Results 71 to 80 of about 315,042 (319)
Être femme et écrivain au XIXe siècle : un statut encore incertain [PDF]
Revue Roumaine d’Etudes Francophones, 2020 Reading is dangerous act for a woman – just remember the fate of Emma Bovary. Writing is even worse. Being a woman and a writer in the 19th century is completely undesirable, because femininity and celebrity are two incompatible concepts.
BACALI Mihaela
doaj
International Journal of Surgery Case Reports, 2015 Gallbladder duplication is a rare congenital malformation that occurs in about one in 4000 births. Congenital anomalies of the gallbladder and anatomical variations of their positions are associated with an increased risk of complications after laparoscopic cholecystectomy.We report the case of a double gallbladder in a fifty-six year old man.
openaire +2 more sources
Somatic mutational landscape in von Hippel–Lindau familial hemangioblastoma
Molecular Oncology, EarlyView.The causes of central nervous system (CNS) hemangioblastoma in Von Hippel–Lindau (vHL) disease are unclear. We used Whole Exome Sequencing (WES) on familial hemangioblastoma to investigate events that underlie tumor development. Our findings suggest that VHL loss creates a permissive environment for tumor formation, while additional alterations ...
Maja Dembic +5 more
wiley +1 more source
A Case of Carcinoma Arising in a Duplication of the Sigmoid Colon [PDF]
, 2002 A rare case of carcinoma in a duplication of the sigmoid colon is presented. A 61-year-old woman was admitted complaining of left epigastric pain and a mass.After several examinations including barium enema, tumor resection with left hemicolectomy was ...
島田, 良 +4 more
core
Localization of an accessory helicase at the replisome is critical in sustaining efficient genome duplication [PDF]
, 2010 © The Author(s) 2010. Published by Oxford University PressGenome duplication requires accessory helicases to displace proteins ahead of advancing replication forks.
Lloyd, RG +11 more
core +1 more source
Frontiers in Genetics, 2013 Copy number variations (CNVs) are associated with many complex diseases. Next generation sequencing data enable one to identify precise CNV breakpoints to better under the underlying molecular mechanisms and to design more efficient assays.
Yinghua eWu +4 more
doaj +1 more source
Molecular Oncology, EarlyView.EXOSC10, an essential nuclear RNA exosome‐associated 3′‐5′ exoribonuclease, is inhibited by the anticancer drug 5‐fluorouracil (5‐FU), and EXOSC10 depletion increases 5‐FU sensitivity. The colon‐cancer variant EXOSC10S402T, located in a proteolysis motif, is stable and nuclear but nonfunctional in vivo.
Radhika Sain +10 more
wiley +1 more source
CNV and nervous system diseases - what's new? [PDF]
, 2008 Several new genomic disorders caused by copy number variation (CNV) of genes whose dosage is critical for the physiological function of the nervous system have been recently identified.
Gu, W., Lupski, J. R.
core +1 more source
Molecular Oncology, EarlyView.Intratumour heterogeneity complicates precision management of advanced endometrial cancer. Circulating tumor DNA (ctDNA) offers a minimally invasive strategy to capture tumor evolution and therapeutic resistance. Here, we compare tumor‐agnostic NGS with tumor‐informed ddPCR, outlining their relative sensitivity, concordance, and clinical implications ...
Carlos Casas‐Arozamena +15 more
wiley +1 more source
Multiple Submission, Duplicate Submission and Duplicate Publication
Balkan Medical Journal, 2013 Committee on Publication Ethics (COPE). http://publicationethics. org/case/duplicate-submission-manuscript-%E2%80%98plant- and-soil%E2%80%99-plso5942-and-%E2%80%98applied-soil- ecology%E2%80%99-apsoil-d-0 (access: 01 December 2012)
openaire +5 more sources