关注
Sebastian Hollizeck
Sebastian Hollizeck
Peter MacCallum Cancer Center
在 petermac.org 的电子邮件经过验证
标题
引用次数
引用次数
年份
An evolutionarily conserved function of polycomb silences the MHC class I antigen presentation pathway and enables immune evasion in cancer
ML Burr, CE Sparbier, KL Chan, YC Chan, A Kersbergen, EYN Lam, ...
Cancer cell 36 (4), 385-401. e8, 2019
4782019
RET solvent front mutations mediate acquired resistance to selective RET inhibition in RET-driven malignancies
BJ Solomon, L Tan, JJ Lin, SQ Wong, S Hollizeck, K Ebata, BB Tuch, ...
Journal of Thoracic Oncology 15 (4), 541-549, 2020
2372020
Human RIPK1 deficiency causes combined immunodeficiency and inflammatory bowel diseases
Y Li, M Führer, E Bahrami, P Socha, M Klaudel-Dreszler, A Bouzidi, Y Liu, ...
Proceedings of the National Academy of Sciences 116 (3), 970-975, 2019
1682019
Human TGF-β1 deficiency causes severe inflammatory bowel disease and encephalopathy
D Kotlarz, B Marquardt, T Barøy, WS Lee, L Konnikova, S Hollizeck, ...
Nature genetics 50 (3), 344-348, 2018
1302018
Intestinal inflammation and dysregulated immunity in patients with inherited caspase-8 deficiency
AS Lehle, HF Farin, B Marquardt, BE Michels, T Magg, Y Li, Y Liu, ...
Gastroenterology 156 (1), 275-278, 2019
1062019
Non-genetic determinants of malignant clonal fitness at single-cell resolution
KA Fennell, D Vassiliadis, EYN Lam, LG Martelotto, JJ Balic, S Hollizeck, ...
Nature 601 (7891), 125-131, 2022
982022
Proteome analysis of human neutrophil granulocytes from patients with monogenic disease using data-independent acquisition*[S]
P Grabowski, S Hesse, S Hollizeck, M Rohlfs, U Behrends, R Sherkat, ...
Molecular & Cellular Proteomics 18 (4), 760-772, 2019
622019
Myb-like, SWIRM, and MPN domains 1 (MYSM1) deficiency: Genotoxic stress-associated bone marrow failure and developmental aberrations
E Bahrami, M Witzel, T Racek, J Puchałka, S Hollizeck, N Greif-Kohistani, ...
Journal of Allergy and Clinical Immunology 140 (4), 1112-1119, 2017
502017
Novel Mutations in RASGRP1 are Associated with Immunodeficiency, Immune Dysregulation, and EBV-Induced Lymphoma
I Somekh, B Marquardt, Y Liu, M Rohlfs, S Hollizeck, M Karakukcu, E Unal, ...
Journal of Clinical Immunology 38, 699-710, 2018
462018
Impact on clinical decision making of next-generation sequencing in pediatric epilepsy in a tertiary epilepsy referral center
H Hoelz, C Herdl, L Gerstl, M Tacke, K Vill, C von Stuelpnagel, I Rost, ...
Clinical EEG and neuroscience 51 (1), 61-69, 2020
402020
Genetic deficiency and biochemical inhibition of ITK affect human Th17, Treg, and innate lymphoid cells
A Eken, M Cansever, I Somekh, Y Mizoguchi, N Zietara, FZ Okus, ...
Journal of Clinical Immunology 39, 391-400, 2019
362019
CARMIL2 deficiency presenting as very early onset inflammatory bowel disease
T Magg, A Shcherbina, D Arslan, MM Desai, S Wall, V Mitsialis, R Conca, ...
Inflammatory Bowel Diseases 25 (11), 1788-1795, 2019
332019
Human FCHO1 deficiency reveals role for clathrin-mediated endocytosis in development and function of T cells
M Łyszkiewicz, N Ziętara, L Frey, U Pannicke, M Stern, Y Liu, Y Fan, ...
Nature communications 11 (1), 1031, 2020
302020
Lymphocytic interstitial pneumonia and follicular bronchiolitis in children: A registry‐based case series
F Prenzel, J Harfst, N Schwerk, F Ahrens, E Rietschel, S Schmitt‐Grohé, ...
Pediatric Pulmonology 55 (4), 909-917, 2020
202020
NOX1 regulates collective and planktonic cell migration: insights from patients with pediatric-onset IBD and NOX1 deficiency
R Khoshnevisan, M Anderson, S Babcock, S Anderson, D Illig, ...
Inflammatory Bowel Diseases 26 (8), 1166-1176, 2020
172020
Alternative splicing rescues loss of common gamma chain function and results in IL-21R-like deficiency
D Illig, M Navratil, J Kelečić, R Conca, I Hojsak, O Jadrešin, M Ćorić, ...
Journal of clinical immunology 39, 207-215, 2019
92019
Valosin-containing protein-regulated endoplasmic reticulum stress causes NOD2-dependent inflammatory responses
M Ghalandary, Y Li, T Fröhlich, T Magg, Y Liu, M Rohlfs, S Hollizeck, ...
Scientific Reports 12 (1), 3906, 2022
32022
Prospective cohort study of genomic newborn screening: BabyScreen+ pilot study protocol
S Lunke, SE Bouffler, L Downie, J Caruana, DJ Amor, A Archibald, ...
BMJ open 14 (4), e081426, 2024
22024
Defects in Signal Recognition Particle (SRP) Components Reveal an Essential and Non-Redundant Role for Granule Biogenesis and Differentiation of Neutrophil Granulocytes
Y Mizoguchi, S Hesse, M Linder, N Zietara, M Lyszkiewicz, Y Liu, ...
Blood 134, 216, 2019
22019
Human FCH domain only 1 (FCHO1) deficiency reveals an essential role for clathrin-mediated endocytosis for the development and function of T cells
M Lyszkiewicz, N Zietara, L Frey, U Pannicke, Y Liu, Y Fan, J Puchalka, ...
EUROPEAN JOURNAL OF IMMUNOLOGY 49, 29-30, 2019
22019
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