Results 21 to 30 of about 44,175 (160)

Mâtürîdî-Hanefî Aidiyetin Osmanlı’daki İzdüşümleri

open access: yesCumhuriyet İlahiyat Dergisi, 2016
Mâtürîdîlik bir Osmanlı kimliğidir ve bu kimlik zannedildiği gibi son dönemle de sınırlı değildir; bütün bir Osmanlı tarihi boyunca biçimsel olarak varlığını korumuştur.
Mehmet Kalaycı
doaj   +1 more source

Exosomal lncRNA CHL1-AS1 Derived from Peritoneal Macrophages Promotes the Progression of Endometriosis via the miR-610/MDM2 Axis

open access: yesInternational Journal of Nanomedicine, 2021
Background Exosomes secreted by peritoneal macrophages (pMφ) are deeply involved in the development of endometriosis (EMs). Exosomes can mediate cell-to-cell communication by transferring biological molecules.
Ting Liu   +5 more
semanticscholar   +1 more source

HAWC J2227+610 and Its Association with G106.3+2.7, a New Potential Galactic PeVatron [PDF]

open access: yesAstrophysical Journal, 2020
We present the detection of very-high-energy gamma-ray emission above 100 TeV from HAWC J2227+610 with the High-Altitude Water Cherenov Gamma-Ray Observatory (HAWC) observatory.
A. Albert   +99 more
semanticscholar   +1 more source

Sâlih Nâbî'nin Felsefe-i Mûsikî İsimli Eseri Üzerine Bir Değerlendirme

open access: yesCumhuriyet İlahiyat Dergisi, 2018
Sâlih Nâbî (ö. 1332/ 1914), Osmanlı’nın son dönemlerinde yaşayan tıbbiye mezunu bir Türk mûsikîsi meraklısıdır. 1910 yılında Felsefe-i Mûsikî isimli bir eser kaleme almış, bu çalışmasında mûsikînin insan ruhu üzerindeki etkisi, mûsikî tarihi ve kendi ...
Mehmet Tıraşcı
doaj   +1 more source

Association of congenital cardiovascular malformation and neuropsychiatric phenotypes with 15q11.2 (BP1–BP2) deletion in the UK Biobank

open access: yesEuropean Journal of Human Genetics, 2020
Deletion of a non-imprinted 500kb genomic region at chromosome 15q11.2, between breakpoints 1 and 2 of the Prader–Willi/Angelman locus (BP1–BP2 deletion), has been associated in previous studies with phenotypes including congenital cardiovascular ...
S. Williams   +9 more
semanticscholar   +1 more source

Kur’ân-ı Kerîm’deki Sarf ‘Udûllerinin Anlama Etkisi

open access: yesCumhuriyet İlahiyat Dergisi, 2018
Bu makalede, üslûp bilimin ve belâgatin önemli konuları arasında yer alan ‘udûl olgusu ele alınmıştır. Ses, sözcük ve gramer yönleriyle ‘udûl üç kategoriye ayrılır.
Yaşar Daşkıran
doaj   +1 more source

The mTORC1/4E-BP1 axis represents a critical signaling node during fibrogenesis

open access: yesNature Communications, 2019
Myofibroblasts are the key effector cells responsible for excessive extracellular matrix deposition in multiple fibrotic conditions, including idiopathic pulmonary fibrosis (IPF). The PI3K/Akt/mTOR axis has been implicated in fibrosis, with pan-PI3K/mTOR
Hannah V. Woodcock   +23 more
semanticscholar   +1 more source

Should We Report 15q11.2 BP1-BP2 Deletions and Duplications in the Prenatal Setting?

open access: yesJournal of Clinical Medicine, 2020
Copy number variations of the 15q11.2 region at breakpoints 1-2 (BP1-BP2) have been associated with variable phenotypes and low penetrance. Detection of such variations in the prenatal setting can result in significant parental anxiety.
I. Maya   +9 more
semanticscholar   +1 more source

4E-BP1 Protects Neurons from Misfolded Protein Stress and Parkinson's Disease Toxicity by Inducing the Mitochondrial Unfolded Protein Response

open access: yesJournal of Neuroscience, 2020
Decline of protein quality control in neurons contributes to age-related neurodegenerative disorders caused by misfolded proteins. 4E-BP1 is a key node in the regulation of protein synthesis, as activated 4E-BP1 represses global protein translation ...
S. Dastidar   +7 more
semanticscholar   +1 more source

Treatment-resistant psychotic symptoms and the 15q11.2 BP1–BP2 (Burnside-Butler) deletion syndrome: case report and review of the literature

open access: yesTranslational Psychiatry, 2020
The 15q11.2 BP1-BP2 (Burnside-Butler) deletion is a rare copy number variant impacting four genes ( NIPA1, NIPA2, CYFIP1, and TUBGCP5 ), and carries increased risks for developmental delay, intellectual disability, and neuropsychiatric disorders ...
M. Farrell   +15 more
semanticscholar   +1 more source

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