Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Lauren Kam"'
Autor:
Emily H Belarmino, Michelle Carfagno, Lauren Kam, Kene-Chukwu Ifeagwu, Miriam E Nelson, Rebecca A Seguin-Fowler
Publikováno v:
Public Health Nutrition, Vol 27 (2024)
Abstract Objective: To better understand how the public defines ‘healthy’ foods and to determine whether the public considers sustainability, implicitly and explicitly, in the context of healthy eating. Design: We conducted a content analysis
Externí odkaz:
https://doaj.org/article/90e093e380554594a5f74d5d32d5e1a4
Autor:
Li Cai, Danny Overman, Carrie Wilson, Binbin Huang, Dan Wang, Ying Wang, Jodie William, Melissa Calvert, Caron Glotzbach, Lauren Kam-Morgan, Anjen Chenn
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101566- (2024)
Externí odkaz:
https://doaj.org/article/de41b6265c7f4c9d80972b6b13dfb56c
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101635- (2024)
Externí odkaz:
https://doaj.org/article/e20c6423a0d840d1882b9b4148c0b12e
Autor:
Shethah R. Morgan, Jessica Whiteley, Emma Donald, John Smith, Marcia T. Eisenberg, Eddie Kallam, Lauren Kam-Morgan
Publikováno v:
Clinical Medicine Insights: Pathology, Vol 2012, Iss 5, Pp 15-22 (2012)
Externí odkaz:
https://doaj.org/article/9286e993e21849fb9ee3e3542ee13bd5
Autor:
Mohammad Haque, Lauren Kaminsky, Raz Abdulqadir, Jessica Engers, Evgeny Kovtunov, Manmeet Rawat, Rana Al-Sadi, Thomas Y. Ma
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
BackgroundDefective intestinal epithelial tight junction (TJ), characterized by an increase in intestinal TJ permeability, has been shown to play a critical role in the pathogenesis of inflammatory bowel disease (IBD). Tumor necrosis factor-α (TNF-
Externí odkaz:
https://doaj.org/article/3d6dadc85d734c34991bd87666b04db4
Isocitrate dehydrogenase 1 and 2 (IDH1 and IDH2) are the most frequently mutated metabolic genes in human cancer. They encode cytosolic and mitochondrial enzymes that catalyze the conversion of isocitrate to a-ketoglutarate (αKG), a key component in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29b38d3582bdaae4554ac21abe8bb718
https://europepmc.org/articles/PMC6216322/
https://europepmc.org/articles/PMC6216322/
Autor:
Scott Hood, Jordan Riojas, Carissa Best, Danny Overman, Dylan Rutledge, Li Cai, Kaitlyn Barker, Marcia Eisenberg, Eddie Kallam, Lauren Kam-Morgan
Publikováno v:
Journal of Clinical Epigenetics.
The Epi proColon® test is the first and only FDA-approved molecular blood test for colorectal cancer (CRC) screening. The high-sensitivity Real-Time PCR method detects a hypermethylated promoter region of the Septin 9 gene (SEPT9) shown to be associ
Autor:
Marcia Eisenberg, Lauren Kam-Morgan, Bruce Horten, Hawazin Faruki, D. Neil Hayes, Matthew D. Wilkerson, Gregory Mayhew, Charles M. Perou, Scott Parker, Cheng Fan, Myla Lai-Goldman
Publikováno v:
Archives of Pathology & Laboratory Medicine. 140:536-542
Context A histologic classification of lung cancer subtypes is essential in guiding therapeutic management. Objective To complement morphology-based classification of lung tumors, a previously developed lung subtyping panel (LSP) of 57 genes was test
Autor:
Yangming Cao, Lauren Kam-Morgan, Bifen Chen, Henry T. Lynch, Jay P. Marshall, Maura Pieretti, Nada H. Khattar
Publikováno v:
American Journal of Gastroenterology. 97:1822-1827
The clinical differentiation between hereditary nonpolyposis colorectal cancer (HNPCC) and attenuated familial adenomatous polyposis (AFAP) is very difficult. The 62-yr-old proband presented with duodenal adenocarcinoma. His history of subtotal colec
Autor:
Dharam P. Chauhan, Matthew C. Cayouette, Lauren Kam-Morgan, C. Richard Boland, Luigi Laghi, Giancarlo Marra, John M. Carethers, Cameron G. Binnie, Minoru Koi, Michael C. Luce, Mary T. Hawn, Sajeev P. Cherian
Publikováno v:
Gastroenterology. 109:1368-1374
Background & Aims : Hereditary nonpolyposis colorectal cancer (HNPCC) has been linked recently to a defect in repairing mismatched nucleotides in DNA. The aim of this study was to screen for germline mutations that result in prematurely truncated pro