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British Dental Journal
|
November 22, 2014
Consensus statement: Oral health and elite sport performance
I 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 sequencing
Guosheng 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 comparison
Blair 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 Humans
Olga 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 esophagectomy
J 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 Palsy
Isdin 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 properties
M 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 nystagmus
Mervyn 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 families
R 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-/- mice
Bryn D Webb, Sherin Shaaban, Harald Gaspar, et al.
Page
of 97
Search research articles
Search
Showing results (921-930 of 964) with videos related to
Sort By:
Page
of 97
British Dental Journal
|
November 22, 2014
Consensus statement: Oral health and elite sport performance
I 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 sequencing
Guosheng 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 comparison
Blair 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 Humans
Olga 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 esophagectomy
J 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 Palsy
Isdin 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 properties
M 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 nystagmus
Mervyn 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 families
R 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-/- mice
Bryn D Webb, Sherin Shaaban, Harald Gaspar, et al.
Page
of 97