Correction to 'The thymocyte-specific RNA-binding protein Arpp21 provides TCR repertoire diversity by binding to the 3’-UTR and promoting Rag1 mRNA expression'

Autor: Meng Xu, Taku Ito-Kureha, Hyun-Seo Kang, Aleksandar Chernev, Timsse Raj, Kai P. Hoefig, Christine Hohn, Florian Giesert, Yinhu Wang, Wenliang Pan, Natalia Ziętara, Tobias Straub, Regina Feederle, Carolin Daniel, Barbara Adler, Julian König, Stefan Feske, George C. Tsokos, Wolfgang Wurst, Henning Urlaub, Michael Sattler, Jan Kisielow, F. Gregory Wulczyn, Marcin Łyszkiewicz, Vigo Heissmeyer

Publikováno v: Nature Communications, Vol 15, Iss 1, Pp 1-3 (2024)

Externí odkaz: https://doaj.org/article/9e89d380ba524171be8ac6b2c5c274ad

Characterising a homozygous two‐exon deletion in UQCRH: comparing human and mouse phenotypes

Autor: Silvia Vidali, Raffaele Gerlini, Kyle Thompson, Jill E Urquhart, Jana Meisterknecht, Juan Antonio Aguilar‐Pimentel, Oana V Amarie, Lore Becker, Catherine Breen, Julia Calzada‐Wack, Nirav F Chhabra, Yi‐Li Cho, Patricia da Silva‐Buttkus, René G Feichtinger, Kristine Gampe, Lillian Garrett, Kai P Hoefig, Sabine M Hölter, Elisabeth Jameson, Tanja Klein‐Rodewald, Stefanie Leuchtenberger, Susan Marschall, Philipp Mayer‐Kuckuk, Gregor Miller, Manuela A Oestereicher, Kristina Pfannes, Birgit Rathkolb, Jan Rozman, Charlotte Sanders, Nadine Spielmann, Claudia Stoeger, Marten Szibor, Irina Treise, John H Walter, Wolfgang Wurst, Johannes A Mayr, Helmut Fuchs, Ulrich Gärtner, Ilka Wittig, Robert W Taylor, William G Newman, Holger Prokisch, Valerie Gailus‐Durner, Martin Hrabě de Angelis

Publikováno v: EMBO Molecular Medicine, Vol 13, Iss 12, Pp 1-19 (2021)

Abstract Mitochondrial disorders are clinically and genetically diverse, with isolated complex III (CIII) deficiency being relatively rare. Here, we describe two affected cousins, presenting with recurrent episodes of severe lactic acidosis, hyperamm

Externí odkaz: https://doaj.org/article/341f02162d414b2e9fd51d3fc242e6ba

Characterising a homozygous two‐exon deletion in UQCRH : comparing human and mouse phenotypes

Autor: Elisabeth Jameson, Johannes A. Mayr, Manuela A. Oestereicher, John H. Walter, Juan Antonio Aguilar-Pimentel, Wolfgang Wurst, William G. Newman, Stefanie Leuchtenberger, Patricia da Silva-Buttkus, Jill E. Urquhart, Helmut Fuchs, Ilka Wittig, Robert W. Taylor, Silvia Vidali, René G. Feichtinger, Jana Meisterknecht, Martin Hrabě de Angelis, Lore Becker, Philipp Mayer-Kuckuk, Kai P. Hoefig, Yi-Li Cho, Catherine Breen, Nadine Spielmann, Marten Szibor, Raffaele Gerlini, Irina Treise, Lillian Garrett, Nirav Florian Chhabra, Oana V. Amarie, Kyle Thompson, Charlotte Sanders, Susan Marschall, Jan Rozman, Holger Prokisch, Kristine Gampe, Birgit Rathkolb, Sabine M. Hölter, Kristina Pfannes, Gregor Miller, Tanja Klein-Rodewald, Valerie Gailus-Durner, Julia Calzada-Wack, Ulrich Gärtner, Claudia Stoeger

Publikováno v: EMBO Molecular Medicine
Newman, W, Urquhart, J, Breen, C, Walter, J & Jameson, E 2021, ' Characterising a homozygous two-exon deletion in UQCRH: comparing human and mouse phenotypes ', EMBO Molecular Medicine, vol. 13, no. 12, e14397 . https://doi.org/10.15252/emmm.202114397
EMBO Mol. Med.:e14397 (2021)
EMBO molecular medicine 13(12), e14397 (2021). doi:10.15252/emmm.202114397
EMBO Molecular Medicine, Vol 13, Iss 12, Pp n/a-n/a (2021)

Mitochondrial disorders are clinically and genetically diverse, with isolated complex III (CIII) deficiency being relatively rare. Here, we describe two affected cousins, presenting with recurrent episodes of severe lactic acidosis, hyperammonaemia,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54043c9e401c3918feb0aba8928fcbc2
https://doi.org/10.15252/emmm.202114397

Induced miR‐99a expression represses Mtor cooperatively with miR‐150 to promote regulatory T‐cell differentiation

Autor: Anian Hiekel, K. Mark Ansel, Sebastian C. Warth, Vigo Heissmeyer, Ludger Klein, Karsten Kretschmer, Kai P. Hoefig, Sonja Schallenberg, Ksenija Jovanovic

Publikováno v: EMBO J. 34, 1195-1213 (2015)

Peripheral induction of regulatory T (Treg) cells provides essential protection from inappropriate immune responses. CD4 + T cells that lack endogenous miRNAs are impaired to differentiate into Treg cells, but the relevant miRNAs are unknown. We perf

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6090dde0e3a119de3023b0951aa06bb8
https://doi.org/10.15252/embj.201489589

A robust methodology to study urine microRNA as tumor marker: microRNA-126 and microRNA-182 are related to urinary bladder cancer

Autor: Alfred C. Feller, Georg Sczakiel, Dieter Jocham, Hartmut Merz, Jens M. Warnecke, Merle Hanke, Ingo Kausch, Kai P. Hoefig

Publikováno v: Urologic Oncology: Seminars and Original Investigations. 28:655-661

Objectives MicroRNAs have been shown to be related to specific types of malignant cell growth. In case of urothelial bladder cancer (BCa), novel noninvasive diagnosis is particularly required and it is attractive to consider, as urine is an easily av

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::203e0d91fb6e301d90ea26599dc8c1f8
https://doi.org/10.1016/j.urolonc.2009.01.027