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Items: 1 to 20 of 80

1.
Absence of the RING domain in MID1 results in patterning defects in the developing human brain
Sarah Frank, Elisa Gabassi, Stephan Käseberg, Marco Bertin, Lea Zografidou, Daniela Pfeiffer, Heiko Brennenstuhl, Sven Falk, Marisa Karow, Susann Schweiger
Life Sci Alliance. 2024 Apr; 7(4): e202302288. Published online 2024 Jan 18. doi: 10.26508/lsa.202302288
PMCID:
PMC10796562
AbstractArticlePDF–2.9M
2.
Opitz GBBB syndrome with total anomalous pulmonary venous connection: A new MID1 gene variant
Maryangel Perea‐Cabrera, Javier T. Granados‐Riveron, Begoña Segura‐Stanford, Liliana M. Moreno‐Vargas, Diego Prada‐Gracia, Mari C. Moran‐Espinosa, Julio Erdmenger, Hector Diaz‐Garcia, Rocío Sánchez‐Urbina
Mol Genet Genomic Med. 2023 Sep; 11(9): e2234. Published online 2023 Jul 27. doi: 10.1002/mgg3.2234
PMCID:
PMC10496055
AbstractArticlePDF–12M
3.
The role of anillin/Mid1p during medial division and cytokinesis: from fission yeast to cancer cells
Imane M. Rezig, Wandiahyel G. Yaduma, Gwyn W. Gould, Christopher J. McInerny
Cell Cycle. 2023; 22(6): 633–644. Published online 2022 Nov 25. doi: 10.1080/15384101.2022.2147655
PMCID:
PMC9980708
AbstractArticlePDF–1.4M
4.
A Genetics-First Approach Revealed Monogenic Disorders in Patients With ARM and VACTERL Anomalies
Romy van de Putte, Gabriel C. Dworschak, Erwin Brosens, Heiko M. Reutter, Carlo L. M. Marcelis, Rocio Acuna-Hidalgo, Nehir E. Kurtas, Marloes Steehouwer, Sally L. Dunwoodie, Eberhard Schmiedeke, Stefanie Märzheuser, Nicole Schwarzer, Alice S. Brooks, Annelies de Klein, Cornelius E. J. Sloots, Dick Tibboel, Giulia Brisighelli, Anna Morandi, Maria F. Bedeschi, Michael D. Bates, Marc A. Levitt, Alberto Peña, Ivo de Blaauw, Nel Roeleveld, Han G. Brunner, Iris A. L. M. van Rooij, Alexander Hoischen
Front Pediatr. 2020; 8: 310. Published online 2020 Jun 23. doi: 10.3389/fped.2020.00310
PMCID:
PMC7324789
AbstractArticlePDF–233K
5.
Two Novel Pathogenic MID1 Variants and Genotype-Phenotype Correlation Reanalysis in X-Linked Opitz G/BBB Syndrome
Nuno Maia, Maria J. Nabais Sá, Nataliya Tkachenko, Gabriela Soares, Isabel Marques, Bárbara Rodrigues, Ana M. Fortuna, Rosário Santos, Arjan P.M. de Brouwer, Paula Jorge
Mol Syndromol. 2017 Dec; 9(1): 45–51. Published online 2017 Aug 29. doi: 10.1159/000479177
PMCID:
PMC5803688
AbstractArticlePDF–1.0M
6.
Molecular Dynamics Simulation Reveals Insights into the Mechanism of Unfolding by the A130T/V Mutations within the MID1 Zinc-Binding Bbox1 Domain
Yunjie Zhao, Chen Zeng, Michael A. Massiah
PLoS One. 2015; 10(4): e0124377. Published online 2015 Apr 13. doi: 10.1371/journal.pone.0124377
PMCID:
PMC4395243
AbstractArticlePDF–3.3M
7.
XLOS-Observed Mutations of MID1 Bbox1 Domain Cause Domain Unfolding
Katharine M. Wright, Kuanlin Wu, Omotolani Babatunde, Haijuan Du, Michael A. Massiah
PLoS One. 2014; 9(9): e107537. Published online 2014 Sep 12. doi: 10.1371/journal.pone.0107537
PMCID:
PMC4162623
AbstractArticlePDF–1.2M
8.
X-linked Opitz G/BBB Syndrome: Identification of a Novel Mutation and Prenatal Diagnosis in a Korean Family
Hyun-Jung Cho, Mee-Yong Shin, Kang-Mo Ahn, Sang Il Lee, Hee-Jin Kim, Chang-Seok Ki, Jong-Won Kim
J Korean Med Sci. 2006 Oct; 21(5): 790–793. Published online 2006 Oct 31. doi: 10.3346/jkms.2006.21.5.790
PMCID:
PMC2721984
AbstractArticlePDF–114K
9.
Widely variable endogenous retroviral methylation levels in human placenta
Daphne Reiss, Ying Zhang, Dixie L. Mager
Nucleic Acids Res. 2007 Jul; 35(14): 4743–4754. Published online 2007 Jul 7. doi: 10.1093/nar/gkm455
PMCID:
PMC1950553
AbstractArticlePDF–385K
10.
Opitz G/BBB syndrome in Xp22: mutations in the MID1 gene cluster in the carboxy-terminal domain.
K Gaudenz, E Roessler, N Quaderi, B Franco, G Feldman, D L Gasser, B Wittwer, J Horst, E Montini, J M Opitz, A Ballabio, M Muenke
Am J Hum Genet. 1998 Sep; 63(3): 703–710. doi: 10.1086/302010
Correction in:
Am J Hum Genet, volume 63 on page 1571
PMCID:
PMC1377398
Abstract
11.
The Opitz syndrome gene product, MID1, associates with microtubules
Susann Schweiger, John Foerster, Tanja Lehmann, Vanessa Suckow, Yves A. Muller, Gerald Walter, Theresa Davies, Helen Porter, Hans van Bokhoven, Peter W. Lunt, Peter Traub, Hans-Hilger Ropers
Proc Natl Acad Sci U S A. 1999 Mar 16; 96(6): 2794–2799. doi: 10.1073/pnas.96.6.2794
PMCID:
PMC15848
AbstractArticlePDF–255K
12.
Erdr1 Drives Macrophage Programming via Dynamic Interplay with YAP1 and Mid1
Yuhang Wang
Immunohorizons. 2024 Feb 1; 8(2): 198–213. Published online 2024 Feb 23. doi: 10.4049/immunohorizons.2400004
PMCID:
PMC10916360
AbstractArticlePDF–2.5M
13.
TRIM18-Regulated STAT3 Signaling Pathway via PTP1B Promotes Renal Epithelial–Mesenchymal Transition, Inflammation, and Fibrosis in Diabetic Kidney Disease
Qi Chen, Chan Gao, Ming Wang, Xiao Fei, Ning Zhao
Front Physiol. 2021; 12: 709506. Published online 2021 Aug 9. doi: 10.3389/fphys.2021.709506
PMCID:
PMC8381599
AbstractArticlePDF–4.4M
14.
Osterix promotes the migration and angiogenesis of breast cancer by upregulation of S100A4 expression
Shuang Qu, Jiahui Wu, Qianyi Bao, Bing Yao, Rui Duan, Xiang Chen, Lingyun Li, Hongyan Yuan, Yucui Jin, Changyan Ma
J Cell Mol Med. 2019 Feb; 23(2): 1116–1127. Published online 2018 Nov 18. doi: 10.1111/jcmm.14012
PMCID:
PMC6349213
AbstractArticlePDF–2.4M
15.
Resveratrol induces dephosphorylation of Tau by interfering with the MID1-PP2A complex
Susann Schweiger, Frank Matthes, Karen Posey, Eva Kickstein, Stephanie Weber, Moritz M. Hettich, Sandra Pfurtscheller, Dan Ehninger, Rainer Schneider, Sybille Krauß
Sci Rep. 2017; 7: 13753. Published online 2017 Oct 23. doi: 10.1038/s41598-017-12974-4
PMCID:
PMC5653760
AbstractArticlePDF–2.6M
16.
A hormone-dependent feedback-loop controls androgen receptor levels by limiting MID1, a novel translation enhancer and promoter of oncogenic signaling
Andrea Köhler, Ümmühan Demir, Eva Kickstein, Sybille Krauss, Johanna Aigner, Beatriz Aranda-Orgillés, Antonios I Karagiannidis, Clemens Achmüller, Huajie Bu, Andrea Wunderlich, Michal-Ruth Schweiger, Georg Schaefer, Susann Schweiger, Helmut Klocker, Rainer Schneider
Mol Cancer. 2014; 13: 146. Published online 2014 Jun 9. doi: 10.1186/1476-4598-13-146
PMCID:
PMC4074869
AbstractArticlePDF–1.8M
17.
EXOME SEQUENCING AND DIFFUSION TENSOR IMAGING IN DEVELOPMENTAL DISABILITIES
Senthil K Sundaram, AHM M Huq, Tammy Hsia, Harry T Chugani
Pediatr Res. Author manuscript; available in PMC 2015 Mar 1.
Published in final edited form as: Pediatr Res. 2014 Mar; 75(3): 443–447. Published online 2013 Dec 6. doi: 10.1038/pr.2013.234
PMCID:
PMC3943710
AbstractArticlePDF–397K
18.
The MID1 E3 Ligase Catalyzes the Polyubiquitination of Alpha4 (α4), a Regulatory Subunit of Protein Phosphatase 2A (PP2A): NOVEL INSIGHTS INTO MID1-MEDIATED REGULATION of PP2A
Haijuan Du, Yongzhao Huang, Manar Zaghlula, Erica Walters, Timothy C. Cox, Michael A. Massiah
J Biol Chem. 2013 Jul 19; 288(29): 21341–21350. Published online 2013 Jun 5. doi: 10.1074/jbc.M113.481093
PMCID:
PMC3774402
AbstractArticlePDF–1.7M
19.
NMR Studies of the C-Terminus of alpha4 Reveal Possible Mechanism of Its Interaction with MID1 and Protein Phosphatase 2A
Haijuan Du, Michael A. Massiah
PLoS One. 2011; 6(12): e28877. Published online 2011 Dec 14. doi: 10.1371/journal.pone.0028877
PMCID:
PMC3237570
AbstractArticlePDF–1.0M
20.
Protein Phosphatase 2A (PP2A)-specific Ubiquitin Ligase MID1 Is a Sequence-dependent Regulator of Translation Efficiency Controlling 3-Phosphoinositide-dependent Protein Kinase-1 (PDPK-1)
Beatriz Aranda-Orgillés, Désirée Rutschow, Raphael Zeller, Antonios I. Karagiannidis, Andrea Köhler, Changwei Chen, Timothy Wilson, Sven Krause, Stefan Roepcke, David Lilley, Rainer Schneider, Susann Schweiger
J Biol Chem. 2011 Nov 18; 286(46): 39945–39957. Published online 2011 Sep 19. doi: 10.1074/jbc.M111.224451
PMCID:
PMC3220588
AbstractArticlePDF–2.6M

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