Zobrazeno 1 - 10
of 264
pro vyhledávání: '"Lips, C"'
Protein modification with poly-ubiquitin chains is a crucial process involved in a myriad of cellular pathways. Chain synthesis requires two steps: substrate modification with ubiquitin (priming) followed by repetitive ubiquitin-to-ubiquitin attachme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=mdc______med::eef5dcd32d939d2f5a5449ea2d107025
http://edoc.mdc-berlin.de/19426/1/19426oa.pdf
http://edoc.mdc-berlin.de/19426/1/19426oa.pdf
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
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
Publikováno v:
European Journal of Surgery. Jun99, Vol. 165 Issue 6, p535-538. 4p.
Autor:
Van Wijk, Jeroen P H, Dreijerink, K. M A, Pieterman, C. R C, Lips, C. J M, Zelissen, P. M J, Valk, G. D.
Publikováno v:
Van Wijk, J P H, Dreijerink, K M A, Pieterman, C R C, Lips, C J M, Zelissen, P M J & Valk, G D 2012, ' Increased prevalence of impaired fasting glucose in MEN1 gene mutation carriers ', Clinical Endocrinology, vol. 76, no. 1, pp. 67-71 . https://doi.org/10.1111/j.1365-2265.2011.04166.x
Clinical Endocrinology, 76(1), 67-71. Wiley-Blackwell
Clinical Endocrinology, 76(1), 67-71. Wiley-Blackwell
Objective Multiple endocrine neoplasia type 1 (MEN1) is a hereditary syndrome characterized by parathyroid, gastroenteropancreatic, pituitary and adrenal tumours. Cardiovascular disease has been identified as an important cause of death in MEN1 patie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::35c2b98b5e3ae774a6e9d55f1922b68b
https://research.vumc.nl/en/publications/1aa33f36-e758-4e0e-999c-419394152d7c
https://research.vumc.nl/en/publications/1aa33f36-e758-4e0e-999c-419394152d7c
Autor:
Hes, F. J., Van der Luijt, R. B., Janssen, A. L.W., Zewald, R. A., De Jong, G. J., Lenders, J. W., Links, T. P., Luyten, G. P.M., Sijmons, R. H., Eussen, H. J., Halley, D. J.J., Lips, C. J.M., Pearson, P. L., van den Ouweland, A. M.W., Majoor-Krakauer, D. F.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3848::7461b503fd4d15c3be65ee85e2496836
https://biblio.vub.ac.be/vubir/(52e7ad94-a4c1-4844-ab22-b2edbba91763).html
https://biblio.vub.ac.be/vubir/(52e7ad94-a4c1-4844-ab22-b2edbba91763).html
Autor:
Brandi, M, Gagel, R, Angeli, A, Bilezikian, J, Beck-Peccoz, P, Bordi, C, Conte-Devolx, B, Falchetti, A, Gheri, R, Libroia, A, Lips, C, Lombardi, G, Mannelli, M, Pacini, F, Ponder, B, Raue, F, Skogseid, B, Tamburrano, G, Thakker, R, Thompson, N, Tomassetti, P, Tonelli, F, Wells, SA, Marx, S
Publikováno v:
The Journal of clinical endocrinology and metabolism. 86(12)
This is a consensus statement from an international group, mostly of clinical endocrinologists. MEN1 and MEN2 are hereditary cancer syndromes. The commonest tumors secrete PTH or gastrin in MEN1, and calcitonin or catecholamines in MEN2. Management s
Autor:
Dreijerink, K. M.A., Roijers, J. F.M., Jansen-Schillhorn van Veen, J. M., Neijt, J. P., Van Vroonhoven, Th J.M.V., Lips, C. J.M.
Publikováno v:
Nederlands Tijdschrift voor Geneeskunde, 144(51), 2437-2442. Bohn Stafleu van Loghum
MEN-I is an autosomal dominantly inherited disorder, characterised by the occurrence of multiple tumours, particularly in the parathyroid glands, the pancreatic islets, the pituitary gland and the adrenal glands, as well as by neuroendocrine carcinoi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::a4f4cbb825feda1593101f429bebfeab
https://research.vumc.nl/en/publications/8694ba64-c3fa-4f36-9a65-e7ae09368396
https://research.vumc.nl/en/publications/8694ba64-c3fa-4f36-9a65-e7ae09368396