A basal body microtubule singlet-to-doublet transition in Plasmodium male gametogenesis. [PDF]
Yang S +8 more
europepmc +1 more source
Men at risk: occupation and male infertility.
P. Claman
semanticscholar +1 more source
A Generic and Subgeneric Synopsis of the Male Ants of the United States [PDF]
M. R. Smith
openalex +1 more source
Analysis of Soluble Interleukin‐2 Receptor as a Prognostic Biomarker in NMOSD and MOGAD
ABSTRACT Objective Soluble interleukin‐2 receptor (sIL‐2R) is a biomarker for T cell activity. T cells are involved in neuromyelitis optica spectrum disorders (NMOSD) and myelin oligodendrocyte glycoprotein antibody‐associated disease (MOGAD) pathogenesis. However, sIL‐2R has so far not been evaluated in these conditions.
Philipp Klyscz +8 more
wiley +1 more source
Predictors for Acceptance of Sexual Aggression Myths Among People Using Cyberporn: Cross-Sectional Study. [PDF]
Ben Brahim F +3 more
europepmc +1 more source
Lifestyle causes of male infertility
D. Durairajanayagam
semanticscholar +1 more source
Nerve Excitability in Asymptomatic Carriers and Amyotrophic Lateral Sclerosis Patients With C9orf72
ABSTRACT Objective We investigated the effects of C9orf72 mutation carriership on peripheral nerve excitability in asymptomatic individuals from families with a history of C9orf72 amyotrophic lateral sclerosis (ALS) and patients. Methods We included 47 asymptomatic individuals from families with a history of C9orf72 ALS, of whom 23 were carriers (C9 ...
Diederik J. L. Stikvoort García +3 more
wiley +1 more source
Understanding the impact of streptozotocin on diabetic male infertility: perspectives from rodent models and pharmacological networking. [PDF]
Asghar MA +8 more
europepmc +1 more source
The Male of the Parthenogenetic May‐Fly, Ameletus Ludens [PDF]
James G. Needham
openalex +1 more source
ABSTRACT Objective Paroxysmal kinesigenic dyskinesia (PKD) is the most common hereditary paroxysmal movement disorder. The PRRT2 gene is the first identified causative gene and accounts for the majority of PKD. In this study, we investigated the pathogenicity of PRRT2 variants in the splice regions. Methods Patients with clinically suspected PKD and no
Jiao‐Jiao Xu +5 more
wiley +1 more source

