Results 81 to 90 of about 246,792 (294)

Genetic damages in radiation workers of radiology centers in Bushehr port

Iranian South Medical Journal, 2004
Unstable genetic aberrations might provide a good marker for assessing genetic damage in populations exposed to low levels of ionizing radiation.The frequency of these aberrations was estimated in peripheral lymphocytes from hospital workers in Bushehr ...
Gholamreza Khamisipour, Abdolmajid Tamjidi, Akram Tamjidi, Iraj Nabipour   +3 more
doaj  

Chromosomal rearrangements caused by gamma-irradiation in winter wheat cells

Biosystems Diversity, 2017
In this article we report the results of our investigation into several cytogenetic parameters of variability in mutation induction of modern winter wheat varieties and some connections between the means of cytogenetic indices and different doses of ...
M. M. Nazarenko, O. O. Izhboldin
doaj   +1 more source

Spatial and Volumetric Characteristics of Glioblastoma: Associations With Clinical Presentation and Survival

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective We aim to comprehensively analyze how regional tumor and edema characteristics are associated with clinical presentations and survival outcomes in a large cohort of glioblastoma patients. Methods Patients with IDH‐wildtype glioblastoma who received brain MRI from 2010 to 2023 were included.
Daniel J. Zhou, Marc Jaskir, Julian Gal, Yombe Fonkeu, Christos Davatzikos, MacLean P. Nasrallah, Jose Garcia, Rubo Xing, Stephen J. Bagley, Arati Desai, Richard E. Phillips, Steven Tobochnik, Colin A. Ellis, James J. Gugger, Nishant Sinha, Joel M. Stein, Kathryn A. Davis   +16 more
wiley   +1 more source

Tumors of bone

, 2015
Bone tumors constitute a heterogeneous group of neoplasms of skeletal origin. Benign cartilage tumors include osteochondroma, subungual exostosis, bizarre parosteal osteochondromatous proliferation (BPOP), chondromas, synovial chondromatosis ...
Mandahl, Nils,, Mertens, Fredrik,, Lund University.   +2 more
core   +2 more sources

Chromosomal Aberrations Associated with Clonal Evolution and Leukemic Transformation in Fanconi Anemia: Clinical and Biological Implications [PDF]

, 2012
Fanconi anaemia (FA) is an inherited disease with congenital and developmental abnormalities, bone marrow failure, and extreme risk of leukemic transformation.
Holger Tönnies, Stefan Meyer, Tönnies, Holger, Heidemarie Neitzel, Meyer, Stefan; id_orcid, Meyer, Stefan, Neitzel, Heidemarie, Tönnies, H, Neitzel, H   +8 more
core   +1 more source

Neurologic Manifestations of Long COVID Affect Adult Females More Severely Than Males

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To characterize differences in neurologic manifestations of postacute sequelae of SARS‐CoV‐2 infection (Neuro‐PASC) between females and males. Methods Cross‐sectional study of the first consecutive 261 posthospitalization Neuro‐PASC (PNP) and 2068 nonhospitalized Neuro‐PASC (NNP) patients evaluated at the Neuro‐COVID clinic between ...
Hannah Kopinsky, Melissa Lopez, Janet Miller, Millenia Jimenez, Eric M. Liotta, Igor J. Koralnik   +5 more
wiley   +1 more source

Chromosomal aberrations of isolated gp100-positive cells.

, 2014
(A) CGH profiles of gp100-positive cells (n = 57 cells, all displaying chromosomal aberrations in metaphase CGH). The histogram displays the percentage of cells with specific chromosomal alterations.
Anja Ulmer (524176), Sebastian Scheitler (524178), Stefan Schanz (524182), Claus Garbe (48881), Tanja Fehm (23618), Gerhard Fierlbeck (524184), Helmut Breuninger (191128), Isabelle Hodak (524177), Murat Yildiz (524179), Zbigniew Czyz (524180), Klaus Dietz (44087), Petra Lehnert (524181), Bernhard Polzer (503745), Christoph A. Klein (503744), Christian Hafner (332556), Martin Röcken (524183)   +15 more
core   +1 more source

Augmenting and Assaying Nav1.1 Protein Quantity for Dravet Syndrome Therapy

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Dravet Syndrome (DS) is a developmental and epileptic encephalopathy predominantly caused by heterozygous loss‐of‐function variants in SCN1A, which encodes Nav1.1. Conserved upstream open reading frames (uORFs) in SCN1A were validated to regulate translation in reporter assays, demonstrating the therapeutic viability of increasing Nav1.1 from ...
Aiswarya Saravanan, Jordan Safran, Anna Loughman, Grace Lin, Shivanshi Vaid, Dana Allababidi, Peter M. Tessier, Louis T. Dang   +7 more
wiley   +1 more source

The distribution of HBV integration sites, mutational status of selected tumor suppressor genes and numbers of chromosomal aberrations identified in the 25 patients whose samples were assayed using aCGH assay.

, 2012
W/O = without mutation; Low aberration number = less than 100 chromosomal aberrations; High aberration number = more than 100 chromosomal aberrations.
Hui Zhuang (139189), Ziwei Yang (139177), Jinlin Hou (59138), Malcolm A. McCrae (139183), Weijie Li (139178), Jiangbo Zhang (139180), Xiangmei Chen (139185), Pei-Jer Chen (53402), Xiaojun Li (138162), Chunhui Xu (139181), Suzhen Jiang (139176), Yongfeng Wang (139179), Fengmin Lu (139191)   +12 more
core   +1 more source

Clinical Impact of MGMT Promoter Methylation in IDH‐Mutant Gliomas: Influence of Threshold Selection and Clinical Confounding

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background The clinical relevance of MGMT promoter methylation in IDH‐mutant gliomas remains controversial in the era of molecular classification. We aimed to systematically evaluate its clinical relevance by integrating quantitative assessment, cutoff exploration, and adjustment for clinical confounding.
Haihui Jiang, Linxi Cao, Xiaodong Chen, Siqi Tong, Qinghui Zhu, Jun Yang, Song Lin, Yong Cui   +7 more
wiley   +1 more source