Results 61 to 70 of about 22,189 (264)

LİSELERDE ÇALIŞAN ÖĞRETMENLERDE ÖRGÜTSEL BAĞLILIK İLE ÖRGÜTSEL SESSİZLİK ARASINDAKİ İLİŞKİNİN SAPTANMASI

open access: yesYakın Doğu Üniversitesi İlahiyat Fakültesi Dergisi, 2017
Bu  çalışmanın  amacı,  liselerde  çalışan  öğretmenlerin  Örgütsel Bağlılık ile Örgütsel Sessizlik arasındaki ilişkilerinin duygusal bağlılıklarını karşılaştırmaya çalışmaktır.
Süleyman Doğan, Ahmet Sevgin
doaj  

A multimodal characterization of low-dimensional thalamocortical structural connectivity patterns

open access: yesCommunications Biology
The human thalamus is a heterogeneous subcortical structure coordinating whole-brain activity. Investigations of its internal organization reveal differentiable subnuclei, however, a consensus on subnuclei boundaries remains absent.
Alexandra John   +8 more
doaj   +1 more source

Lymphatic Abnormalities in Noonan Syndrome Extend Beyond Clinically Apparent Disease

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Lymphatic disease represents a well‐described manifestation of Noonan syndrome (NS), yet the full phenotypic spectrum remains incompletely characterized, especially in asymptomatic individuals. We conducted a cross‐sectional study including 10 individuals with NS (four with peripheral lymphedema and six without) and 10 age‐ and sex‐matched ...
Inger Norlyk Sheyanth   +7 more
wiley   +1 more source

Lise Follier-Morales [PDF]

open access: yesNouvelles de l'estampe, 2011
Cela fait trente ans que vous gravez ; pouvez-vous nous rappeler les principaux jalons de votre carriere et les techniques que vous pratiquez ? C’est en 1982, grâce a Maxime Preaud, qui etait a l’epoque responsable du fonds du XVIIeme siecle au sein du departement des Estampes et de la photographie de la Bibliotheque nationale et pratiquait la gravure,
openaire   +2 more sources

Streamlining Diagnosis of Bardet–Biedl Syndrome: New Diagnostic Algorithm With Updated Criteria

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Considerable advances have been made in our understanding of Bardet–Biedl syndrome (BBS), particularly in its core clinical features and molecular genetics, warranting an update to the existing diagnostic criteria framework. Using a rigorous, evidence‐based, and consensus‐driven process, a multidisciplinary group of international experts and ...
Jeremy J. Pomeroy   +16 more
wiley   +1 more source

Neurocognitive dynamics and behavioral differences of symmetry and asymmetry processing in working memory: insights from fNIRS

open access: yesScientific Reports
Symmetry is a ubiquitous property of the visual world. It facilitates cognitive processing and fosters aesthetic appeal. Despite its importance to aesthetic experience and perceptual prominence, the integration of symmetry in working memory remains ...
Izabela Maria Sztuka, Simone Kühn
doaj   +1 more source

A Case of Multiple Mitochondrial Dysfunctions Syndrome 1 and Review of the Literature

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Multiple mitochondrial dysfunctions syndrome 1 (MMDS1, MIM #605711) due to NFU1 gene defects is an ultra‐rare autosomal recessive inborn error of metabolism associated with reduced function of NFU1 iron–sulfur cluster (ISC) scaffold protein.
Charles R. DiFalco   +6 more
wiley   +1 more source

Probabilistic Modeling of Lunar Topography for Exosphere Simulations and Implications for Helium, Neon, and Argon

open access: yesThe Planetary Science Journal
We introduce a numerically efficient approach to include lunar surface topography in Monte Carlo exosphere simulations by sampling slope and azimuth angles from latitude-dependent Lunar Orbiter Laser Altimeter distributions and rotating particle release ...
Alexander Peschel   +3 more
doaj   +1 more source

Ocular and Systemic Findings in COL2A1 and COL11A1 Stickler Syndrome

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Stickler syndrome is most commonly caused by variants in COL2A1 and COL11A1 genes. The purpose of this study was to describe genetic variants and phenotypes in COL2A1 and COL11A1 Stickler syndrome. We performed a retrospective genotype–phenotype evaluation of COL2A1 and COL11A1 Stickler syndrome subjects. Thirty‐two subjects with COL2A1 and 13
Aileen G. MacLachlan   +5 more
wiley   +1 more source

The link between ports and industry [PDF]

open access: yesE3S Web of Conferences
Little attention has been devoted to the relationship between ports and industrial development. This presentation advances the hypothesis that port-industrial zones are now engaged in global competition, whereas they were originally conceived within ...
Frémont Antoine
doaj   +1 more source

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