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Results 91 to 100 of about 24,581 (266)

Genome‐Wide Assessment Reveals Ancestral Differences in Homozygosity Patterns Potentially Linked to Parkinson's Disease Etiology

Movement Disorders, EarlyView.
Abstract Background Recessive genetic variation and extended runs of homozygosity (ROHs) may contribute to the unexplained heritability of Parkinson's disease (PD), particularly in diverse and understudied populations. Objective We conducted the first large‐scale, multi‐ancestral investigation of PD to examine the impact of genome‐wide homozygosity on ...
Kathryn Step +680 more
wiley +1 more source

Author Correction: Sustainable production of graphene from petroleum coke using electrochemical exfoliation

npj 2D Materials and Applications, 2021
Sanjit Saha +9 more
doaj +1 more source

Influence of chain length of amido betaines and amine degree of diamines on the binary supramolecular assembly and viscosity dynamics of amido betaine/diamine coacervates

JCIS Open
Recently, there has been growing interest in the hierarchical assemblies of zwitterionic betaine amphiphiles across various fields due to their utility as stimuli-responsive materials.
Yu-Ting Lin +7 more
doaj +1 more source

[Review of] Gerri Hirshey. Nowhere to Run: The Story of Soul Music [PDF]

, 1987
Gerri Hirshey\u27s book was conceived, according to her preface, as a series of literary spotlights, illuminating the world of Soul Music and the musicians whose performances and recordings created it. In its final form, the book became a collection of
Eive, Gloria
core +1 more source

Discordance of Dopaminergic Dysfunction and Subcortical Atrophy by α‐Synuclein Status in Sporadic and Genetic Parkinson's Disease

Movement Disorders, EarlyView.
Abstract Background Parkinson's disease (PD) is characterized by predominantly neuronal α‐synuclein pathology and dopaminergic dysfunction. Cerebrospinal fluid (CSF) seeding amplification assays (SAA) detect α‐synuclein aggregates in vivo, but not all patients with PD have a positive SAA.
Michael Tran Duong +186 more
wiley +1 more source

Current Literature [PDF]

, 1990
Material appearing below is thought to be of particular interest to Linacre Quarterly readers because of its moral, religious, or philosophic content. The medical literature constitutes the primary but not the sole source of such material.
Catholic Physicians\u27 Guild
core +1 more source

Clinical, Genetic, and Imaging Characteristics of SCA27B: Insights from a Large Dutch Cohort

Movement Disorders, EarlyView.
Abstract Background Deep intronic GAA repeat expansions in intron 1 of the FGF14 gene were identified in 2023 as cause of late‐onset cerebellar ataxia. Since then, GAA‐FGF14‐related ataxia (SCA27B) has emerged as one of the most common genetic causes of late‐onset cerebellar ataxia.
Teije H. van Prooije +26 more
wiley +1 more source

Spartan Daily, January 18, 1939 [PDF]

, 1939
Volume 27, Issue 65https://scholarworks.sjsu.edu/spartandaily/2855/thumbnail ...
San Jose State University, School of Journalism and Mass Communications
core +2 more sources

Increased Serum Neurofilament Light Chain Levels in Parkinson's Disease Patients Carrying the p.A53T SNCA Mutation: Data from the Parkinson's Progression Markers Initiative Study

Movement Disorders, EarlyView.
Abstract Background Serum neurofilament light chain (NfL) levels, a marker of axonal damage, are generally elevated in neurodegenerative conditions, but results in idiopathic Parkinson's disease (iPD) have been inconsistent. The p.A53T SNCA mutation usually leads to a severe form of PD.
Nikolaos Papagiannakis +213 more
wiley +1 more source

Spartan Daily, June 4, 1945 [PDF]

, 1945
Volume 33, Issue 148https://scholarworks.sjsu.edu/spartandaily/3628/thumbnail ...
San Jose State University, School of Journalism and Mass Communications
core +1 more source

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