Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Mohd-Manzor Nur Fariha"'
Autor:
Geetha Letchumanan, Natasya Abdullah, Muhamad Marlini, Nizam Baharom, Blair Lawley, Mohd Rahman Omar, Fathima Begum Syed Mohideen, Faizul Helmi Addnan, Mohd Manzor Nur Fariha, Zarini Ismail, Siva Gowri Pathmanathan
Publikováno v:
Frontiers in Cellular and Infection Microbiology, Vol 12 (2022)
Evidence of gut microbiota involvement in regulating glucose metabolism and type 2 diabetes mellitus (T2DM) progression is accumulating. The understanding of microbial dysbiosis and specific alterations of gut microbiota composition that occur during
Externí odkaz:
https://doaj.org/article/8fa3677669b041cf949f65b0e060a259
Autor:
Marlini, Abdul Rahman Amin, Ngatiman M. Hairulhisyam, Raman Nur Fatin Aqilah, Mohd Manzor Nur Fariha, Beth L. Mallard, Fergus Shanahan, Antony M. Wheatley, Muhamad
Publikováno v:
International Journal of Molecular Sciences; Volume 24; Issue 13; Pages: 10774
The hepatic matrisome is involved in the remodeling phase of liver regeneration. As the gut microbiota has been implicated in liver regeneration, we investigated its role in liver regeneration focusing on gene expression of the hepatic matrisome afte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=multidiscipl::3d668b31a7feb35f87365a99ec724ca1
Akademický článek
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Akademický článek
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Autor:
Muhammad, Amalin Kamilah, Aqilah Raman, Nur Fatin, Rahman, Hayati Abdul, Mohd Manzor, Nur Fariha
Publikováno v:
Malaysian Journal of Science, Health & Technology; 2020 Special Issue, Vol. 6, p15-22, 8p
Publikováno v:
Journal of Cellular and Molecular Medicine
Human chorion-derived stem cells (hCDSC) were previously shown to demonstrate multipotent properties with promising angiogenic characteristics in monolayer-cell culture system. In our study, we investigated the angiogenic capability of hCDSC in 3-dim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::086894ba912f93e6b17661f93e38d8c7
https://doi.org/10.1111/jcmm.12051
https://doi.org/10.1111/jcmm.12051
Autor:
A R Hayati, Ay Eeng Tan, Kien Hui Chua, Simat Siti Fatimah, Geok Chin Tan, Mohd Manzor Nur Fariha
Publikováno v:
Microvascular Research. 86:21-29
Background Particular attention has been directed towards human amnion mesenchymal stem cells (HAMCs) due to their accessibility, availability and immunomodulatory properties. Therefore, the aim of the present study was to determine the temporal chan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4284f802a518562f2d40bd9c387ff871
https://doi.org/10.1016/j.mvr.2012.12.004
https://doi.org/10.1016/j.mvr.2012.12.004
Publikováno v:
Cytotherapy. 13:582-593
Background aims Fetal membrane from human placenta tissue has been described as a potential source of stem cells. Despite abundant literature on amnion stem cells, there are limited studies on the stem cell properties of chorion-derived stem cells. M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e58584185b4ae5edcfab70c01697cbad
https://doi.org/10.3109/14653249.2010.549121
https://doi.org/10.3109/14653249.2010.549121
Publikováno v:
Archives of Medical Research. 42:291-300
Background and Aims Placenta as a fetomaternal organ is a potential source of fetal as well as maternal stem cells. This present study describes novel properties of the cells isolated from the maternal part of term placenta membrane, the decidua basa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::966cf06203e52cdc345d85df27d26e55
https://doi.org/10.1016/j.arcmed.2011.06.005
https://doi.org/10.1016/j.arcmed.2011.06.005
Publikováno v:
Cell biology international. 36(12)
Cell-based therapy using stem cells has emerged as one of the pro-angiogenic methods to enhance blood vessel growth and sprouting in ischaemic conditions. This study investigated the endogenous and induced angiogenic characteristics of hCDSC (human c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::838d23805abfae975e1ab659dc8fe81a
https://pubmed.ncbi.nlm.nih.gov/22957758
https://pubmed.ncbi.nlm.nih.gov/22957758