日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

The Experience of a Tertiary Reference Center in Central Anatolia with Children Carrying ZAP-70 Variants, Including Two Novel Variants

安纳托利亚中部一家三级参考中心在携带 ZAP-70 变异体(包括两种新变异体)的儿童中的经验

Göktaş, Serdar; Kalaycik Sengul, Ozlem; Erdem, Şerife; Eke Güngör, Hatice; Babayeva, Royala; Bilgic-Eltan, Sevgi; Güzel, Turan; Dörterler, Koray; Rohlfs, Meino; Özcan, Alper; Yilmaz, Ebru; Karakukcu, Musa; Akar, Haluk Himmet; Karakoc-Aydiner, Elif; Özen, Ahmet; Elmas, Muhsin; Patiroğlu, Türkan; Doğan, Muhammet E; Baş, Hasan; Taylor, Naomi; Baris, Safa; Klein, Christoph; Eken, Ahmet; Ünal, Ekrem

Beyond Dermatological Findings: Multisystem Involvement in Prolidase Deficiency

除了皮肤科表现之外:脯氨酸酶缺乏症的多系统受累

Gungoren, Ezgi Yalcin; Meric, Zeynep; Sefer, Asena Pinar; Deveci Ozkan, Asuman; Can, Salim; Babayeva, Royala; Kasap, Nurhan; Nain, Ercan; Ozek Yucel, Esra; Kiykim, Ayca; Bilgic-Eltan, Sevgi; Yucelten, Ayse Deniz; Karakoc-Aydiner, Elif; Ozen, Ahmet; Baris, Safa

Rapamycin Controls Lymphoproliferation and Reverses T-Cell Responses in a Patient with a Novel STIM1 Loss-of-Function Deletion

雷帕霉素控制淋巴细胞增殖并逆转患有新型 STIM1 功能丧失缺失的患者的 T 细胞反应

Ibrahim Serhat Karakus, Mehmet Cihangir Catak, Alexandra Frohne, Feyza Bayram Catak, Melek Yorgun Altunbas, Royala Babayeva, Sevgi Kostel Bal, Sevgi Bilgic Eltan, Ezgi Yalcin Gungoren, Fehim Esen, Itir Ebru Zemheri, Elif Karakoc-Aydiner, Ahmet Ozen, Suar Caki-Kilic, Michael J Kraakman, Kaan Boztug, 

DIAPH1-Deficiency is Associated with Major T, NK and ILC Defects in Humans

DIAPH1 缺陷与人类 T 细胞、NK 细胞和 ILC 细胞的主要缺陷相关

Azizoglu, Zehra Busra; Babayeva, Royala; Haskologlu, Zehra Sule; Acar, Mustafa Burak; Ayaz-Guner, Serife; Okus, Fatma Zehra; Alsavaf, Mohammad Bilal; Can, Salim; Basaran, Kemal Erdem; Canatan, Mehmed Fatih; Ozcan, Alper; Erkmen, Hasret; Leblebici, Can Berk; Yilmaz, Ebru; Karakukcu, Musa; Kose, Mehmet; Canoz, Ozlem; Özen, Ahmet; Karakoc-Aydiner, Elif; Ceylaner, Serdar; Gümüş, Gülsüm; Per, Huseyin; Gumus, Hakan; Canatan, Halit; Ozcan, Servet; Dogu, Figen; Ikinciogullari, Aydan; Unal, Ekrem; Baris, Safa; Eken, Ahmet

Correction to: DIAPH1-Deficiency is Associated with Major T, NK and ILC Defects in Humans

更正:DIAPH1 缺陷与人类主要 T 细胞、NK 细胞和 ILC 细胞缺陷相关

Azizoglu, Zehra Busra; Babayeva, Royala; Haskologlu, Zehra Sule; Acar, Mustafa Burak; Ayaz-Guner, Serife; Okus, Fatma Zehra; Alsavaf, Mohammad Bilal; Can, Salim; Basaran, Kemal Erdem; Canatan, Mehmed Fatih; Ozcan, Alper; Erkmen, Hasret; Leblebici, Can Berk; Yilmaz, Ebru; Karakukcu, Musa; Kose, Mehmet; Canoz, Ozlem; Özen, Ahmet; Karakoc-Aydiner, Elif; Ceylaner, Serdar; Gümüş, Gülsüm; Per, Huseyin; Gumus, Hakan; Canatan, Halit; Ozcan, Servet; Dogu, Figen; Ikinciogullari, Aydan; Unal, Ekrem; Baris, Safa; Eken, Ahmet

Biallelic NFATC1 mutations cause an inborn error of immunity with impaired CD8+ T-cell function and perturbed glycolysis

双等位基因 NFATC1 突变会导致先天性免疫缺陷,导致 CD8+ T 细胞功能受损和糖酵解紊乱

Sevgi Kostel Bal, Sarah Giuliani, Jana Block, Peter Repiscak, Christoph Hafemeister, Tala Shahin, Nurhan Kasap, Bernhard Ransmayr, Yirun Miao, Cheryl van de Wetering, Alexandra Frohne, Raul Jimenez Heredia, Michael Schuster, Samaneh Zoghi, Vanessa Hertlein, Marini Thian, Aleksandr Bykov, Royala Baba

Severe allergic dysregulation due to a gain of function mutation in the transcription factor STAT6

STAT6转录因子功能获得性突变导致的严重过敏性失调

Safa Baris ,Mehdi Benamar ,Qian Chen ,Mehmet Cihangir Catak ,Mónica Martínez-Blanco ,Muyun Wang ,Jason Fong ,Michel J Massaad ,Asena Pinar Sefer ,Altan Kara ,Royala Babayeva ,Sevgi Bilgic Eltan ,Ayse Deniz Yucelten ,Emine Bozkurtlar ,Leyla Cinel ,Elif Karakoc-Aydiner ,Yumei Zheng ,Hao Wu ,Ahmet Ozen ,Klaus Schmitz-Abe ,Talal A Chatila

Expanding the clinical and immunological phenotypes of PAX1-deficient SCID and CID patients

扩展PAX1缺陷型SCID和CID患者的临床和免疫学表型

Nalan Yakici,Alexandra Y Kreins,Mehmet Cihangir Catak,Royala Babayeva,Baran Erman,Heather Kenney,Hatice Eke Gungor,Pablo A Cea,Tomoki Kawai,Marita Bosticardo,Ottavia Maria Delmonte,Stuart Adams,Yu-Tong Fan,Francesca Pala,Ayberk Turkyilmaz,Evey Howley,Austen Worth,Hakan Kot,Asena Pinar Sefer,Altan Kara,Alper Bulutoglu,Sevgi Bilgic-Eltan,Melek Yorgun Altunbas,Feyza Bayram Catak,Ibrahim Serhat Karakus,Emrah Karatay,Sidem Didar Tekeoglu,Metin Eser,Davut Albayrak,Senol Citli,Ayca Kiykim,Elif Karakoc-Aydiner,Ahmet Ozen,Sujal Ghosh,Holger Gohlke,Fazil Orhan,Luigi D Notarangelo,E Graham Davies,Safa Baris

Corrigendum to "Expanding the clinical and immunological phenotypes of PAX1-deficient SCID and CID patients" [Clinical Immunology 255 (2023) 109757]

对“扩展 PAX1 缺陷型 SCID 和 CID 患者的临床和免疫表型”的更正 [临床免疫学 255 (2023) 109757]

Yakici, Nalan; Kreins, Alexandra Y; Catak, Mehmet Cihangir; Babayeva, Royala; Erman, Baran; Kenney, Heather; Eke-Gungor, Hatice; Cea, Pablo A; Kawai, Tomoki; Bosticardo, Marita; Delmonte, Ottavia Maria; Adams, Stuart; Fan, Yu-Tong; Pala, Francesca; Turkyilmaz, Ayberk; Howley, Evey; Worth, Austen; Kot, Hakan; Sefer, Asena Pinar; Kara, Altan; Bulutoglu, Alper; Bilgic-Eltan, Sevgi; Yorgun Altunbas, Melek; Bayram Catak, Feyza; Karakus, Ibrahim Serhat; Karatay, Emrah; Tekeoglu, Sidem Didar; Eser, Metin; Albayrak, Davut; Citli, Senol; Kiykim, Ayca; Karakoc-Aydiner, Elif; Ozen, Ahmet; Ghosh, Sujal; Gohlke, Holger; Orhan, Fazil; Notarangelo, Luigi D; Davies, E Graham; Baris, Safa