Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
---|---|---|---|
1 |
Material Type: Artigo
|
The importance of motivation in selecting undergraduate medical students for extracurricular research programmesOmmering, Belinda W C ; Van Blankenstein, Floris M ; van Diepen, Merel ; Gruis, Nelleke A ; Kool, Ada ; Dekker, Friedo W Shankar, Pathiyil RaviPloS one, 2021-11, Vol.16 (11), p.e0260193-e0260193 [Periódico revisado por pares]United States: Public Library of ScienceTexto completo disponível |
|
2 |
Material Type: Artigo
|
Magnetic Resonance Imaging Surveillance Detects Early-Stage Pancreatic Cancer in Carriers of a p16-Leiden MutationVasen, Hans F.A ; Wasser, Martin ; van Mil, Anneke ; Tollenaar, Rob A ; Konstantinovski, Marja ; Gruis, Nelleke A ; Bergman, Wilma ; Hes, Frederik J ; Hommes, Daniel W ; Offerhaus, G. Johan A ; Morreau, Hans ; Bonsing, Bert A ; de Vos tot Nederveen Cappel, Wouter HGastroenterology (New York, N.Y. 1943), 2011-03, Vol.140 (3), p.850-856 [Periódico revisado por pares]United States: Elsevier IncTexto completo disponível |
|
3 |
Material Type: Artigo
|
Promoter CpG Island Hypermethylation in Dysplastic Nevus and Melanoma: CLDN11 as an Epigenetic Biomarker for MalignancyGao, Linda ; van den Hurk, Karin ; Moerkerk, Peter T.M. ; Goeman, Jelle J. ; Beck, Samuel ; Gruis, Nelleke A. ; van den Oord, Joost J. ; Winnepenninckx, Véronique J. ; van Engeland, Manon ; van Doorn, RemcoJournal of investigative dermatology, 2014-12, Vol.134 (12), p.2957-2966 [Periódico revisado por pares]United States: Elsevier IncTexto completo disponível |
|
4 |
Material Type: Artigo
|
The absence of multiple atypical nevi in germline CDKN2A mutations: Comment on “Hereditary melanoma: Update on syndromes and management: Genetics of familial atypical multiple mole melanoma syndrome”Ipenburg, Norbertus Anton, MD ; Gruis, Nelleke A., PhD ; Bergman, Wilma, MD, PhD ; van Kester, Marloes Sophia, MD, PhDJournal of the American Academy of Dermatology, 2016-10, Vol.75 (4), p.e157-e157 [Periódico revisado por pares]United States: Elsevier IncTexto completo disponível |
|
5 |
Material Type: Artigo
|
Increased Risk of Cancer Other Than Melanoma in CDKN2A Founder Mutation (p16-Leiden)-Positive Melanoma FamiliesDE SNOO, Femke A ; BISHOP, D. Timothy ; WILLEMZE, Rein ; BREUNING, Martijn H ; GRUIS, Nelleke A ; BERGMAN, Wilma ; VAN LEEUWEN, Inge ; VAN DER DRIFT, Clasine ; VAN NIEUWPOORT, Frans A ; OUT-LUITING, Coby J ; VASEN, Hans F ; TER HUURNE, Jeanet A. C ; FRANTS, Rune RClinical cancer research, 2008-11, Vol.14 (21), p.7151-7157 [Periódico revisado por pares]Philadelphia, PA: American Association for Cancer ResearchTexto completo disponível |
|
6 |
Material Type: Artigo
|
Histologic features of melanoma associated with CDKN2A genotypeSargen, Michael R., MD ; Kanetsky, Peter A., PhD, MPH ; Newton-Bishop, Julia, MD, FMedSci ; Hayward, Nicholas K., PhD ; Mann, Graham J., MBBS, PhD ; Gruis, Nelleke A., PhD ; Tucker, Margaret A., MD ; Goldstein, Alisa M., PhD ; Bianchi-Scarra, Giovanna, PhD ; Puig, Susana, MD ; Elder, David E., MB, ChB, FRCPAJournal of the American Academy of Dermatology, 2015-03, Vol.72 (3), p.496-507.e7 [Periódico revisado por pares]United States: Elsevier IncTexto completo disponível |
|
7 |
Material Type: Artigo
|
Clinical and histologic characteristics of malignant melanoma in families with a germline mutation in CDKN2Avan der Rhee, Jasper I., MD ; Krijnen, Pieta, PhD ; Gruis, Nelleke A., PhD ; de Snoo, Femke A., MD, PhD ; Vasen, Hans F.A., MD, PhD ; Putter, Hein, PhD ; Kukutsch, Nicole A., MD, PhD ; Bergman, Wilma, MD, PhDJournal of the American Academy of Dermatology, 2011-08, Vol.65 (2), p.281-288 [Periódico revisado por pares]New York, NY: Elsevier IncTexto completo disponível |
|
8 |
Material Type: Artigo
|
Melanocortin-1 Receptor Gene Variants Determine the Risk of Nonmelanoma Skin Cancer Independently of Fair Skin and Red HairBastiaens, Maarten T. ; Huurne, Jeannet A. C. ter ; Kielich, Christine ; Gruis, Nelleke A. ; Westendorp, Rudi G.J. ; Vermeer, Bert Jan ; Bavinck, Jan Nico BouwesAmerican journal of human genetics, 2001-04, Vol.68 (4), p.884-894 [Periódico revisado por pares]Chicago, IL: Elsevier IncTexto completo disponível |
|
9 |
Material Type: Artigo
|
A Cell Cycle Regulator Potentially Involved in Genesis of Many Tumor TypesKamb, Alexander ; Gruis, Nelleke A. ; Weaver-Feldhaus, Jane ; Liu, Qingyun ; Harshman, Keith ; Tavtigian, Sean V. ; Stockert, Elisabeth ; Day, Rufus S. ; Johnson, Bruce E. ; Skolnick, Mark H.Science (American Association for the Advancement of Science), 1994-04, Vol.264 (5157), p.436-440 [Periódico revisado por pares]Washington, DC: American Society for the Advancement of ScienceTexto completo disponível |
|
10 |
Material Type: Artigo
|
POT1 loss-of-function variants predispose to familial melanomaRobles-Espinoza, Carla Daniela ; Harland, Mark ; Ramsay, Andrew J ; Aoude, Lauren G ; Quesada, Víctor ; Ding, Zhihao ; Pooley, Karen A ; Pritchard, Antonia L ; Tiffen, Jessamy C ; Petljak, Mia ; Palmer, Jane M ; Symmons, Judith ; Johansson, Peter ; Stark, Mitchell S ; Gartside, Michael G ; Snowden, Helen ; Montgomery, Grant W ; Martin, Nicholas G ; Liu, Jimmy Z ; Choi, Jiyeon ; Makowski, Matthew ; Brown, Kevin M ; Dunning, Alison M ; Keane, Thomas M ; López-Otín, Carlos ; Gruis, Nelleke A ; Hayward, Nicholas K ; Bishop, D Timothy ; Newton-Bishop, Julia A ; Adams, David JNature genetics, 2014-05, Vol.46 (5), p.478-481 [Periódico revisado por pares]United States: Nature Publishing GroupTexto completo disponível |