Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Bayram, Toraman"'
Autor:
Ilknur Tosun, Esra Özkaya, Neşe Kaklikkaya, Faruk Aydin, Bayram Toraman, Celal Kurtuluş Buruk
Publikováno v:
Mikrobiyoloji Bulteni. 54:191-202
Carbapenems are used in the treatment of infections caused by multidrug-resistant bacteria and colistin (polymyxin E) is used as the last choice of antimicrobial agent in those resistant to carbapenems. The worldwide and increased use of colistin, wh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::021fc67ce25f22b818e8f77b3005a0f8
https://doi.org/10.5578/mb.69021
https://doi.org/10.5578/mb.69021
Publikováno v:
Volume: 8, Issue: 3 420-427
The European Research Journal
The European Research Journal
Intellectual disability (ID) is a lifelong condition that begins during the developmental period, and characterized by significant limitations in intellectual functioning and adaptive behavior including social, conceptual and practical skills. In the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c065ad22021b85a0cf467a261731744
https://dergipark.org.tr/tr/pub/eurj/issue/69432/924346
https://dergipark.org.tr/tr/pub/eurj/issue/69432/924346
Publikováno v:
American journal of medical genetics. Part AREFERENCES. 185(6)
Bartsocas-Papas syndrome (BPS) is a rare autosomal recessive disorder characterized by popliteal pterygia, syndactyly, ankyloblepharon, filiform bands between the jaws, cleft lip and palate, and genital malformations. Most of the BPS cases reported t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cde1d60670d13f5937eb048de9c941bf
https://pubmed.ncbi.nlm.nih.gov/33713555
https://pubmed.ncbi.nlm.nih.gov/33713555
Autor:
Ersan Kalay, Hüseyin Okan Soykam, Gokhan Yildiz, Tuba Dinçer, Samiye Çilem Bilginer, Zeynep Göker, Bayram Toraman, Bekir Ergüner, Selma Tural Hesapçıoğlu, Sema Kandil, Serbülent Ünsal, Burak Kaan Kasap
Publikováno v:
The journal of gene medicineREFERENCES. 23(4)
BACKGROUND Genetic etiologies of autism spectrum disorders (ASD) are complex, and the genetic factors identified so far are very diverse. In complex genetic diseases such as ASD, de novo or inherited chromosomal abnormalities are valuable findings fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ff786f7d5d084a9342370513d92d218
https://pubmed.ncbi.nlm.nih.gov/33591602
https://pubmed.ncbi.nlm.nih.gov/33591602
Autor:
Esra, Özkaya, Celal Kurtuluş, Buruk, İlknur, Tosun, Bayram, Toraman, Neşe, Kaklıkkaya, Faruk, Aydın
Publikováno v:
Mikrobiyoloji bulteni. 54(2)
Carbapenems are used in the treatment of infections caused by multidrug-resistant bacteria and colistin (polymyxin E) is used as the last choice of antimicrobial agent in those resistant to carbapenems. The worldwide and increased use of colistin, wh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4c56b8683552a29577d818c84201f07c
https://pubmed.ncbi.nlm.nih.gov/32723275
https://pubmed.ncbi.nlm.nih.gov/32723275
Publikováno v:
Annals of Medical Research. 29:334
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6584db51674412e29abe8021218753ef
https://doi.org/10.5455/annalsmedres.2021.06.438
https://doi.org/10.5455/annalsmedres.2021.06.438
Autor:
Tuba Dinçer, Nurten A. Akarsu, Bayram Toraman, İdris Er, Yavuz Dodurga, Gülden Yorgancıoğlu-Budak, Adem Yıldırım, Özmert M.A. Özdemir, Nuran Sabir, C. Nur Semerci, Akgün Ölmez, Ersan Kalay
Publikováno v:
European Journal of Human Genetics. 25:1118-1125
Microcephalic primordial dwarfism (MPD) is a group of autosomal recessive inherited single-gene disorders with intrauterine and postnatal global growth failure. Seckel syndrome is the most common form of the MPD. Ten genes are known with Seckel syndr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ee9d34b5ad23572a65139b09ce9ed8b
https://doi.org/10.1038/ejhg.2017.120
https://doi.org/10.1038/ejhg.2017.120
Publikováno v:
Cell biology internationalREFERENCES. 44(3)
Receptor-interacting serine/threonine kinase 4 (RIPK4) and transforming growth factor-β 1 (TGF-β1) play critical roles in the development and maintenance of the epidermis. A negative correlation between the expression patterns of RIPK4 and TGF-β s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78b87ab6c658cd2fb8cd787f85d434c7
https://pubmed.ncbi.nlm.nih.gov/31825120
https://pubmed.ncbi.nlm.nih.gov/31825120
Autor:
Ece Altun, Savas Yayli, Bayram Toraman, Deniz Aksu Arica, Ersan Kalay, Leyla Baykal Selçuk, Sevgi Bahadir
Publikováno v:
Acta Dermatovenerologica Croatica
Volume 25
Issue 3
Volume 25
Issue 3
Pemphigus vulgaris (PV) is a life-threatening, autoimmune blistering disease of the skin and mucous membranes. The relationship between PV and human leukocyte antigen (HLA) has been studied in several reports. Previous reports have demonstrated that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::1326595b5c5963a62df0378e6f5a22a7
https://pubmed.ncbi.nlm.nih.gov/29252170
https://pubmed.ncbi.nlm.nih.gov/29252170
Autor:
Ersan Kalay, Bayram Toraman, Tuba Dinçer, Gülay Karagüzel, Emel Gül Açıkgöz, Ahmet Karagüzel, Ayşenur Ökten
Publikováno v:
Gene. 513:202-208
Congenital adrenal hyperplasia (CAH) is a group of autosomal recessively inherited disorders characterized by impaired production of adrenal steroids. Approximately 95% of all CAH are caused by mutations of the CYP21A2 that encodes 21-hydroxylase. In
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d24c569436868615ed1d71f4f4d60fab
https://doi.org/10.1016/j.gene.2012.10.059
https://doi.org/10.1016/j.gene.2012.10.059