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G Hunter

Showing results (921-930 of 964) with videos related to

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British Dental Journal|November 22, 2014
Consensus statement: Oral health and elite sport performanceI Needleman, P Ashley, P Fine, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 14, 2014
Temporal patterns of gene expression in developing maize endosperm identified through transcriptome sequencingGuosheng Li, Dongfang Wang, Ruolin Yang, et al.
The American Journal of Gastroenterology|January 18, 2007
Office-based unsedated small-caliber endoscopy is equivalent to conventional sedated endoscopy in screening and surveillance for Barrett's esophagus: a randomized and blinded comparisonBlair A Jobe, John G Hunter, Eugene Y Chang, et al.
The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences|June 10, 2020
In Vivo Quasi-Elastic Light Scattering Eye Scanner Detects Molecular Aging in HumansOlga Minaeva, Srikant Sarangi, Danielle M Ledoux, et al.
Diseases of the Esophagus : Official Journal of the International Society for Diseases of the Esophagus|February 25, 2015
Significant understaging is seen in clinically staged T2N0 esophageal cancer patients undergoing esophagectomyJ P Dolan, T Kaur, B S Diggs, et al.
American Journal of Ophthalmology|June 24, 2022
Nasal Transposition of the Split Lateral Rectus Muscle for Strabismus Associated With Bilateral 3<sup>rd</sup>-Nerve PalsyIsdin Oke, Birgit Lorenz, Sotirios Basiakos, et al.
Blood|December 15, 1995
BB-10010: an active variant of human macrophage inflammatory protein-1 alpha with improved pharmaceutical propertiesM G Hunter, L Bawden, D Brotherton, et al.
Brain : a Journal of Neurology|February 10, 2011
The clinical and molecular genetic features of idiopathic infantile periodic alternating nystagmusMervyn G Thomas, Moira Crosier, Susan Lindsay, et al.
American Journal of Medical Genetics|December 11, 1996
Simpson-Golabi-Behmel syndrome: genotype/phenotype analysis of 18 affected males from 7 unrelated familiesR M Hughes-Benzie, G Pilia, J Y Xuan, et al.
American Journal of Human Genetics|July 10, 2012
HOXB1 founder mutation in humans recapitulates the phenotype of Hoxb1-/- miceBryn D Webb, Sherin Shaaban, Harald Gaspar, et al.
Pageof 97

Showing results (921-930 of 964) with videos related to

Sort By:
Pageof 97
British Dental Journal|November 22, 2014
Consensus statement: Oral health and elite sport performanceI Needleman, P Ashley, P Fine, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 14, 2014
Temporal patterns of gene expression in developing maize endosperm identified through transcriptome sequencingGuosheng Li, Dongfang Wang, Ruolin Yang, et al.
The American Journal of Gastroenterology|January 18, 2007
Office-based unsedated small-caliber endoscopy is equivalent to conventional sedated endoscopy in screening and surveillance for Barrett's esophagus: a randomized and blinded comparisonBlair A Jobe, John G Hunter, Eugene Y Chang, et al.
The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences|June 10, 2020
In Vivo Quasi-Elastic Light Scattering Eye Scanner Detects Molecular Aging in HumansOlga Minaeva, Srikant Sarangi, Danielle M Ledoux, et al.
Diseases of the Esophagus : Official Journal of the International Society for Diseases of the Esophagus|February 25, 2015
Significant understaging is seen in clinically staged T2N0 esophageal cancer patients undergoing esophagectomyJ P Dolan, T Kaur, B S Diggs, et al.
American Journal of Ophthalmology|June 24, 2022
Nasal Transposition of the Split Lateral Rectus Muscle for Strabismus Associated With Bilateral 3<sup>rd</sup>-Nerve PalsyIsdin Oke, Birgit Lorenz, Sotirios Basiakos, et al.
Blood|December 15, 1995
BB-10010: an active variant of human macrophage inflammatory protein-1 alpha with improved pharmaceutical propertiesM G Hunter, L Bawden, D Brotherton, et al.
Brain : a Journal of Neurology|February 10, 2011
The clinical and molecular genetic features of idiopathic infantile periodic alternating nystagmusMervyn G Thomas, Moira Crosier, Susan Lindsay, et al.
American Journal of Medical Genetics|December 11, 1996
Simpson-Golabi-Behmel syndrome: genotype/phenotype analysis of 18 affected males from 7 unrelated familiesR M Hughes-Benzie, G Pilia, J Y Xuan, et al.
American Journal of Human Genetics|July 10, 2012
HOXB1 founder mutation in humans recapitulates the phenotype of Hoxb1-/- miceBryn D Webb, Sherin Shaaban, Harald Gaspar, et al.
Pageof 97