Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Heinrich, Schrewe"'
Autor:
Marco Eijken, A. Michaela Krautzberger, Manuela Scholze-Wittler, Bianca Boers-Sijmons, Marijke Koedam, Barbara Kosiol, Heinrich Schrewe, Johannes P. van Leeuwen, Bram C. van der Eerden
Publikováno v:
Bone Reports, Vol 22, Iss , Pp 101792- (2024)
Vasorin (Vasn) is a pleiotropic molecule involved in various physiological and pathological conditions, including cancer. Vasn has also been detected in bone cells of developing skeletal tissues but no function for Vasn in bone metabolism has been im
Externí odkaz:
https://doaj.org/article/fb30148d48904876972ed4fe2a7c03eb
Autor:
Jürgen Stumm, Pedro Vallecillo-García, Sophie Vom Hofe-Schneider, David Ollitrault, Heinrich Schrewe, Aris N. Economides, Giovanna Marazzi, David A. Sassoon, Sigmar Stricker
Publikováno v:
Stem Cell Research, Vol 32, Iss , Pp 8-16 (2018)
Fibro-adipogenic progenitors (FAPs) are resident mesenchymal progenitors in adult skeletal muscle that support muscle repair, but also give rise to fibrous and adipose infiltration in response to disease and chronic injury. FAPs are identified using
Externí odkaz:
https://doaj.org/article/998eb6efcebd4550a4742b5099f18bf3
Autor:
Anne-Laure Bonnet, Catherine Chaussain, Isabelle Broutin, Gaël Y. Rochefort, Heinrich Schrewe, Céline Gaucher
Publikováno v:
Frontiers in Medicine, Vol 5 (2018)
First described in 1988, vasorin (VASN) is a transmembrane glycoprotein expressed during early mouse development, and with a less extent, in various organs and tissues (e.g., kidney, aorta, and brain) postnatally. Vasn KO mice die after 3 weeks of li
Externí odkaz:
https://doaj.org/article/b41eea45aaf84f48a3f4585f1bba24cf
Autor:
Teng-Wei Huang, Amrita A. Iyer, Melissa M. McGovern, Jeanne M. Manalo, Kevin K. Ohlemiller, Navish A. Bosquez Huerta, Heinrich Schrewe, Benjamin Deneen, Junsung Woo, Andrew K. Groves, Fredrick A. Pereira
Publikováno v:
J Neurosci
The Journal of Neuroscience
The Journal of Neuroscience
Mediator protein complex subunit 12 (Med12) is a core component of the basal transcriptional apparatus and plays a critical role in the development of many tissues. Mutations in Med12 are associated with X-linked intellectual disability syndromes and
Autor:
Matthieu M Vermeren, Qifeng Zhang, Elizabeth Smethurst, Anne Segonds-Pichon, Heinrich Schrewe, Michael J O Wakelam
Publikováno v:
PLoS ONE, Vol 11, Iss 9, p e0162814 (2016)
Phospholipase D2 (PLD2) is an enzyme that produces phosphatidic acid (PA), a lipid messenger molecule involved in a number of cellular events including, through its membrane curvature properties, endocytosis. The PLD2 knock out (PLD2KO) mouse has bee
Externí odkaz:
https://doaj.org/article/08c6d72cd8164d30b2a4638761b5cd4a
Autor:
Loïc Louvet, Gaëlle Lenglet, A. Michaela Krautzberger, Romuald Mentaverri, Frédéric Hague, Clara Kowalewski, Nassim Mahtal, Julie Lesieur, Anne‐Laure Bonnet, Caroline Andrique, Céline Gaucher, Cathy Gomila, Heinrich Schrewe, Pierre‐Louis Tharaux, Said Kamel, Catherine Chaussain, Isabelle Six
Publikováno v:
Journal of Cellular Physiology
Journal of Cellular Physiology, 2022, ⟨10.1002/jcp.30838⟩
Journal of Cellular Physiology, 2022, ⟨10.1002/jcp.30838⟩
International audience; Within the cardiovascular system, the protein vasorin (Vasn) is predominantly expressed by vascular smooth muscle cells (VSMCs) in the coronary arteries and the aorta. Vasn knockout (Vasn(-/-) ) mice die within 3 weeks of birt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::127ad9bb4d4cd3e79beff4793a7792cb
https://u-picardie.hal.science/hal-03740510
https://u-picardie.hal.science/hal-03740510
Autor:
Farhat L Khanim, Rachel E Hayden, Jane Birtwistle, Alessia Lodi, Stefano Tiziani, Nicholas J Davies, Jon P Ride, Mark R Viant, Ulrich L Gunther, Joanne C Mountford, Heinrich Schrewe, Richard M Green, Jim A Murray, Mark T Drayson, Chris M Bunce
Publikováno v:
PLoS ONE, Vol 4, Iss 12, p e8147 (2009)
BackgroundThe majority of acute myeloid leukaemia (AML) patients are over sixty years of age. With current treatment regimens, survival rates amongst these, and also those younger patients who relapse, remain dismal and novel therapies are urgently r
Externí odkaz:
https://doaj.org/article/9636c763c1a443abb133d3874ed80303
Autor:
Joanna Segal, Lillian Garrett, Manuela Scholze-Wittler, Dirk H. Busch, Bernd Timmermann, Eckhard Wolf, Markus Ralser, Thure Adler, Nana-Maria Grüning, Martin Hrabě de Angelis, Helmut Fuchs, Jan Rozman, Thomas Klopstock, Antje Krüger, Julia Calzada-Wack, Michael Mülleder, Sabine M. Hölter, Steve Michel, Hans Lehrach, Ingo Voigt, Ludger Hartmann, Mariia Yuneva, Frauke Neff, Ildiko Racz, Lore Becker, Martin Klingenspor, Ralf Fischer, Wolfgang Wurst, Heinrich Schrewe, Valerie Gailus-Durner, Beata Lukaszewska‐McGreal, Birgit Rathkolb
Publikováno v:
Journal of Inherited Metabolic Disease
Journal of inherited metabolic disease 42(5), 839-849 (2019). doi:10.1002/jimd.12105
J. Inherit. Metab. Dis. 42, 839-849 (2019)
Journal of inherited metabolic disease 42(5), 839-849 (2019). doi:10.1002/jimd.12105
J. Inherit. Metab. Dis. 42, 839-849 (2019)
Triosephosphate isomerase (TPI) deficiency is a fatal genetic disorder characterized by hemolytic anemia and neurological dysfunction. Although the enzyme defect in TPI was discovered in the 1960s, the exact etiology of the disease is still debated.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8cc9b7daee234fa033a69f5666742a4f
https://mediatum.ub.tum.de/doc/1539484/document.pdf
https://mediatum.ub.tum.de/doc/1539484/document.pdf
Autor:
Sigmar Stricker, David Sassoon, Sophie vom Hofe-Schneider, Pedro Vallecillo Garcia, David Ollitrault, Jürgen Stumm, Aris N. Economides, Heinrich Schrewe, Giovanna Marazzi
Publikováno v:
Stem Cell Research
Stem Cell Research, Elsevier, 2018, 32, pp.8-16. ⟨10.1016/j.scr.2018.08.010⟩
Stem Cell Research, Vol 32, Iss, Pp 8-16 (2018)
Stem Cell Research, Elsevier, 2018, 32, pp.8-16. ⟨10.1016/j.scr.2018.08.010⟩
Stem Cell Research, Vol 32, Iss, Pp 8-16 (2018)
Fibro-adipogenic progenitors (FAPs) are resident mesenchymal progenitors in adult skeletal muscle that support muscle repair, but also give rise to fibrous and adipose infiltration in response to disease and chronic injury. FAPs are currently identif
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b92da3c92aa7bf01aaebb28bbe4ee30
https://hal.sorbonne-universite.fr/hal-01908913
https://hal.sorbonne-universite.fr/hal-01908913
Autor:
María Sánchez-Díaz, Heinrich Schrewe, Jasper Mullenders, Markus Schober, Leonela Amoasii, Iannis Aifantis, Ramya Raviram, Stephanie Lau, Maria Guillamot, Pedro P. Rocha, Beatriz Aranda-Orgilles, Avik Choudhuri, Ricardo Saldaña-Meyer, Eirini Trompouki, Eric Wang, Aristotelis Tsirigos, Jane A. Skok, Kun Wang, Leonard I. Zon, Anne Fassl, Nan Zhang, Danny Reinberg, Piotr Sicinski, Clarisse Kayembe
Publikováno v:
Cell Stem Cell
Hematopoietic-specific transcription factors require coactivators to communicate with the general transcription machinery and establish transcriptional programs that maintain hematopoietic stem cell (HSC) self-renewal, promote differentiation, and pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe77e3d89e8ccee1fbb37099beeba41c
https://hdl.handle.net/11858/00-001M-0000-002C-A8BC-C
https://hdl.handle.net/11858/00-001M-0000-002C-A8BC-C