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Jay Shendure

Showing results (351-360 of 437) with videos related to

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American Journal of Human Genetics|December 25, 2012
Exome sequencing identifies mutations in CCDC114 as a cause of primary ciliary dyskinesiaMichael R Knowles, Margaret W Leigh, Lawrence E Ostrowski, et al.
Nature Genetics|August 13, 2013
GRIN2A mutations cause epilepsy-aphasia spectrum disordersGemma L Carvill, Brigid M Regan, Simone C Yendle, et al.
JAMA Pediatrics|June 11, 2021
Comparison of Symptoms and RNA Levels in Children and Adults With SARS-CoV-2 Infection in the Community SettingErin Chung, Eric J Chow, Naomi C Wilcox, et al.
American Journal of Human Genetics|October 9, 2012
Whole-exome capture and sequencing identifies HEATR2 mutation as a cause of primary ciliary dyskinesiaAmjad Horani, Todd E Druley, Maimoona A Zariwala, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 4, 2015
Accelerating matchmaking of novel dysmorphology syndromes through clinical and genomic characterization of a large cohortRanad Shaheen, Nisha Patel, Hanan Shamseldin, et al.
American Journal of Human Genetics|May 1, 2012
Haploinsufficiency of SF3B4, a component of the pre-mRNA spliceosomal complex, causes Nager syndromeFrancois P Bernier, Oana Caluseriu, Sarah Ng, et al.
American Journal of Human Genetics|January 6, 2015
MAT2A mutations predispose individuals to thoracic aortic aneurysmsDong-chuan Guo, Limin Gong, Ellen S Regalado, et al.
Developmental Cell|August 15, 2023
Single-cell census of human tooth development enables generation of human enamelAmmar Alghadeer, Sesha Hanson-Drury, Anjali P Patni, et al.
Emerging Infectious Diseases|October 24, 2024
Clinical and Genomic Epidemiology of Coxsackievirus A21 and Enterovirus D68 in Homeless Shelters, King County, Washington, USA, 2019-2021Sarah N Cox, Amanda M Casto, Nicholas M Franko, et al.
Cell Host & Microbe|August 25, 2015
Regional Isolation Drives Bacterial Diversification within Cystic Fibrosis LungsPeter Jorth, Benjamin J Staudinger, Xia Wu, et al.
Pageof 44

Showing results (351-360 of 437) with videos related to

Sort By:
Pageof 44
American Journal of Human Genetics|December 25, 2012
Exome sequencing identifies mutations in CCDC114 as a cause of primary ciliary dyskinesiaMichael R Knowles, Margaret W Leigh, Lawrence E Ostrowski, et al.
Nature Genetics|August 13, 2013
GRIN2A mutations cause epilepsy-aphasia spectrum disordersGemma L Carvill, Brigid M Regan, Simone C Yendle, et al.
JAMA Pediatrics|June 11, 2021
Comparison of Symptoms and RNA Levels in Children and Adults With SARS-CoV-2 Infection in the Community SettingErin Chung, Eric J Chow, Naomi C Wilcox, et al.
American Journal of Human Genetics|October 9, 2012
Whole-exome capture and sequencing identifies HEATR2 mutation as a cause of primary ciliary dyskinesiaAmjad Horani, Todd E Druley, Maimoona A Zariwala, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 4, 2015
Accelerating matchmaking of novel dysmorphology syndromes through clinical and genomic characterization of a large cohortRanad Shaheen, Nisha Patel, Hanan Shamseldin, et al.
American Journal of Human Genetics|May 1, 2012
Haploinsufficiency of SF3B4, a component of the pre-mRNA spliceosomal complex, causes Nager syndromeFrancois P Bernier, Oana Caluseriu, Sarah Ng, et al.
American Journal of Human Genetics|January 6, 2015
MAT2A mutations predispose individuals to thoracic aortic aneurysmsDong-chuan Guo, Limin Gong, Ellen S Regalado, et al.
Developmental Cell|August 15, 2023
Single-cell census of human tooth development enables generation of human enamelAmmar Alghadeer, Sesha Hanson-Drury, Anjali P Patni, et al.
Emerging Infectious Diseases|October 24, 2024
Clinical and Genomic Epidemiology of Coxsackievirus A21 and Enterovirus D68 in Homeless Shelters, King County, Washington, USA, 2019-2021Sarah N Cox, Amanda M Casto, Nicholas M Franko, et al.
Cell Host & Microbe|August 25, 2015
Regional Isolation Drives Bacterial Diversification within Cystic Fibrosis LungsPeter Jorth, Benjamin J Staudinger, Xia Wu, et al.
Pageof 44