İçeriğe geç
akaturk Akademik ölçüm

Makale detayı · 2016 · article

Identification of Polycystic Ovary Syndrome PCOS Specific Genes in Cumulus and Mural Granulosa Cells

Dergi PLOS ONE
ISSN1932-6203
YÖKSİS OpenAlex Açık erişim · gold Üst %10
Yıl2016
Atıf43OpenAlex
Atıf38Semantic Scholar · 1 etkili
Yüzdelik%94,7
FWCI5,191,00 = dünya ortalaması
Scopus (SJR)Q1
WoS (JCR)Q1

Veri kaynağı ayrımı

  • YÖKSİSYÖKSİS makale kaydı
  • YÖKSİS dergi adıPLOS ONE
  • Katalog eşleşmesi (ISSN)PLOS ONE
  • OpenAlexOpenAlex zenginleştirmesi (özet, atıf, konular)
  • Semantic Scholaratıf sayısı (OpenAlex ile birleştirilmez)

Özet

OpenAlex İngilizce

Polycystic ovary syndrome (PCOS) is a metabolic and endocrine disorder which affects women of reproductive age with prevalence of 8-18%. The oocyte within the follicle is surrounded by cumulus cells (CCs), which connect with mural granulosa cells (MGCs) that are responsible for secreting steroid hormones. The main aim of this study is comparing gene expression profiles of MGCs and CCs in PCOS and control samples to identify PCOS-specific differentially expressed genes (DEGs). In this study, two microarray databases were searched for mRNA expression microarray studies performed with CCs and MGCs obtained from PCOS patients and control samples. Three independent studies were selected to be integrated with naive meta-analysis since raw meta-data from these studies were found to be highly correlated. DEGs in these somatic cells were identified for PCOS and control groups. This study enabled us to reveal dysregulation in MAPK (mitogen activated protein kinase), insulin and Wnt signaling pathways between CCs and MGCs in PCOS. The meta-analysis results together with qRT-PCR validations provide evidence that molecular signaling is dysregulated through MGCs and CCs in PCOS, which is important for follicle and oocyte maturation and may contribute to the pathogenesis of the syndrome.

Konular

Atıflar

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

43atıfOpenAlex · cited_by_count (önbellek / veritabanı)

Yerel katalogda bu makaleye atıf yapan 2 yayın (OpenAlex referans eşleşmesi; tam dünya listesi değildir).

  1. 2025 Custom exome panel revealed new mutations in MAPK14 and novel mutation in RUNX2 gene in patients with PCOSAtıf 1 · OpenAlex
  2. 2024 Custom exome panel revealed new mutations in MAPK14 and novel mutation in RUNX2 gene in patients with PCOSAtıf 0 · OpenAlex

Yazarlar

9
  1. Alp Aydos 1
  2. Aykut Gürel 2
  3. Yasemin Öztemur Islakoğlu 3
  4. Senem Noyan 4
  5. Bağdagül Gökçe 5
  6. Tolga Ecemiş 6
  7. Cemil Kaya 7
  8. Arif Tarık Aksu 8
  9. BALA GÜR DEDEOĞLU ANKARA ÜNİVERSİTESİ 9