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A C Smith

Showing results (381-390 of 442) with videos related to

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Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology|November 20, 2012
MALT lymphoma in labial salivary gland biopsy from Sjögren syndrome: importance of follow-up in early detectionA Keszler, L I Adler, M S Gandolfo, et al.
Clinical Genetics|June 1, 2018
A ZPR1 mutation is associated with a novel syndrome of growth restriction, distinct craniofacial features, alopecia, and hypoplastic kidneysY A Ito, A C Smith, K D Kernohan, et al.
Psychiatry Research|April 30, 2013
Polymorphisms in schizophrenia candidate gene UFD1L may contribute to cognitive deficitsVanessa K Ota, Arthur A Berberian, Ary Gadelha, et al.
Revista Brasileira De Psiquiatria (Sao Paulo, Brazil : 1999)|March 9, 2017
Catechol-O-methyltransferase (COMT) polymorphisms modulate working memory in individuals with schizophrenia and healthy controlsCamila T Matsuzaka, Denise Christofolini, Vanessa K Ota, et al.
Plos One|March 19, 2025
Inter-rater reliability of stress signatures in exfoliated primary dentition - Improving scientific rigor and reproducibility in histological data collectionSimone A M Lemmers, Mona Le Luyer, Samantha J Stoll, et al.
Human Genetics|December 6, 2001
Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndromeN Liburd, M Ghosh, S Riazuddin, et al.
Journal of Medical Genetics|August 3, 2004
Genomic imprinting of PPP1R9A encoding neurabin I in skeletal muscle and extra-embryonic tissuesK Nakabayashi, S Makino, S Minagawa, et al.
BMC Gastroenterology|July 22, 2009
Interrelationship between TP53 gene deletion, protein expression and chromosome 17 aneusomy in gastric adenocarcinomaAndré S Khayat, Adriana C Guimarães, Danielle Q Calcagno, et al.
Neuroscience|June 27, 2012
Analysis of SNAP25 mRNA expression and promoter DNA methylation in brain areas of Alzheimer's Disease patientsT K Furuya, P N O Silva, S L M Payão, et al.
Clinical Genetics|January 16, 2015
LIMS2 mutations are associated with a novel muscular dystrophy, severe cardiomyopathy and triangular tonguesJodi Warman Chardon, A C Smith, J Woulfe, et al.
Pageof 45

Showing results (381-390 of 442) with videos related to

Sort By:
Pageof 45
Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology|November 20, 2012
MALT lymphoma in labial salivary gland biopsy from Sjögren syndrome: importance of follow-up in early detectionA Keszler, L I Adler, M S Gandolfo, et al.
Clinical Genetics|June 1, 2018
A ZPR1 mutation is associated with a novel syndrome of growth restriction, distinct craniofacial features, alopecia, and hypoplastic kidneysY A Ito, A C Smith, K D Kernohan, et al.
Psychiatry Research|April 30, 2013
Polymorphisms in schizophrenia candidate gene UFD1L may contribute to cognitive deficitsVanessa K Ota, Arthur A Berberian, Ary Gadelha, et al.
Revista Brasileira De Psiquiatria (Sao Paulo, Brazil : 1999)|March 9, 2017
Catechol-O-methyltransferase (COMT) polymorphisms modulate working memory in individuals with schizophrenia and healthy controlsCamila T Matsuzaka, Denise Christofolini, Vanessa K Ota, et al.
Plos One|March 19, 2025
Inter-rater reliability of stress signatures in exfoliated primary dentition - Improving scientific rigor and reproducibility in histological data collectionSimone A M Lemmers, Mona Le Luyer, Samantha J Stoll, et al.
Human Genetics|December 6, 2001
Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndromeN Liburd, M Ghosh, S Riazuddin, et al.
Journal of Medical Genetics|August 3, 2004
Genomic imprinting of PPP1R9A encoding neurabin I in skeletal muscle and extra-embryonic tissuesK Nakabayashi, S Makino, S Minagawa, et al.
BMC Gastroenterology|July 22, 2009
Interrelationship between TP53 gene deletion, protein expression and chromosome 17 aneusomy in gastric adenocarcinomaAndré S Khayat, Adriana C Guimarães, Danielle Q Calcagno, et al.
Neuroscience|June 27, 2012
Analysis of SNAP25 mRNA expression and promoter DNA methylation in brain areas of Alzheimer's Disease patientsT K Furuya, P N O Silva, S L M Payão, et al.
Clinical Genetics|January 16, 2015
LIMS2 mutations are associated with a novel muscular dystrophy, severe cardiomyopathy and triangular tonguesJodi Warman Chardon, A C Smith, J Woulfe, et al.
Pageof 45