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368 results for Methionine+-+genetics

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The Brain-Derived Neurotrophic Factor Val66Met Polymorphism Moderates an Effect of Physical Activity on Working Memory Performance
Author / Creator:Erickson, Kirk I. ; Banducci, Sarah E. ; Weinstein, Andrea M. ; MacDonald, Angus W. ; Ferrell, Robert E. ; Halder, Indrani ; Flory, Janine D. ; Manuck, Stephen B.
Publisher:Los Angeles, CA: SAGE Publications
Journal title:Psychological science, 2013-09, Vol.24 (9), p.1770-1779
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A genetic model of methionine restriction extends Drosophila health- and lifespan
Author / Creator:Parkhitko, Andrey A. ; Wang, Lin ; Filine, Elizabeth ; Jouandin, Patrick ; Leshchiner, Dmitry ; Binari, Richard ; Asara, John M. ; Rabinowitz, Joshua D. ; Perrimon, Norbert
Publisher:United States: National Academy of Sciences
Journal title:Proceedings of the National Academy of Sciences - PNAS, 2021-10, Vol.118 (40), p.1-12
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Inhibition of PRC2 Activity by a Gain-of-Function H3 Mutation Found in Pediatric Glioblastoma
Author / Creator:Lewis, Peter W. ; Müller, Manuel M. ; Koletsky, Matthew S. ; Cordero, Francisco ; Lin, Shu ; Banaszynski, Laura A. ; Garcia, Benjamin A. ; Muir, Tom W. ; Becher, Oren J. ; Allis, C. David
Publisher:United States: American Association for the Advancement of Science
Journal title:Science (American Association for the Advancement of Science), 2013-05, Vol.340 (6134), p.857-861
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Histone H3K36 mutations promote sarcomagenesis through altered histone methylation landscape
Author / Creator:Lu, Chao ; Jain, Siddhant U. ; Hoelper, Dominik ; Bechet, Denise ; Molden, Rosalynn C. ; Ran, Leili ; Murphy, Devan ; Venneti, Sriram ; Hameed, Meera ; Pawel, Bruce R. ; Wunder, Jay S. ; Dickson, Brendan C. ; Lundgren, Stefan M. ; Jani, Krupa S. ; De Jay, Nicolas ; Papillon-Cavanagh, Simon ; Andrulis, Irene L. ; Sawyer, Sarah L. ; Grynspan, David ; Turcotte, Robert E. ; Nadaf, Javad ; Fahiminiyah, Somayyeh ; Muir, Tom W. ; Majewski, Jacek ; Thompson, Craig B. ; Chi, Ping ; Garcia, Benjamin A. ; Allis, C. David ; Jabado, Nada ; Lewis, Peter W.
Publisher:United States: American Association for the Advancement of Science
Journal title:Science (American Association for the Advancement of Science), 2016-05, Vol.352 (6287), p.844-849
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H3K27M induces defective chromatin spread of PRC2-mediated repressive H3K27me2/me3 and is essential for glioma tumorigenesis
Author / Creator:Harutyunyan, Ashot S. ; Krug, Brian ; Chen, Haifen ; Papillon-Cavanagh, Simon ; Zeinieh, Michele ; De Jay, Nicolas ; Deshmukh, Shriya ; Chen, Carol C. L. ; Belle, Jad ; Mikael, Leonie G. ; Marchione, Dylan M. ; Li, Rui ; Nikbakht, Hamid ; Hu, Bo ; Cagnone, Gael ; Cheung, Warren A. ; Mohammadnia, Abdulshakour ; Bechet, Denise ; Faury, Damien ; McConechy, Melissa K ; Pathania, Manav ; Jain, Siddhant U. ; Ellezam, Benjamin ; Weil, Alexander G. ; Montpetit, Alexandre ; Salomoni, Paolo ; Pastinen, Tomi ; Lu, Chao ; Lewis, Peter W. ; Garcia, Benjamin A. ; Kleinman, Claudia L. ; Jabado, Nada ; Majewski, Jacek
Publisher:London: Nature Publishing Group UK
Journal title:Nature communications, 2019-03, Vol.10 (1), p.1262-13, Article 1262
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Guidelines for diagnosis and management of the cobalamin-related remethylation disorders cblC, cblD, cblE, cblF, cblG, cblJ and MTHFR deficiency
Author / Creator:Huemer, Martina ; Diodato, Daria ; Schwahn, Bernd ; Schiff, Manuel ; Bandeira, Anabela ; Benoist, Jean-Francois ; Burlina, Alberto ; Cerone, Roberto ; Couce, Maria L. ; Garcia-Cazorla, Angeles ; la Marca, Giancarlo ; Pasquini, Elisabetta ; Vilarinho, Laura ; Weisfeld-Adams, James D. ; Kožich, Viktor ; Blom, Henk ; Baumgartner, Matthias R. ; Dionisi-Vici, Carlo
Publisher:Dordrecht: Springer Netherlands
Journal title:Journal of inherited metabolic disease, 2017-01, Vol.40 (1), p.21-48
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MFN2 agonists reverse mitochondrial defects in preclinical models of Charcot-Marie-Tooth disease type 2A
Author / Creator:Rocha, Agostinho G. ; Franco, Antonietta ; Krezel, Andrzej M. ; Rumsey, Jeanne M. ; Alberti, Justin M. ; Knight, William C. ; Biris, Nikolaos ; Zacharioudakis, Emmanouil ; Janetka, James W. ; Baloh, Robert H. ; Kitsis, Richard N. ; Mochly-Rosen, Daria ; Townsend, R. Reid ; Gavathiotis, Evripidis ; Dorn, Gerald W.
Publisher:United States: The American Association for the Advancement of Science
Journal title:Science (American Association for the Advancement of Science), 2018-04, Vol.360 (6386), p.336-341
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Evolution of bidirectional costly mutualism from byproduct consumption
Author / Creator:Harcombe, William R. ; Chacón, Jeremy M. ; Adamowicz, Elizabeth M. ; Chubiz, Lon M. ; Marx, Christopher J.
Publisher:United States: National Academy of Sciences
Journal title:Proceedings of the National Academy of Sciences - PNAS, 2018-11, Vol.115 (47), p.12000-12004
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Long-term effects of tafamidis for the treatment of transthyretin familial amyloid polyneuropathy
Author / Creator:Coelho, Teresa ; Maia, Luis F. ; da Silva, Ana Martins ; Cruz, Márcia W. ; Planté-Bordeneuve, Violaine ; Suhr, Ole B. ; Conceiçao, Isabel ; Schmidt, Hartmut H.-J. ; Trigo, Pedro ; Kelly, Jeffery W. ; Labaudinière, Richard ; Chan, Jason ; Packman, Jeff ; Grogan, Donna R.
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Journal of neurology, 2013-11, Vol.260 (11), p.2802-2814
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Interaction between stress and the BDNF Val66Met polymorphism in depression: a systematic review and meta-analysis
Author / Creator:Hosang, Georgina M ; Shiles, Celia ; Tansey, Katherine E ; McGuffin, Peter ; Uher, Rudolf
Publisher:England: BioMed Central
Journal title:BMC medicine, 2014-01, Vol.12, p.7-7
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Methionine in Proteins: It’s Not Just for Protein Initiation Anymore
Author / Creator:Lim, Jung Mi ; Kim, Geumsoo ; Levine, Rodney L.
Publisher:New York: Springer US
Journal title:Neurochemical research, 2019-01, Vol.44 (1), p.247-257
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BDNF pro-peptide actions facilitate hippocampal LTD and are altered by the common BDNF polymorphism Val66Met
Author / Creator:Mizui, Toshiyuki ; Ishikawa, Yasuyuki ; Kumanogoh, Haruko ; Lume, Maria ; Matsumoto, Tomoya ; Hara, Tomoko ; Yamawaki, Shigeto ; Takahashi, Masami ; Shiosaka, Sadao ; Itami, Chiaki ; Uegaki, Koichi ; Saarma, Mart ; Kojima, Masami
Publisher:United States: National Academy of Sciences
Journal title:Proceedings of the National Academy of Sciences - PNAS, 2015-06, Vol.112 (23), p.E3067-E3074
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Histone H3 lysine-to-methionine mutants as a paradigm to study chromatin signaling
Author / Creator:Herz, Hans-Martin ; Morgan, Marc ; Gao, Xin ; Jackson, Jessica ; Rickels, Ryan ; Swanson, Selene K. ; Florens, Laurence ; Washburn, Michael P. ; Eissenberg, Joel C. ; Shilatifard, Ali
Publisher:United States: American Association for the Advancement of Science
Journal title:Science (American Association for the Advancement of Science), 2014-08, Vol.345 (6200), p.1065-1070
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Specific detection of methionine 27 mutation in histone 3 variants (H3K27M) in fixed tissue from high-grade astrocytomas
Author / Creator:Bechet, Denise ; Gielen, Gerrit G. H. ; Korshunov, Andrey ; Pfister, Stefan M. ; Rousso, Caterina ; Faury, Damien ; Fiset, Pierre-Olivier ; Benlimane, Naciba ; Lewis, Peter W. ; Lu, Chao ; David Allis, C. ; Kieran, Mark W. ; Ligon, Keith L. ; Pietsch, Torsten ; Ellezam, Benjamin ; Albrecht, Steffen ; Jabado, Nada
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Acta neuropathologica, 2014-11, Vol.128 (5), p.733-741
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Deletion of the initial methionine codon of the Tmem95 gene causes subfertility, but not complete infertility, in male mice
Author / Creator:Inoue, Naokazu ; Wada, Ikuo
Publisher:United States: Society for the Study of Reproduction
Journal title:Biology of reproduction, 2022-03, Vol.106 (3), p.378-381
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Evidence of H3 K27M mutations in posterior fossa ependymomas
Author / Creator:Gessi, Marco ; Capper, David ; Sahm, Felix ; Huang, Kristin ; von Deimling, Andreas ; Tippelt, Stephan ; Fleischhack, Gudrun ; Scherbaum, Daniel ; Alfer, Joachim ; Juhnke, Björn-Ole ; von Hoff, Katja ; Rutkowski, Stefan ; Warmuth-Metz, Monika ; Chavez, Lukas ; Pfister, Stefan M. ; Pietsch, Torsten ; Jones, David T. W. ; Sturm, Dominik
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Acta neuropathologica, 2016-10, Vol.132 (4), p.635-637
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Adult Brainstem Gliomas With H3K27M Mutation: Radiology, Pathology, and Prognosis
Author / Creator:Daoud, Elena V ; Rajaram, Veena ; Cai, Chunyu ; Oberle, Robert J ; Martin, Gregory R ; Raisanen, Jack M ; White, Charles L ; Foong, Chan ; Mickey, Bruce E ; Pan, Edward ; Hatanpaa, Kimmo J
Publisher:England: Oxford University Press
Journal title:Journal of neuropathology and experimental neurology, 2018-04, Vol.77 (4), p.302-311
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Deep learning tools predict variants in disordered regions with lower sensitivity
Author / Creator:Luppino, Federica ; Lenz, Swantje ; Chow, Chi Fung Willis ; Toth-Petroczy, Agnes
Publisher:England: BioMed Central Ltd
Journal title:BMC genomics, 2025-04, Vol.26 (1), p.367-16, Article 367
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Brain-Derived Neurotrophic Factor Val66Met Human Polymorphism Impairs the Beneficial Exercise-Induced Neurobiological Changes in Mice
Author / Creator:Ieraci, Alessandro ; Madaio, Alessandro I ; Mallei, Alessandra ; Lee, Francis S ; Popoli, Maurizio
Publisher:England: Nature Publishing Group
Journal title:Neuropsychopharmacology (New York, N.Y.), 2016-12, Vol.41 (13), p.3070-3079
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Incorporation of non-canonical amino acids into the developing murine proteome
Author / Creator:Calve, Sarah ; Witten, Andrew J. ; Ocken, Alexander R. ; Kinzer-Ursem, Tamara L.
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2016-08, Vol.6 (1), p.32377-32377, Article 32377
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The Brain-Derived Neurotrophic Factor Val66Met Polymorphism Moderates an Effect of Physical Activity on Working Memory Performance

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A genetic model of methionine restriction extends Drosophila health- and lifespan

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Inhibition of PRC2 Activity by a Gain-of-Function H3 Mutation Found in Pediatric Glioblastoma

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Histone H3K36 mutations promote sarcomagenesis through altered histone methylation landscape

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H3K27M induces defective chromatin spread of PRC2-mediated repressive H3K27me2/me3 and is essential for glioma tumorigenesis

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Guidelines for diagnosis and management of the cobalamin-related remethylation disorders cblC, cblD, cblE, cblF, cblG, cblJ and MTHFR deficiency

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MFN2 agonists reverse mitochondrial defects in preclinical models of Charcot-Marie-Tooth disease type 2A

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Evolution of bidirectional costly mutualism from byproduct consumption

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Long-term effects of tafamidis for the treatment of transthyretin familial amyloid polyneuropathy

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Interaction between stress and the BDNF Val66Met polymorphism in depression: a systematic review and meta-analysis

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Methionine in Proteins: It’s Not Just for Protein Initiation Anymore

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BDNF pro-peptide actions facilitate hippocampal LTD and are altered by the common BDNF polymorphism Val66Met

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Histone H3 lysine-to-methionine mutants as a paradigm to study chromatin signaling

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Specific detection of methionine 27 mutation in histone 3 variants (H3K27M) in fixed tissue from high-grade astrocytomas

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Deletion of the initial methionine codon of the Tmem95 gene causes subfertility, but not complete infertility, in male mice

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Evidence of H3 K27M mutations in posterior fossa ependymomas

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Adult Brainstem Gliomas With H3K27M Mutation: Radiology, Pathology, and Prognosis

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Deep learning tools predict variants in disordered regions with lower sensitivity

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Brain-Derived Neurotrophic Factor Val66Met Human Polymorphism Impairs the Beneficial Exercise-Induced Neurobiological Changes in Mice

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Incorporation of non-canonical amino acids into the developing murine proteome

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