Zobrazeno 1 - 10
of 51
pro vyhledávání: '"H Haluk Akar"'
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:
Türkan Patıroğlu, H. Haluk Akar
Publikováno v:
Turkish Journal of Hematology, Vol 33, Iss 4, Pp 339-345 (2016)
We studied the frequencies of human leukocyte antigen alleles (A, B, and DRB1) in 90 patients with acute lymphoblastic leukemia (ALL) and then compared them with 126 controls in this study. Although the frequencies of the A*03 allele, the DRB1*03 all
Externí odkaz:
https://doaj.org/article/d9cde09195ab4fc48f9633d55036e6d9
Autor:
Mikdat Yildiz, H. Haluk Akar
Publikováno v:
Paediatrica Indonesiana, Vol 59, Iss 5, Pp 271-5 (2019)
Background Atopic dermatitis (AD) is the most common chronic inflammatory skin disease in the pediatric population. The pathophysiology of AD is complex and not clearly understood. The role of lipoxin B4 (LXB4), an anti-inflammatory mediator, has not
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a03bd7acda897e2fbba219f814fbd2f5
https://paediatricaindonesiana.org/index.php/paediatrica-indonesiana/article/view/2227
https://paediatricaindonesiana.org/index.php/paediatrica-indonesiana/article/view/2227
Autor:
Gülen Tüysüz, Lale Olcay, Ferda Ozkinay, Murat Söker, Hüseyin Onay, Turkan Patiroglu, Ugur Ozbek, Şebnem Yılmaz, Ali Bay, Tiraje Celkan, Hamiyet Hekimci Özdemir, Zeynep Karakas, Nihal Karadaş, Mehmet Akif Yesilipek, Hüseyin Tokgöz, Gonul Aydogan, Talia Ileri, Baris Yilmaz, Yeşim Oymak, Serap Karaman, Zuhal Keskin Yildirim, Vedat Uygun, Umran Caliskan, Berna Atabay, Burcu Akıncı, Ayse Metin, Tuba Hilkay Karapınar, Yusuf Ziya Aral, Müge Gökçe, Zühre Kaya, Ayca Kiykim, Gülsün Karasu, Bilge Özsait Selçuk, Alphan Kupesiz, H. Haluk Akar, Deniz Yilmaz Karapinar, Yurdanur Kilinç, Gül Nihal Özdemir
WOS: 000478208700001
PubMed ID: 31321910
Background Severe congenital neutropenia is a rare disease, and autosomal dominantly inherited ELANE mutation is the most frequently observed genetic defect in the registries from North America and W
PubMed ID: 31321910
Background Severe congenital neutropenia is a rare disease, and autosomal dominantly inherited ELANE mutation is the most frequently observed genetic defect in the registries from North America and W
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3957b5a6f3bf8948d4de62234d0e2999
https://hdl.handle.net/20.500.12605/15940
https://hdl.handle.net/20.500.12605/15940
Autor:
Andrew P. Stubbs, Mirjam van der Burg, Dik C. van Gent, Turkan Patiroglu, Jacob Rozmus, Robert A. Holt, Jacques J.M. van Dongen, Klaus Schwarz, Ingrid Pico-Knijnenburg, Erik J. Simons, H. Haluk Akar, Ricardo Leite, Myriam Ricarda Lorenz, David van Zessen, René L. Warren, Isabel S. Jerchel, Hanna IJspeert, Nicole S. Verkaik, Angela Wawer
Publikováno v:
Blood, 128(5), 650-659. American Society of Hematology
Repair of DNA double-strand breaks (DSBs) by the nonhomologous end-joining pathway (NHEJ) is important not only for repair of spontaneous breaks but also for breaks induced in developing lymphocytes during V(D)J (variable [V], diversity [D], and join
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea7abaa5d07c6364e3fac57a280901fc
https://doi.org/10.1182/blood-2016-02-701029
https://doi.org/10.1182/blood-2016-02-701029
Publikováno v:
Türk Kardiyoloji Derneği Arşivi, Vol 44, Iss 4, Pp 342-345 (2016)
Summary– Dedicator of cytokinesis 8 protein (DOCK8) deficiency is an autosomal recessive, inherited form of hyper-immunoglobulin E (hyper-IgE) syndrome, characterized by persistent cutaneous viral infections, elevated IgE, eosinophilia, and allergi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::754999ca0f50c0dec363a9a6382907d6
https://jag.journalagent.com/z4/download_fulltext.asp?pdir=tkd&un=TKDA-26511
https://jag.journalagent.com/z4/download_fulltext.asp?pdir=tkd&un=TKDA-26511
Publikováno v:
SiSli Etfal Hastanesi Tip Bulteni / The Medical Bulletin of Sisli Hospital. :255-259
Objective: Hashimoto’s thyroiditis (HT) is an autoimmune thyroid disease resulting from complex interactions between genetic and environmental factors. The Human Leukocyte Antigen (HLA) genes have been found to be involved in the susceptibility to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::504b97fb853ed4798ab80bc8d1a22af4
https://doi.org/10.5350/semb.20151005010345
https://doi.org/10.5350/semb.20151005010345
Publikováno v:
Allergologia et Immunopathologia. 43:538-542
The pathogenesis of exercise-induced bronchoconstriction (EIB) in asthma is incompletely understood. The role of exhaled breath condensate (EBC) annexin A5, which is an anti-inflammatory mediator, has not been investigated. The purpose of this study
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1adb522182d6366d2a1a2208aab3154c
https://doi.org/10.1016/j.aller.2014.10.003
https://doi.org/10.1016/j.aller.2014.10.003
Publikováno v:
Acta Microbiologica en Immunologica Hungarica, 62(3), 267-274. Akadémiai Kiadó
The hyper-immunoglobulin M (HIGM) syndrome is a heterogeneous group of genetic disorders characterized by recurrent infections, decreased serum levels of immunoglobulin G (IgG) and IgA, and normal/increased serum levels of IgM. Herein, we describe th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8b67a2d3f02bfd5d07a742a52137d7c
https://doi.org/10.1556/030.62.2015.3.4
https://doi.org/10.1556/030.62.2015.3.4
Autor:
Ekrem Unal, H. Haluk Akar, M. Akif Ozdemir, Yenan T. Bryceson, Henrich Schlums, Siobhan O. Burns, Samuel C. C. Chiang, Turkan Patiroglu, Shahnaz Bibi, Kimberly Gilmour, Musa Karakukcu
Publikováno v:
Clinical Immunology. 159:58-62
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30023b90e1d3e82f9595320a7d57b043
https://doi.org/10.1016/j.clim.2015.04.015
https://doi.org/10.1016/j.clim.2015.04.015