Zobrazeno 1 - 10
of 65
pro vyhledávání: '"Wautot, V."'
Autor:
Mornex, F. *, Girard, N., Merle, P., Béziat, C., Kubas, A., Wautot, V., Khodri, M., Trepo, C.
Publikováno v:
In Cancer / Radiothérapie 2005 9(6):470-476
Autor:
Lemmes, I, Van de Ven, W, Kas, K, Zhang, C, Giraud, S, Wautot, V, Buisson, N, Pugeat, M, Peix, J, Caldener, A, Parente, F, Quincey, D, Courseaux, A, Carle, G, Gaudray, P, De Wit, M, Lips, C, Hoppener, J, Khodaei, S, Grant, A, Weber, G, Teh, B, Farnebo, F, Kytola, S, Grimmond, S
The search for the gene whose mutations predispose individuals to multiple endocrine neoplasia type 1 (MEN-1) started in 1988 when the MEN1 locus was assigned to 11q13, close to PYGM. It came to an end with the recent identification of a gene express
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1064::df5820c200b5412e4876e564d1292260
https://doi.org/10.1046/j.1365-2796.1998.00347.x
https://doi.org/10.1046/j.1365-2796.1998.00347.x
Autor:
Lemmens, I, VandeVen, W, Kas, K, Zhang, C, Giraud, S, Wautot, V, Buisson, N, DeWitte, K, Salandre, J, Lenoir, G, Pugeat, M, Calender, A, Parente, F, Quincey, D, Gaudray, P, DeWit, M, Lips, C, Hoppener, J, Khodaei, S, Grant, A, Weber, G, Kytola, S, Teh, B, Farnebo, F, Phelan, C
Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disorder characterised by tumours of the parathyroids, pancreas and anterior pituitary that represents one of the familial cancer syndromes. The MEN1 locus has been previously locali
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1064::dc9d0099615807782721eb39895f2f8c
https://ora.ox.ac.uk/objects/uuid:e87ca893-dab6-4315-9635-ec3abd395dca
https://ora.ox.ac.uk/objects/uuid:e87ca893-dab6-4315-9635-ec3abd395dca
Autor:
Lemmens, I, Merregaert, J, Van de Ven, W, Kas, K, Zhang, C, Giraud, S, Wautot, V, Buisson, N, De Witte, K, Salandre, J, Lenoir, G, Calender, A, Parente, F, Quincey, D, Courseaux, A, Carle, G, Gaudray, P, De Wit, M, Lips, C, Höppener, J, Khodaei, S, Grant, A, Weber, G, Kytölä, S, Thakker, R
Publikováno v:
Genomics. 44(1)
Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant familial cancer syndrome characterized by parathyroid, pancreatic, and anterior pituitary tumors. The MEN1 locus has been previously localized to chromosome 11q13, and a 2-Mb gene-ri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::ad8f9f0c0fc8e90ff2c8a7e52f1e18cf
http://ora.ox.ac.uk/objects/uuid:aafdadee-ae7b-4f47-bfa8-142822328d48
http://ora.ox.ac.uk/objects/uuid:aafdadee-ae7b-4f47-bfa8-142822328d48
Autor:
Lemmens, I, VandeVen, WJM, Kas, K, Zhang, CX, Giraud, S, Wautot, V, Buisson, N, DeWitte, K, Salandre, J, Lenoir, G, Pugeat, M, Calender, A, Parente, F, Quincey, D, Gaudray, P, DeWit, MJ, Lips, CJM, Hoppener, JWM, Khodaei, S, Grant, AL, Weber, G, Kytola, S, Teh, BT, Farnebo, F, Phelan, C, Hayward, N, Larsson, C, Pannett, AAJ, Forbes, SA, Bassett, JHD, Thakker, RV
Publikováno v:
HUMAN MOLECULAR GENETICS. 6(7)
Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disorder characterised by tumours of the parathyroids, pancreas and anterior pituitary that represents one of the familial cancer syndromes. The MEN1 locus has been previously locali
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1064::ad58eb3787abf6d3ec573995860cff9d
http://ora.ox.ac.uk/objects/uuid:e87ca893-dab6-4315-9635-ec3abd395dca
http://ora.ox.ac.uk/objects/uuid:e87ca893-dab6-4315-9635-ec3abd395dca
Akademický článek
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Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
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Autor:
Touch, S., Hatime, M., Elmorabit, B., Merle, P., Tanguy, R., Diaz, O., Wautot, V., Enachescu, C., Elkhoti, Y., Mornex, F.
Publikováno v:
In Cancer / Radiothérapie September 2012 16(5-6):520-520
Autor:
Hatime, M., Elmorabit, B., Touch, S., Merle, P., Tanguy, R., Diaz, O., Wautot, V., Enachescu, C., Elkhoti, Y., Mornex, F.
Publikováno v:
In Cancer / Radiothérapie September 2012 16(5-6):519-519
Autor:
Elmorabit, B., Touch, S., Hatime, M., Tanguy, R., Diaz, O., Wautot, V., Enachescu, C., Couraud, S., Mornex, F.
Publikováno v:
In Cancer / Radiothérapie September 2012 16(5-6):514-515