Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Muhammet Ensar Dogan"'
Autor:
Zahra Heydari, Maria Peshkova, Zeynep Burcin Gonen, Ianos Coretchi, Ahmet Eken, Arzu Hanım Yay, Muhammet Ensar Dogan, Nuriye Gokce, Hilal Akalin, Nastasia Kosheleva, Daniela Galea-Abdusa, Mariana Ulinici, Valentina Vorojbit, Anastasia Shpichka, Stanislav Groppa, Massoud Vosough, Mihail Todiras, Denis Butnaru, Yusuf Ozkul, Peter Timashev
Publikováno v:
Journal of Molecular Medicine. 101:51-63
Extracellular vesicles (EVs) are produced by various cells and exist in most biological fluids. They play an important role in cell-cell signaling, immune response, and tumor metastasis, and also have theranostic potential. They deliver many function
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::191165b79988ef43700d848d658073c4
https://doi.org/10.1007/s00109-022-02276-2
https://doi.org/10.1007/s00109-022-02276-2
Autor:
Veysel Gok, Hayato Tada, Muhammet Ensar Dogan, Ummü Alakus Sari, Kübra Aslan, Alper Ozcan, Ebru Yilmaz, Fatih Kardas, Musa Karakukcu, Halit Canatan, Cigdem Karakukcu, Munis Dundar, Akihiro Inazu, Ekrem Unal
Publikováno v:
Clinica Chimica Acta. 529:61-66
© 2022Background: Sitosterolemia, also known as phytosterolemia, results from increased intestinal absorption of plant sterols and decreased intestinal and biliary excretion of sterols, resulting in increased levels of plant sterols in the plasma. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5cb52a9c4aef71595131a1cd902afc31
https://doi.org/10.1016/j.cca.2022.02.001
https://doi.org/10.1016/j.cca.2022.02.001
Autor:
Hamit Acer, Gül Demet Özçora, Mehmet Canpolat, Muhammet Ensar Doğan, Zehra Filiz Kahraman, Sefer Kumandaş
Publikováno v:
The Journal of Pediatric Academy, Vol 5, Iss 3, Pp 93-98 (2024)
Cockayne syndrome (CS) is a rare, severe, genetic neurodegenerative disorder. To better understand the condition, this article aimed to discuss the clinical manifestations and prognosis of CS. This clinical study was a retrospective review of the med
Externí odkaz:
https://doaj.org/article/0339ff09e8e446eba93d577fdbea35ca
Autor:
Alperen Vural, Murat Salih Güneş, Keziban Korkmaz Bayram, Yusuf Ozkul, Mehmet İlhan Şahin, Muhammet Ensar Dogan, Meltem Cerrah Gunes, Sevda Yesim Ozdemir, Fatma Aybuga, Arslan Bayram
Publikováno v:
Journal of Neurogenetics. 35:45-57
The characteristic feature of noise-induced hearing loss (NIHL) is the loss or malfunction of the outer hair cells (OHC) and the inner hair cells (IHC) of the cochlea. 90-95% of the spiral ganglion neurons, forming the cell bodies of cochlear nerve,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cae48e7780139508b4acbed61c34504b
https://doi.org/10.1080/01677063.2021.1904922
https://doi.org/10.1080/01677063.2021.1904922
Introduction Paroxysmal exercise-induced dyskinesia (PED) is characterized by repeated episodes of involuntary movement disorders that are typically caused by prolonged walking or running and mostly caused by SLC2A1 gene mutations. Phenotypes vary fr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7915d11fe5354f92d805031055918449
https://avesis.erciyes.edu.tr/publication/details/f9b3d7f8-7cb2-41de-8204-d4048a611ff7/oai
https://avesis.erciyes.edu.tr/publication/details/f9b3d7f8-7cb2-41de-8204-d4048a611ff7/oai
Autor:
Hilal Akalin, Yakut Erdem, Munis Dundar, Muhammet Ensar Dogan, Nuriye Gokce, Sevgi Ozmen, Yusuf Ozkul
Background: In this study, expression level analysis of genes associated with Attention Deficit Hyperactivity Disorder (ADHD) (SLC6A3, SLC6A4, SLC1A2, VMAT2, MAOA, COMT, GLYAT, GRM5, DRD4, TPH1, and ADRA2C) by pre-treatment and post-treatment with At
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e8670ad4dd0e7eae5dc5a4baaaf7402a
https://doi.org/10.21203/rs.3.rs-440720/v1
https://doi.org/10.21203/rs.3.rs-440720/v1
Autor:
Ahmet Eken, Neslihan Günay, Ismail Dursun, Ayşe Seda Pınarbaşı, Hülya Akgün, Muammer Hakan Poyrazoğlu, Munis Dundar, Sibel Yel, Aynur Gencer Balaban, Muhammet Ensar Dogan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3391c5169975e98118db50db75b160e1
https://avesis.erciyes.edu.tr/publication/details/231c4cff-31bc-4fcd-aff9-880f6d508762/oai
https://avesis.erciyes.edu.tr/publication/details/231c4cff-31bc-4fcd-aff9-880f6d508762/oai
Autor:
Ekrem Unal, Christoph Klein, Başaknur Akyildiz, Turkan Patiroglu, Hakan Poyrazoglu, Maximilam Witzel, Muhammet Ensar Dogan, Meino Rohlfs, Ayşenur Paç Kısaarslan
Publikováno v:
Journal of pediatric hematology/oncology. 43(3)
Various autoimmune diseases may be associated with primary immune deficiencies. We reported a case with a loss-of-function mutation in DNASE1L3, a gene described previously in families with systemic lupus erythematosus. In addition, the patient showe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe3f9e0efb56cbbf6cf09ddcd8972922
https://pubmed.ncbi.nlm.nih.gov/32205782
https://pubmed.ncbi.nlm.nih.gov/32205782
Autor:
Kursad Unluhizarci, Yusuf Ozkul, Cetin Saatci, Hilal Akalin, Mehmet Nuri Ozbek, Ayca Dundar, Ruken Yıldırım, Mustafa Akkus, Ulviye Kazimli, Gamze Çelmeli, Mesut Parlak, Munis Dundar, Meltem Cerrah Gunes, Ruslan Bayramov, Nihal Hatipoglu, Sercan Kenanoglu, Ismail Dundar, Oya Ercan, Muge Gulcihan Onal, Muhammet Ensar Dogan
Congenital adrenal hyperplasia (CAH) is an autosomal recessive genetic disorder due to presence of mutations in the genes involved in the metabolism of steroid hormones in adrenal gland. There are two main forms of CAH, classic form and non-classic f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2568b91a63a8e7eb36cb380f795b4c76
https://avesis.erciyes.edu.tr/publication/details/432f24c9-eb76-412a-9753-92cc7f802027/oai
https://avesis.erciyes.edu.tr/publication/details/432f24c9-eb76-412a-9753-92cc7f802027/oai
Autor:
Mehmet Serdar Kutuk, Munis Dundar, Mahmut Tuncay Ozgun, Sadan Tutus, Muhammet Ensar Dogan, Ozguc Altun
Publikováno v:
Journal of Clinical Ultrasound. 45:267-276
Objective The aim of this study was to assess the sonographic (US) characteristics, associated malformations, chromosomal status, and perinatal outcomes of fetuses with an upper extremity malformation (UEM) detected by US examination. Methods The dat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::56dcf2ace5f291957fedefd0f869e038
https://doi.org/10.1002/jcu.22429
https://doi.org/10.1002/jcu.22429