
Yan, Q1
Matheson, C2
Lopez, O3
-
58
-
-
0028874195
-
Developing motor neurons rescued from programmed and axotomy-induced cell death by GDNF
-
R Oppenheim L Houenou J Johnson Developing motor neurons rescued from programmed and axotomy-induced cell death by GDNF Nature 373 1995 344 346
-
(1995)
Nature
, vol.373
, pp. 344-346
-
-
Oppenheim, R1
Houenou, L2
Johnson, J3
-
59
-
-
0028979805
-
The gene coding for glial cell line derived neurotrophic factor (GDNF) maps to chromosome 5p12-p13.1
-
D Schindelhauer S Schuffenhauer T Gasser The gene coding for glial cell line derived neurotrophic factor (GDNF) maps to chromosome 5p12-p13.1 Genomics 28 1995 605 607
-
(1995)
Genomics
, vol.28
, pp. 605-607
-
-
Schindelhauer, D1
Schuffenhauer, S2
Gasser, T3
-
60
-
-
0029901727
-
Renal agenesis and the absence of enteric neurons in mice lacking GDNF
-
M Sanches I Silos-Santiago J Firsen Renal agenesis and the absence of enteric neurons in mice lacking GDNF Nature 382 1996 70 73
-
(1996)
Nature
, vol.382
, pp. 70-73
-
-
Sanches, M1
Silos-Santiago, I2
Firsen, J3
-
61
-
-
15844426332
-
Defects in enteric innervation and kidney development in mice lacking GDNF
-
J Pichel L Shen H Sheng Defects in enteric innervation and kidney development in mice lacking GDNF Nature 382 1996 73 76
-
(1996)
Nature
, vol.382
, pp. 73-76
-
-
Pichel, J1
Shen, L2
Sheng, H3
-
62
-
-
15844384629
-
Renal and neuronal abnormalities in mice lacking GDNF
-
M Moore R Klein I Farinas Renal and neuronal abnormalities in mice lacking GDNF Nature 382 1996 76 79
-
(1996)
Nature
, vol.382
, pp. 76-79
-
-
Moore, M1
Klein, R2
Farinas, I3
-
63
-
-
0027374562
-
Expression of the c-ret proto-oncogene during mouse embryogenesis
-
B Pachnis V Mankoo F Costantini Expression of the c-ret proto-oncogene during mouse embryogenesis Development 119 1993 1005 1007
-
(1993)
Development
, vol.119
, pp. 1005-1007
-
-
Pachnis V Mankoo, B1
Costantini, F2
-
64
-
-
0027930997
-
Developmental expression of the RET protooncogene
-
N Avantaggiato V Dathan M Grieco Developmental expression of the RET protooncogene Cell Growth Diff 5 1994 305 311
-
(1994)
Cell Growth Diff
, vol.5
, pp. 305-311
-
-
Avantaggiato V Dathan, N1
Grieco, M2
-
65
-
-
0028896367
-
Spatial and temporal expression of the ret proto-oncogene product in embryonic, infant and adult rat tissues
-
T Tsuzuki M Takahashi N Asai Spatial and temporal expression of the ret proto-oncogene product in embryonic, infant and adult rat tissues Oncogene 10 1995 191 198
-
(1995)
Oncogene
, vol.10
, pp. 191-198
-
-
Tsuzuki, T1
Takahashi, M2
Asai, N3
-
66
-
-
0030024846
-
Embryonic expression of glial cell-derived neurotrophic factor (GDNF) suggests multiple developmental roles in neural differentiation and epithelial-mesenchymal interactions
-
H Hellmich L Kos ES Cho Embryonic expression of glial cell-derived neurotrophic factor (GDNF) suggests multiple developmental roles in neural differentiation and epithelial-mesenchymal interactions Mech Dev 54 1996 95 105
-
(1996)
Mech Dev
, vol.54
, pp. 95-105
-
-
Hellmich, H1
Kos, L2
Cho, ES3
-
67
-
-
0029119781
-
Diversity of RET proto-oncogene mutations in familial and sporadic Hirschsprung's disease
-
A Attie T Pelet P Edery Diversity of RET proto-oncogene mutations in familial and sporadic Hirschsprung's disease Hum Mol Genet 4 1995 1381 1386
-
(1995)
Hum Mol Genet
, vol.4
, pp. 1381-1386
-
-
Attie T Pelet, A1
Edery, P2
-
68
-
-
0029069528
-
Mutation analysis of the RET receptor tyrosine kinase in Hirschsprung's disease
-
M Angrist S Bolk B Thiel Mutation analysis of the RET receptor tyrosine kinase in Hirschsprung's disease Hum Mol Genet 4 1995 821 830
-
(1995)
Hum Mol Genet
, vol.4
, pp. 821-830
-
-
Angrist, M1
Bolk, S2
Thiel, B3
-
69
-
-
0030962660
-
Mutation analysis of the RET, the endothelin-B receptor, and the endothelin-3 genes in sporadic patients with Hirschsprung's disease
-
T Kusafuka Y Wang P Puri Mutation analysis of the RET, the endothelin-B receptor, and the endothelin-3 genes in sporadic patients with Hirschsprung's disease J Pediatr Surg 32 1997 501 504
-
(1997)
J Pediatr Surg
, vol.32
, pp. 501-504
-
-
Kusafuka, T1
Wang, Y2
Puri, P3
-
70
-
-
16944365710
-
Frequency of RET mutations in long- and short-segment Hirschsprung disease
-
M Seri L Yin V Barone Frequency of RET mutations in long- and short-segment Hirschsprung disease Hum Mutat 9 1997 243 249
-
(1997)
Hum Mutat
, vol.9
, pp. 243-249
-
-
Seri, M1
Yin, L2
Barone, V3
-
71
-
-
0029924529
-
Exclusion of linkage between RET and neuronal intestinal dysplasia type B
-
D Barone V Weber Y Luo Exclusion of linkage between RET and neuronal intestinal dysplasia type B Am J Med Genet 62 1996 195 198
-
(1996)
Am J Med Genet
, vol.62
, pp. 195-198
-
-
Barone V Weber, D1
Luo, Y2
-
72
-
-
0030014485
-
Congenital central hypoventilation syndrome: Mutation analysis of the receptor tyrosine kinase RET
-
S Bolk M Angrist S Schwartz Congenital central hypoventilation syndrome: Mutation analysis of the receptor tyrosine kinase RET Am J Med Genet 63 1996 603 609
-
(1996)
Am J Med Genet
, vol.63
, pp. 603-609
-
-
Bolk, S1
Angrist, M2
Schwartz, S3
-
73
-
-
0024465081
-
Molecular biology and biochemistry of the endothelins
-
M Yanagisawa T Masaki Molecular biology and biochemistry of the endothelins TIBS 10 1989 374 378
-
(1989)
TIBS
, vol.10
, pp. 374-378
-
-
Yanagisawa, M1
Masaki, T2
-
74
-
-
0028609612
-
Interaction of endothelin-3 with endothelin-B receptor is essential for development of epidermal melanocytes and enteric neurons
-
AG Baynash K Hosoda A Giaid Interaction of endothelin-3 with endothelin-B receptor is essential for development of epidermal melanocytes and enteric neurons Cell 79 1994 1277 1285
-
(1994)
Cell
, vol.79
, pp. 1277-1285
-
-
Baynash, AG1
Hosoda, K2
Giaid, A3
-
75
-
-
0028844260
-
Interstitial deletion of the endothelin-B receptor in the spotting lethal (sl) rat
-
I Ceccherini AL Zhang I Matera Interstitial deletion of the endothelin-B receptor in the spotting lethal (sl) rat Hum Mol Genet 4 1995 2089 2096
-
(1995)
Hum Mol Genet
, vol.4
, pp. 2089-2096
-
-
Ceccherini, I1
Zhang, AL2
Matera, I3
-
76
-
-
0030033185
-
Null mutation of endothelin receptor type B in spotting lethal rats causes aganglionic megacolon and white coat color
-
CE Gariepy M Cass DT Yanagisawa Null mutation of endothelin receptor type B in spotting lethal rats causes aganglionic megacolon and white coat color Proc Natl Acad Sci USA 93 1996 867 872
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 867-872
-
-
Gariepy, CE1
Cass DT Yanagisawa, M2
-
77
-
-
0028862473
-
Mutation of the endothelin-receptor B gene in Waardenburg-Hirschsprung disease
-
T Attie M Till A Pelet Mutation of the endothelin-receptor B gene in Waardenburg-Hirschsprung disease Hum Mol Genet 4 1995 2407 2409
-
(1995)
Hum Mol Genet
, vol.4
, pp. 2407-2409
-
-
Attie, T1
Till, M2
Pelet, A3
-
78
-
-
85119793739
-
Novel mutations of the endothelinreceptor B gene in Hirschsprung disease
-
T Kusafuka Y Wang P Puri Novel mutations of the endothelinreceptor B gene in Hirschsprung disease Hum Mol Genet 4 1995 2407 2409
-
(1995)
Hum Mol Genet
, vol.4
, pp. 2407-2409
-
-
Kusafuka, T1
Wang, Y2
Puri, P3
-
79
-
-
0030070810
-
Endothelin-B receptor mutations in patients with isolated Hirschsprung disease from a non-inbred population
-
A Auricchio G Casari A Staiano Endothelin-B receptor mutations in patients with isolated Hirschsprung disease from a non-inbred population Hum Mol Genet 5 1996 351 354
-
(1996)
Hum Mol Genet
, vol.5
, pp. 351-354
-
-
Auricchio, A1
Casari, G2
Staiano, A3
-
80
-
-
9044220230
-
Heterozygous endothelin receptor B (EDNRB) mutations in isolated Hirschsprung disease
-
J Amiel D Attie T Jan Heterozygous endothelin receptor B (EDNRB) mutations in isolated Hirschsprung disease Hum Mol Genet 5 1996 355 357
-
(1996)
Hum Mol Genet
, vol.5
, pp. 355-357
-
-
Amiel, J1
Attie T Jan, D2
-
81
-
-
85119795348
-
-
InoueMHosodaKImuraKet al: Mutational analysis of the endothelin-B receptor gene in Japanese Hirschsprung disease. J Pediatr Surg (in press)
-
-
-
-
82
-
-
8044257726
-
Mutations of the endothelin-B receptor and endothelin-3 genes in Hirschsprung's disease
-
P Kusafuka T Puri Mutations of the endothelin-B receptor and endothelin-3 genes in Hirschsprung's disease Pediatr Surg Int 12 1997 19 23
-
(1997)
Pediatr Surg Int
, vol.12
, pp. 19-23
-
-
Kusafuka T Puri, P1
-
83
-
-
8044261417
-
The RET proto-oncogene: A challenge to our understanding of disease pathogenesis
-
T Kusafuka P Puri The RET proto-oncogene: A challenge to our understanding of disease pathogenesis Pediatr Surg Int 12 1997 11 18
-
(1997)
Pediatr Surg Int
, vol.12
, pp. 11-18
-
-
Kusafuka, T1
Puri, P2
-
84
-
-
0027992642
-
ECE-1: A membrane-bound metalloproteinase that catalyzes the proteolytic activation of big endothelin-1
-
D Xu N Emoto A Giaid ECE-1: A membrane-bound metalloproteinase that catalyzes the proteolytic activation of big endothelin-1 Cell 78 1994 473 485
-
(1994)
Cell
, vol.78
, pp. 473-485
-
-
Xu, D1
Emoto, N2
Giaid, A3
-
85
-
-
85119786396
-
Endothelins in development of neural crest derived tissues
-
M Yanagisawa Endothelins in development of neural crest derived tissues Presented at the 2nd International Meeting: Hirschsprung's and Related Neurocristopathies October 1995 Cleveland, OH
-
(1995)
-
-
Yanagisawa, M1
-
86
-
-
0031017089
-
Human homology and candidate genes for the dominant megacolon locus, a mouse model of Hirschsprung disease
-
A Pingault V Puliti M Prehu Human homology and candidate genes for the dominant megacolon locus, a mouse model of Hirschsprung disease Genomics 39 1997 86 89
-
(1997)
Genomics
, vol.39
, pp. 86-89
-
-
Pingault V Puliti, A1
Prehu, M2
-
87
-
-
0028301090
-
The oncogenic versions of the Ret and Trk tyrosine kinases bind Shc and Grb2 adaptor proteins
-
M Borrello G Pelicci E Arighi The oncogenic versions of the Ret and Trk tyrosine kinases bind Shc and Grb2 adaptor proteins Oncogene 9 1994 1661 1668
-
(1994)
Oncogene
, vol.9
, pp. 1661-1668
-
-
Borrello, M1
Pelicci, G2
Arighi, E3
-
88
-
-
0028982261
-
The RET receptor protein tyrosine kinase associates with the SH2-containing adaptor protein Grb10
-
A Pandey H Duan P Fiore The RET receptor protein tyrosine kinase associates with the SH2-containing adaptor protein Grb10 J Biol Chem 270 1995 21461 21463
-
(1995)
J Biol Chem
, vol.270
, pp. 21461-21463
-
-
Pandey, A1
Duan, H2
Fiore, P3
-
89
-
-
0029050368
-
Loss of function effect of RET mutations causing Hirschsprung's disease
-
B Pasini MG Borrello A Greco Loss of function effect of RET mutations causing Hirschsprung's disease Nature Genet 10 1995 35 40
-
(1995)
Nature Genet
, vol.10
, pp. 35-40
-
-
Pasini, B1
Borrello, MG2
Greco, A3
-
90
-
-
15844405218
-
Molecular heterogeneity of RET loss of function in Hirschsprung's disease
-
F Carlomagno G Vita M Berlingieri Molecular heterogeneity of RET loss of function in Hirschsprung's disease EMBO J 15 1996 2717 2725
-
(1996)
EMBO J
, vol.15
, pp. 2717-2725
-
-
Carlomagno, F1
Vita, G2
Berlingieri, M3
-
91
-
-
0029798406
-
Mechanism of RET dysfunction by Hirschsprung mutations affecting its extracellular domain
-
T Iwashita H Murakami N Asai Mechanism of RET dysfunction by Hirschsprung mutations affecting its extracellular domain Hum Mol Genet 5 1996 1577 1580
-
(1996)
Hum Mol Genet
, vol.5
, pp. 1577-1580
-
-
Iwashita, T1
Murakami, H2
Asai, N3
-
92
-
-
4644256817
-
The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2
-
C Eng D Clayton I Schuffenecker The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2 JAMA 276 1996 1575 1579
-
(1996)
JAMA
, vol.276
, pp. 1575-1579
-
-
Eng, C1
Clayton, D2
Schuffenecker, I3
-
93
-
-
0020314519
-
Hirschsprung's disease in a family with multiple endocrine neoplasia type 2
-
M Verdy A Weber C Roy Hirschsprung's disease in a family with multiple endocrine neoplasia type 2 J Pediatr Gastroenterol Nutr 1 1982 603 607
-
(1982)
J Pediatr Gastroenterol Nutr
, vol.1
, pp. 603-607
-
-
Verdy, M1
Weber, A2
Roy, C3
-
94
-
-
0028566385
-
Diverse phenotypes associated with axon 10 mutations of the RET proto-oncogene
-
L Mulligan C Eng T Attie Diverse phenotypes associated with axon 10 mutations of the RET proto-oncogene Hum Mol Genet 3 1994 2163 2167
-
(1994)
Hum Mol Genet
, vol.3
, pp. 2163-2167
-
-
Mulligan, L1
Eng, C2
Attie, T3
-
95
-
-
0028916234
-
Mutation analysis of multiple endocrine neoplasia type 2A associated with Hirschsprung's disease
-
M Borst J Van Camp M Peacock Mutation analysis of multiple endocrine neoplasia type 2A associated with Hirschsprung's disease Surgery 117 1995 386 391
-
(1995)
Surgery
, vol.117
, pp. 386-391
-
-
Borst, M1
Van Camp, J2
Peacock, M3
-
96
-
-
0029823617
-
Clinical presentations and RET protooncogene mutations in seven multiple endocrine neoplasia type 2 kindreds
-
R Blank C Sklar A Dimich Clinical presentations and RET protooncogene mutations in seven multiple endocrine neoplasia type 2 kindreds Cancer 78 1996 1996 2003
-
(1996)
Cancer
, vol.78
, pp. 1996-2003
-
-
Blank, R1
Sklar, C2
Dimich, A3
-
97
-
-
0030739287
-
Biological properties of RET with cysteine mutations correlate with multiple endocrine neoplasia type 2A, familial medullary thyroid carcinoma, and Hirschsprung's disease phenotype
-
S Ito T Iwashita N Asai Biological properties of RET with cysteine mutations correlate with multiple endocrine neoplasia type 2A, familial medullary thyroid carcinoma, and Hirschsprung's disease phenotype Cancer Res 57 1997 2870 2872
-
(1997)
Cancer Res
, vol.57
, pp. 2870-2872
-
-
Ito, S1
Iwashita, T2
Asai, N3
|