Kết quả tìm kiếm - Anthony Antonellis
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Predicting the pathogenicity of aminoacyl-tRNA synthetase mutations Bằng Stephanie N. Oprescu, Laurie B. Griffin, Asim A. Beg, Anthony Antonellis
Được phát hành 2016Revisão -
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Compound heterozygosity for loss-of-function <i>FARSB</i> variants in a patient with classic features of recessive aminoacyl-tRNA synthetase-related disease Bằng Anthony Antonellis, Stephanie N. Oprescu, Laurie B. Griffin, Amer Heider, Andrea Amalfitano, Jeffrey W. Innis
Được phát hành 2018Artigo -
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Determinants of the Development of Diabetes (Maturity-Onset Diabetes of the Young-3) in Carriers of <i>HNF-1</i>α Mutations Bằng Tomasz Klupa, James H. Warram, Anthony Antonellis, Marcus G. Pezzolesi, Moonsuk Nam, Maciej T. Małecki, Alessandro Doria, Stephen S. Rich, Andrzej S. Królewski
Được phát hành 2002Artigo -
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An evolutionarily conserved intronic region controls the spatiotemporal expression of the transcription factor Sox10 Bằng James R. Dutton, Anthony Antonellis, Thomas J. Carney, Frederico S. L. M. Rodrigues, William J. Pavan, Andrew Ward, Robert N. Kelsh
Được phát hành 2008Artigo -
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An assessment of mechanisms underlying peripheral axonal degeneration caused by aminoacyl-tRNA synthetase mutations Bằng Morgane Stum, Heather M. McLaughlin, Erica L. Kleinbrink, Kathy E. Miers, Susan L. Ackerman, Kevin L. Seburn, Anthony Antonellis, Robert W. Burgess
Được phát hành 2010Artigo -
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Functional Analyses of Glycyl-tRNA Synthetase Mutations Suggest a Key Role for tRNA-Charging Enzymes in Peripheral Axons Bằng Anthony Antonellis, Shih-Queen Lee-Lin, Amy S. Wasterlain, Paul Leo, Martha Quezado, Lev G. Goldfarb, Kyungjae Myung, Shawn M. Burgess, Kenneth H. Fischbeck, Eric D. Green
Được phát hành 2006Artigo -
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Exome sequencing identifies a significant variant in methionyl-tRNA synthetase (<i>MARS</i>) in a family with late-onset CMT2 Bằng Michael Gonzalez, Heather M. McLaughlin, Henry Houlden, Min Guo, Yo‐Tsen Liu, Marios Hadjivassilious, Fiorella Speziani, Xiang‐Lei Yang, Anthony Antonellis, Mary M. Reilly, Stephan Züchner
Được phát hành 2013Artigo -
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Identification of Neural Crest and Glial Enhancers at the Mouse Sox10 Locus through Transgenesis in Zebrafish Bằng Anthony Antonellis, Jimmy Huynh, Shih-Queen Lee-Lin, Ryan M. Vinton, Gabriel Renaud, Stacie K. Loftus, Gene Elliot, Tyra G. Wolfsberg, Eric D. Green, Andrew S. McCallion, William J. Pavan
Được phát hành 2008Artigo -
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Charcot-Marie-Tooth–Linked Mutant GARS Is Toxic to Peripheral Neurons Independent of Wild-Type GARS Levels Bằng William W. Motley, Kevin L. Seburn, Mir Hussain Nawaz, Kathy E. Miers, Jun Cheng, Anthony Antonellis, Eric D. Green, Kevin Talbot, Xiang‐Lei Yang, Kenneth H. Fischbeck, Robert W. Burgess
Được phát hành 2011Artigo -
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Phenotypic spectrum of disorders associated with glycyl-tRNA synthetase mutations Bằng Kumaraswamy Sivakumar, Theodoros Kyriakides, Imke Puls, Garth A. Nicholson, Benoît Funalot, Anthony Antonellis, Nyamkhishig Sambuughin, Kyproula Christodoulou, John L. Beggs, Eleni Zamba‐Papanicolaou, Victor Ionâşescu, Marinos C. Dalakas, Eric D. Green, Kenneth H. Fischbeck, Lev G. Goldfarb
Được phát hành 2005Artigo -
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A Recurrent loss-of-function alanyl-tRNA synthetase (AARS ) mutation in patients with charcot-marie-tooth disease type 2N (CMT2N) Bằng Heather M. McLaughlin, Reiko Sakaguchi, William Giblin, Thomas E. Wilson, Leslie G. Biesecker, James R. Lupski, Kevin Talbot, Jeffery M. Vance, Stephan Züchner, Yi‐Chung Lee, Marina Kennerson, Ya‐Ming Hou, Garth A. Nicholson, Anthony Antonellis
Được phát hành 2011Artigo -
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<i>Gpnmb</i> is a melanoblast‐expressed, MITF‐dependent gene Bằng Stacie K. Loftus, Anthony Antonellis, Ivana Matera, Gabriel Renaud, Laura L. Baxter, Duncan Reid, Tyra G. Wolfsberg, Yidong Chen, Chenwei Wang, Megana Prasad, Seneca L. Bessling, Andrew S. McCallion, Eric D. Green, Dorothy C. Bennett, William J. Pavan
Được phát hành 2008Artigo -
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SOX10 directly modulates ERBB3 transcription via an intronic neural crest enhancer Bằng Megana Prasad, Xylena Reed, David U. Gorkin, Julia C. Cronin, Anthony R. McAdow, Kristopher H. Chain, Chani J. Hodonsky, Erin A. Jones, John Svaren, Anthony Antonellis, Stephen L. Johnson, Stacie K. Loftus, William J. Pavan, Andrew S. McCallion
Được phát hành 2011Artigo -
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A Loss-of-Function Variant in the Human Histidyl-tRNA Synthetase (<i>HARS</i>) Gene is Neurotoxic In Vivo Bằng Aimée Vester, Gisselle A. Vélez-Ruiz, Heather M. McLaughlin, NISC Comparative Sequencing Program, James R. Lupski, Kevin Talbot, Jeffery M. Vance, Stephan Züchner, Ricardo H. Roda, Kenneth H. Fischbeck, Leslie G. Biesecker, Garth A. Nicholson, Asim A. Beg, Anthony Antonellis
Được phát hành 2012Artigo -
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Glycyl tRNA Synthetase Mutations in Charcot-Marie-Tooth Disease Type 2D and Distal Spinal Muscular Atrophy Type V Bằng Anthony Antonellis, Rachel E. Ellsworth, Nyamkhishig Sambuughin, Imke Puls, Annette Abel, Shih-Queen Lee-Lin, Albena Jordanova, Ivo Kremensky, Kyproula Christodoulou, Lefkos Middleton, Kumaraswamy Sivakumar, Victor Ionâşescu, Benoît Funalot, Jeffery M. Vance, Lev G. Goldfarb, Kenneth H. Fischbeck, Eric D. Green
Được phát hành 2003Artigo
Công cụ tìm kiếm:
Các môn học liên quan
Biology
Genetics
Gene
Mutation
Phenotype
Medicine
Loss function
Disease
RNA
Allele
Complementation
Transfer RNA
Cell biology
Compound heterozygosity
Exome sequencing
Pathology
Transcription factor
Diabetes mellitus
Endocrinology
Internal medicine
Zebrafish
Aminoacyl tRNA synthetase
Exome
Missense mutation
Mutant
Neuroscience
Peripheral neuropathy
SOX10
Atrophy
Bioinformatics