| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Actin polymerisation after FCγR stimulation of human fibroblasts is BCL10 independent
|
Garcia-Gomez, Sonia
|
|
2016
|
163 |
C |
p. 120-122
3 p.
|
artikel
|
| 2 |
Altered signaling in systemic juvenile idiopathic arthritis monocytes
|
Macaubas, Claudia
|
|
2016
|
163 |
C |
p. 66-74
9 p.
|
artikel
|
| 3 |
B cell development in chromosome 22q11.2 deletion syndrome
|
Derfalvi, Beata
|
|
2016
|
163 |
C |
p. 1-9
9 p.
|
artikel
|
| 4 |
Clinical and structural impact of mutations affecting the residue Phe367 of FOXP3 in patients with IPEX syndrome
|
Colobran, Roger
|
|
2016
|
163 |
C |
p. 60-65
6 p.
|
artikel
|
| 5 |
Correlation of bone marrow abnormalities, peripheral lymphocyte subsets and clinical features in uncomplicated common variable immunodeficiency (CVID) patients
|
Lougaris, Vassilios
|
|
2016
|
163 |
C |
p. 10-13
4 p.
|
artikel
|
| 6 |
Deep intronic mis-splicing mutation in JAK3 gene underlies T−B+NK− severe combined immunodeficiency phenotype
|
Stepensky, Polina
|
|
2016
|
163 |
C |
p. 91-95
5 p.
|
artikel
|
| 7 |
Differential expression of sema3A and sema7A in a murine model of multiple sclerosis: Implications for a therapeutic design
|
Gutiérrez-Franco, Ana
|
|
2016
|
163 |
C |
p. 22-33
12 p.
|
artikel
|
| 8 |
Editorial Board
|
|
|
2016
|
163 |
C |
p. IFC-
1 p.
|
artikel
|
| 9 |
Hypomorphic function and somatic reversion of DOCK8 cause combined immunodeficiency without hyper-IgE
|
Kienzler, Anne-Kathrin
|
|
2016
|
163 |
C |
p. 17-21
5 p.
|
artikel
|
| 10 |
IRAK-4 deficiency as a cause for familial fatal invasive infection by Streptococcus pneumoniae
|
Grazioli, Serge
|
|
2016
|
163 |
C |
p. 14-16
3 p.
|
artikel
|
| 11 |
Mimotope mimicking epidermal growth factor receptor alleviates mononuclear cell infiltration in exocrine glands induced by muscarinic acetylcholine 3 receptor
|
Yang, Lin
|
|
2016
|
163 |
C |
p. 111-119
9 p.
|
artikel
|
| 12 |
Molecular and immunological characterization of DNA ligase IV deficiency
|
Jiang, Jinqiu
|
|
2016
|
163 |
C |
p. 75-83
9 p.
|
artikel
|
| 13 |
Next generation sequencing revealed DNA ligase IV deficiency in a “developmentally normal” patient with massive brain Epstein–Barr virus-positive diffuse large B-cell lymphoma
|
Sharapova, Svetlana O.
|
|
2016
|
163 |
C |
p. 108-110
3 p.
|
artikel
|
| 14 |
Restoration of t cell substes of patients with type 1 diabetes mellitus by microencapsulated human umbilical cord Wharton jelly-derived mesenchymal stem cells: An in vitro study
|
Montanucci, Pia
|
|
2016
|
163 |
C |
p. 34-41
8 p.
|
artikel
|
| 15 |
Siglec-1-positive plasmacytoid dendritic cells (pDCs) in human peripheral blood: A semi-mature and myeloid-like subset imbalanced during protective and autoimmune responses
|
Wilhelm, Theresa R.
|
|
2016
|
163 |
C |
p. 42-51
10 p.
|
artikel
|
| 16 |
Soluble SEMA4D/CD100: A novel immunoregulator in infectious and inflammatory diseases
|
Maleki, Kimia T.
|
|
2016
|
163 |
C |
p. 52-59
8 p.
|
artikel
|
| 17 |
The low EOMES/TBX21 molecular phenotype in multiple sclerosis reflects CD56+ cell dysregulation and is affected by immunomodulatory therapies
|
McKay, Fiona C.
|
|
2016
|
163 |
C |
p. 96-107
12 p.
|
artikel
|
| 18 |
Uncoupling complement C1s activation from C1q binding in apoptotic cell phagocytosis and immunosuppressive capacity
|
Colonna, Lucrezia
|
|
2016
|
163 |
C |
p. 84-90
7 p.
|
artikel
|
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