-
1
-
-
0031981819
-
Mutations of the RET-GDNF signalling pathway in Ondine's curse
-
Amiel J, Salomon R, Attié T, Pelet A, Mokhtari M, Trang H, Gaultier C, Munnich A, Lyonnet S (1998): Mutations of the RET-GDNF signalling pathway in Ondine's curse. Am J Hum Genet 62:715-717.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 715-717
-
-
Amiel, J.1
Salomon, R.2
Attié, T.3
Pelet, A.4
Mokhtari, M.5
Trang, H.6
Gaultier, C.7
Munnich, A.8
Lyonnet, S.9
-
2
-
-
0030983548
-
TrnR2, a novel receptor that mediates Neurturin and GDNF signalling through Ret
-
Baloh R, Tansey M, Golden J, Creedon D, Heuckeroth R, Keck C, Zimonjic D, Popescu N, Johnson Jr E, Milbrandt J (1997): TrnR2, a novel receptor that mediates Neurturin and GDNF signalling through Ret. Neuron 18:793-802.
-
(1997)
Neuron
, vol.18
, pp. 793-802
-
-
Baloh, R.1
Tansey, M.2
Golden, J.3
Creedon, D.4
Heuckeroth, R.5
Keck, C.6
Zimonjic, D.7
Popescu, N.8
Johnson, E.9
Milbrandt, J.10
-
3
-
-
0030014485
-
Congenital central hypoventilation syndrome: Mutation analysis of the receptor tyrosine kinase RET
-
Bolk S, Angrist M, Schwartz S, Silvestri J, Weese-Mayer D, Chakravarti A (1996a): Congenital central hypoventilation syndrome: Mutation analysis of the receptor tyrosine kinase RET. Am J Hum Genet 63:603609.
-
(1996)
Am J Hum Genet
, vol.63
, pp. 603609
-
-
Bolk, S.1
Angrist, M.2
Schwartz, S.3
Silvestri, J.4
Weese-Mayer, D.5
Chakravarti, A.6
-
4
-
-
0030017530
-
Endothelin-3 framehift mutation in congenital central hypoventilation syndrome
-
Bolk S, Angrist M, Xie J, Yanagisawa M, Silvestri J, Weese-Mayer D, Chakravarti A (1996b): Endothelin-3 framehift mutation in congenital central hypoventilation syndrome. Nat Genet 13:395-396.
-
(1996)
Nat Genet
, vol.13
, pp. 395-396
-
-
Bolk, S.1
Angrist, M.2
Xie, J.3
Yanagisawa, M.4
Silvestri, J.5
Weese-Mayer, D.6
Chakravarti, A.7
-
5
-
-
0028135127
-
A newborn with ring chromosome 10, aganglionic megacolon, and renal hypoplasia
-
Calebrese C, Franchi PG, Stuppia L, Mingarelli R, Rossi C, Ramenghi L, Marino M, Morizio M, Peila E, Antonucci A, Palka G (1994): A newborn with ring chromosome 10, aganglionic megacolon, and renal hypoplasia. J Med Genet 31:804-806.
-
(1994)
J Med Genet
, vol.31
, pp. 804-806
-
-
Calebrese, C.1
Franchi, P.G.2
Stuppia, L.3
Mingarelli, R.4
Rossi, C.5
Ramenghi, L.6
Marino, M.7
Morizio, M.8
Peila, E.9
Antonucci, A.10
Palka, G.11
-
6
-
-
0027977002
-
A single missense mutation in the tyrosine kinase catalytic domain of the RET proto-oncogene is associated with multiple endocrine neoplasia type 2B
-
Carlson K, Dou S, Chi D, Scavarda N, Toshima K, Jackson C, Wells S, Goodfellow P, Donis Keller H (1994): A single missense mutation in the tyrosine kinase catalytic domain of the RET proto-oncogene is associated with multiple endocrine neoplasia type 2B. Proc Natl Acad Sei (USA) 91:1579-1583.
-
(1994)
Proc Natl Acad Sei (USA)
, vol.91
, pp. 1579-1583
-
-
Carlson, K.1
Dou, S.2
Chi, D.3
Scavarda, N.4
Toshima, K.5
Jackson, C.6
Wells, S.7
Goodfellow, P.8
Donis Keller, H.9
-
7
-
-
0027303248
-
Mutations in the RET protooncogene are associated with MEN 2A and FMTC
-
Donis-Keller H, Dou S, Chi D, Carlson K, Toshima K, Lairmore T, Howe J, Moley J, Goodfellow P, Wells A (1993): Mutations in the RET protooncogene are associated with MEN 2A and FMTC. Hum Molec Genet 7:851-856.
-
(1993)
Hum Molec Genet
, vol.7
, pp. 851-856
-
-
Donis-Keller, H.1
Dou, S.2
Chi, D.3
Carlson, K.4
Toshima, K.5
Lairmore, T.6
Howe, J.7
Moley, J.8
Goodfellow, P.9
Wells, A.10
-
8
-
-
15844422453
-
GDNF signalling through the Ret receptor tyrosine kinase
-
Durbec P, Marcos-Gutierrez C, Kilkenny C, Grigoriou M, Wartiowaara K, Suvanto P, Smith P, Ponder B, Costantini F, Saarma M, Sariola H, Pachnis V (1996): GDNF signalling through the Ret receptor tyrosine kinase. Nature 381:789-793.
-
(1996)
Nature
, vol.381
, pp. 789-793
-
-
Durbec, P.1
Marcos-Gutierrez, C.2
Kilkenny, C.3
Grigoriou, M.4
Wartiowaara, K.5
Suvanto, P.6
Smith, P.7
Ponder, B.8
Costantini, F.9
Saarma, M.10
Sariola, H.11
Pachnis, V.12
-
9
-
-
0027972513
-
Mutations of the RET protooncogene in Hirschsprung"s disease
-
Edery P, Lyonnet S, Mulligan L, Pelet A, Dow E, Abel L, Holder S, NihoulFekete C, Ponder B, Munnich A (1994): Mutations of the RET protooncogene in Hirschsprung"s disease. Nature 367:378-380.
-
(1994)
Nature
, vol.367
, pp. 378-380
-
-
Edery, P.1
Lyonnet, S.2
Mulligan, L.3
Pelet, A.4
Dow, E.5
Abel, L.6
Holder, S.7
Nihoulfekete, C.8
Ponder, B.9
Munnich, A.10
-
10
-
-
0028006092
-
Point mutation within the tyrosine kinase domain of the RET proto-oncogene in multiple endocrine neoplasia type 2B and related sporadic tumors
-
Eng C, Smith D, Mulligan L, Nagai M, Healey C, Ponder M, Gardner E, Sheumann G, Jackson C, Tunnacliffe A, Ponder B (1994): Point mutation within the tyrosine kinase domain of the RET proto-oncogene in multiple endocrine neoplasia type 2B and related sporadic tumors. Hum Molec Genet 3:237-241.
-
(1994)
Hum Molec Genet
, vol.3
, pp. 237-241
-
-
Eng, C.1
Smith, D.2
Mulligan, L.3
Nagai, M.4
Healey, C.5
Ponder, M.6
Gardner, E.7
Sheumann, G.8
Jackson, C.9
Tunnacliffe, A.10
Ponder, B.11
-
11
-
-
0030024846
-
Embryonic expression of glial cell-line derived neurtrophic factor (GDNF) suggests multiple developmental roles in neural differentiation and epithelialmesenchymal interactions
-
Hellmich HL, Kos L, Cho ES, Mahon KA, Zimmer A (1996): Embryonic expression of glial cell-line derived neurtrophic factor (GDNF) suggests multiple developmental roles in neural differentiation and epithelialmesenchymal interactions. Mech Dev 54:95-105.
-
(1996)
Mech Dev
, vol.54
, pp. 95-105
-
-
Hellmich, H.L.1
Kos, L.2
Cho, E.S.3
Mahon, K.A.4
Zimmer, A.5
-
12
-
-
0028174024
-
A mutation in the RET proto-oncogene associated with endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma
-
Hofstra R, Landsvater R, Ceccherini I, Stülp R, Stelwagen T, Luo Y, Pasini B, Höppener J, Ploos van Amstel H, Romeo G, Lips C, Buys C (1994): A mutation in the RET proto-oncogene associated with endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma. Nature 367:375-376.
-
(1994)
Nature
, vol.367
, pp. 375-376
-
-
Hofstra, R.1
Landsvater, R.2
Ceccherini, I.3
Stülp, R.4
Stelwagen, T.5
Luo, Y.6
Pasini, B.7
Höppener, J.8
Van Ploos Amstel, H.9
Romeo, G.10
Lips, C.11
Buys, C.12
-
13
-
-
16944365682
-
A GPI-linked protein that interacts with Ret to form a candidate neurturin receptor
-
Klein R, Sherman D, Ho W, Stone D, Bennett G, Moffat B, Vandlen R, Simmons L, Gu Q, Hongo J, Devaux B, Poulsen K, Armanini M, Nozaki C, Asai N, Goddard A, Phillips H, Henderson C, Takahashi M, Rosen-thal A (1997): A GPI-linked protein that interacts with Ret to form a candidate neurturin receptor. Nature 387:717-721.
-
(1997)
Nature
, vol.387
, pp. 717-721
-
-
Klein, R.1
Sherman, D.2
Ho, W.3
Stone, D.4
Bennett, G.5
Moffat, B.6
Vandlen, R.7
Simmons, L.8
Gu, Q.9
Hongo, J.10
Devaux, B.11
Poulsen, K.12
Armanini, M.13
Nozaki, C.14
Asai, N.15
Goddard, A.16
Phillips, H.17
Henderson, C.18
Takahashi, M.19
Rosen-thal, A.20
more..
-
14
-
-
0029827559
-
Neurturin, a relative of glial-cell-line-derived neurotrophic factor
-
Kotzbauer P, Lampe P, Heuckeroth R, Golden J, Creedon D, Johnson Jr E, Milbrandt J (1996): Neurturin, a relative of glial-cell-line-derived neurotrophic factor. Nature 384:467-470.
-
(1996)
Nature
, vol.384
, pp. 467-470
-
-
Kotzbauer, P.1
Lampe, P.2
Heuckeroth, R.3
Golden, J.4
Creedon, D.5
Johnson, E.6
Milbrandt, J.7
-
15
-
-
15844384629
-
Renal and neuronal abnormalities in mice lacking GDNF
-
Moore M, Klain R, Farinas I, Sauer H, Armanini M, Phillips H, Reichart L, Ryan A, 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.1
Klain, R.2
Farinas, I.3
Sauer, H.4
Armanini, M.5
Phillips, H.6
Reichart, L.7
Ryan, A.8
Carver-Moore, K.9
Rosenthal, A.10
-
16
-
-
0027231568
-
Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A
-
Mulligan L, Kwok J, Healey C, Eisdon M, Eng C, Gardner E, Love D, Mole S, Moore J, Papi L, Ponder M, Telenius H, Tunnacliffe A, Ponder B (1993): Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A. Nature 363:458-460.
-
(1993)
Nature
, vol.363
, pp. 458-460
-
-
Mulligan, L.1
Kwok, J.2
Healey, C.3
Eisdon, M.4
Eng, C.5
Gardner, E.6
Love, D.7
Mole, S.8
Moore, J.9
Papi, L.10
Ponder, M.11
Telenius, H.12
Tunnacliffe, A.13
Ponder, B.14
-
17
-
-
0028199074
-
Specific mutations of the RET proto-oncogene are related to disease phenotype in MEN 2A and FMTC
-
Mulligan L, Eng C, Healey C, Clayton D, Kwok J, Gardner E, Ponder M, Frilling A, Jackson C, Lehnert H, Neumann H, Thibodeau S, Ponder BAJ (1994): Specific mutations of the RET proto-oncogene are related to disease phenotype in MEN 2A and FMTC. Nat Genet 6:70-74.
-
(1994)
Nat Genet
, vol.6
, pp. 70-74
-
-
Mulligan, L.1
Eng, C.2
Healey, C.3
Clayton, D.4
Kwok, J.5
Gardner, E.6
Ponder, M.7
Frilling, A.8
Jackson, C.9
Lehnert, H.10
Neumann, H.11
Thibodeau, S.12
Ponder, B.A.J.13
-
18
-
-
0028850090
-
-
Nakahara S, Yokomori K, Tamura K, Oku K, Tsuchida Y (1995): Hirschsprung's disease associated with Ondine's curse: A special subgroup? J Pediatr Surg 30:1481-1484.
-
(1995)
Hirschsprung's Disease Associated with Ondine's Curse: a Special Subgroup? J Pediatr Surg
, vol.30
, pp. 1481-1484
-
-
Nakahara, S.1
Yokomori, K.2
Tamura, K.3
Oku, K.4
Tsuchida, Y.5
-
19
-
-
0027374562
-
Expression of the c-ret protooncogene during mouse embryogenesis
-
Pachnis V, Mankoo B, Costantini F (1993): Expression of the c-ret protooncogene during mouse embryogenesis. Development 119:1005-1017.
-
(1993)
Development
, vol.119
, pp. 1005-1017
-
-
Pachnis, V.1
Mankoo, B.2
Costantini, F.3
-
20
-
-
15844426332
-
Defects in enteric innervation and kidney development in mice lacking GDNF
-
Pichel J, Shen L, Hui S, Granholm A, Drago J, Grinberg A, Lee E, Huang S, Saarma M, Hoffer B, 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.1
Shen, L.2
Hui, S.3
Granholm, A.4
Drago, J.5
Grinberg, A.6
Lee, E.7
Huang, S.8
Saarma, M.9
Hoffer, B.10
Sariola, H.11
Westphal, H.12
-
21
-
-
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, Pasini B, Bocciardi R, Lerone M, Kääriäinen H, Martuciello G (1994): Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirschsprung's disease. Nature 367:377-378.
-
(1994)
Nature
, vol.367
, pp. 377-378
-
-
Romeo, G.1
Ronchetto, P.2
Luo, Y.3
Barone, V.4
Sen, M.5
Ceccherini, I.6
Pasini, B.7
Bocciardi, R.8
Lerone, M.9
Kääriäinen, H.10
Martuciello, G.11
-
22
-
-
0029901727
-
Renal agenesis and the absence of enteric neurons in mice lacking GDNF
-
Sanchez M, Silos-Santiago I, Frisen J, He B, Lira S, 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.1
Silos-Santiago, I.2
Frisen, J.3
He, B.4
Lira, S.5
Barbacid, M.6
-
24
-
-
0028174023
-
Defects in the kidney and enteric nervous system of mice lacking the tyrosine kinase receptor Ret
-
Schuchardt A, D'Agati V, Larsson-Blomberg L, Costantini F, Pachnis V (1994): Defects in the kidney and enteric nervous system of mice lacking the tyrosine kinase receptor Ret. Nature 367:380-383.
-
(1994)
Nature
, vol.367
, pp. 380-383
-
-
Schuchardt, A.1
D'Agati, V.2
Larsson-Blomberg, L.3
Costantini, F.4
Pachnis, V.5
-
25
-
-
0028939138
-
Isolation and characterization of a chicken homolog of the c-ret proto-oncogene
-
Schuchardt A, Srinivas S, Pacnhis V, Costantini F (1995): Isolation and characterization of a chicken homolog of the c-ret proto-oncogene. Oncogene 10:641-649.
-
(1995)
Oncogene
, vol.10
, pp. 641-649
-
-
Schuchardt, A.1
Srinivas, S.2
Pacnhis, V.3
Costantini, F.4
-
26
-
-
0030007849
-
Localization of glial cell line-derived neurotrophic factor (GDNF) mRNA in embryonic rat by in situ hybridization
-
Suvanto P, Hiltunen JO, Arumäe U, Moshnyakov M, Sariola H, Sainio K, Saarma M (1996): Localization of glial cell line-derived neurotrophic factor (GDNF) mRNA in embryonic rat by in situ hybridization. Eur J Neurosci 8:816-822.
-
(1996)
Eur J Neurosci
, vol.8
, pp. 816-822
-
-
Suvanto, P.1
Hiltunen, J.O.2
Arumäe, U.3
Moshnyakov, M.4
Sariola, H.5
Sainio, K.6
Saarma, M.7
-
27
-
-
0025164766
-
Characterization of ret proto-oncogene mRNAs encoding two isoforms of the protein product in a human neuroblastoma cell line
-
Tahira T, Ishizaka Y, Itoh F, Sugimura T, Nagao M (1990): Characterization of ret proto-oncogene mRNAs encoding two isoforms of the protein product in a human neuroblastoma cell line. Oncogene 5:97-102.
-
(1990)
Oncogene
, vol.5
, pp. 97-102
-
-
Tahira, T.1
Ishizaka, Y.2
Itoh, F.3
Sugimura, T.4
Nagao, M.5
-
28
-
-
15844406351
-
Functional receptor for GDNF encoded by the c-ret proto-oncogene
-
Trupp M, Arenas E, Fainziciber M, Nilsson A, Sieber B, Grigoriou M, Kilkenny C, Salazar-Grueso E, Pachnis V, Arumäes U, Sariola H, Saarma M, Ibanez CF (1996): Functional receptor for GDNF encoded by the c-ret proto-oncogene. Nature 381:785-789.
-
(1996)
Nature
, vol.381
, pp. 785-789
-
-
Trupp, M.1
Arenas, E.2
Fainziciber, M.3
Nilsson, A.4
Sieber, B.5
Grigoriou, M.6
Kilkenny, C.7
Salazar-Grueso, E.8
Pachnis, V.9
Arumäes, U.10
Sariola, H.11
Saarma, M.12
Ibanez, C.F.13
-
29
-
-
0028896367
-
Spatial and temporal expression of the ret proto-oncogene product in embryonic, infant and adult rat tissues
-
Tsuzuki T, Takahashi M, Asai N, Iwashita T, Matsuyama M, Asai J (1995): Spatial and temporal expression of the ret proto-oncogene product in embryonic, infant and adult rat tissues. Oncogene 10:191-198.
-
(1995)
Oncogene
, vol.10
, pp. 191-198
-
-
Tsuzuki, T.1
Takahashi, M.2
Asai, N.3
Iwashita, T.4
Matsuyama, M.5
Asai, J.6
-
30
-
-
0027270603
-
Ondine-Hirschsprung syndrome (Haddad syndrome): Further delineation in two cases and review of the literature
-
Verloes A, Elmer C, Lacombe D, Heinrichs C, Rebuffat E, Démarquez J, Moncla A, Adam E (1993): Ondine-Hirschsprung syndrome (Haddad syndrome): Further delineation in two cases and review of the literature. Eur J Pediatr 152:75-77.
-
(1993)
Eur J Pediatr
, vol.152
, pp. 75-77
-
-
Verloes, A.1
Elmer, C.2
Lacombe, D.3
Heinrichs, C.4
Rebuffat, E.5
Démarquez, J.6
Moncla, A.7
Adam, E.8
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