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Makale detayı · 2022 · article

Next-generation sequencing of prolidase gene identifies novel and common variants associated with low prolidase in coronary artery ectasia

Dergi Molecular Biology Reports
ISSN0301-4851
YÖKSİS OpenAlex
Yıl2022
Atıf6OpenAlex
Atıf6Semantic Scholar
Yüzdelik%63,1
FWCI0,421,00 = dünya ortalaması
Scopus (SJR)Q2
WoS (JCR)Q3
DOI10.1007/s11033-022-08142-1 OpenAlexOpenAlex kaydı

Veri kaynağı ayrımı

  • YÖKSİSYÖKSİS makale kaydı
  • YÖKSİS dergi adıMolecular Biology Reports
  • Katalog eşleşmesi (ISSN)Molecular Biology Reports
  • OpenAlexOpenAlex zenginleştirmesi (özet, atıf, konular)
  • Semantic Scholaratıf sayısı (OpenAlex ile birleştirilmez)

Özet

Özet henüz derlenmedi; DergiPark / OpenAlex kuyruğu işlenince burada görünecek.

Konular

Atıflar

OpenAlex cited_by_count. WoS veya Scopus atıf sayısı değildir; o kaynaklar için ayrı kolon yoktur.

6atıfOpenAlex · cited_by_count (önbellek / veritabanı)

Yerel katalogda bu makaleye atıf yapan 12 yayın (OpenAlex referans eşleşmesi; tam dünya listesi değildir).

  1. 2025 Next-generation sequencing of CCR5, CXCR4, and IFNAR1 variants in relation to HIV-1 disease progression and ART responseAtıf 6 · OpenAlex
  2. 2025 Next-generation sequencing of CCR5, CXCR4, and IFNAR1 variants in relation to HIV-1 disease progression and ART responseAtıf 6 · OpenAlex
  3. 2025 Next-generation sequencing of CCR5, CXCR4, and IFNAR1 variants in relation to HIV-1 disease progression and ART responseAtıf 6 · OpenAlex
  4. 2025 Endothelin-converting Enzyme-1b Genetic Variants Increase the Risk of Coronary Artery EctasiaAtıf 2 · OpenAlex
  5. 2024 Endothelin-converting Enzyme-1b Genetic Variants Increase the Risk of Coronary Artery EctasiaAtıf 2 · OpenAlex
  6. 2024 Endothelin-converting Enzyme-1b Genetic Variants Increase the Risk of Coronary Artery EctasiaAtıf 2 · OpenAlex
  7. 2024 Endothelin-converting Enzyme-1b Genetic Variants Increase the Risk of Coronary Artery EctasiaAtıf 2 · OpenAlex
  8. 2026 A next‐generation sequencing–based pharmacogenetic study of ABCB1 , ABCC1 , and ABCC2 variants associated with antiseizure medication response in Turkish epilepsy patientsAtıf 0 · OpenAlex
  9. 2026 A next‐generation sequencing–based pharmacogenetic study of ABCB1 , ABCC1 , and ABCC2 variants associated with antiseizure medication response in Turkish epilepsy patientsAtıf 0 · OpenAlex
  10. 2026 Evaluation of dopamine transporter gene variations in Turkish children with attention deficit hyperactivity disorder treated with methylphenidate adverse effectsAtıf 0 · OpenAlex

Yazarlar

9
  1. KÜBRA ÇİĞDEM PEKKOÇ UYANIK 1
  2. EZGİ IRMAK ASLAN 2
  3. ONUR KILIÇARSLAN 3
  4. Ozgur Selim Er 4
  5. SERHAN ÖZYILDIRIM İSTANBUL ÜNİVERSİTESİ-CERRAHPAŞA 5
  6. FATİH YANAR 6
  7. AHMET YILDIZ 7
  8. OĞUZ ÖZTÜRK 8
  9. HÜLYA YILMAZ AYDOĞAN 9