Arama Sonuçları - Caleb Webber
- Gösterilen 1 - 20 sonuçlar arası kayıtlar. 39
- Sonraki Sayfaya Git
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1
The Roles of FMRP-Regulated Genes in Autism Spectrum Disorder: Single- and Multiple-Hit Genetic Etiologies Yazar: Julia Steinberg, Caleb Webber
Baskı/Yayın Bilgisi 2013Artigo -
2
Addressing variability in iPSC-derived models of human disease: guidelines to promote reproducibility Yazar: Viola Volpato, Caleb Webber
Baskı/Yayın Bilgisi 2020Revisão -
3
Phenotype Ontologies and Cross-Species Analysis for Translational Research Yazar: Peter N. Robinson, Caleb Webber
Baskı/Yayın Bilgisi 2014Revisão -
4
Unbiased Functional Clustering of Gene Variants with a Phenotypic-Linkage Network Yazar: Frantisek Honti, Stephen Meader, Caleb Webber
Baskı/Yayın Bilgisi 2014Artigo -
5
Haploinsufficiency predictions without study bias Yazar: Julia Steinberg, Frantisek Honti, Stephen Meader, Caleb Webber
Baskı/Yayın Bilgisi 2015Artigo -
6
Bias of Selection on Human Copy-Number Variants Yazar: Duc-Quang Nguyen, Caleb Webber, Chris P. Ponting
Baskı/Yayın Bilgisi 2006Artigo -
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Laplacian eigenmaps and principal curves for high resolution pseudotemporal ordering of single-cell RNA-seq profiles Yazar: Kieran R. Campbell, Chris P. Ponting, Caleb Webber
Baskı/Yayın Bilgisi 2015Pré-impressão -
8
GAT: a simulation framework for testing the association of genomic intervals Yazar: Andreas Heger, Caleb Webber, Martin Goodson, Chris P. Ponting, Gerton Lunter
Baskı/Yayın Bilgisi 2013Artigo -
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Diagnostically relevant facial gestalt information from ordinary photos Yazar: Quentin RV. Ferry, Julia Steinberg, Caleb Webber, David Fitzpatrick, Chris P. Ponting, Andrew Zisserman, Christoffer Nellåker
Baskı/Yayın Bilgisi 2014Artigo -
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Extensive microRNA-mediated crosstalk between lncRNAs and mRNAs in mouse embryonic stem cells Yazar: Jennifer Y. Tan, Tamara Sirey, Frantisek Honti, Bryony Graham, Allison Piovesan, Matthias Merkenschlager, Caleb Webber, Chris P. Ponting, Ana Claudia Marques
Baskı/Yayın Bilgisi 2015Artigo -
15
A single-cell atlas of the human substantia nigra reveals cell-specific pathways associated with neurological disorders Yazar: Devika Agarwal, Cynthia Sandor, Viola Volpato, Tara M. Caffrey, Jimena Monzón‐Sandoval, Rory Bowden, Javier Alegre‐Abarrategui, Richard Wade‐Martins, Caleb Webber
Baskı/Yayın Bilgisi 2020Artigo -
16
Expression profiling of mouse subplate reveals a dynamic gene network and disease association with autism and schizophrenia Yazar: 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
Baskı/Yayın Bilgisi 2013Artigo -
17
RNA sequencing reveals MMP2 and TGFB1 downregulation in LRRK2 G2019S Parkinson's iPSC-derived astrocytes Yazar: 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
Baskı/Yayın Bilgisi 2019Artigo -
18
Transcriptomic profiling of purified patient-derived dopamine neurons identifies convergent perturbations and therapeutics for Parkinson’s disease Yazar: 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
Baskı/Yayın Bilgisi 2016Artigo -
19
Network Topologies and Convergent Aetiologies Arising from Deletions and Duplications Observed in Individuals with Autism Yazar: 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
Baskı/Yayın Bilgisi 2013Artigo -
20
Natural genetic variation caused by small insertions and deletions in the human genome Yazar: 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
Baskı/Yayın Bilgisi 2011Artigo
Arama Araçları:
İlgili Konular
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