Martijn C. Nawijn

ORCID: 0000-0003-3372-6521
Publications
Citations
Views
---
Saved
---
About
Contact & Profiles
Research Areas
  • Asthma and respiratory diseases
  • IL-33, ST2, and ILC Pathways
  • Allergic Rhinitis and Sensitization
  • Single-cell and spatial transcriptomics
  • Chronic Obstructive Pulmonary Disease (COPD) Research
  • Neonatal Respiratory Health Research
  • Pediatric health and respiratory diseases
  • Immune Cell Function and Interaction
  • Cancer Mechanisms and Therapy
  • Eosinophilic Esophagitis
  • Epigenetics and DNA Methylation
  • Food Allergy and Anaphylaxis Research
  • Wnt/β-catenin signaling in development and cancer
  • Dermatology and Skin Diseases
  • Respiratory and Cough-Related Research
  • Peptidase Inhibition and Analysis
  • SARS-CoV-2 and COVID-19 Research
  • Mast cells and histamine
  • Respiratory viral infections research
  • Inhalation and Respiratory Drug Delivery
  • COVID-19 Clinical Research Studies
  • T-cell and B-cell Immunology
  • Cancer-related gene regulation
  • Immune Response and Inflammation
  • Cancer-related molecular mechanisms research

University Medical Center Groningen
2016-2025

University of Groningen
2016-2025

Institute for Asthma and Allergy
2010-2024

Dialyse Centrum Groningen
2020-2024

Duke University
2021

University College London
2021

Wellcome Sanger Institute
2020

Odense University Hospital
2017

The Netherlands Cancer Institute
2004-2009

Oncode Institute
2004-2008

Carly G.K. Ziegler Samuel J. Allon Sarah K. Nyquist Ian M. Mbano Vincent N. Miao and 95 more Constantine N. Tzouanas Yuming Cao Ashraf S. Yousif Julia Bals Blake M. Hauser Jared Feldman Christoph Muus Marc H. Wadsworth Samuel W. Kazer Travis K. Hughes Benjamin A. Doran G. James Gatter Marko Vukovic Faith Taliaferro Benjamin E. Mead Zhiru Guo Jennifer Wang Delphine Gras Magali Plaisant Meshal Ansari Ilias Angelidis Heiko Adler Jennifer M. S. Sucre Chase J. Taylor Brian Lin Avinash Waghray Vanessa Mitsialis Daniel F. Dwyer Kathleen M. Buchheit Joshua A. Boyce Nora A. Barrett Tanya M. Laidlaw Shaina L. Carroll Lucrezia Colonna Victor Tkachev Christopher W. Peterson Alison Yu Hengqi Zheng Hannah P. Gideon Caylin G. Winchell Philana Ling Lin Colin D. Bingle Scott B. Snapper Jonathan A. Kropski Fabian J. Theis Herbert B. Schiller Laure‐Emmanuelle Zaragosi Pascal Barbry Alasdair Leslie Hans‐Peter Kiem JoAnne L. Flynn Sarah M. Fortune Bonnie Berger Robert W. Finberg Leslie S. Kean Manuel Garber Aaron G. Schmidt Daniel Lingwood Alex K. Shalek José Ordovás-Montañés Nicholas E. Banovich Pascal Barbry Alvis Brāzma Tushar J. Desai Thu Elizabeth Duong Oliver Eickelberg Christine S. Falk Michael Farzan Ian A. Glass Muzlifah Haniffa Péter Horváth Deborah Hung Naftali Kaminski Mark A. Krasnow Jonathan A. Kropski Malte Kühnemund Robert Lafyatis Haeock Lee Sylvie Leroy Sten Linnarson Joakim Lundeberg Kerstin Meyer Alexander Misharin Martijn C. Nawijn Marko Nikolić José Ordovás-Montañés Dana Pe’er Joseph E. Powell Stephen R. Quake Jayaraj Rajagopal Purushothama Rao Tata Emma L. Rawlins Aviv Regev Paul A. Reyfman Mauricio Rojas

There is pressing urgency to understand the pathogenesis of severe acute respiratory syndrome coronavirus clade 2 (SARS-CoV-2), which causes disease COVID-19. SARS-CoV-2 spike (S) protein binds angiotensin-converting enzyme (ACE2), and in concert with host proteases, principally transmembrane serine protease (TMPRSS2), promotes cellular entry. The cell subsets targeted by tissues factors that regulate ACE2 expression remain unknown. Here, we leverage human, non-human primate, mouse...

10.1016/j.cell.2020.04.035 article EN cc-by Cell 2020-04-27

The recent advent of methods for high-throughput single-cell molecular profiling has catalyzed a growing sense in the scientific community that time is ripe to complete 150-year-old effort identify all cell types human body. Human Cell Atlas Project an international collaborative aims define terms distinctive profiles (such as gene expression profiles) and connect this information with classical cellular descriptions location morphology). An open comprehensive reference map state cells...

10.7554/elife.27041 article EN cc-by eLife 2017-12-05
Joana P. Bernardes Neha Mishra Florian Tran Thomas Bahmer Lena Best and 95 more Johanna I. Blase Dora Bordoni Jeanette Franzenburg Ulf Geisen Jonathan Josephs‐Spaulding Philipp Köhler Axel Künstner Elisa Rosati Anna C. Aschenbrenner Petra Bächer Nathan Baran Teide Jens Boysen Burkhard Brandt Niklas Bruse Jonathan Dörr Andreas Dräger Gunnar Elke David Ellinghaus Julia Fischer Michael Förster André Franke Sören Franzenburg Norbert Frey Anette Friedrichs Janina Fuß Andreas Glück Jacob Hamm Finn Hinrichsen Marc P. Hoeppner Simon Imm Ralf Junker Sina Kaiser Ying H. Kan Rainer Knoll Christoph Lange Georg Laue Clemens Lier Matthias Lindner Γεώργιος Μαρίνος Robert Markewitz Jacob Nattermann Rainer Noth Peter Pickkers Klaus F. Rabe Alina Renz Christoph Röcken Jan Rupp Annika Schaffarzyk Alexander Scheffold Jonas Schulte-Schrepping Domagoj Schunk Dirk Skowasch Thomas Ulas Klaus‐Peter Wandinger Michael Wittig Johannes Zimmermann Hauke Busch Bimba F. Hoyer Christoph Kaleta Jan Heyckendorf Matthijs Kox Jan Rybniker Stefan Schreiber Joachim L. Schultze Philip Rosenstiel Nicholas E. Banovich Tushar J. Desai Oliver Eickelberg Muzlifa Haniffa Péter Horváth Jonathan A. Kropski Robert Lafyatis Joakim Lundeberg Kerstin B. Meyer Martijn C. Nawijn Marko Nikolić José Ordovas Montañes Dana Pe’er Purushothama Rao Tata Emma L. Rawlins Aviv Regev Paul A. Reyfman Christos Samakovlis Joachim L. Schultze Alex K. Shalek Douglas P. Shepherd Jason R. Spence Sarah A. Teichmann Fabian J. Theis Alexander M. Tsankov Maarten van den Berge Michael von Papen Jeffrey A. Whitsett Laure‐Emmanuelle Zaragosi Angel Angelov

10.1016/j.immuni.2020.11.017 article EN publisher-specific-oa Immunity 2020-11-26
Lisa Sikkema Ciro Ramírez-Suástegui Daniel Strobl Tessa E. Gillett Luke Zappia and 92 more Elo Madissoon Nikolay S. Markov Laure‐Emmanuelle Zaragosi Yuge Ji Meshal Ansari Marie‐Jeanne Arguel Leonie Apperloo Martin Banchero Christophe Bécavin Marijn Berg Evgeny Chichelnitskiy Mei-I Chung Antoine Collin Aurore Gay Janine Gote-Schniering Baharak Hooshiar Kashani Kemal İnecik Manu Jain Theodore S. Kapellos Tessa Kole Sylvie Leroy Christoph H. Mayr Amanda J. Oliver Michael von Papen Lance Peter Chase J. Taylor Thomas Walzthoeni Chuan Xu Linh T. Bui Carlo De Donno Leander Dony Alen Faiz Minzhe Guo Austin J. Gutierrez Lukas Heumos Ni Huang Ignacio L. Ibarra Nathan D. Jackson Preetish Kadur Lakshminarasimha Murthy Mohammad Lotfollahi Tracy Tabib Carlos Talavera‐López Kyle J. Travaglini Anna Wilbrey-Clark Kaylee B. Worlock Masahiro Yoshida Yuexin Chen James S. Hagood Ahmed Agami Péter Horváth Joakim Lundeberg Charles‐Hugo Marquette Gloria Pryhuber Chistos Samakovlis Xin Sun Lorraine B. Ware Kun Zhang Maarten van den Berge Yohan Bossé Tushar J. Desai Oliver Eickelberg Naftali Kaminski Mark A. Krasnow Robert Lafyatis Marko Nikolić Joseph E. Powell Jayaraj Rajagopal Mauricio Rojas Orit Rozenblatt–Rosen Max A. Seibold Dean Sheppard Douglas P. Shepherd Don D. Sin Wim Timens Alexander M. Tsankov Jeffrey A. Whitsett Yan Xu Nicholas E. Banovich Pascal Barbry Thu Elizabeth Duong Christine S. Falk Kerstin B. Meyer Jonathan A. Kropski Dana Pe’er Herbert B. Schiller Purushothama Rao Tata Joachim L. Schultze Sara A. Teichmann Alexander V. Misharin Martijn C. Nawijn Malte D. Luecken Fabian J. Theis

Single-cell technologies have transformed our understanding of human tissues. Yet, studies typically capture only a limited number donors and disagree on cell type definitions. Integrating many single-cell datasets can address these limitations individual the variability present in population. Here we integrated Human Lung Cell Atlas (HLCA), combining 49 respiratory system into single atlas spanning over 2.4 million cells from 486 individuals. The HLCA presents consensus re-annotation with...

10.1038/s41591-023-02327-2 article EN cc-by Nature Medicine 2023-06-01

Cellular diversity of the lung endothelium has not been systematically characterized in humans. We provide a reference atlas human endothelial cells (ECs) to facilitate better understanding phenotypic and composition comprising endothelium.We reprocessed control single-cell RNA sequencing (scRNAseq) data from 6 datasets. EC populations were through iterative clustering with subsequent differential expression analysis. Marker genes validated by fluorescent microscopy situ hybridization....

10.1161/circulationaha.120.052318 article EN cc-by-nc-nd Circulation 2021-05-25

In recent years, functional genomics approaches combining genetic information with bulk RNA-sequencing data have identified the downstream expression effects of disease-associated risk factors through so-called quantitative trait locus (eQTL) analysis. Single-cell creates enormous opportunities for mapping eQTLs across different cell types and in dynamic processes, many which are obscured when using methods. Rapid increase throughput reduction cost per now allow this technology to be applied...

10.7554/elife.52155 article EN cc-by eLife 2020-03-09

The EMBL-EBI Expression Atlas is an added value knowledge base that enables researchers to answer the question of where (tissue, organism part, developmental stage, cell type) and under which conditions (disease, treatment, gender, etc) a gene or protein interest expressed. brings together data from >4500 expression studies >65 different species, across tissues. It makes these freely available in easy visualise form, after expert curation accurately represent intended experimental design,...

10.1093/nar/gkab1030 article EN cc-by Nucleic Acids Research 2021-11-19

ABSTRACT Organ- and body-scale cell atlases have the potential to transform our understanding of human biology. To capture variability present in population, these must include diverse demographics such as age ethnicity from both healthy diseased individuals. The growth size number single-cell datasets, combined with recent advances computational techniques, for first time makes it possible generate comprehensive large-scale through integration multiple datasets. Here, we integrated Human...

10.1101/2022.03.10.483747 preprint EN cc-by-nd bioRxiv (Cold Spring Harbor Laboratory) 2022-03-11

The Pim family of proto-oncogenes encodes a distinct class serine/threonine kinases consisting PIM1, PIM2, and PIM3. Although the genes are evolutionarily highly conserved, contribution PIM proteins to mammalian development is unclear. PIM1-deficient mice were previously described but showed only minor phenotypic aberrations. To assess role in physiology, compound knockout generated. Mice lacking expression Pim1, Pim2, Pim3 viable fertile. However, PIM-deficient show profound reduction body...

10.1128/mcb.24.13.6104-6115.2004 article EN Molecular and Cellular Biology 2004-06-16

GATA-3 is a zinc-finger transcription factor that essential for both early T cell development and Th2 differentiation. To quantify expression during in vivo the mouse, gene was targeted by insertion of lacZ reporter homologous recombination embryonic stem (ES) cells. Although we could detect GATA-3+ cells throughout thymus, proportions varied considerably between distinct differentiation stages. The two periods TCR α β recombination, which occur quiescent or slowly dividing cells, were...

10.1002/(sici)1521-4141(199906)29:06<1912::aid-immu1912>3.0.co;2-d article EN European Journal of Immunology 1999-06-01

Studies of SOCS-1-deficient mice have implicated Socs-1 in the suppression JAK-STAT (Janus tyrosine kinase-signal transducers and activators transcription) signaling T cell development. It has been suggested that levels protein may be regulated through proteasome pathway. Here we show interacts with members Pim family serine/threonine kinases thymocytes. Coexpression results phosphorylation stabilization protein. The are significantly reduced Pim-1(-/-), Pim-2(-/-) as compared wild-type...

10.1073/pnas.042035699 article EN Proceedings of the National Academy of Sciences 2002-02-19

Recent data indicate a role for airway epithelial necroptosis, regulated form of necrosis, and the associated release damage-associated molecular patterns (DAMPs) in development chronic obstructive pulmonary disease (COPD). DAMPs can activate pattern recognition receptors (PRRs), triggering innate immune responses. We hypothesized that cigarette smoke (CS)-induced necroptosis DAMP initiate inflammation COPD. Human bronchial BEAS-2B cells were exposed to extract (CSE), necrotic cell death...

10.1152/ajplung.00174.2015 article EN AJP Lung Cellular and Molecular Physiology 2015-12-31
Coming Soon ...