Search Results - "van Zelm, M.C"

Abnormalities in CD57 + cytotoxic T cells and Vδ1 + γδT cells in subclinical celiac disease in childhood are affected by cytomegalovirus. The Generation R Study by Jansen, M.A.E, van den Heuvel, D, Jaddoe, V.W.V, van Zelm, M.C, Moll, H.A

“…Abstract Celiac disease (CD) is a digestive and autoimmune disorder driven by an immune response to modified gluten peptides. Affected intestines show…”
Get full text

Estimating human age from T-cell DNA rearrangements by Zubakov, D., Liu, F., van Zelm, M.C., Vermeulen, J., Oostra, B.A., van Duijn, C.M., Driessen, G.J., van Dongen, J.J.M., Kayser, M., Langerak, A.W.

“…Predicting human phenotypes from genotypes is a newly emerging field with relevance for personalized medicine [1] and forensics [2]. However, only a few…”
Get full text

Basal [Ca.sup.2+] signaling is particularly increased in mutated chronic lymphocytic leukemia by Muggen, A.F, Pillai, S.Y, Kil, L.P, van Zelm, M.C, van Dongen, J.J.M, Hendriks, R.W, Langerak, A.W

“…On the basis of somatic hypermutation status of their B-cell antigen receptor (BCR) genes, chronic lymphocytic leukemia (CLL) patients can be divided into…”
Get full text

Is there a pathogenic role for IgE in psoriasis? by Heeringa, J.J., van Zelm, M.C.

“…Linked Article: Yan et al. Br J Dermatol 2016; 175:122–133…”
Get full text

Persistent polyclonal B-cell lymphocytosis: extensively proliferated CD27+IgM+IgD+ memory B cells with a distinctive immunophenotype by Berkowska, M A, Grosserichter-Wagener, C, Adriaansen, H J, de Ridder, D, Mirani-Oostdijk, K P, Agteresch, H J, Böttcher, S, Orfao, A, van Dongen, J J M, van Zelm, M C

Get full text

Artemis splice defects cause atypical SCID and can be restored in vitro by an antisense oligonucleotide by IJspeert, H, Lankester, A C, van den Berg, J M, Wiegant, W, van Zelm, M C, Weemaes, C M R, Warris, A, Pan-Hammarström, Q, Pastink, A, van Tol, M J D, van Dongen, J J M, van Gent, D C, van der Burg, M

“…Artemis deficiency is known to result in classical T−B− severe combined immunodeficiency (SCID) in case of Artemis null mutations, or Omenn's syndrome in case…”
Get full text

B-cell maturation and antibody responses in individuals carrying a mutated CD19 allele by Artac, H, Reisli, I, Kara, R, Pico-Knijnenburg, I, Adin-Çinar, S, Pekcan, S, Jol-van der Zijde, C M, van Tol, M J D, Bakker-Jonges, L E, van Dongen, J J M, van der Burg, M, van Zelm, M C

“…Homozygous CD19 mutations lead to an antibody deficiency due to disruption of the CD19 complex and consequent impaired signaling by the B-cell antigen…”
Get full text

Antibody-deficiency and acute nephritic syndrome in a patient with homozygous disruption of CD81 gene (ESID Plenary Session VI: Novel Primary Immunodeficiencies and Late breakers) by van Zelm, M.C.

Get full text

Novel mutations in a Japanese patient with CD 19 deficiency by Kanegane, H, Agematsu, K, Futatani, T, Sira, M.M, Suga, K, Sekiguchi, T, van Zelm, M.C, Miyawaki, T

Get full text