Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Hulya Tosun Yildirim"'
Autor:
Hulya Tosun Yildirim, Dondu Nergiz, Canan Sadullahoglu, Zelal Akgunduz, Senay Yildirim, Selen Dogan, Cem Sezer
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 63, Iss 3, Pp 412-417 (2020)
Background: Cyclin D1, a member of the cyclin protein family, is instrumental in the cell cycle due to its influence on the progression from G1 to the S phase. Its overexpression causes reduced doubling time and is also associated with clonogenic gro
Externí odkaz:
https://doaj.org/article/8925e7c70fb64e9f880d29623e503321
Autor:
Hikmet Tekin Nacaroglu, Demet Can, Canan Sule Unsal Karkiner, Yontem Yaman, Hudaver Alper, Hulya Tosun Yildirim, Paul W. Bishop
Publikováno v:
Dermatologica Sinica, Vol 33, Iss 4, Pp 231-233 (2015)
Juvenile xanthogranuloma is a non-Langerhans cell histiocytosis seen most commonly in childhood and adolescence. Extracutaneous involvement is rare. We report an interesting and extremely rare case of systemic (skin, lung, spleen, and colon) “juven
Externí odkaz:
https://doaj.org/article/044178a95a4a40dc99277fe327cef89d
Publikováno v:
Case Reports in Oncological Medicine, Vol 2015 (2015)
Although rare, malignant melanoma may occur in children. Childhood melanomas account for only 0.3–3% of all melanomas. In particular the presence of congenital melanocytic nevi is associated with an increased risk of development of melanoma. We her
Externí odkaz:
https://doaj.org/article/4b5a8fef786e44f28f288fc4bddb8ea3
Autor:
Gulden Diniz, Hulya Tosun Yildirim, Sarenur Gokben, Gul Serdaroglu, Filiz Hazan, Kanay Yararbas, Ajlan Tukun
Publikováno v:
Case Reports in Genetics, Vol 2014 (2014)
Limb-girdle muscular dystrophy type 2D (LGMD-2D) is caused by autosomal recessive defects in the alpha-sarcoglycan gene located on chromosome 17q21. In this study, we present a child with alpha-sarcoglycanopathy and describe a novel deletion in the a
Externí odkaz:
https://doaj.org/article/618f2184db734d698034b3e6335a6d39
Autor:
Ayse Nur Akinel, Sibel Berker Karauzum, Oznur Tokta, Hulya Tosun Yildirim, Bahar Akkaya, Funda Tayfun Küpesiz, Ceren Hangul
Publikováno v:
Turk patoloji dergisi. 38(3)
OBJECTIVE DUX4 is an embryonic transcription factor (TF) later silenced in somatic tissues, while active in germline testis cells. Re-expression in somatic cells has been revealed to be present in pathologic conditions such as dystrophy, leukemia, an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3ff11ec5344d92735dbd8d3a794098d
https://pubmed.ncbi.nlm.nih.gov/34854471
https://pubmed.ncbi.nlm.nih.gov/34854471
Autor:
Ayse Pinar Ercetin, Hulya Tosun Yildirim, Ayse Banu Demir, Irfan Karaca, Nur Olgun, Çiğdem Ecevit, Safiye Aktaş, Bengü Demirağ, Ahmet Çelik, Ayşe Erbay
Publikováno v:
Journal of Pediatric Hematology/Oncology. 41:7-12
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Hepatoblastoma (HB) is the most common liver malignancy in children. The prognosis changes according to the histologic subtypes of HB. In the present study, we aimed to characterize the expression level of selected microRNAs (miRNAs) in
Hepatoblastoma (HB) is the most common liver malignancy in children. The prognosis changes according to the histologic subtypes of HB. In the present study, we aimed to characterize the expression level of selected microRNAs (miRNAs) in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8861c4905339b0048df3e5005355d3cb
https://doi.org/10.1097/mph.0000000000001234
https://doi.org/10.1097/mph.0000000000001234
Autor:
Hulya Tosun Yildirim
Publikováno v:
Journal of Dr. Behcet Uz Children s Hospital.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9894ff0e1eed26a9069e7b05b463633f
https://doi.org/10.5222/buchd.2020.69772
https://doi.org/10.5222/buchd.2020.69772
Autor:
Dinc, Suren, Hulya Tosun, Yildirim, Irem, Atalay, Alper, Sayiner, Mustafa, Yildirim, Arsenal Sezgin, Alikanoglu, Cem, Sezer
Publikováno v:
Journal of B.U.ON. : official journal of the Balkan Union of Oncology. 23(6)
HMGB1, the most important member of the high mobility group box protein family, is a nuclear protein with different functions in the cell; it has a role in cancer progression, angiogenesis, invasion, and metastasis development. We studied the express
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a767a74bf6396dee3125314f5b569692
https://pubmed.ncbi.nlm.nih.gov/30610817
https://pubmed.ncbi.nlm.nih.gov/30610817
Publikováno v:
Journal of Dr Behcet Uz Children s Hospital.
Childhood soft tissue sarcomas are heterogenous and be quite varied in apperance. Especially, these neoplasms known as "small round cell tumor" group, with their hyperchromatic nuclei and monotonous small and limited cytoplasm. These neoplasms share
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd2a103430e3737e9fc5bcf710a0f925
https://doi.org/10.5222/buchd.2019.98698
https://doi.org/10.5222/buchd.2019.98698
Publikováno v:
Journal of Dr Behcet Uz Children s Hospital.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2d9fccc07fdd9ff0f5c76b1f08113c33
https://doi.org/10.5222/buchd.2018.53386
https://doi.org/10.5222/buchd.2018.53386