Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Henrike L Sczakiel"'
Autor:
Cristina Lopez, Nikolai Schleussner, Stephan H. Bernhart, Kortine Kleinheinz, Stephanie Sungalee, Henrike L. Sczakiel, Helene Kretzmer, Umut H. Toprak, Selina Glaser, Rabea Wagener, Ole Ammerpohl, Susanne Bens, Maciej Giefing, Juan C. Gonzalez Sanchez, Gordana Apic, Daniel Hubschmann, Martin Janz, Markus Kreuz, Anja Mottok, Judith M. Muller, Julian Seufert, Steve Hoffmann, Jan O. Korbel, Robert B. Russell, Roland Schule, Lorenz Trumper, Wolfram Klapper, Bernhard Radlwimmer, Peter Lichter, Ralf Kuppers, Matthias Schlesner, Stephan Mathas, Reiner Siebert
Publikováno v:
Haematologica, Vol 108, Iss 2 (2022)
Histone methylation-modifiers, such as EZH2 and KMT2D, are recurrently altered in B-cell lymphomas. To comprehensively describe the landscape of alterations affecting genes encoding histone methylation-modifiers in lymphomagenesis we investigated who
Externí odkaz:
https://doaj.org/article/3d3b5d4cbb534e4eb3816d334f4e9a3c
Autor:
Aline Azabdaftari, Henrike L. Sczakiel, Magdalena Danyel, Benno Kohlmaier, Christoph J. Mache, Amelie Stalke, Eva‐Doreen Pfister, Julia Thumfart, Stephan Henning, A. S. Knisely, Philip Bufler
Publikováno v:
Liver International. 43:1089-1095
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e50c48572e709a62c5c7e54e4f60fb0e
https://doi.org/10.1111/liv.15563
https://doi.org/10.1111/liv.15563
Autor:
Henrike L. Sczakiel, Max Zhao, Brigitte Wollert-Wulf, Magdalena Danyel, Nadja Ehmke, Corinna Stoltenburg, Nadirah Damseh, Motee Al-Ashhab, Tugce B. Balci, Matthew Osmond, Andrea Andrade, Jens Schallner, Joseph Porrmann, Kimberly McDonald, Mingjuan Liao, Henry Oppermann, Konrad Platzer, Nadine Dierksen, Majid Mojarrad, Atieh Eslahi, Behnaz Bakaeean, Daniel G. Calame, James R. Lupski, Zahra Firoozfar, Seyed Mohammad Seyedhassani, Seyed Ahmad Mohammadi, Najwa Anwaar, Fatima Rahman, Dominik Seelow, Martin Janz, Denise Horn, Reza Maroofian, Felix Boschann
FINCA syndrome [MIM: 618278] is an autosomal recessive multisystem disorder characterized by fibrosis, neurodegeneration and cerebral angiomatosis. To date, 13 patients from nine families with biallelic NHLRC2 variants have been published. In all of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::57f4c30e125d8e7b4b33e25f77fcc089
http://edoc.mdc-berlin.de/23362/1/23362oa.pdf
http://edoc.mdc-berlin.de/23362/1/23362oa.pdf
Autor:
Felix Boschann, Daniel Acero Moreno, Martin A. Mensah, Henrike L. Sczakiel, Karolina Skipalova, Manuel Holtgrewe, Stefan Mundlos, Björn Fischer-Zirnsak
Publikováno v:
Journal of Human Genetics
Bilateral laryngeal abductor paralysis is a rare entity and the second most common cause of stridor in newborns. So far, no conclusive genetic or chromosomal aberration has been reported for X-linked isolated bilateral vocal cord paralysis, also refe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7f06b471bc1c0335941a2b9e68709b8
https://doi.org/10.1038/s10038-022-01018-z
https://doi.org/10.1038/s10038-022-01018-z
Autor:
Martin A. Mensah, Henri Niskanen, Alexandre P. Magalhaes, Shaon Basu, Martin Kircher, Henrike L. Sczakiel, Alisa M. V. Reiter, Jonas Elsner, Peter Meinecke, Saskia Biskup, Brian H. Y. Chung, Gregor Dombrowsky, Christel Eckmann-Scholz, Marc Phillip Hitz, Alexander Hoischen, Paul-Martin Holterhus, Wiebke Hülsemann, Kimia Kahrizi, Vera M. Kalscheuer, Anita Kan, Mandy Krumbiegel, Ingo Kurth, Jonas Leubner, Ann Carolin Longardt, Jörg D. Moritz, Hossein Najmabadi, Karolina Skipalova, Lot Snijders Blok, Andreas Tzschach, Eberhard Wiedersberg, Martin Zenker, Carla Garcia-Cabau, René Buschow, Xavier Salvatella, Matthew L. Kraushar, Stefan Mundlos, Almuth Caliebe, Malte Spielmann, Denise Horn, Denes Hnisz
Publikováno v:
Nature
Nature, 614, 7948, pp. 564-571
Nature, 614, 564-571
Nature, 614, 7948, pp. 564-571
Nature, 614, 564-571
Thousands of genetic variants in protein-coding genes have been linked to disease. However, the functional impact of most variants is unknown as they occur within intrinsically disordered protein regions that have poorly defined functions1–3. Intri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7d44f81500de5059b7ca491edb8534c
http://hdl.handle.net/2445/200283
http://hdl.handle.net/2445/200283
Autor:
Cristina, Lopez, Nikolai, Schleussner, Stephan H, Bernhart, Kortine, Kleinheinz, Stephanie, Sungalee, Henrike L, Sczakiel, Helene, Kretzmer, Umut H, Toprak, Selina, Glaser, Rabea, Wagener, Ole, Ammerpohl, Susanne, Bens, Maciej, Giefing, Juan C Gonzalez, Sanchez, Gordana, Apic, Daniel, Hubschmann, Martin, Janz, Markus, Kreuz, Anja, Mottok, Judith M, Muller, Julian, Seufert, Steve, Hoffmann, Jan O, Korbel, Robert B, Russell, Roland, Schule, Lorenz, Trumper, Wolfram, Klapper, Bernhard, Radlwimmer, Peter, Lichter, Ralf, Kuppers, Matthias, Schlesner, Stephan, Mathas, Reiner, Siebert
Publikováno v:
Haematologica.
Histone methylation-modifiers, like EZH2 and KMT2D, are recurrently altered in B-cell lymphomas. To comprehensively describe the landscape of alterations affecting genes encoding histone methylation-modifiers in lymphomagenesis we investigated whole
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9674233f991554afd14bb4f5decea79d
https://pubmed.ncbi.nlm.nih.gov/35522148
https://pubmed.ncbi.nlm.nih.gov/35522148
Autor:
Mariantonia Costanza, Wilhelm Woessmann, Claus Scheidereit, Suzanne D. Turner, Michael Hummel, Stephan Mathas, Linda von Hoff, Georg Lenz, Michael Grau, Antonia Niedobitek, Christian Hinze, Henrike L Sczakiel, Chiara Romagnani, Christine Damm-Welk, Franziska Hummel, Bernd Dörken, Korinna Jöhrens, Olaf Merkel, Huan-Chang Liang, Patrick R. Griffin, Martin Janz, Bernd Gillissen, Roberto Piva, Ioannis Anagnostopoulos, Dagmar Stoiber, Eva Kaergel, Pawel Durek, Lukas Kenner, Nikolai Schleussner
Publikováno v:
Leukemia
BASE-Bielefeld Academic Search Engine
BASE-Bielefeld Academic Search Engine
Transcription factor AP-1 is constitutively activated and IRF4 drives growth and survival in ALK(+) and ALK(–) anaplastic large cell lymphoma (ALCL). Here we demonstrate high-level BATF and BATF3 expression in ALCL. Both BATFs bind classical AP-1 m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83a31559cec1df4c83d4f1852b904093
https://www.repository.cam.ac.uk/handle/1810/274128
https://www.repository.cam.ac.uk/handle/1810/274128