Results 251 to 260 of about 536,745 (332)

GENOTYPIC AND PHENOTYPIC CORRELATION AND PATH ANALYSIS FOR LODGING RESISTANCE TRAITS IN BREAD WHEAT (Triticum aestivum L.)

, 2007
Z. I. Sarker, A. K. M. Shamsuddin, Lutfur Rahman, R. Ara   +3 more
openalex   +2 more sources

Acoustic Measures Capture Speech Dysfunction in Spinocerebellar Ataxia

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Spinocerebellar ataxias (SCA) are hereditary cerebellar degenerative disorders with a common feature of dysarthria, involving impaired phonatory and articulatory control of speech, thereby affecting social communication. In this study, we investigated whether acoustic measures could objectively measure speech dysfunction and identify
Zena Fadel, Charlotte Hennessey, Hannah Lee, Pia Parekh, Sheng‐Han Kuo, Ami Kumar   +5 more
wiley   +1 more source

Genetic dissection of nutrient element enrichment in <i>Saccharum officinarum</i> L. for deciphering the food health. [PDF]

Front Plant Sci
Fan L, Chachar Z, Chen M, Li Y, Chen J, He H, Wen J, Gul S, Lai R, Qi Y.   +9 more
europepmc   +1 more source

Age‐Related Characteristics of SYT1‐Associated Neurodevelopmental Disorder

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objectives We describe the clinical manifestations and developmental abilities of individuals with SYT1‐associated neurodevelopmental disorder (Baker‐Gordon syndrome) from infancy to adulthood. We further describe the neuroradiological and electrophysiological characteristics of the condition at different ages, and explore the associations ...
Sam G. Norwitz, Josefine Eck, Joel S. Winston, Kate Baker   +3 more
wiley   +1 more source

Genomewide association and prediction of phenotypic stability in barley. [PDF]

Plant Genome
Neyhart JL, Gutierrez L, Smith KP.
europepmc   +1 more source

Discovery and Targeted Proteomic Studies Reveal Striatal Markers Validated for Huntington's Disease

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Clinical trials for Huntington's disease (HD) enrolling persons before clinical motor diagnosis (CMD) lack validated biomarkers. This study aimed to conduct an unbiased discovery analysis and a targeted examination of proteomic biomarkers scrutinized by clinical validation. Methods Cerebrospinal fluid was obtained from PREDICT‐HD and
Daniel Chelsky, Cara Joyce, H. Jeremy Bockholt, Paul A. Rudnick, William H. Adams, Fiona McAllister, Justin W. Smock, Michael A. Newton, Jane S. Paulsen   +8 more
wiley   +1 more source

CDKN2B Inhibits Vascular Smooth Muscle Phenotypic Switching in Corpus Spongiosum Surrounding the Urethral Plate in Hypospadias. [PDF]

Biomedicines
Huang J, Xu Z, Huang J, Yin X, Huang Y, Chen F.   +5 more
europepmc   +1 more source

Heritability, Phenotypic and Genetic Correlations Between Type Ratings and Milk Fat Production in Ayrshire Cattle

, 1963
D.F. Butcher, Ralph Mitchell, I.D. Porterfield, R.S. Dunbar   +3 more
openalex   +1 more source

Evaluation of the Efficacy and Safety of Satralizumab in a Pregnant NMOSD Patient With AQP4/MOG‐IgG Dual Seropositive: A Case Report

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Neuromyelitis Optica Spectrum Disorder (NMOSD) is a chronic autoimmune neuroinflammatory disease, typically characterized by antibodies against aquaporin 4 (AQP4‐IgG) or myelin oligodendrocyte glycoprotein (MOG‐IgG). Simultaneous seropositivity for both antibodies in a single patient is exceedingly rare.
Yeting Luo, Shuhua Xie, Xianghong Liu
wiley   +1 more source

An Integrative Genetic Strategy for Identifying Causal Genes at Quantitative Trait Loci in Chickens. [PDF]

Animals (Basel)
Ishikawa A.
europepmc   +1 more source