Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Behzad Zaker"'
Autor:
Behzad Zaker, Mohammadreza Ardalan
Publikováno v:
Journal of Cardiovascular and Thoracic Research, Vol 12, Iss 3, Pp 165-171 (2020)
Vascular calcification is a high prevalent complication that arises as a consequence of impaired calcium and phosphate balance amongst cardiovascular patients. Multiple inducer/ inhibitory molecules and pathways as well as genetic background and life
Externí odkaz:
https://doaj.org/article/4d92cdd026594fa09de81f86d9d86e35
Autor:
Sepideh Zununi Vahed, Alessandra Cremaschi, Behzad Zaker, Seyed Sadroddin Rasi Hashemi, Mohammadreza Ardalan
Publikováno v:
Journal of Nephropharmacology, Vol 10, Iss 2, Pp e17-e17 (2021)
A plasma protease, ADAMTS13, cleaves the von Willebrand factor (VWF) and its deficiency is associated with the pathogenesis of thrombotic thrombocytopenic purpura (TTP). According to the Human Gene Mutation Database (HGMD), about 150 mutations have b
Externí odkaz:
https://doaj.org/article/0810cf76275e44a89d5a8af4be7ea1ef
Autor:
Jalal Etemadi, Taraneh Majidi, Roza Motavalli, Mortaza Bonyadi, Sepideh Zununi Vahed, Behzad Zaker, Mohammadreza Ardalan
Publikováno v:
Journal of Nephropathology, Vol 7, Iss 2, Pp 45-50 (2018)
Background: Familial Mediterranean Fever (FMF) is the most common inherited autoinflammatory disease. Kidney involvement in FMF is usually attributed to secondary amyloidosis. Non-amyloid glomerular involvement has also been reported. Objectives: We
Externí odkaz:
https://doaj.org/article/90795cc33c404c11a5b63ee62064d2ed
Akademický článek
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Publikováno v:
Pathology - Research and Practice. 243:154344
Background/aim: Despite the attractive anticancer effects, poor solubility and low bioavailability have restricted the clinical application of curcumin. Recent findings show that gemini nano-curcumin (Gemini-Cur) significantly improves cellular uptak
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2fab83bda0e7b7549fca8e98d6348f7
https://doi.org/10.1016/j.prp.2023.154344
https://doi.org/10.1016/j.prp.2023.154344
Autor:
Seyed Sadroddin Rasi Hashemi, Alessandra Cremaschi, Mohammadreza Ardalan, Behzad Zaker, Sepideh Zununi Vahed
Publikováno v:
Journal of Nephropharmacology, Vol 10, Iss 2, Pp e17-e17 (2021)
A plasma protease, ADAMTS13, cleaves the von Willebrand factor (VWF) and its deficiency is associated with the pathogenesis of thrombotic thrombocytopenic purpura (TTP). According to the Human Gene Mutation Database (HGMD), about 150 mutations have b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dcc472f712dc2e3037c613b3c9b84adb
https://jnephropharmacology.com/PDF/npj-10373
https://jnephropharmacology.com/PDF/npj-10373
Autor:
Sepideh Zununi Vahed, Behzad Zaker, Jalal Etemadi, Roza Motavalli, Mohammadreza Ardalan, Taraneh Majidi, Mortaza Bonyadi
Publikováno v:
Journal of Nephropathology. 7:45-50
Background: Familial Mediterranean Fever (FMF) is the most common inherited autoinflammatory disease. Kidney involvement in FMF is usually attributed to secondary amyloidosis. Non-amyloid glomerular involvement has also been reported. Objectives: We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::16584341d5c9620164163ca9340cfaaf
https://doi.org/10.15171/jnp.2018.13
https://doi.org/10.15171/jnp.2018.13
Autor:
Mohammadreza Ardalan, Behzad Zaker
Publikováno v:
Journal of Cardiovascular and Thoracic Research
Journal of Cardiovascular and Thoracic Research, Vol 12, Iss 3, Pp 165-171 (2020)
Journal of Cardiovascular and Thoracic Research, Vol 12, Iss 3, Pp 165-171 (2020)
Vascular calcification is a high prevalent complication that arises as a consequence of impaired calcium and phosphate balance amongst cardiovascular patients. Multiple inducer/ inhibitory molecules and pathways as well as genetic background and life
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6038cf38ee50589dddc9bf1b93f4bbc4
https://pubmed.ncbi.nlm.nih.gov/33123321
https://pubmed.ncbi.nlm.nih.gov/33123321
Autor:
Koorosh Kamali, Behzad Zaker-Kandjani, Hossein Najmabadi, Mehdi Banan, Hadi Bayat, Parvaneh Daneshmand, Azita Azarkeivan, Pegah Namdar-Aligoodarzi
Publikováno v:
Hemoglobin. 37(5)
Recently, five genetic modifiers [β-globin mutations, coinheritance of α-thalassemia (α-thal), XmnI polymorphism and single nucleotide polymorphisms (SNPs) in the BCL11A and HBS1L-MYB loci] were used to predict the β-thal major (β-TM) or β-thal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ddc6eaf9e4eb8905518ac5eecd539883
https://pubmed.ncbi.nlm.nih.gov/23805990
https://pubmed.ncbi.nlm.nih.gov/23805990