نتائج البحث - Brendan D. Galvin
- يعرض 1 - 4 نتائج من 4
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Activating mutations in the extracellular domain of the fibroblast growth factor receptor 2 function by disruption of the disulfide bond in the third immunoglobulin-like domain حسب Scott C. Robertson, April N. Meyer, Kristen C. Hart, Brendan D. Galvin, Melanie K. Webster, Daniel J. Donoghue
منشور في 1998Artigo -
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A High-Quality De novo Genome Assembly from a Single Mosquito Using PacBio Sequencing حسب Sarah B. Kingan, Haynes Heaton, Juliana Cudini, Christine Lambert, Primo Baybayan, Brendan D. Galvin, Richard Durbin, Jonas Korlach, Mara Lawniczak
منشور في 2019Artigo -
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Resolving the full spectrum of human genome variation using Linked-Reads حسب Patrick Marks, Sarah Garcia, Álvaro Martínez Barrio, Kamila Belhocine, Jorge Bernate, Rajiv Bharadwaj, Keith P. Bjornson, Claudia Catalanotti, Josh Delaney, Adrian Fehr, Ian T. Fiddes, Brendan D. Galvin, Haynes Heaton, Jill Herschleb, Christopher M. Hindson, Esty Holt, Cassandra B. Jabara, Susanna Jett, Nikka Keivanfar, Sofia Kyriazopoulou-Panagiotopoulou, Monkol Lek, Bill K. Lin, Adam J. Lowe, Shazia Mahamdallie, Shamoni Maheshwari, Tony Makarewicz, Jamie L. Marshall, Francesca Meschi, Christopher J. O'Keefe, Heather Ordonez, Pranav Patel, Andrew Price, Ariel Royall, Elise Ruark, Sheila Seal, Michael Schnall-Levin, Preyas Shah, David Stafford, Stephen R. Williams, Indira Wu, Andrew Wei Xu, Nazneen Rahman, Daniel G. MacArthur, Deanna M. Church
منشور في 2019Artigo
أدوات البحث:
موضوعات ذات صلة
Biology
Gene
Genetics
Mutation
Biochemistry
Computational biology
DNA sequencing
Fibroblast growth factor
Fibroblast growth factor receptor
Fibroblast growth factor receptor 2
Genome
Molecular biology
Point mutation
Receptor
Receptor tyrosine kinase
Reference genome
Tyrosine kinase
1000 Genomes Project
Apert syndrome
Chemistry
Comparative genomics
Contig
Craniosynostosis
Crouzon syndrome
Cysteine
Demography
Enzyme
Exome
Exome sequencing
Fibroblast growth factor receptor 1