Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Ozdal Etlik"'
Autor:
Vatan Barisik, Hüseyin Anıl Korkmaz, Utku Karaarslan, Dinçer Atila, Filiz Hazan, C Eraslan, Behzat Özkan, Melek Yildiz, Ozdal Etlik, E S Ata
Publikováno v:
ResearcherID
WOS: 000451246700003
PubMed ID: 31149275
Objective. Ectopic posterior pituitary gland (EPP) is usually characterized by an abnormal pituitary stalk and hypoplasia of the anterior hypophysis. The genetic mechanisms involved in the developmen
PubMed ID: 31149275
Objective. Ectopic posterior pituitary gland (EPP) is usually characterized by an abnormal pituitary stalk and hypoplasia of the anterior hypophysis. The genetic mechanisms involved in the developmen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b93c9574ad89d09d75f936e489ceab5
https://doi.org/10.4183/aeb.2018.300
https://doi.org/10.4183/aeb.2018.300
Autor:
Behzat Özkan, Erhan Pariltay, Esra Ataman, Filiz Hazan, Korcan Demir, Erhan Ozbek, Ozdal Etlik
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 29
Aarskog-Scott syndrome (ASS) is a rare X-linked recessive genetic disorder caused by FGD1 mutations. FGD1 regulates the actin cytoskeleton and regulates cell growth and differentiation by activating the c-Jun N-terminal kinase signaling cascade. ASS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86ee17b019cc6072e3da6540834627c4
https://doi.org/10.1515/jpem-2015-0482
https://doi.org/10.1515/jpem-2015-0482
Publikováno v:
Molecular and Cellular Probes. 24:138-141
Spinal muscular atrophy (SMA), the leading genetic cause of death in childhood, is an autosomal recessive neuromuscular disorder characterized by progressive muscle weakness, associated with deletions of the survival motor neuron 1 (SMN1) gene. Appro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54f65e349e4501d666120397846977c2
https://doi.org/10.1016/j.mcp.2009.12.001
https://doi.org/10.1016/j.mcp.2009.12.001
Publikováno v:
Molecular and Cellular Probes. 22:71-75
Achondroplasia is the most common form of dwarfism and has an incidence of approximately 1/7500. In more than 98% of cases, the disease is associated with a G to A or G to C substitution at nucleotide position 1138 (p.G380R) of the fibroblast growth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16a9c5739ec90dfa50a9180d7344c10f
https://doi.org/10.1016/j.mcp.2007.06.002
https://doi.org/10.1016/j.mcp.2007.06.002
Publikováno v:
Genetic Testing. 11:463-466
Recently, an acquired somatic point mutation (p.V617F) in a highly conserved residue of the pseudokinase domain of the JAK2 tyrosine kinase was shown to be associated with myeloproliferative disorders. Because of the clinical importance of this mutat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::041920ae07e3aad20a423b01e925d3b8
https://doi.org/10.1089/gte.2007.0051
https://doi.org/10.1089/gte.2007.0051
Autor:
Ahmet Tomur, Ozdal Etlik
Publikováno v:
Electronic Journal of General Medicine. 3:21-28
Aim: The aim was to investigate the interactions of hyperbaric oxygenation (HBO) and sulphur dioxide (SO2) inhalation (at 10 ppm, one hour daily for 45 days) on lipoperoxidation and fragility of RBC membranes. Methods: Malonyldialdehyde (MDA) levels,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bc06a9493df48b411d45d06867c8f175
https://doi.org/10.29333/ejgm/82356
https://doi.org/10.29333/ejgm/82356
Publikováno v:
Experimental and Molecular Pathology. 83:1-3
Single-nucleotide polymorphisms in the genes that code for coagulation factors V (factor V Leiden) and II (prothrombin, G20210A), as well as the methylenetetrahydrofolate reductase (MTHFR, C677T) gene, have been implicated in the majority of cases of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98581be512323c0ddd187eec5bcd51aa
https://doi.org/10.1016/j.yexmp.2006.12.006
https://doi.org/10.1016/j.yexmp.2006.12.006
Publikováno v:
Journal of Urology. 158:2296-2299
The aim of this research was to compare the protective effects of mesna, hyperbaric oxygenation (HBO), and their combination in cyclophosphamide-induced hemorrhagic cystitis in guinea pigs. Following one dose of i.p. 21.5 mg./kg. mesna administration
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d356ebee7ee9c779ff540f574f2634e3
https://doi.org/10.1016/s0022-5347(01)68238-7
https://doi.org/10.1016/s0022-5347(01)68238-7
Publikováno v:
Analytical biochemistry. 441(2)
Single-nucleotide polymorphism (SNP) genotyping is widely used in genetic association studies to characterize genetic factors underlying inherited traits. Despite many recent advances in high-throughput SNP genotyping, inexpensive and flexible method
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1975928c31aca3b561b4f43ce3a71830
https://pubmed.ncbi.nlm.nih.gov/23872005
https://pubmed.ncbi.nlm.nih.gov/23872005
Publikováno v:
Genetic Testing. 8:381-383
Factor V Leiden and prothrombin G20210A are clinically relevant genetic risk factors for venous thrombosis. Molecular diagnostic testing for factor V Leiden and prothrombin G20210A is widespread, and laboratories use a variety of technical approaches
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b6e56301435f9266f6709e132d96ed3
https://doi.org/10.1089/gte.2004.8.381
https://doi.org/10.1089/gte.2004.8.381