Zobrazeno 1 - 10
of 544
pro vyhledávání: '"Haploview"'
Publikováno v:
Molecular Biology Reports. 49:321-329
Endometriosis is a multifactorial estrogen dependent gynecological disease characterized by implantation of functional endometrial tissue at ectopic positions. Though this disease is benign, it is associated with an increased risk of malignant transf
Autor:
Sanjana Mehrotra, Archna Pruthi, Rashim Mannan, Nanamika Thakur, Vipin Kumar, Rajeev Kumar Pandey
Publikováno v:
Human Immunology. 82:791-797
Background IL6 is an important candidate gene implicated in the pathogenesis of glaucoma. The present study assessed the genetic association of −174G > C and −572G > C polymorphisms in the IL6 promoter region with primary open angle glaucoma (POA
Publikováno v:
Experimental Physiology. 106:1839-1848
NEW FINDINGS What is the central question of this study? Vascular endothelial growth factor A (VEGFA) is an important growth factor involved in changes in the bronchial microvascular and airway inflammation in chronic obstructive pulmonary disease (C
Publikováno v:
Journal of Advanced Engineering Trends. 40:61-69
The pre-processing phase is a crucial step to prepare any data for deep considerable analysis. Genome-wide data is considered big data; dealing with such data is not an easy task and still poses a significant challenge. Th
Autor:
Antonella Insalaco, Marianna Nicoletta Rossi, Manuela Pardeo, Emanuela Sacco, Chiara Passarelli, Denise Pires Marafon, Giusi Prencipe, Ivan Caiello, Claudia Bracaglia, Chiara Perrone, Fabrizio De Benedetti, Giulia Marucci, Anna Tulone
Publikováno v:
Arthritis & Rheumatology. 73:1053-1061
OBJECTIVE To evaluate the impact of early treatment and IL1RN genetic variants on the response to anakinra in systemic juvenile idiopathic arthritis (JIA). METHODS Response to anakinra was defined as achievement of clinically inactive disease (CID) a
Autor:
Sravya Thumoju, Akhter Husain, Rajeshwari Rajeshwari, Vasavi Mohan, Srinivas Reddy Gosla, Praveen Kumar Neela
Publikováno v:
Indonesian Biomedical Journal, Vol 13, Iss 1, Pp 27-33 (2021)
BACKGROUND: Cleft lip palate is a common congenital anomaly with multifactorial etiology. Many high-risk markers at different loci were reported to be involved in its etiology. Advanced genetic research led to the discovery of evidence of a new linka
Publikováno v:
Molecular & Cellular Toxicology
Background The interferon-induced transmembrane (IFITM) protein family consists of interferon-stimulated genes (ISGs) that show potent antiviral capacity against a broad range of viruses. Many studies have been performed to investigate an association
Publikováno v:
International Journal of Medical Sciences
Papillary thyroid carcinoma (PTC) is the major subtype of thyroid cancer, accounting for 75%-85% of all thyroid malignancies. This study aimed to identify the association between the interactions of single nucleotide polymorphisms (SNPs) in RAS famil
Publikováno v:
Cancer Cell International, Vol 21, Iss 1, Pp 1-9 (2021)
Cancer Cell International
Cancer Cell International
Background The study aimed to evaluate the relationship of IL-1B/IL-1RN polymorphisms to the predisposition of head and neck cancer (HNC) in a Chinese Han population. Methods Nine single-nucleotide polymorphisms (SNPs) in IL-1B/IL-1RN were genotyped
Autor:
Muhammad Farooq Sabar, Iqbal Bano, Raheela Aslam, Muhammad Ayoub, Samra Kousar, Muhammad Usman Ghani, Ahmad Ali Shahid, Mariam Shahid, Tayyab Husnain, Saba Altaf
Publikováno v:
The Clinical Respiratory Journal. 15:374-381
INTRODUCTION Various genome wide association studies have manifested that Major Histocompatibility Complex (MHC) region on chromosome 6p21 houses many potential candidate genes for asthma. OBJECTIVE This Case-Control association study was planned to