Zobrazeno 1 - 10
of 11 515
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56cd9b90a915500a6b94ae161c9617da
https://doi.org/10.1016/j.jare.2021.02.001
https://doi.org/10.1016/j.jare.2021.02.001
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12ebba11afdbd36734c3bae434ef5c8f
http://europepmc.org/articles/PMC8666522
http://europepmc.org/articles/PMC8666522
Autor:
Gao, Weifeng1,2 (AUTHOR), Cui, Wenxiao1,2 (AUTHOR), Wu, Fangchun1,2 (AUTHOR), Chen, Huiying1,2 (AUTHOR), Liu, Simin1,2 (AUTHOR), Guan, Mengyun1,2 (AUTHOR), Saqib, Hafiz Sohaib Ahmed1,2 (AUTHOR), Ye, Shaopan1,2 (AUTHOR), Ikhwanuddin, Mhd2,3 (AUTHOR), Ma, Hongyu1,2 (AUTHOR) mahy@stu.edu.cn
Publikováno v:
Fishes (MDPI AG). Jan2023, Vol. 8 Issue 1, p18. 12p.
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ce398e93a37f62c38df6650111fa1628
https://pubmed.ncbi.nlm.nih.gov/34901814
https://pubmed.ncbi.nlm.nih.gov/34901814
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02c1d2f69764af92d5eeec228197e1ac
http://europepmc.org/articles/PMC7738939
http://europepmc.org/articles/PMC7738939
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d8abedcde529bbc301ff618bf119fca
http://europepmc.org/articles/PMC6085508
http://europepmc.org/articles/PMC6085508
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6e8194abfdee6062e46b6d83d012b36
https://doi.org/10.1016/j.ebiom.2018.03.003
https://doi.org/10.1016/j.ebiom.2018.03.003
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1cc91e37a594f232f77c5afc102e84b
https://doi.org/10.1016/j.gene.2017.12.022
https://doi.org/10.1016/j.gene.2017.12.022
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Pekkoc Uyanik, Kubra Cigdem1,2 (AUTHOR), Kalayci Yigin, Aysel1 (AUTHOR), Dogangun, Burak3 (AUTHOR), Seven, Mehmet1 (AUTHOR) mimseven@istanbul.edu.tr
Publikováno v:
Immunological Investigations. May2022, Vol. 51 Issue 4, p766-777. 12p.