Ziele und Wege biologischer Forschung : beleuchtet an der Hand einer Gerüstbildungsmechanik
, 1892 Friedrich Dreyer
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Alkane biosynthesis gene expression and its increased production in recombinant cyanobacteria
FEBS Open Bio, EarlyView.The transcription and mRNA structures of the alkane biosynthesis genes ado/aar were analysed in the representative cyanobacteria PCC 6803 and SK1‐2‐1, which produce C17H36 and C15H32, respectively. PCC 6803 transconjugants carrying these genes showed a 1.8‐ to 2.3‐fold increase in C17H36 production.
Misato Nagao +4 more
wiley +1 more source
Clinical utility of cerebrospinal fluid biomarkers measured by LUMIPULSE® system
Annals of Clinical and Translational Neurology, Volume 9, Issue 12, Page 1898-1909, December 2022., 2022 Abstract Objectives Cerebrospinal fluid (CSF) biomarkers of Alzheimer's disease (AD) are well‐established in research settings, but their use in routine clinical practice remains a largely unexploited potential. Here, we examined the relationship between CSF biomarkers, measured by a fully automated immunoassay platform, and brain β‐amyloid (Aβ ...
Hisashi Nojima +9 more
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Data for the problem of evolution in man. I. A first study of the variability and correlation of the hand [PDF]
, 1900 Mitch Whiteley, Karl Pearson
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FEBS Open Bio, EarlyView.SLC7A11 frequently migrates faster in SDS‐PAGE. The present study found that the high hydrophobicity of SLC7A11 causes its anomalous migration in SDS‐PAGE with a low concentration of acrylamide gel. Replacing isoleucine with asparagine reduced hydrophobicity and restored its normal migration at 55 kDa, revealing the role of hydrophobicity and gel ...
Nsengiyumva Emmanuel +13 more
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Clinical heterogeneity in a family with flail arm syndrome and review of hnRNPA1‐related spectrum
Annals of Clinical and Translational Neurology, Volume 9, Issue 12, Page 1910-1917, December 2022., 2022 Abstract Objective Flail arm syndrome (FAS) is one of the atypical subtypes of amyotrophic lateral sclerosis (ALS). Mutations in hnRNPA1 encoding heterogeneous nuclear ribonucleoprotein (hnRNP) A1 are a rare genetic cause of ALS. Herein, marked clinical heterogeneity of FAS in a pedigree with a known hnRNPA1 variant was described to raise early ...
Xiaochen Han +5 more
wiley +1 more source
123. A REMARKABLE CASE OF APHASIA. ACUTE AND COMPLETE EMBOLIC SOFTENING OF THE LEFT MOTOR-VOCAL SPEECH CENTER (BROCAʼS CONVOLUTION) IN A RIGHT-HANDED MAN; TRANSIENT MOTOR APHASIA, MARKED INABILITY TO NAME OBJECTS, AND ESPECIALLY PERSONS, CONSIDERABLE AGRAPHIA AND SLIGHT WORD-BLINDNESS [PDF]
, 1899 Byrom Branrwell, Jelliffe
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Hemorrhage and thrombosis hand in hand
Annals of Saudi Medicine, 2012 Ashish Bhalla +4 more
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