Unal O

Title : Optimization of Phellinus hartigii extracts: Biological activities, and phenolic content analysis - Unal_2025_BMC.Complement.Med.Ther_25_113

Author(s) : Unal O , Gurgen A , Krupodorova T , Sevindik M , Kabaktepe S , Akata I

Ref : BMC Complement Med Ther , 25 :113 , 2025

Abstract :

PubMedSearch : Unal_2025_BMC.Complement.Med.Ther_25_113

PubMedID: 40133842

Title : Bioactivity of the Gray Knight Mushroom Tricholoma terreum (Agaricomycetes): Antioxidant, Antiproliferative, and Enzyme Inhibition Potential - Sevindik_2025_Int.J.Med.Mushrooms_27_75

Author(s) : Sevindik M , Bal C , Unal O , Eraslan EC

Ref : Int J Med Mushrooms , 27 :75 , 2025

Abstract :

PubMedSearch : Sevindik_2025_Int.J.Med.Mushrooms_27_75

PubMedID: 40743719

Title : Optimization of Phellinus hartigii extracts: Biological activities, and phenolic content analysis - Unal_2025_BMC.Complement.Med.Ther_25_113

Author(s) : Unal O , Gurgen A , Krupodorova T , Sevindik M , Kabaktepe S , Akata I

Ref : BMC Complement Med Ther , 25 :113 , 2025

Abstract :

PubMedSearch : Unal_2025_BMC.Complement.Med.Ther_25_113

PubMedID: 40133842

Title : Bioactivity of the Gray Knight Mushroom Tricholoma terreum (Agaricomycetes): Antioxidant, Antiproliferative, and Enzyme Inhibition Potential - Sevindik_2025_Int.J.Med.Mushrooms_27_75

Author(s) : Sevindik M , Bal C , Unal O , Eraslan EC

Ref : Int J Med Mushrooms , 27 :75 , 2025

Abstract :

PubMedSearch : Sevindik_2025_Int.J.Med.Mushrooms_27_75

PubMedID: 40743719

Title : Optimization of Phellinus hartigii extracts: Biological activities, and phenolic content analysis - Unal_2025_BMC.Complement.Med.Ther_25_113

Author(s) : Unal O , Gurgen A , Krupodorova T , Sevindik M , Kabaktepe S , Akata I

Ref : BMC Complement Med Ther , 25 :113 , 2025

Abstract :

PubMedSearch : Unal_2025_BMC.Complement.Med.Ther_25_113

PubMedID: 40133842

Title : Bioactivity of the Gray Knight Mushroom Tricholoma terreum (Agaricomycetes): Antioxidant, Antiproliferative, and Enzyme Inhibition Potential - Sevindik_2025_Int.J.Med.Mushrooms_27_75

Author(s) : Sevindik M , Bal C , Unal O , Eraslan EC

Ref : Int J Med Mushrooms , 27 :75 , 2025

Abstract :

PubMedSearch : Sevindik_2025_Int.J.Med.Mushrooms_27_75

PubMedID: 40743719

Title : Progressive deafness-dystonia due to SERAC1 mutations: A study of 67 cases - Maas_2017_Ann.Neurol_82_1004

Author(s) : Maas RR , Iwanicka-Pronicka K , Kalkan Ucar S , Alhaddad B , AlSayed M , Al-Owain MA , Al-Zaidan HI , Balasubramaniam S , Baric I , Bubshait DK , Burlina A , Christodoulou J , Chung WK , Colombo R , Darin N , Freisinger P , Garcia Silva MT , Grunewald S , Haack TB , van Hasselt PM , Hikmat O , Horster F , Isohanni P , Ramzan K , Kovacs-Nagy R , Krumina Z , Martin-Hernandez E , Mayr JA , McClean P , de Meirleir L , Naess K , Ngu LH , Pajdowska M , Rahman S , Riordan G , Riley L , Roeben B , Rutsch F , Santer R , Schiff M , Seders M , Sequeira S , Sperl W , Staufner C , Synofzik M , Taylor RW , Trubicka J , Tsiakas K , Unal O , Wassmer E , Wedatilake Y , Wolff T , Prokisch H , Morava E , Pronicka E , Wevers RA , de Brouwer AP , Wortmann SB

Ref : Annals of Neurology , 82 :1004 , 2017

Abstract :

PubMedSearch : Maas_2017_Ann.Neurol_82_1004

PubMedID: 29205472

Gene_locus related to this paper: human-SERAC1

Title : Progressive deafness-dystonia due to SERAC1 mutations: A study of 67 cases - Maas_2017_Ann.Neurol_82_1004

Author(s) : Maas RR , Iwanicka-Pronicka K , Kalkan Ucar S , Alhaddad B , AlSayed M , Al-Owain MA , Al-Zaidan HI , Balasubramaniam S , Baric I , Bubshait DK , Burlina A , Christodoulou J , Chung WK , Colombo R , Darin N , Freisinger P , Garcia Silva MT , Grunewald S , Haack TB , van Hasselt PM , Hikmat O , Horster F , Isohanni P , Ramzan K , Kovacs-Nagy R , Krumina Z , Martin-Hernandez E , Mayr JA , McClean P , de Meirleir L , Naess K , Ngu LH , Pajdowska M , Rahman S , Riordan G , Riley L , Roeben B , Rutsch F , Santer R , Schiff M , Seders M , Sequeira S , Sperl W , Staufner C , Synofzik M , Taylor RW , Trubicka J , Tsiakas K , Unal O , Wassmer E , Wedatilake Y , Wolff T , Prokisch H , Morava E , Pronicka E , Wevers RA , de Brouwer AP , Wortmann SB

Ref : Annals of Neurology , 82 :1004 , 2017

Abstract :

PubMedSearch : Maas_2017_Ann.Neurol_82_1004

PubMedID: 29205472

Gene_locus related to this paper: human-SERAC1

Title : Progressive deafness-dystonia due to SERAC1 mutations: A study of 67 cases - Maas_2017_Ann.Neurol_82_1004

Author(s) : Maas RR , Iwanicka-Pronicka K , Kalkan Ucar S , Alhaddad B , AlSayed M , Al-Owain MA , Al-Zaidan HI , Balasubramaniam S , Baric I , Bubshait DK , Burlina A , Christodoulou J , Chung WK , Colombo R , Darin N , Freisinger P , Garcia Silva MT , Grunewald S , Haack TB , van Hasselt PM , Hikmat O , Horster F , Isohanni P , Ramzan K , Kovacs-Nagy R , Krumina Z , Martin-Hernandez E , Mayr JA , McClean P , de Meirleir L , Naess K , Ngu LH , Pajdowska M , Rahman S , Riordan G , Riley L , Roeben B , Rutsch F , Santer R , Schiff M , Seders M , Sequeira S , Sperl W , Staufner C , Synofzik M , Taylor RW , Trubicka J , Tsiakas K , Unal O , Wassmer E , Wedatilake Y , Wolff T , Prokisch H , Morava E , Pronicka E , Wevers RA , de Brouwer AP , Wortmann SB

Ref : Annals of Neurology , 82 :1004 , 2017

Abstract :

PubMedSearch : Maas_2017_Ann.Neurol_82_1004

PubMedID: 29205472

Gene_locus related to this paper: human-SERAC1

Title : Two Turkish siblings with MEGDEL syndrome due to novel SERAC1 gene mutation - Unal_2015_Turk.J.Pediatr_57_388

Author(s) : Unal O , Ozgul RK , Yucel D , Yalnizoglu D , Tokatli A , Sivri HS , Hismi B , Coskun T , Dursun A

Ref : Turk J Pediatr , 57 :388 , 2015

Abstract :

PubMedSearch : Unal_2015_Turk.J.Pediatr_57_388

PubMedID: 27186703

Gene_locus related to this paper: human-SERAC1

Title : Two Turkish siblings with MEGDEL syndrome due to novel SERAC1 gene mutation - Unal_2015_Turk.J.Pediatr_57_388

Author(s) : Unal O , Ozgul RK , Yucel D , Yalnizoglu D , Tokatli A , Sivri HS , Hismi B , Coskun T , Dursun A

Ref : Turk J Pediatr , 57 :388 , 2015

Abstract :

PubMedSearch : Unal_2015_Turk.J.Pediatr_57_388

PubMedID: 27186703

Gene_locus related to this paper: human-SERAC1

Title : Two Turkish siblings with MEGDEL syndrome due to novel SERAC1 gene mutation - Unal_2015_Turk.J.Pediatr_57_388

Author(s) : Unal O , Ozgul RK , Yucel D , Yalnizoglu D , Tokatli A , Sivri HS , Hismi B , Coskun T , Dursun A

Ref : Turk J Pediatr , 57 :388 , 2015

Abstract :

PubMedSearch : Unal_2015_Turk.J.Pediatr_57_388

PubMedID: 27186703

Gene_locus related to this paper: human-SERAC1

Unal O

References (12)

1. Optimization of Phellinus hartigii extracts: Biological activities, and phenolic content analysis - Unal_2025_BMC.Complement.Med.Ther_25_113

2. Bioactivity of the Gray Knight Mushroom Tricholoma terreum (Agaricomycetes): Antioxidant, Antiproliferative, and Enzyme Inhibition Potential - Sevindik_2025_Int.J.Med.Mushrooms_27_75

3. Optimization of Phellinus hartigii extracts: Biological activities, and phenolic content analysis - Unal_2025_BMC.Complement.Med.Ther_25_113

4. Bioactivity of the Gray Knight Mushroom Tricholoma terreum (Agaricomycetes): Antioxidant, Antiproliferative, and Enzyme Inhibition Potential - Sevindik_2025_Int.J.Med.Mushrooms_27_75

5. Optimization of Phellinus hartigii extracts: Biological activities, and phenolic content analysis - Unal_2025_BMC.Complement.Med.Ther_25_113

6. Bioactivity of the Gray Knight Mushroom Tricholoma terreum (Agaricomycetes): Antioxidant, Antiproliferative, and Enzyme Inhibition Potential - Sevindik_2025_Int.J.Med.Mushrooms_27_75

7. Progressive deafness-dystonia due to SERAC1 mutations: A study of 67 cases - Maas_2017_Ann.Neurol_82_1004

8. Progressive deafness-dystonia due to SERAC1 mutations: A study of 67 cases - Maas_2017_Ann.Neurol_82_1004

9. Progressive deafness-dystonia due to SERAC1 mutations: A study of 67 cases - Maas_2017_Ann.Neurol_82_1004

10. Two Turkish siblings with MEGDEL syndrome due to novel SERAC1 gene mutation - Unal_2015_Turk.J.Pediatr_57_388

11. Two Turkish siblings with MEGDEL syndrome due to novel SERAC1 gene mutation - Unal_2015_Turk.J.Pediatr_57_388

12. Two Turkish siblings with MEGDEL syndrome due to novel SERAC1 gene mutation - Unal_2015_Turk.J.Pediatr_57_388