Martin C Wapenaar
Martin C Wapenaar
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A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21
DA Van Heel, L Franke, KA Hunt, R Gwilliam, A Zhernakova, M Inouye, ...
Nature genetics 39 (7), 827-829, 2007
Newly identified genetic risk variants for celiac disease related to the immune response
KA Hunt, A Zhernakova, G Turner, GAR Heap, L Franke, M Bruinenberg, ...
Nature genetics 40 (4), 395, 2008
Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications.
JT Den Dunnen, PM Grootscholten, E Bakker, LA Blonden, HB Ginjaar, ...
American journal of human genetics 45 (6), 835, 1989
Myosin IXB variant increases the risk of celiac disease and points toward a primary intestinal barrier defect
AJ Monsuur, PIW de Bakker, BZ Alizadeh, A Zhernakova, MR Bevova, ...
Nature genetics 37 (12), 1341-1344, 2005
Isolation of probes detecting restriction fragment length polymorphisms from X chromosome-specific libraries: potential use for diagnosis of Duchenne muscular dystrophy
MH Hofker, MC Wapenaar, N Goor, E Bakker, GJB Van Ommen, ...
Human genetics 70 (2), 148-156, 1985
Associations with tight junction genes PARD3 and MAGI2 in Dutch patients point to a common barrier defect for coeliac disease and ulcerative colitisAn unusual case of ascites
MC Wapenaar, AJ Monsuur, AA van Bodegraven, RK Weersma, ...
Gut 57 (4), 463-467, 2008
A deletion hot spot in the Duchenne muscular dystrophy gene
MC Wapenaar, T Kievits, KA Hart, S Abbs, LAJ Blonden, JT Den Dunnen, ...
Genomics 2 (2), 101-108, 1988
A gene from the Xp22. 3 region shares homology with voltage-gated chloride channels
MA Slegtenhorst, M T. Bassl, G Borsanil, MC Wapenaar, GB Ferrero, ...
Human Molecular Genetics 3 (4), 547-552, 1994
A high resolution deletion map of human chromosome Xp22
L Schaefer, GB Ferrero, A Grillo, MT Bassi, EJ Roth, MC Wapenaar, ...
Nature genetics 4 (3), 272-279, 1993
A microarray screen for novel candidate genes in coeliac disease pathogenesis
B Diosdado, MC Wapenaar, L Franke, KJ Duran, MJ Goerres, M Hadithi, ...
Gut 53 (7), 944-951, 2004
The X chromosome shows less genetic variation at restriction sites than the autosomes.
MH Hofker, MI Skraastad, AA Bergen, MC Wapenaar, E Bakker, ...
American journal of human genetics 39 (4), 438, 1986
High resoluation deletion breakpoint mapping in the DMD gene by whole cosmid hybridization
LAJ Blonden, JT Dunnen, HMB Paassen, MC Wapenaar, ...
Nucleic acids research 17 (14), 5611-5621, 1989
The interferon gamma gene in celiac disease: augmented expression correlates with tissue damage but no evidence for genetic susceptibility
MC Wapenaar, MJ van Belzen, JH Fransen, AF Sarasqueta, RHJ Houwen, ...
Journal of autoimmunity 23 (2), 183-190, 2004
Functional characterization of mutations in the myosin Vb gene associated with microvillus inclusion disease
AM Szperl, MR Golachowska, M Bruinenberg, R Prekeris, ...
Journal of pediatric gastroenterology and nutrition 52 (3), 307, 2011
Direct nonradioactive in situ hybridization of somatic cell hybrid DNA to human lymphocyte chromosomes
T Kievits, P Devilee, J Wiegant, MC Wapenaar, CJ Cornelisse, ...
Cytometry: The Journal of the International Society for Analytical Cytology …, 1990
Association analysis of MYO9B gene polymorphisms with celiac disease in a Swedish/Norwegian cohort
SS Amundsen, AJ Monsuur, MC Wapenaar, BA Lie, J Ek, ...
Human immunology 67 (4-5), 341-345, 2006
Characterization ofCxorf5 (71-7A), a novel human cDNA mapping to Xp22 and encoding a protein containing coiled-coil α-helical domains
L De Conciliis, A Marchitiello, MC Wapenaar, G Borsani, S Giglio, ...
Genomics 51 (2), 243-250, 1998
The genes for X-linked ocular albinism (OA1) and microphthalmia with linear skin defects (MLS): cloning and characterization of the critical regions
MC Wapenaar, MT Bassl, L Schaefer, A Grillo, GB Ferrero, AC Chlnault, ...
Human molecular genetics 2 (7), 947-952, 1993
Deletions within the pseudoautosomal region help map three new markers and indicate a possible role of this region in linear growth.
A Henke, M Wapenaar, GJ Van Ommen, P Maraschio, G Camerino, ...
American journal of human genetics 49 (4), 811, 1991
Generation and fluorescent in situ hybridization mapping of yeast artificial chromosomes of 1p, 17p, 17q, and 19q from a hybrid cell line by high-density screening of an …
MS Driesen, JG Dauwerse, MC Wapenaar, EJ Meershoek, P Mollevanger, ...
Genomics 11 (4), 1079-1087, 1991
Il sistema al momento non può eseguire l'operazione. Riprova più tardi.
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