Zobrazeno 1 - 10
of 1 291
pro vyhledávání: '"AcademicSubjects/SCI01140"'
Autor:
Ilse H Stalis, Jeanette C. Papp, Cynthia C. Steiner, Steven M. Thomas, Lindsay C. Sidak-Loftis, Sugandha Dandekar, Jessica Martin Judson, Leona G. Chemnick, Michael N Romanov, Kelli Walker, Michael Mace, Oliver A. Ryder
Publikováno v:
Journal of Heredity
Parthenogenesis is a relatively rare event in birds, documented in unfertilized eggs from columbid, galliform, and passerine females with no access to males. In the critically endangered California condor, parentage analysis conducted utilizing polym
Autor:
Nathan V. Whelan, Caitlin A Redak, Jeffrey T. Garner, Ashantye' S Williams, Kenneth M. Halanych
Publikováno v:
Journal of Heredity
The southeastern United States is home to some of the richest biodiversity in the world. Over the last 200 years, however, rapid industrialization and urbanization have threatened many natural areas, including freshwater habitats. River impoundments
Autor:
Wesley Thompson, Katharine Evans, Daniel Thomas, Evangelos J. Vandoros, Erin Crowley, Ana-Maria Leonte, Annette Hughes, Daniele Sohier, Benjamin Bastin, David Crabtree, M Joseph Benzinger
Publikováno v:
Journal of AOAC International
Background The Thermo Scientific™ SureTect™ Salmonella species PCR Assay utilizes Solaris™ reagents for performing PCR for the rapid and specific detection of Salmonella species in a broad range of foods and select environmental surfaces. Objec
Publikováno v:
Journal of AOAC International
Background Stable carbon isotope analysis of sugars in honey by LC–isotope ratio mass spectrometry (IRMS) is a useful tool for detecting adulteration of honey with extraneous sugar. Purity criteria based on 13C/12C ratios of saccharides in honey, d
Autor:
David C. Whiteman, Thomas L. Vaughan, Bradley J. Kendall, Puya Gharahkhani, Stuart MacGregor, Jue-Sheng Ong
Publikováno v:
Human Molecular Genetics
Symptoms related with gastro-esophageal reflux disease (GERD) were previously shown to be linked with increased risk for the 2019 coronavirus disease (COVID-19). We aim to interrogate the possibility of a shared genetic basis between GERD and COVID-1
Publikováno v:
Mutagenesis
Hepatocellular carcinoma (HCC) is still one of the most common malignancies worldwide. The accuracy of biomarkers for predicting the prognosis of HCC and the therapeutic effect is not satisfactory. N6-methyladenosine (m6A) methylation regulators play
Autor:
Janani Srinivasa Vasudevan, Akshay Kanakan, Rajesh Pandey, Partha Chattopadhyay, Ranjeet Maurya
Publikováno v:
Briefings in Functional Genomics
Infectious diseases are potential drivers for human evolution, through a complex, continuous and dynamic interaction between the host and the pathogen/s. It is this dynamic interaction that contributes toward the clinical outcome of a pathogenic dise
Autor:
Christopher Shaw, Youn-Bok Lee, Do-Young Lee, Claire Troakes, Emma L. Scotter, Jean-Marc Gallo, Boris Rogelj, Jacqueline C. Mitchell
Publikováno v:
Human Molecular Genetics
Transactive response DNA binding protein 43 (TDP-43) is an RNA processing protein central to the pathogenesis of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD). Nuclear TDP-43 mislocalizes in patients to the cytoplasm, where it
Autor:
Gregory M. Findlay
Publikováno v:
Human Molecular Genetics
The application of genomics to medicine has accelerated the discovery of mutations underlying disease and has enhanced our knowledge of the molecular underpinnings of diverse pathologies. As the amount of human genetic material queried via sequencing
Autor:
Gonzalo Perez-Siles, Melina Ellis, Andrew Burgess, Megan H. Brewer, Steve Vucic, Ramesh K Narayanan, Garth A. Nicholson, Marina L. Kennerson, Brent Neumann, Carolyn Ly
Publikováno v:
Human Molecular Genetics
Charcot–Marie-Tooth (CMT) is a commonly inherited, non-fatal neurodegenerative disorder that affects sensory and motor neurons in patients. More than 90 genes are known to cause axonal and demyelinating forms of CMT. The p.R158H mutation in the pyr