Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Seth L. Ness"'
Autor:
Seth L. Ness, Abigail Bangerter, Nikolay V. Manyakov, David Lewin, Matthew Boice, Andrew Skalkin, Shyla Jagannatha, Meenakshi Chatterjee, Geraldine Dawson, Matthew S. Goodwin, Robert Hendren, Bennett Leventhal, Frederick Shic, Jean A. Frazier, Yvette Janvier, Bryan H. King, Judith S. Miller, Christopher J. Smith, Russell H. Tobe, Gahan Pandina
Publikováno v:
Frontiers in Neuroscience, Vol 13 (2019)
Objective: The Janssen Autism Knowledge Engine (JAKE®) is a clinical research outcomes assessment system developed to more sensitively measure treatment outcomes and identify subpopulations in autism spectrum disorder (ASD). Here we describe JAKE an
Externí odkaz:
https://doaj.org/article/233046f661aa4d178f578093c00aae2b
Autor:
Seth L. Ness, Nikolay V. Manyakov, Abigail Bangerter, David Lewin, Shyla Jagannatha, Matthew Boice, Andrew Skalkin, Geraldine Dawson, Yvette M. Janvier, Matthew S. Goodwin, Robert Hendren, Bennett Leventhal, Frederick Shic, Walter Cioccia, Gahan Pandina
Publikováno v:
Frontiers in Neuroscience, Vol 11 (2017)
Objective: To test usability and optimize the Janssen Autism Knowledge Engine (JAKE®) system's components, biosensors, and procedures used for objective measurement of core and associated symptoms of autism spectrum disorder (ASD) in clinical trials
Externí odkaz:
https://doaj.org/article/3507e7bff0bc4373ac2c4c58a52656f3
Autor:
Raju Kucherlapati, Timothy D. Jenkins, Wolfgang Liedtke, Winfried Edelmann, Seth L. Ness, Anil K. Rustgi
Publikováno v:
Journal of Biological Chemistry. 273:23904-23911
Keratins are intermediate filaments of epithelial cells. Mutations in keratin genes expressed in skin lead to human disorders, including epidermolysis bullosa simplex and epidermolytic hyperkeratosis. We examined the role of keratin 4 (K4) in maintai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b982e9554150dc9c3f20f0dc28198e7
https://doi.org/10.1074/jbc.273.37.23904
https://doi.org/10.1074/jbc.273.37.23904
Autor:
Thomas B. Friedman, Anne C. Madeo, Karen B. Avraham, Carmen C. Brewer, Tamar Ben-Yosef, Robert J. Desnick, Seth L. Ness, Judith P. Willner, Ruth Kornreich, A Bar-Lev, Andrew J. Griffith
Publikováno v:
Journal of medical genetics. 40(10)
Usher syndrome (USH) is an autosomal recessive disorder comprising of bilateral sensorineural hearing loss, progressive loss of vision due to retinitis pigmentosa (RP), and variable vestibular dysfunction. It is the most frequent cause of deafness an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c79e8b0fa1313afcd06bb392652caa4
https://pubmed.ncbi.nlm.nih.gov/14569126
https://pubmed.ncbi.nlm.nih.gov/14569126
Autor:
Anil K. Lalwani, Susan Bellman, Melvin D. Schloss, Zahoor Ahmed, Richard J.H. Smith, Seth L. Ness, Arabandi Ramesh, Sheikh Riazuddin, Thomas B. Friedman, Robert C. Polomeno, Edward R. Wilcox, C. R. Srikumari Srisailpathy, Julie M. Bork, Saima Riazuddin, Vazken M. Der Kaloustian, Walter E. Nance, Graeme Wistow, Shaheen N. Khan, Linda M. Peters, Dilip Desmukh, Xue-Zhong Liu, Zubair M. Ahmed, Robert J. Morell, Andrew J. Griffith, S. L. Bernstein, Maria Bitner-Glindzicz, X. Cindy Li, Sigrid Wayne
Genes causing nonsyndromic autosomal recessive deafness (DFNB12) and deafness associated with retinitis pigmentosa and vestibular dysfunction (USH1D) were previously mapped to overlapping regions of chromosome 10q21-q22. Seven highly consanguineous f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b2acf26b9bb7e65139c9a2f9e49d2fd
https://europepmc.org/articles/PMC1234923/
https://europepmc.org/articles/PMC1234923/
Publikováno v:
Otolaryngology - Head and Neck Surgery. 129:P93
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::db5b0cc573b9093e57cb44413bbf9587
https://doi.org/10.1016/s0194-5998(03)00933-1
https://doi.org/10.1016/s0194-5998(03)00933-1