Zobrazeno 1 - 10
of 55
pro vyhledávání: '"Ali, Sazci"'
Publikováno v:
Brain Disorders, Vol 3, Iss , Pp 100013- (2021)
Amyotrophic Lateral Sclerosis (ALS) is a devastating neurodegenerative disease caused by the death of motor neurons in the late stage of life and there is currently no effective treatment. To date, there has been much research into the association of
Externí odkaz:
https://doaj.org/article/c2c533c0d5d24b43bab5e1b6e075f38a
Autor:
Ali Sazci, Halil Atilla Idrisoglu
Publikováno v:
Clinical Parkinsonism & Related Disorders, Vol 1, Iss , Pp 52-53 (2019)
We report a pregnancy in a patient with Parkinson's disease with PARK2 mutations. Although pregnancy is uncommon in patients with Parkinson's disease, an early-onset Parkinson's patient with three silent and two missense mutations in the PARK2 gene i
Externí odkaz:
https://doaj.org/article/dc30f90eb80d4d4684ea4e401564f09c
Publikováno v:
Current Pharmaceutical Biotechnology. 21:1176-1185
Background: In the last decade, there have been accumulating data that the use of medicinal plants could bring additional benefits to the supportive treatment of various diseases. Nigella sativa (N. sativa, family Ranunculaceae) is one of these plant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a84ccd4064cd4fe83a49ff25f664e463
https://doi.org/10.2174/1389201021666200430120453
https://doi.org/10.2174/1389201021666200430120453
Publikováno v:
Molecular Biology Reports. 46:3411-3416
WOS: 000470332600078 PubMed ID: 30980267 RELN gene encodes a large extracellular matrix protein which is critical for neuronal migration, cell positioning and cell-cell interactions. It also controls the synaptic plasticity of neurons for initiation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b60288147fc7abd77dcb12b2e7cca670
https://doi.org/10.1007/s11033-019-04803-w
https://doi.org/10.1007/s11033-019-04803-w
Autor:
Saide Betül Arslan Satılmış, Emin Emre Kurt, Ebru Perim Akçay, Ali Sazci, Ahmet Cevdet Ceylan
Publikováno v:
The journal of gene medicineREFERENCES. 23(2)
Background X-linked intellectual disability type Nascimento (XIDTN) is a disorder of the ubiquitin-proteasome pathway of protein degradation controlled by the UBE2A gene. The disease is characterized by intellectual disability, speech impairment, dys
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e98ae9b6680c1daf0cd17c675775e52d
https://pubmed.ncbi.nlm.nih.gov/33368912
https://pubmed.ncbi.nlm.nih.gov/33368912
Publikováno v:
Neuroscience Bulletin. 35:362-364
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4119209804b0f026ba7c21f328204e1b
https://doi.org/10.1007/s12264-018-0287-6
https://doi.org/10.1007/s12264-018-0287-6
Autor:
Goncagül Haklar, Ali Sazci, Murat Akgül, Levent Türkeri, Ozgur Baykan, Nihal Uren, Ali Yaman, Emel Ergul, Ilker Tinay
Publikováno v:
Clinical Laboratory. 65
BACKGROUND Bladder cancer is an important health problem which ranks 4th among most frequently seen cancer types in men. In our study we aimed to investigate the correlations among urothelial type bladder cancer polymorphisms, ApaI, BsmI, FokI, and T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::211415a5f6feccd0e31701cd5c5f06cb
https://doi.org/10.7754/clin.lab.2018.180339
https://doi.org/10.7754/clin.lab.2018.180339
Publikováno v:
Biomedical Reports. 5:506-510
The transcription factor 4 (TCF4) gene encodes a helix-loop-helix transcription factor protein, which initiates neuronal differentiation and is primarily expressed during nervous system development. The aim of the present study is to investigate the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::486fd25857bc85d153dee57e0aff9701
https://doi.org/10.3892/br.2016.742
https://doi.org/10.3892/br.2016.742
Autor:
Nihal Uren, Hakan Uzunoglu, Çağrı Triyaki, Oktay Yirmibesoglu, Ertuğrul Kargi, Emel Ergul, Tugcan Korak, Ali Sazci, N. Zafer Utkan
Publikováno v:
Biomedical Reports. 4:369-373
Nibrin, encoded by the NBN gene, participates in DNA repair. Mutations in the NBN gene lead to Nijemen breakage syndrome, which may result in several types of diseases, particularly susceptibility to cancer, including breast cancer. Polymorphic varia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::643b7373ee20fd11bb4a5b0502d33489
https://doi.org/10.3892/br.2016.579
https://doi.org/10.3892/br.2016.579
Autor:
Nihal Uren, Ali Sazci, Turgay Şimşek, Nihat Zafer Utkan, Tugcan Korak, Emel Ergul, Nuh Zafer Cantürk
Publikováno v:
Volume: 47, Issue: 3 97-100
İstanbul Journal of Pharmacy
İstanbul Journal of Pharmacy
Apolipoprotein E (ApoE) is an important secretory glycoprotein, and also a ligand for LDL receptors and ApoE receptors. It is involved in lipid transport and catabolism, nerve regeneration, immune system regulation, and cell proliferation. Moreover,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6a186988959ecde15fe133a5a7678b9
https://dergipark.org.tr/tr/pub/iujp/issue/31365/346507
https://dergipark.org.tr/tr/pub/iujp/issue/31365/346507
