Bildiriler
1.
Identifying differentially expressed genes based on nonnegative factorization using gene expression data of glioblastoma stem cells
Güven Emine, Akçay Sevinç, Yayın Yeri: International Congress of Engineering and Natural Sciences Studies, Ankara, Turkey, 08.05.2021
Uluslararası
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2.
Rare and Precious: Elastin gene diseases
Akçay Sevinç, Yayın Yeri: 9th Molecular Biology and Biotechnology Congress,
Ulusal
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3.
In silico investigation of molecular mechanisms in patients with pulmonary arterial hypertension affecting the severity of COVID-19
Akçay Sevinç, Yayın Yeri: Ankara International Congress on Scientific Research-VII,
Uluslararası
Tam metin bildiri
4.
Increased expression of mutant elastin alleles in autosomal dominant cutis laxa is normalized by transforming growth factor beta treatment.
Akçay Sevinç, Urban Zsolt, Lawrence Elizabeth, Yayın Yeri: The American Society of Human Genetics, 66th Annual Meeting, Vancouver,
Uluslararası
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5.
A partial elastin gene duplication in supravalvular aortic stenosis
Akçay Sevinç, Yayın Yeri: IV. International Congress on Applied Biological Sciences, Eskisehir, Turkey,
Uluslararası
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6.
Molecular analysis of elastin gene mutations in autosomal dominant cutis laxa.
Akçay Sevinç, Yayın Yeri: 7th International Molecular Biology and Biotechnology Congress, Konya, Turkey,
Uluslararası
Özet bildiri
7.
Heritable disorders associated with TGFβ signaling
Akçay Sevinç, Yayın Yeri: International African Conference on Current Studies of Science, Technology& Social Sciences, Johannesburg, South Africa,
Uluslararası
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8.
Investigation of potential key biomarkers and pathways related to idiopathic pulmonary fibrosis based on bioinformatics methods.
Akçay Sevinç, Yayın Yeri: 6th International Congress on Veterinary and Animal Sciences.,
Uluslararası
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9.
Genotype-dependent alterations in TGFβ signaling in ELN-related cutis laxa.
Akçay Sevinç, Urban Zsolt, Yayın Yeri: The American Society of Human Genetics, 65th Annual Meeting, Baltimore,
Uluslararası
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10.
Mutation-specific TGFβ Signaling Changes in Patients with ELN-Related Cutis Laxa.
Akçay Sevinç, Urban Zsolt, Yayın Yeri: Gordon Research Seminar on Elastin, Elastic Fibers & Microfibrills, Biddeford, ME,
Uluslararası
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11.
Novel ELN mutations and vascular phenotype in autosomal dominant cutis laxa
Akçay Sevinç, Urban Zsolt, Yayın Yeri: The American Society of Human Genetics, 63rd Annual Meeting, Boston, MA,,
Uluslararası
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12.
TGFβ signaling in patients with ELN-related cutis laxa
Akçay Sevinç, Urban Zsolt, Yayın Yeri: American Society for Matrix Biology, Biennial Meeting, Cleveland, OH,
Uluslararası
13.
Sarcopenia: Genetic determination, risk factors and public health significance.
Akçay Sevinç, Yayın Yeri: Çukurova 7th International Scientific Researches Conference,
Uluslararası
Tam metin bildiri
14.
Autosomal dominant cutis laxa and supravalvular aortic stenosis: clinical, molecular and mutational aspects
Akçay Sevinç, Yayın Yeri: 2nd International European Conference on Interdisciplinary Scientific Researches,
Uluslararası
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15.
Identification of Potential Key Biomarkers and Pathways Involved in Pulmonary Arterial Hypertension by in silico analysis
Akçay Sevinç, Yayın Yeri: 10. Ulusal Moleküler Biyoloji ve Biyoteknoloji Kongresi,
Ulusal
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