Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Intan Razari"'
Autor:
Alim El-Hakim, Inswasti Cahyani, Muhammad Zulfikar Arief, Gilang Akbariani, Asep Muhamad Ridwanuloh, Syam Budi Iryanto, Ratih Rahayu, Daeng Deni Mardaeni, Vincentius Budhyanto, Yusnita, Wening Sari, Anggi Pn Hidayati, Intan Razari, Silviatun Nihayah, Kinasih Prayuni, Chandra Utomo, Ratih Asmana Ningrum, Susanti Susanti, Ahmad Utomo
Publikováno v:
Epigenetics, Vol 19, Iss 1 (2024)
Stunting is the result of chronic malnutrition due to the lack of micronutrient-based methyl donors required for epigenetic programming during the first 1000 days of life. Methylation studies using bisulfite conversion from blood DNA are invasive and
Externí odkaz:
https://doaj.org/article/3616bc19696942f48ac5c10b113cd092
Publikováno v:
Makara Journal of Health Research, Vol 23, Iss 2, Pp 149-153 (2023)
Background: Asthma is a multifactorial disease that encompasses a multitude of genetic and environmental factors. One such factor is the disintegrin and metalloprotein-33 (ADAM33) gene, which is correlated with asthma and bronchial hyperresponsivenes
Externí odkaz:
https://doaj.org/article/09b48ca04dd046ce90061dfb38f2941c
Autor:
Abdul Salam M. Sofro, Soedarsono Soedarsono, Yenni Zulhamidah, Intan Razari, Rika Yuliwulandari, Kinasih Prayuni, Retno Susilowati, Katsushi Tokunaga
Publikováno v:
Pharmacogenomics. 22:157-163
Background: Owing to the high resistance rate of tuberculosis (TB) to isoniazid, which is metabolized by N-acetyltransferase 2 (NAT2), we investigated the associations between NAT2 variants and multidrug-resistant (MDR)-TB. Materials & methods: The a
Publikováno v:
Environmental Toxicology and Pharmacology. 65:14-17
Genetic variations in the glutathione S-transferase genes GSTT1 and GSTM1 have been widely studied, and homozygous deletions or null genotypes have been reported in different populations. Previous studies suggest that individuals who are homozygous-n
Autor:
Rika, Yuliwulandari, Kinasih, Prayuni, Intan, Razari, Retno W, Susilowati, Yenni, Zulhamidah, Soedarsono, Soedarsono, Abdul Salam M, Sofro, Katsushi, Tokunaga
Publikováno v:
Pharmacogenomics. 22(3)
Publikováno v:
Medical Laboratory Technology Journal. 7:66
The rs1800629 polymorphism plays a crucial role in the pathogenesis of infectious and autoimmune diseases. Meanwhile, tuberculosis (TB) remains a health primary infectious disease in Indonesia. The purpose of this study is to evaluate the HRM method
Publikováno v:
Medical Journal of Indonesia, Vol 26, Iss 1 (2017)
Background: Arylamine N-acetyltransferase 2 (NAT2) polymorphism was previously reported to have association with the risk of drug toxicities and the development of various diseases. Previous research on the Indonesian population, especially Javanese
Autor:
Taisei Mushiroda, Intan Razari, Erna Kristin, Hideki Yanai, Aziza Ariyani, Subagyo, Britanto Dani Wicaksono, Syafrizal, Surakameth Mahasirimongkol, Kencono Viyati, Rika Yuliwulandari, Eva Sri Diana, Suci Setiawati, Retno Susilowati, Kinasih Prayuni, Katsushi Tokunaga
Publikováno v:
Journal of Human Genetics. 61:533-537
Drug-induced liver injury (DILI) is the most common adverse drug reaction in the treatment of tuberculosis (TB). Several studies showed that patients with TB and the slow-acetylator phenotype caused by NAT2 variants are highly susceptible to DILI cau
Autor:
Helwiah Umniyati, Kinasih Prayuni, Rika Yuliwulandari, Kencono Viyati, Retno Susilowati, Intan Razari
Publikováno v:
Annals of human geneticsREFERENCES. 83(6)
Background N-acetyltransferase 2 (NAT2) is a key enzyme involved in the phase II metabolism of aromatic amines and heterocyclic aromatic amines present in a wide range of xenobiotics. The aim of this study was to investigate the NAT2 polymorphism in
Publikováno v:
Medical Journal of Indonesia; Mar2017, Vol. 26 Issue 1, p7-13, 7p