Results 241 to 250 of about 586,704 (319)

Global genetic diversity of Infectious Salmon Anemia Virus (ISAV) a scoping review protocol. [PDF]

PLoS One
Thapa PC, Raquib A, Mears K, Sanchez J, Saksida S, Hammell KL, Thakur KK.   +6 more
europepmc   +1 more source

An Analysis for IDH‐Mutant Grade 4 Astrocytoma Based on WHO CNS 5: Implication of Clinical Practice

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Purpose There is ongoing debate regarding the therapeutic approach and prognosis for IDH‐mutant grade 4 astrocytoma, a newly defined subtype of diffuse glioma in the 2021 WHO classification system for central nervous system tumors (WHO CNS 5). The aim of this study was to explore the clinical outcome and prognosticators for newly diagnosed IDH‐
Xianxin Qiu, Liping Liang, Lingchao Chen, Pengjie Hong, Wanzun Lin, Jiabing Liu, Zhirui Zhou, Wenjia Zhu, Tianqi Wu, Mingyuan Pan, Yihua Zhong, Jing Gao, Zhiyong Qin, Yang Wang   +13 more
wiley   +1 more source

Genetic Diversity and Metabolic Profile of Tibetan Medicinal Plant <i>Saussurea obvallata</i>. [PDF]

Genes (Basel)
Zhang S, Wang S, Wang S, Su H, De J.
europepmc   +1 more source

Tools for assessment of genetic and phenotypic diversity

, 1988
M. Lefort-Buson, Catherine Damerval
openalex   +1 more source

Analysis of the genetic diversity and phylogenetic relationship of Italian isolates of feline immunodeficiency virus indicates a high prevalence and heterogeneity of subtype B.

, 1997
Mauro Pistello, Daniela Mauro, E Nicoletti, Giovanni Cammarota, M. Joan Curcio, M Bendinelli, Donatella Matteucci   +6 more
openalex   +1 more source

Pathway Analyses of Inherited Neuropathies Identify Putative Common Mechanisms of Axon Degeneration

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Inherited neuropathies (IN) are associated with over 100 different genetic mutations presenting with a variety of phenotypes. This complexity suggests multiple pathways may converge onto a limited number of downstream pathways to effect axonal injury.
Christopher R. Cashman, Craig Blackstone, Reza Sadjadi   +2 more
wiley   +1 more source

Genetic diversity analysis and core germplasm construction of tea plants in Lu'an. [PDF]

BMC Plant Biol
Wang Y, Peng H, Tong X, Ding X, Song C, Ma T, Wang H, Wei W, Chen C, Zhu J, Liu D.   +10 more
europepmc   +1 more source

Fetal Akinesia/Hypokinesia and Arthrogryposis of Neuromuscular Origin: Etiologic Groups, Genetics, and Phenotypic Spectrum

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To provide a comprehensive clinical and genetic characterization of individuals with arthrogryposis multiplex congenita (AMC), focusing on the distribution of genetic etiologies across the neuromuscular spectrum and comparing myogenic and neurogenic subtypes. Methods A total of 105 individuals with AMC were clinically and genetically
Florencia Pérez‐Vidarte, Berta Estévez‐Arias, Leslie Matalonga, Delia Yubero, Anna Codina, Carlos Ortez, Julita Medina, Lidia DeSena DeCabo, Laura Carrera‐García, Jesica Expósito‐Escudero, Cristina Jou, Eduardo F. Tizzano, Andres Nascimento, Daniel Natera‐de Benito   +13 more
wiley   +1 more source

Genetic diversity of norovirus in Shenzhen Based on continuous surveillance from 2016 to 2022. [PDF]

Front Cell Infect Microbiol
Wang X, Liu W, Hu M, Ma H, He Y, Wang B, Li K, Zhang R, Fu J, Zhang H, Chen L, Zhao X, Aimaiti B, Song H, Ren H, Hu X.   +15 more
europepmc   +1 more source

Phenotyping Healthcare Use 2–3 Decades Before the First Multiple Sclerosis Demyelinating Event

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Phenotype hospital, physician, and emergency department (ED) visits by diagnoses and specialty up to 29 years pre‐multiple sclerosis (MS) onset versus a matched population without MS. Methods We identified people with MS (PwMS) using population‐based administrative data from Ontario, Canada (1991–2020).
Helen Tremlett, Karl Everett, Colleen J. Maxwell, Feng Zhu, Ayesha Asaf, Ping Li, Kyla A. McKay, Yinshan Zhao, Ruth Ann Marrie   +8 more
wiley   +1 more source