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G Hunter

Showing results (951-960 of 964) with videos related to

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Genome Research|June 16, 2000
Comparative genome sequence analysis of the Bpa/Str region in mouse and ManA M Mallon, M Platzer, R Bate, et al.
Biorxiv : the Preprint Server for Biology|September 24, 2024
Gene identification for ocular congenital cranial motor neuron disorders using human sequencing, zebrafish screening, and protein binding microarraysJulie A Jurgens, Paola M Matos Ruiz, Jessica King, et al.
The Journal of Biological Chemistry|May 29, 1999
Identification of amino acid residues critical for aggregation of human CC chemokines macrophage inflammatory protein (MIP)-1alpha, MIP-1beta, and RANTES. Characterization of active disaggregated chemokine variantsL G Czaplewski, J McKeating, C J Craven, et al.
Investigative Ophthalmology & Visual Science|March 31, 2025
Gene Identification for Ocular Congenital Cranial Motor Neuron Disorders Using Human Sequencing, Zebrafish Screening, and Protein Binding MicroarraysJulie A Jurgens, Paola M Matos Ruiz, Jessica King, et al.
The New England Journal of Medicine|May 29, 2009
Radiofrequency ablation in Barrett's esophagus with dysplasiaNicholas J Shaheen, Prateek Sharma, Bergein F Overholt, et al.
Human Genetics|October 15, 2021
TUBB3 Arg262His causes a recognizable syndrome including CFEOM3, facial palsy, joint contractures, and early-onset peripheral neuropathyMary C Whitman, Brenda J Barry, Caroline D Robson, et al.
Gastroenterology|June 18, 2011
Durability of radiofrequency ablation in Barrett's esophagus with dysplasiaNicholas J Shaheen, Bergein F Overholt, Richard E Sampliner, et al.
Nature Genetics|October 3, 2006
Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmusPatrick Tarpey, Shery Thomas, Nagini Sarvananthan, et al.
The New England Journal of Medicine|October 17, 2019
Randomized Trial of Medical versus Surgical Treatment for Refractory HeartburnStuart J Spechler, John G Hunter, Karen M Jones, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 21, 2024
Expanding the genetics and phenotypes of ocular congenital cranial dysinnervation disordersJulie A Jurgens, Brenda J Barry, Wai-Man Chan, et al.
Pageof 97

Showing results (951-960 of 964) with videos related to

Sort By:
Pageof 97
Genome Research|June 16, 2000
Comparative genome sequence analysis of the Bpa/Str region in mouse and ManA M Mallon, M Platzer, R Bate, et al.
Biorxiv : the Preprint Server for Biology|September 24, 2024
Gene identification for ocular congenital cranial motor neuron disorders using human sequencing, zebrafish screening, and protein binding microarraysJulie A Jurgens, Paola M Matos Ruiz, Jessica King, et al.
The Journal of Biological Chemistry|May 29, 1999
Identification of amino acid residues critical for aggregation of human CC chemokines macrophage inflammatory protein (MIP)-1alpha, MIP-1beta, and RANTES. Characterization of active disaggregated chemokine variantsL G Czaplewski, J McKeating, C J Craven, et al.
Investigative Ophthalmology & Visual Science|March 31, 2025
Gene Identification for Ocular Congenital Cranial Motor Neuron Disorders Using Human Sequencing, Zebrafish Screening, and Protein Binding MicroarraysJulie A Jurgens, Paola M Matos Ruiz, Jessica King, et al.
The New England Journal of Medicine|May 29, 2009
Radiofrequency ablation in Barrett's esophagus with dysplasiaNicholas J Shaheen, Prateek Sharma, Bergein F Overholt, et al.
Human Genetics|October 15, 2021
TUBB3 Arg262His causes a recognizable syndrome including CFEOM3, facial palsy, joint contractures, and early-onset peripheral neuropathyMary C Whitman, Brenda J Barry, Caroline D Robson, et al.
Gastroenterology|June 18, 2011
Durability of radiofrequency ablation in Barrett's esophagus with dysplasiaNicholas J Shaheen, Bergein F Overholt, Richard E Sampliner, et al.
Nature Genetics|October 3, 2006
Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmusPatrick Tarpey, Shery Thomas, Nagini Sarvananthan, et al.
The New England Journal of Medicine|October 17, 2019
Randomized Trial of Medical versus Surgical Treatment for Refractory HeartburnStuart J Spechler, John G Hunter, Karen M Jones, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 21, 2024
Expanding the genetics and phenotypes of ocular congenital cranial dysinnervation disordersJulie A Jurgens, Brenda J Barry, Wai-Man Chan, et al.
Pageof 97