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Andrew E Timms

Showing results (1-10 of 47) with videos related to

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Communicative & Integrative Biology|June 30, 2010
KLHDC8B in Hodgkin lymphoma and possibly twinningAndrew E Timms, Marshall S Horwitz
G3 (Bethesda, Md.)|December 7, 2017
Optimizing Genomic Methods for Mapping and Identification of Candidate Variants in ENU Mutagenesis Screens Using Inbred MiceKrista A Geister, Andrew E Timms, David R Beier
G3 (Bethesda, Md.)|June 5, 2016
Mutations in Dnaaf1 and Lrrc48 Cause Hydrocephalus, Laterality Defects, and Sinusitis in MiceSeungshin Ha, Anna M Lindsay, Andrew E Timms, et al.
BMC Genomics|November 11, 2015
Variant mapping and mutation discovery in inbred mice using next-generation sequencingJabier Gallego-Llamas, Andrew E Timms, Krista A Geister, et al.
International Journal of Molecular Sciences|March 29, 2023
Transcriptomic Signatures of Single-Suture Craniosynostosis PhenotypesSamantha Lapehn, Jonas A Gustafson, Andrew E Timms, et al.
The Journal of Thoracic and Cardiovascular Surgery|April 22, 2019
Transcriptome profiling reveals activation of inflammation and apoptosis in the neonatal striatum after deep hypothermic circulatory arrestLan N Tu, Andrew E Timms, Nataliya Kibiryeva, et al.
Plos One|July 22, 2016
Improvement of ENU Mutagenesis Efficiency Using Serial Injection and Mismatch Repair Deficiency MiceJabier Gallego-Llamas, Andrew E Timms, Rose Pitstick, et al.
American Journal of Medical Genetics. Part A|January 18, 2018
Bi-allelic mutations of CCDC88C are a rare cause of severe congenital hydrocephalusGaia Ruggeri, Andrew E Timms, Chi Cheng, et al.
Translational Vision Science & Technology|April 18, 2022
Machine Learning Prediction of Non-Coding Variant Impact in Human Retinal cis-Regulatory ElementsLeah S VandenBosch, Kelsey Luu, Andrew E Timms, et al.
Journal of Hematology & Oncology|April 24, 2014
Heritable GATA2 mutations associated with familial AML-MDS: a case report and review of literatureJuehua Gao, Ryan D Gentzler, Andrew E Timms, et al.
Pageof 5

Showing results (1-10 of 47) with videos related to

Sort By:
Pageof 5
Communicative & Integrative Biology|June 30, 2010
KLHDC8B in Hodgkin lymphoma and possibly twinningAndrew E Timms, Marshall S Horwitz
G3 (Bethesda, Md.)|December 7, 2017
Optimizing Genomic Methods for Mapping and Identification of Candidate Variants in ENU Mutagenesis Screens Using Inbred MiceKrista A Geister, Andrew E Timms, David R Beier
G3 (Bethesda, Md.)|June 5, 2016
Mutations in Dnaaf1 and Lrrc48 Cause Hydrocephalus, Laterality Defects, and Sinusitis in MiceSeungshin Ha, Anna M Lindsay, Andrew E Timms, et al.
BMC Genomics|November 11, 2015
Variant mapping and mutation discovery in inbred mice using next-generation sequencingJabier Gallego-Llamas, Andrew E Timms, Krista A Geister, et al.
International Journal of Molecular Sciences|March 29, 2023
Transcriptomic Signatures of Single-Suture Craniosynostosis PhenotypesSamantha Lapehn, Jonas A Gustafson, Andrew E Timms, et al.
The Journal of Thoracic and Cardiovascular Surgery|April 22, 2019
Transcriptome profiling reveals activation of inflammation and apoptosis in the neonatal striatum after deep hypothermic circulatory arrestLan N Tu, Andrew E Timms, Nataliya Kibiryeva, et al.
Plos One|July 22, 2016
Improvement of ENU Mutagenesis Efficiency Using Serial Injection and Mismatch Repair Deficiency MiceJabier Gallego-Llamas, Andrew E Timms, Rose Pitstick, et al.
American Journal of Medical Genetics. Part A|January 18, 2018
Bi-allelic mutations of CCDC88C are a rare cause of severe congenital hydrocephalusGaia Ruggeri, Andrew E Timms, Chi Cheng, et al.
Translational Vision Science & Technology|April 18, 2022
Machine Learning Prediction of Non-Coding Variant Impact in Human Retinal cis-Regulatory ElementsLeah S VandenBosch, Kelsey Luu, Andrew E Timms, et al.
Journal of Hematology & Oncology|April 24, 2014
Heritable GATA2 mutations associated with familial AML-MDS: a case report and review of literatureJuehua Gao, Ryan D Gentzler, Andrew E Timms, et al.
Pageof 5