Detalhe da pesquisa
1.
[Spatio-temporal distribution of COVID-19 in Cologne and associated socio-economic factors in the period from February 2020 to October 2021]. / Die zeitlich-räumliche Verteilung von COVID-19 in Köln und beeinflussende soziale Faktoren im Zeitraum Februar 2020 bis Oktober 2021.
Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz
; 65(9): 853-862, 2022 Sep.
Artigo
em Alemão
| MEDLINE | ID: mdl-35920847
2.
Uncovering chains of infections through spatio-temporal and visual analysis of COVID-19 contact traces.
Comput Graph
; 106: 1-8, 2022 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-35637696
3.
STAT3 gain-of-function mutations associated with autoimmune lymphoproliferative syndrome like disease deregulate lymphocyte apoptosis and can be targeted by BH3 mimetic compounds.
Clin Immunol
; 181: 32-42, 2017 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-28579554
4.
Fatal Lymphoproliferative Disease in Two Siblings Lacking Functional FAAP24.
J Clin Immunol
; 36(7): 684-92, 2016 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-27473539
5.
Deregulation of Fas ligand expression as a novel cause of autoimmune lymphoproliferative syndrome-like disease.
Haematologica
; 100(9): 1189-98, 2015 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-26113417
6.
Next-generation-sequencing-based risk stratification and identification of new genes involved in structural and sequence variations in near haploid lymphoblastic leukemia.
Genes Chromosomes Cancer
; 52(6): 564-79, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-23508829
7.
Combined immunodeficiency with life-threatening EBV-associated lymphoproliferative disorder in patients lacking functional CD27.
Haematologica
; 98(3): 473-8, 2013 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-22801960
8.
Human RAD52 - a novel player in DNA repair in cancer and immunodeficiency.
Haematologica
; 102(2): e69-e72, 2017 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-27979922
9.
Symptom diaries as a digital tool to detect SARS-CoV-2 infections and differentiate between prevalent variants.
Front Public Health
; 10: 1030939, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36452944
10.
Specific antibody deficiency and autoinflammatory disease extend the clinical and immunological spectrum of heterozygous NFKB1 loss-of-function mutations in humans.
Haematologica
; 101(10): e392-e396, 2016 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-27365489
11.
Whole-genome paired-end analysis confirms remarkable genomic stability of atypical teratoid/rhabdoid tumors.
Genes Chromosomes Cancer
; 52(10): 983-5, 2013 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-23929726
12.
Mutated SON putatively causes a cancer syndrome comprising high-risk medulloblastoma combined with café-au-lait spots.
Fam Cancer
; 18(3): 353-358, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30680470
13.
Pediatric ALL relapses after allo-SCT show high individuality, clonal dynamics, selective pressure, and druggable targets.
Blood Adv
; 3(20): 3143-3156, 2019 10 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-31648313
14.
EBV Negative Lymphoma and Autoimmune Lymphoproliferative Syndrome Like Phenotype Extend the Clinical Spectrum of Primary Immunodeficiency Caused by STK4 Deficiency.
Front Immunol
; 9: 2400, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30386345
15.
Congenital embryonal rhabdomyosarcoma caused by heterozygous concomitant PTCH1 and PTCH2 germline mutations.
Eur J Hum Genet
; 26(1): 137-142, 2018 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29230040
16.
Diagnostic challenges in a child with early onset desmoplastic medulloblastoma and homozygous variants in MSH2 and MSH6.
Eur J Hum Genet
; 26(3): 440-444, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29302048
17.
Loss of Pax5 Exploits Sca1-BCR-ABLp190 Susceptibility to Confer the Metabolic Shift Essential for pB-ALL.
Cancer Res
; 78(10): 2669-2679, 2018 05 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-29490943
18.
A novel approach to detect resistance mechanisms reveals FGR as a factor mediating HDAC inhibitor SAHA resistance in B-cell lymphoma.
Mol Oncol
; 10(8): 1232-44, 2016 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-27324824
19.
Next-generation-sequencing of recurrent childhood high hyperdiploid acute lymphoblastic leukemia reveals mutations typically associated with high risk patients.
Leuk Res
; 39(9): 990-1001, 2015 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-26189108
20.
Infection Exposure is a Causal Factor in B-cell Precursor Acute Lymphoblastic Leukemia as a Result of Pax5-Inherited Susceptibility.
Cancer Discov
; 5(12): 1328-43, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26408659