Ушбу иш иқтибос қилган ишлар

12 та иш

Иш: Frequency of mutations in “thrombophilic state” genes in Uzbekistan

1. The homozygous C677T mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for migraine

   Hisanori Kowa, Kenichi Yasui, Takao Takeshima +3

   Мақола20003 иқтибос

   ABIABI:AkademIndex/openalex/2026.other.578799

2. A common genetic variation in the 3'-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis

   SR Poort, FR Rosendaal, PH Reitsma +1

   Мақола19962 иқтибос

   ABIABI:AkademIndex/openalex/2026.other.159717

3. Mutation in blood coagulation factor V associated with resistance to activated protein C

   Rogier M. Bertina, Bobby P. C. Koeleman, Ted Koster +5

   Мақола19942 иқтибос

   ABIABI:AkademIndex/openalex/2026.other.159719

4. Venous thrombosis: a multicausal disease

   FR Rosendaal

   Шарҳ мақола19992 иқтибос

   ABIABI:AkademIndex/openalex/2026.other.159721

5. Сарлавҳасиз

   Бошқа1 иқтибос

   ABIABI:AkademIndex/openalex/2026.other.578793

6. Сарлавҳасиз

   Бошқа1 иқтибос

   ABIABI:AkademIndex/openalex/2026.other.578794

7. Сарлавҳасиз

   Бошқа1 иқтибос

   ABIABI:AkademIndex/openalex/2026.other.578795

8. Сарлавҳасиз

   Бошқа1 иқтибос

   ABIABI:AkademIndex/openalex/2026.other.578796

9. Сарлавҳасиз

   Бошқа1 иқтибос

   ABIABI:AkademIndex/openalex/2026.other.578797

10. Сарлавҳасиз

    Бошқа1 иқтибос

    ABIABI:AkademIndex/openalex/2026.other.578798

11. Сарлавҳасиз

    Бошқа1 иқтибос

    ABIABI:AkademIndex/openalex/2026.other.578800

12. Сарлавҳасиз

    Бошқа1 иқтибос

    ABIABI:AkademIndex/openalex/2026.other.578801