खोज परिणाम - Caleb Webber
- प्रदर्शित 1 - 20 परिणाम 39
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Bias of Selection on Human Copy-Number Variants द्वारा Duc-Quang Nguyen, Caleb Webber, Chris P. Ponting
प्रकाशित 2006Artigo -
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SCANPS: a web server for iterative protein sequence database searching by dynamic programing, with display in a hierarchical SCOP browser द्वारा Terence P. Walsh, Caleb Webber, Stephen M. J. Searle, Shane Sturrock, Geoffrey J. Barton
प्रकाशित 2008Artigo -
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Extensive microRNA-mediated crosstalk between lncRNAs and mRNAs in mouse embryonic stem cells द्वारा Jennifer Y. Tan, Tamara Sirey, Frantisek Honti, Bryony Graham, Allison Piovesan, Matthias Merkenschlager, Caleb Webber, Chris P. Ponting, Ana Claudia Marques
प्रकाशित 2015Artigo -
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A single-cell atlas of the human substantia nigra reveals cell-specific pathways associated with neurological disorders द्वारा Devika Agarwal, Cynthia Sandor, Viola Volpato, Tara M. Caffrey, Jimena Monzón‐Sandoval, Rory Bowden, Javier Alegre‐Abarrategui, Richard Wade‐Martins, Caleb Webber
प्रकाशित 2020Artigo -
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Expression profiling of mouse subplate reveals a dynamic gene network and disease association with autism and schizophrenia द्वारा Anna Hoerder‐Suabedissen, Franziska M. Oeschger, Michelle L. Krishnan, T. Grant Belgard, Weizhi Wang, Sheena Lee, Caleb Webber, Enrico Petretto, A. David Edwards, Zoltán Molnár
प्रकाशित 2013Artigo -
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RNA sequencing reveals MMP2 and TGFB1 downregulation in LRRK2 G2019S Parkinson's iPSC-derived astrocytes द्वारा Heather Booth, Frank Wessely, Natalie Connor‐Robson, Federica Rinaldi, Jane Vowles, Cathy Browne, Samuel Evetts, Joshua Shulman, Sally A. Cowley, Caleb Webber, Richard Wade‐Martins
प्रकाशित 2019Artigo -
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Transcriptomic profiling of purified patient-derived dopamine neurons identifies convergent perturbations and therapeutics for Parkinson’s disease द्वारा Cynthia Sandor, Paul Robertson, Charmaine Lang, Andreas Heger, Heather Booth, Jane Vowles, Lorna Witty, Rory Bowden, Joshua Shulman, Sally A. Cowley, Richard Wade‐Martins, Caleb Webber
प्रकाशित 2016Artigo -
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Network Topologies and Convergent Aetiologies Arising from Deletions and Duplications Observed in Individuals with Autism द्वारा Hyun Ji Noh, Chris P. Ponting, Hannah Boulding, Stephen Meader, Catalina Betancur, Joseph D. Buxbaum, Dalila Pinto, Christian R. Marshall, Anath C. Lionel, Stephen W. Scherer, Caleb Webber
प्रकाशित 2013Artigo -
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Natural genetic variation caused by small insertions and deletions in the human genome द्वारा Ryan E. Mills, W. Stephen Pittard, Julienne M. Mullaney, Umar Farooq, Todd Creasy, Anup Mahurkar, David M. Kemeza, Daniel S. Strassler, Chris P. Ponting, Caleb Webber, Scott E. Devine
प्रकाशित 2011Artigo
खोज साधन:
संबंधित विषय
Biology
Genetics
Gene
Medicine
Neuroscience
Computational biology
Phenotype
Disease
Genome
Genotype
Pathology
Computer science
Gene expression
Cell biology
Single-nucleotide polymorphism
Embryonic stem cell
Internal medicine
Parkinson's disease
Transcriptome
Bioinformatics
Dopamine
Genetic association
Genome-wide association study
Induced pluripotent stem cell
Immunology
Artificial intelligence
Central nervous system
Copy-number variation
Dopaminergic
Evolutionary biology