Results 81 to 90 of about 984,465 (267)

Anomalous Fraunhofer Line Profiles [PDF]

open access: yesNature, 1962
DURING the spring of 1961 we made observations of the H line of Ca(II) in the spectrum of moonlight, with the view of detecting any luminescent radiation which might have been present. The observations were made with the 50-in. reflector of the University of Padua's Observatory at Asiago.
J. F. GRAINGER, J. RING
openaire   +1 more source

Hyperosmotic stress induces PARP1‐mediated HPF1‐dependent mono(ADP‐ribosyl)ation

open access: yesFEBS Letters, EarlyView.
Sorbitol‐induced hyperosmotic stress rapidly induces reversible mono(ADP‐ribosyl)ation (MARylation) on PARP1 without the signs of genotoxic signaling. We show that PARP1 autoMARylation is HPF1 dependent and forms hydroxylamine‐resistant O‐glycosidic linkages.
Anna Georgina Kopasz   +11 more
wiley   +1 more source

An isoform of 14‐3‐3 protein regulates transbilayer lipid movement at the plasma membrane

open access: yesFEBS Letters, EarlyView.
Loss of 14‐3‐3ζ in CHO cells confers resistance to exogenous phosphatidylserine (PS) and impairs endocytosis‐independent inward flip‐flop of fluorescent PS at the plasma membrane. RNAi‐mediated knockdown reproduces this defect, while no additive effect is seen in ATP11C‐deficient cells.
Akiko Yamaji‐Hasegawa   +3 more
wiley   +1 more source

Profile line accuracy in cephalometric radiographs

open access: yesAmerican Journal of Orthodontics and Dentofacial Orthopedics
Introduction This study investigates the accuracy of facial soft-tissue profile lines in lateral cephalometric radiographs by comparing them to true profile lines derived from 3-dimensional photographs.Methods This prospective methodological study was performed on preexisting records of 100 orthodontic patients.
Marie-Laure Arn   +4 more
openaire   +3 more sources

The ubiquitin ligase RNF115 is required for the clearance of damaged lysosomes

open access: yesFEBS Letters, EarlyView.
Upon lysosomal rupture, an E3 ubiquitin ligase RNF115 translocates from the cytosol to the damaged lysosomal membrane. Moreover, RNF115 depletion impairs the clearance of damaged lysosomes, identifying it as a key regulator of lysosomal quality control.
Sae Nakanaga   +3 more
wiley   +1 more source

Data-driven analysis of neutron diffraction line profiles: application to plastically deformed Ta. [PDF]

open access: yesSci Rep, 2022
Tallman AE   +7 more
europepmc   +1 more source

Epigenetic blind spots – the role of DNA methylation dynamics in stem cell‐based models of embryogenesis

open access: yesFEBS Letters, EarlyView.
Embryo‐like structures (stembryos) are an innovative tool, but they are hindered by experimental variability and limited developmental potential. DNA methylation is crucial for mammalian development, but its status in stembryo models is poorly characterized.
Sara Canil   +4 more
wiley   +1 more source

Line Profiles of Faculae and Pores [PDF]

open access: yesHighlights of Astronomy, 1977
Historically, attempts to model the temperature structure of faculae have generally suffered from a rather basic contradiction. Models which were based on center to limb measurements of the continuum contrast of faculae disagree with models that are based on measurements of line profiles in faculae.
openaire   +1 more source

Septin 9 PB domains coordinate centrosome positioning and microtubule acetylation to control epithelial polarity

open access: yesFEBS Letters, EarlyView.
Septin 9 polybasic domains couple phosphoinositide‐rich membrane binding to centrosome positioning, Golgi organization, and microtubule acetylation to control epithelial polarity. Their loss disrupts this axis, causing centrosome mispositioning, Golgi fragmentation, reduced microtubule acetylation, and polarity inversion via upregulation of the ...
Ting ting Cai   +4 more
wiley   +1 more source

Phase-Dependent Line Profiles of VV CEP [PDF]

open access: yesJournal of Astronomy and Space Sciences, 1992
The normalized line profiles of VV Cep have been calculated by integrating the equation of transfer. The Sobolev theory was adopted and the wind velocity distribution was assumed to be V(r)=V∞(1-Rc/r)^(1/2). The peaks of the line profiles for the phase 0.
Kyung-Mee Kim, Kyu-Hong Choi
doaj  

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