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C Murray

Showing results (1251-1260 of 1,465) with videos related to

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The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|January 17, 2025
Familial Oculoauriculovertebral Spectrum: A Genomic Investigation of Autosomal Dominant InheritanceAline L Petrin, Ligiane Alves Machado-Paula, Austin Hinkle, et al.
American Journal of Human Genetics|May 10, 2011
Whole-Exome sequencing identifies FAM20A mutations as a cause of amelogenesis imperfecta and gingival hyperplasia syndromeJames O'Sullivan, Carolina C Bitu, Sarah B Daly, et al.
The Journal of Pediatrics|January 18, 2013
Late-onset sepsis in very low birth weight infants from singleton and multiple-gestation birthsNansi S Boghossian, Grier P Page, Edward F Bell, et al.
Nature Genetics|September 6, 2000
Domain-specific mutations in TGFB1 result in Camurati-Engelmann diseaseA Kinoshita, T Saito, H Tomita, et al.
American Journal of Medical Genetics. Part A|May 17, 2011
Genomic strategy identifies a missense mutation in WD-repeat domain 65 (WDR65) in an individual with Van der Woude syndromeNicholas K Rorick, Akira Kinoshita, Jason L Weirather, et al.
Scientific Reports|October 15, 2022
Pericytes take up and degrade α-synuclein but succumb to apoptosis under cellular stressTaylor J Stevenson, Rebecca H Johnson, Jimmy Savistchenko, et al.
The Lancet. Infectious Diseases|September 3, 2022
The Johns Hopkins University Center for Systems Science and Engineering COVID-19 Dashboard: data collection process, challenges faced, and lessons learnedEnsheng Dong, Jeremy Ratcliff, Tamara D Goyea, et al.
BMC Public Health|February 16, 2024
Perceptions and beliefs of community gatekeepers about genomic risk information in African cleft researchAbimbola M Oladayo, Oluwakemi Odukoya, Veronica Sule, et al.
Nature Medicine|June 1, 2010
Recovery of motoneuron and locomotor function after spinal cord injury depends on constitutive activity in 5-HT2C receptorsKatherine C Murray, Aya Nakae, Marilee J Stephens, et al.
The Journal of Allergy and Clinical Immunology. in Practice|April 18, 2021
Randomized Trial of the Efficacy and Safety of Berotralstat (BCX7353) as an Oral Prophylactic Therapy for Hereditary Angioedema: Results of APeX-2 Through 48 Weeks (Part 2)H James Wedner, Emel Aygören-Pürsün, Jonathan Bernstein, et al.
Pageof 147

Showing results (1251-1260 of 1,465) with videos related to

Sort By:
Pageof 147
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|January 17, 2025
Familial Oculoauriculovertebral Spectrum: A Genomic Investigation of Autosomal Dominant InheritanceAline L Petrin, Ligiane Alves Machado-Paula, Austin Hinkle, et al.
American Journal of Human Genetics|May 10, 2011
Whole-Exome sequencing identifies FAM20A mutations as a cause of amelogenesis imperfecta and gingival hyperplasia syndromeJames O'Sullivan, Carolina C Bitu, Sarah B Daly, et al.
The Journal of Pediatrics|January 18, 2013
Late-onset sepsis in very low birth weight infants from singleton and multiple-gestation birthsNansi S Boghossian, Grier P Page, Edward F Bell, et al.
Nature Genetics|September 6, 2000
Domain-specific mutations in TGFB1 result in Camurati-Engelmann diseaseA Kinoshita, T Saito, H Tomita, et al.
American Journal of Medical Genetics. Part A|May 17, 2011
Genomic strategy identifies a missense mutation in WD-repeat domain 65 (WDR65) in an individual with Van der Woude syndromeNicholas K Rorick, Akira Kinoshita, Jason L Weirather, et al.
Scientific Reports|October 15, 2022
Pericytes take up and degrade α-synuclein but succumb to apoptosis under cellular stressTaylor J Stevenson, Rebecca H Johnson, Jimmy Savistchenko, et al.
The Lancet. Infectious Diseases|September 3, 2022
The Johns Hopkins University Center for Systems Science and Engineering COVID-19 Dashboard: data collection process, challenges faced, and lessons learnedEnsheng Dong, Jeremy Ratcliff, Tamara D Goyea, et al.
BMC Public Health|February 16, 2024
Perceptions and beliefs of community gatekeepers about genomic risk information in African cleft researchAbimbola M Oladayo, Oluwakemi Odukoya, Veronica Sule, et al.
Nature Medicine|June 1, 2010
Recovery of motoneuron and locomotor function after spinal cord injury depends on constitutive activity in 5-HT2C receptorsKatherine C Murray, Aya Nakae, Marilee J Stephens, et al.
The Journal of Allergy and Clinical Immunology. in Practice|April 18, 2021
Randomized Trial of the Efficacy and Safety of Berotralstat (BCX7353) as an Oral Prophylactic Therapy for Hereditary Angioedema: Results of APeX-2 Through 48 Weeks (Part 2)H James Wedner, Emel Aygören-Pürsün, Jonathan Bernstein, et al.
Pageof 147