OpenAlex 988 works 14 author topics
Works
988 works
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YÖKSİS
SJR Q1
JCR Q1
OpenAlex top 1%
OpenAlex 99.5%
No abstract yet.
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YÖKSİS
SJR Q2
JCR Q3
OpenAlex top 1%
OpenAlex 99.7%
Aicardi-Goutières syndrome is an inflammatory disease occurring due to mutations in any of TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR or IFIH1. We report on 374 patients from 299 families with mutations in these seven genes. Most patients conformed to one of two fairly stereotyped clinical profiles; either exhi…
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YÖKSİS
SJR Q1
JCR Q2
OpenAlex top 1%
OpenAlex 99.8%
No abstract yet.
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YÖKSİS
SJR Q1
JCR Q1
OpenAlex top 1%
OpenAlex 99.9%
No abstract yet.
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OpenAlex top 10%
OpenAlex 91.4%
No abstract yet.
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YÖKSİS
SJR Q1
JCR Q2
OpenAlex 82.5%
No abstract yet.
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OpenAlex top 10%
OpenAlex 95.0%
BACKGROUND: Members of the p47 (immunity-related GTPases (IRG) family) GTPases are essential, interferon-inducible resistance factors in mice that are active against a broad spectrum of important intracellular pathogens. Surprisingly, there are no reports of p47 function in humans. RESULTS: Here we show that the p47 G…
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YÖKSİS
SJR Q1
JCR Q1
OpenAlex top 10%
OpenAlex 98.6%
No abstract yet.
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YÖKSİS
SJR Q1
JCR Q1
OpenAlex top 10%
OpenAlex 98.0%
Silica particles induce lung inflammation and fibrosis. Here we show that stimulator of interferon genes (STING) is essential for silica-induced lung inflammation. In mice, silica induces lung cell death and self-dsDNA release in the bronchoalveolar space that activates STING pathway. Degradation of extracellular self…
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YÖKSİS
SJR Q1
JCR Q1
OpenAlex top 10%
OpenAlex 98.0%
Silica particles induce lung inflammation and fibrosis. Here we show that stimulator of interferon genes (STING) is essential for silica-induced lung inflammation. In mice, silica induces lung cell death and self-dsDNA release in the bronchoalveolar space that activates STING pathway. Degradation of extracellular self…
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OpenAlex top 10%
OpenAlex 98.9%
No abstract yet.
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OpenAlex top 10%
OpenAlex 97.5%
Familial Mediterranean fever (FMF) (OMIM #249100) is the most common hereditary autoinflammatory disease in the world. FMF is caused by gain of function mutations of MEFV gene which encodes an immune regulatory protein, pyrin. Over the last few years, we have witnessed several new developments in the pathogenesis, gen…
Academicians
14 academicians
- EDA TAHİR TURANLI 10 author topics
- BANU PEYNİRCİOĞLU 8 author topics
- RAMAZAN GÜNEŞAÇAR 6 author topics
- ECİR ALİ ÇAKMAK 4 author topics
- NESRİN ERKOL 4 author topics
- MUHAMMET MURAT ÇELİK 3 author topics
- VOLKAN YAZAR 3 author topics
- AYÇA ÇAKMAK AYDIN 2 author topics
- DAMLA YILDIRIM DAĞTAŞ 2 author topics
- DUYGU MERVE ÇALIŞKAN 2 author topics
- ELİF GELMEZ 2 author topics
- KIYMET ASLI KİREÇTEPE AYDIN 2 author topics