Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Turkan Patıroglu"'
Autor:
Marcin Łyszkiewicz, Natalia Ziętara, Laura Frey, Ulrich Pannicke, Marcel Stern, Yanshan Liu, Yanxin Fan, Jacek Puchałka, Sebastian Hollizeck, Ido Somekh, Meino Rohlfs, Tuğba Yilmaz, Ekrem Ünal, Musa Karakukcu, Türkan Patiroğlu, Christina Kellerer, Ebru Karasu, Karl-Walter Sykora, Atar Lev, Amos Simon, Raz Somech, Joachim Roesler, Manfred Hoenig, Oliver T. Keppler, Klaus Schwarz, Christoph Klein
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-15 (2020)
FCH domain only 1 (FCHO1) is a key molecule involved in clathrin-mediated endocytosis (CME). Here, the authors report homozygous FCHO1 mutations in individuals with variable T and B cell lymphopenia, which are associated with loss-of-function of FCHO
Externí odkaz:
https://doaj.org/article/74724d48da6d4ad88e09abfe678d8216
Autor:
Firdevs AYDIN, Kemal DENİZ, Süreyya Burcu GÖRKEM, Veysel GÖK, Alper ÖZCAN, Ebru YILMAZ, Ekrem ÜNAL, Musa KARAKÜKÇÜ, Türkan PATIROĞLU, Mehmet Akif ÖZDEMİR, Can ACIPAYAM, Defne AY TUNCEL
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 43, Iss , Pp S31- (2021)
Objective: Rhabdoid tumors, which are rare in childhood, are aggressive cancers. It can be particularly seen in 3 different anatomical regions, mostly in the central nervous system, kidneys, and soft tissue in early childhood. In this study, it was a
Externí odkaz:
https://doaj.org/article/0154714528984f74b8b6314ef38cda86
Autor:
Veysel GOK, Firdevs AYDIN, Alper OZCAN, Ebru YILMAZ, Ekrem UNAL, Musa KARAKUKCU, Türkan PATIROGLU, Mehmet Akif OZDEMIR, Filiz KARAMAN, Orhan GORUKMEZ, Ozlem GORUKMEZ, Atil BISGIN
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 43, Iss , Pp S65- (2021)
Objective: The programmed cell death 1 (PD-1) receptor is an immune checkpoint receptor expressed by activated T cells. PD-1 inhibits the immune system by binding to its ligands expressed on tumor cells. Nivolumab and pembrolizumab are some of the mo
Externí odkaz:
https://doaj.org/article/8fc9fac9b6054cc2b9b1c3e60f6e9bd4
Autor:
Marcin Łyszkiewicz, Natalia Ziętara, Laura Frey, Ulrich Pannicke, Marcel Stern, Yanshan Liu, Yanxin Fan, Jacek Puchałka, Sebastian Hollizeck, Ido Somekh, Meino Rohlfs, Tuğba Yilmaz, Ekrem Ünal, Musa Karakukcu, Türkan Patiroğlu, Christina Kellerer, Ebru Karasu, Karl-Walter Sykora, Atar Lev, Amos Simon, Raz Somech, Joachim Roesler, Manfred Hoenig, Oliver T. Keppler, Klaus Schwarz, Christoph Klein
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-1 (2020)
An amendment to this paper has been published and can be accessed via a link at the top of the paper.
Externí odkaz:
https://doaj.org/article/6a981817becc4e8ca162ede7a2b51a17
Publikováno v:
Revista Espanola de Enfermedades Digestivas, Vol 107, Iss 9, Pp 547-553 (2015)
Backgound and aim: There are some common genetic features between celiac disease (CD) and diabetes mellitus type 1 (DM). However, the genetic risk factors have not been fully clarified for CD and the co-occurrence of CD and DM. KIR (killer immunoglob
Externí odkaz:
https://doaj.org/article/7308c9873f6f4039869294165e48cebf
Autor:
Turkan Patiroglu, H Haluk Akar
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 14, Iss 3 (2015)
Clericuzio-type poikiloderma with neutropenia (PN) is characterized by poikiloderma, non-cyclic neutropenia, recurrent sinopulmonary infections, pachyonychia, and palmo- plantar hyperkeratosis. Mutations in the C16orf57 gene, which is located on chro
Externí odkaz:
https://doaj.org/article/4ecbe879f08246839a95adf2931a2a48
Autor:
Amanda J. Walne, Laura Collopy, Shirleny Cardoso, Alicia Ellison, Vincent Plagnol, Canan Albayrak, Davut Albayrak, Sara Sebnem Kilic, Turkan Patıroglu, Haluk Akar, Keith Godfrey, Tina Carter, Makia Marafie, Ajay Vora, Mikael Sundin, Thomas Vulliamy, Hemanth Tummala, Inderjeet Dokal
Publikováno v:
Haematologica, Vol 101, Iss 10 (2016)
Dyskeratosis congenita is a highly pleotropic genetic disorder. This heterogeneity can lead to difficulties in making an accurate diagnosis and delays in appropriate management. The aim of this study was to determine the underlying genetic basis in p
Externí odkaz:
https://doaj.org/article/633600b395564b04938f38e1ab54d2e9
Publikováno v:
The Saudi Journal of Gastroenterology, Vol 28, Iss 3, Pp 233-238 (2022)
Background: Human leukocyte antigen (HLA)-G, a member of the HLA family, is crucial for fetomaternal tolerance. Transmembrane or circulating/soluble HLA-G (sHLA-G) is elevated in autoimmune conditions and the tumor microenvironment. Circulating sHLA-
Externí odkaz:
https://doaj.org/article/74e1a64327594981a7a60b15efda8539
Autor:
Alper Ozcan, Ekrem Unal, Musa Karakukcu, Abdulhakim Coskun, Mehmet Akif Ozdemir, Turkan Patiroglu
Publikováno v:
İstanbul Kuzey Klinikleri, Vol 7, Iss 3, Pp 255-259 (2020)
OBJECTIVE: Vena cava superior syndrome comprises various symptoms of compression of vena cava superior. The results of increased venous pressure in the upper body may cause edema of the head and neck associated with cyanosis, plethora and distended s
Externí odkaz:
https://doaj.org/article/5e11258ac3864be3a687a2e579b9df61
Publikováno v:
İstanbul Kuzey Klinikleri, Vol 5, Iss 4, Pp 353-356 (2018)
In this report, we examine severe neutropenia secondary to ganciclovir treatment and associated intracranial abscess in a patient with respiratory insufficiency who required intubation due to cytomegalovirus (CMV) pneumonitis. Secondary neutropenia i
Externí odkaz:
https://doaj.org/article/6892903dba714af2a3302d8a91d081ab