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Eda Tahir Turanli

Showing results (11-20 of 27) with videos related to

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Peerj|November 15, 2024
Investigation of multiple sclerosis-related pathways through the integration of genomic and proteomic dataElif Everest, Ege Ülgen, Ugur Uygunoglu, et al.
Paediatrics and International Child Health|January 16, 2019
A 9.5-year-old boy with recurrent neurological manifestations and severe hypertension, treated initially for polyarteritis nodosa, was subsequently diagnosed with adenosine deaminase type 2 deficiency (DADA2) which responded to anti-TNF-αSezgin Sahin, Amra Adrovic, Kenan Barut, et al.
Plos One|October 29, 2024
Profiling of five urinary exosomal miRNAs for the differential diagnosis of patients with diabetic kidney disease and focal segmental glomerulosclerosisSinan Trabulus, Mehmet Seyit Zor, Selma Alagoz, et al.
Biology|September 23, 2022
Transcriptomics and Proteomics Analyses Reveal JAK Signaling and Inflammatory Phenotypes during Cellular Senescence in Blind Mole Rats: The Reflections of Superior BiologyNurcan Inci, Erdogan Oguzhan Akyildiz, Abdullah Alper Bulbul, et al.
Clinical and Experimental Rheumatology|September 28, 2010
The prevalence of Behçet's syndrome, familial Mediterranean fever, HLA-B51 and MEFV gene mutations among ethnic Armenians living in Istanbul, TurkeyEmire Seyahi, Eda Tahir Turanli, Mehmet Serhat Mangan, et al.
American Journal of Medical Genetics. Part A|May 20, 2024
A rare case of uncharacterized autoinflammatory disease: Patient carrying variations in NLRP3 and TNFRSF1A genesOzgur Can Kilinc, Konul Gayibova, Merve Ozkilinc Onen, et al.
Modern Rheumatology Case Reports|August 5, 2023
A case with febrile attacks and vasculopathy associated with ADA2 and MEFV pathogenic variantsKerem Parlar, Eda Tahir Turanli, Eda Nuhoglu Kantarci, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 11, 2019
Spectrum of the neurologic manifestations in childhood-onset cryopyrin-associated periodic syndromeHuseyin Kilic, Sezgin Sahin, Cisem Duman, et al.
Journal of Experimental Zoology. Part A, Comparative Experimental Biology|February 21, 2006
Stable transmission and expression of the hepatitis B virus total genome in hybrid transgenic mice until F10 generationHaydar Bagis, Sezen Arat, Hande Odaman Mercan, et al.
Brain, Behavior, and Immunity|June 17, 2022
Genome-wide analysis of schizophrenia and multiple sclerosis identifies shared genomic loci with mixed direction of effectsMohammad Ahangari, Elif Everest, Tan-Hoang Nguyen, et al.
Pageof 3

Showing results (11-20 of 27) with videos related to

Sort By:
Pageof 3
Peerj|November 15, 2024
Investigation of multiple sclerosis-related pathways through the integration of genomic and proteomic dataElif Everest, Ege Ülgen, Ugur Uygunoglu, et al.
Paediatrics and International Child Health|January 16, 2019
A 9.5-year-old boy with recurrent neurological manifestations and severe hypertension, treated initially for polyarteritis nodosa, was subsequently diagnosed with adenosine deaminase type 2 deficiency (DADA2) which responded to anti-TNF-αSezgin Sahin, Amra Adrovic, Kenan Barut, et al.
Plos One|October 29, 2024
Profiling of five urinary exosomal miRNAs for the differential diagnosis of patients with diabetic kidney disease and focal segmental glomerulosclerosisSinan Trabulus, Mehmet Seyit Zor, Selma Alagoz, et al.
Biology|September 23, 2022
Transcriptomics and Proteomics Analyses Reveal JAK Signaling and Inflammatory Phenotypes during Cellular Senescence in Blind Mole Rats: The Reflections of Superior BiologyNurcan Inci, Erdogan Oguzhan Akyildiz, Abdullah Alper Bulbul, et al.
Clinical and Experimental Rheumatology|September 28, 2010
The prevalence of Behçet's syndrome, familial Mediterranean fever, HLA-B51 and MEFV gene mutations among ethnic Armenians living in Istanbul, TurkeyEmire Seyahi, Eda Tahir Turanli, Mehmet Serhat Mangan, et al.
American Journal of Medical Genetics. Part A|May 20, 2024
A rare case of uncharacterized autoinflammatory disease: Patient carrying variations in NLRP3 and TNFRSF1A genesOzgur Can Kilinc, Konul Gayibova, Merve Ozkilinc Onen, et al.
Modern Rheumatology Case Reports|August 5, 2023
A case with febrile attacks and vasculopathy associated with ADA2 and MEFV pathogenic variantsKerem Parlar, Eda Tahir Turanli, Eda Nuhoglu Kantarci, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 11, 2019
Spectrum of the neurologic manifestations in childhood-onset cryopyrin-associated periodic syndromeHuseyin Kilic, Sezgin Sahin, Cisem Duman, et al.
Journal of Experimental Zoology. Part A, Comparative Experimental Biology|February 21, 2006
Stable transmission and expression of the hepatitis B virus total genome in hybrid transgenic mice until F10 generationHaydar Bagis, Sezen Arat, Hande Odaman Mercan, et al.
Brain, Behavior, and Immunity|June 17, 2022
Genome-wide analysis of schizophrenia and multiple sclerosis identifies shared genomic loci with mixed direction of effectsMohammad Ahangari, Elif Everest, Tan-Hoang Nguyen, et al.
Pageof 3