Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Hilmi, Tozkir"'
Publikováno v:
Clinical Dysmorphology. 32:65-69
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f2246e8b0b0f9b928f9b8114b809ff94
https://doi.org/10.1097/mcd.0000000000000441
https://doi.org/10.1097/mcd.0000000000000441
Autor:
Nuray CAN, Ebru TAŞTEKIN, Tülin DENIZ YALTA, Necdet SÜT, Selma KORKMAZ, Ufuk USTA, Fulya ÖZ PUYAN, Ezgi GENÇ, Mert CEZIK, Busem BINBOĞA TUTUĞ, Osman KÖSTEK, Hilmi TOZKIR
Publikováno v:
Türk Patoloji Dergisi, Vol 34, Iss 2, Pp 134-142 (2018)
Objective: BRAF is the most common mutation in melanoma. The most common subtype is BRAF V600E, followed by V600K. Initially, the authors aimed to investigate whether clinicopathological features of melanoma are associated with BRAF mutations. We the
Externí odkaz:
https://doaj.org/article/c7410c8419314fd996c3fa6d2a221ba6
Publikováno v:
Biochemical and biophysical research communications. 619
TP73 antisense RNA 1 (TP73-AS1) is an oncogenic long non-coding RNA that is activated in several types of cancers. It has been shown that the activity of TP73-AS1 is controlled by several miRNAs, but post-transcriptional mechanisms that regulate TP73
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fae9a5076858e6595161f1e762b81336
https://pubmed.ncbi.nlm.nih.gov/35760009
https://pubmed.ncbi.nlm.nih.gov/35760009
Autor:
Hakan Gurkan, Sinem Yalcintepe, Damla Eker, Hilmi Tozkir, Irfan Cicin, Emine Ikbal Atli, Huseyin Ahmet Tezel, Engin Atli, Selma Demir
Publikováno v:
Tumori Journal. 106:510-517
Background: Recent advances in next-generation sequencing (NGS) technology have enabled multigene testing and changed the diagnostic approach to hereditary gastrointestinal cancer/polyposis syndromes. The aim of this study was to analyze different ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5bf84762a9d8463f68f7e814fc831cb9
https://doi.org/10.1177/0300891620919171
https://doi.org/10.1177/0300891620919171
Publikováno v:
Molecular biology reports. 49(7)
Prostate cancer is a malignant disease that severely affects the health and comfort of the male population. The long non-coding RNA TP73-AS1 has been shown to be involved in the malignant transformation of various human cancers. However, whether TP73
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82d551c33f6742d828c1852a2a1ed69a
https://pubmed.ncbi.nlm.nih.gov/35138524
https://pubmed.ncbi.nlm.nih.gov/35138524
Autor:
Emine Ikbal Atli, Necdet Sut, Drenushe Zhuri, Hakan Gurkan, Işık Görker, Cisem Mail, Sinem Yalcintepe, Damla Eker, Hilmi Tozkir, Yasemiin Ozen, Hazal Sezginer Guler, Selma Demir, Engin Atli
Publikováno v:
Archives of Neuropsychiatry.
Introduction Autism spectrum disorder is a genetically and phenotypically heterogeneous group. Genetic studies carried out to date have suggested that both common and rare genetic variants play a role in the etiology of this disorder. In our study, w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::afc6cf34cb12f1ba64a09896e2eecbcc
https://doi.org/10.29399/npa.27407
https://doi.org/10.29399/npa.27407
Autor:
Selma, Demir, Hilmi, Tozkir, Hakan, Gurkan, E Ikbal, Atli, Sinem, Yalcintepe, Engin, Atli, Y Atakan, Sezer, Damla, Eker, Nermin, Tuncbilek, Ebru, Tastekin, Yasemin, Ozen, Irfan, Cicin
Publikováno v:
Journal of B.U.ON. : official journal of the Balkan Union of Oncology. 25(3)
Pathogenic/likely pathogenic (P/LP) germline variations in BRCA1 and BRCA2 genes are responsible for the majority of hereditary breast and ovarian cancers. This study presents the BRCA1/BRCA2 sequencing and deletion duplication analyses results of of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::123c5a0f40d8e06f297e62b24107685c
https://pubmed.ncbi.nlm.nih.gov/32862574
https://pubmed.ncbi.nlm.nih.gov/32862574
Autor:
Mehmet Celik, Sibel Guldiken, Semra Ayturk, Buket Yilmaz Bulbul, Ahmet Kucukarda, Nuray Can, Ebru Tastekin, Atakan Sezer, Necdet Sut, Armagan Tugrul, Hakan Gurkan, Hilmi Tozkir, Bora Demirkan
Publikováno v:
Journal of Elementology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5663c280057fbeca4846bd9db3b3d441
https://doi.org/10.5601/jelem.2020.25.1.1984
https://doi.org/10.5601/jelem.2020.25.1.1984
Publikováno v:
Balkan Journal of Medical Genetics, Vol 21, Iss 2, Pp 69-72 (2018)
Balkan Journal of Medical Genetics : BJMG
Balkan Journal of Medical Genetics : BJMG
The balanced non-Robertsonian translocation (ROB) associated with acrocentric chromosomes is an unusual phenomenon. We report the case of rare non-ROB involving chromosomes 15 and 22 with cytogenetic and molecular cytogenetic findings of 46,XY,t(15;2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::381f2cc02204091092a5e07a64dcef1c
https://doaj.org/article/232f79beb6a1406fbfc0f75b1589861c
https://doaj.org/article/232f79beb6a1406fbfc0f75b1589861c
Autor:
Ezgi Genc, Nuray Can, Necdet Sut, Hilmi Tozkir, Mert Cezik, Ebru Tastekin, Fulya Oz Puyan, Busem Binboğa Tutuğ, Osman Kostek, Tulin Yalta, Selma Korkmaz, Ufuk Usta
Publikováno v:
Türk Patoloji Dergisi, Vol 34, Iss 2, Pp 158-164 (2018)
Objective BRAF is the most common mutation in melanoma. The most common subtype is BRAF V600E, followed by V600K. Initially, the authors aimed to investigate whether clinicopathological features of melanoma are associated with BRAF mutations. We then
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32f25df8e4a5dcb49c970627a17a73e0
http://www.turkjpath.org/pdf.php3?id=1858
http://www.turkjpath.org/pdf.php3?id=1858