Zobrazeno 1 - 10
of 77
pro vyhledávání: '"HWE, Hardy–Weinberg equilibrium"'
Autor:
Most. Nazma Parvin, Mohammad Safiqul Islam, Mohammed Hanif, Md. Saiful Islam, Md. Abdul Aziz, Mir Md. Abdullah Al-Mamun, Sikder Nahidul Islam Rabbi
Publikováno v:
Journal of Advanced Research
Journal of Advanced Research, Vol 33, Iss, Pp 141-151 (2021)
Journal of Advanced Research, Vol 33, Iss, Pp 141-151 (2021)
Graphical abstract
Introduction Nephrotic syndrome is a common pediatric kidney disease. Investigations on several genetic polymorphisms revealed an inconsistent influence on the resistance of patients to steroids. Objectives This study aimed to
Introduction Nephrotic syndrome is a common pediatric kidney disease. Investigations on several genetic polymorphisms revealed an inconsistent influence on the resistance of patients to steroids. Objectives This study aimed to
Autor:
Seyedeh Maryam Kazemi, Aghil Esmaieli-bandboni, Ziba Veisi Malekshahi, Mohammad Shahbaz Sardood, Mehrdad Hashemi, Keivan Majidzadeh, Maryam Kadkhodazadeh, Rezvan Esmaili, Babak Negahdari
Publikováno v:
Annals of Medicine and Surgery
Objectives Vitamin D deficiency is a driving force of common cancers like breast cancer. Vitamin D receptor (VDR) can play a tumor suppressor role by helping the precise function of vitamin D in cells such as modulation TGF-β signaling pathway. This
Autor:
Laura, Airaksinen, Juliana Xm, Cerqueira, Heini, Huhtala, Päivi, Saavalainen, Dawit A, Yohannes, Markku, Mäki, Kalle, Kurppa, Elina, Kilpeläinen, Anastasia, Shcherban, Aarno, Palotie, Katri, Kaukinen, Katri, Lindfors
Publikováno v:
Journal of Translational Autoimmunity
Purpose and objectives Given their role in homing immune cells to the intestine, CC motif chemokine receptor 9 (CCR9) and its specific ligand CC motif chemokine ligand 25 (CCL25) are interesting candidate genes for celiac disease. These genes are loc
Autor:
Phuntila Tharabenjasin, Panan Suntornsaratoon, Chatchai Muanprasat, Noel Pabalan, Hamdi Jarjanazi
Publikováno v:
Infection, Genetics and Evolution
Background The reported association between an insertion/deletion (I/D) polymorphism in the angiotensin-converting enzyme (ACE) gene and the risk for acute lung injury (ALI)/acute respiratory distress syndrome (ARDS) remains controversial despite the
Publikováno v:
EBioMedicine
EBioMedicine, Vol 33, Iss, Pp 88-93 (2018)
EBioMedicine, Vol 33, Iss, Pp 88-93 (2018)
Base excision repair (BER) is the main mechanism to repair endogenous DNA lesions caused by reactive oxygen species. BER deficiency is linked with cancer susceptibility and premature aging. Single nucleotide polymorphisms (SNPs) within BER genes have
Autor:
Yan Zou, Zhenjian Zhuo, Wei Liu, Jue Tang, Jing He, Tianyou Yang, Jiao Zhang, Ruizhong Zhang, Huimin Xia, Jinhong Zhu
Publikováno v:
EBioMedicine
EBioMedicine, Vol 30, Iss, Pp 113-119 (2018)
EBioMedicine, Vol 30, Iss, Pp 113-119 (2018)
Variations in nucleotide excision repair pathway genes may predispose to initiation of cancers. However, polymorphisms of ERCC1/XPF genes and neuroblastoma risk have not been investigated before. To evaluate the relevance of polymorphisms of ERCC1/XP
Autor:
Marcelo Barciela Brandão, Antonia Teresinha Tresoldi, Celize Cruz Bresciani Almeida, Maria Luisa Ferreira de Miranda, Clarice Weis Arns, Fernando Augusto Lima Marson, Jose Vicente de Pieri, Ester Piacentini Côrrea, José Dirceu Ribeiro, Emílio Carlos Elias Baracat, Marcelo Conrado dos Reis, Juliana Cristina Santiago Bastos, Patricia G. Schlodtmann, Carmen Silvia Bertuzzo, Alfonso Eduardo Alvarez, Mariana Tresoldi das N. Romaneli, Therezinha de Oliveira
Publikováno v:
Gene
Background Acute viral bronchiolitis is the leading cause of hospitalization among infants during the first year of life. Most infants hospitalized for bronchiolitis do not present risk factors and are otherwise healthy. Our objective was to determin
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Autor:
Thomas Makatsoris, Foteini Kalofonou, Anna G. Antonacopoulou, Haralabos P. Kalofonos, Foteinos-Ioannis Dimitrakopoulos, Angelos Koutras, Vassiliki Tzelepi, Anastasia E. Kottorou, Stella Marousi
Publikováno v:
Translational Oncology, Vol 14, Iss 1, Pp 100912-(2021)
Translational Oncology
Translational Oncology
Highlights • NF-κB2 and RELB levels were upregulated in CRC and surrounding stroma compared to non-neoplastic tissue and stroma. • RELB protein expression in the tumour had prognostic value for overall survival. • Tumour RELB gene expression i
Autor:
Xiansheng Zeng, Xindong Chen, Meihua Guo, Qipeng Zhou, Zili Zhang, Mingmei Xiong, Wenju Lu, Defu Li, Jianxing He, Jian Wang
Publikováno v:
Meta Gene
Objective Store operated calcium channels (SOCCs) and Receptor-operated calcium channels (ROCCs) are important pathways participating in regulation of intracellular Ca2 + concentration in various cell types. The purpose of our study is to determine w