Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Neda Z, Ghanem"'
Autor:
Sumayh A. Aldakeel, Neda Z. Ghanem, Amani M. Al-Amodi, Ahoud Khalid Osman, Lubna Ibrahim Al Asoom, Nazish Rafique Ahmed, Noor B. Almandil, Mohammed Shakil Akhtar, Sayed Azeez, J. Francis Borgio
Publikováno v:
Archives of Medical Science, Vol 16, Iss 2, Pp 453-459 (2019)
Externí odkaz:
https://doaj.org/article/05fcbc8def0a4efeb2078da1b383bf02
Publikováno v:
Small GTPases
The Ras homologous (Rho) protein family of GTPases (RhoA, RhoB and RhoC) are the members of the Ras superfamily and regulate cellular processes such as cell migration, proliferation, polarization, adhesion, gene transcription and cytoskeletal structu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2c59a804a063acaf26df22436a778c6
https://doi.org/10.1080/21541248.2021.1951590
https://doi.org/10.1080/21541248.2021.1951590
Publikováno v:
Life sciences. 306
RGPR-p117 was originally discovered as a novel transcription factor, which specifically binds to a nuclear factor I (NFI) consensus motif TTGGC(N)The NRK-52E wild-type cells and RGPR-p117-overexpressing NRK-52E cells were cultured in DMEM containing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d86793a40207648aaf850ae150194b1
https://pubmed.ncbi.nlm.nih.gov/35835253
https://pubmed.ncbi.nlm.nih.gov/35835253
Autor:
J. Francis Borgio, Lubna Ibrahim Al Asoom, Sayed Abdul Azeez, Noor B. Almandil, Ahoud Khalid Osman, Sumayh A Aldakeel, Amani M. Al-Amodi, Mohammed Shakil Akhtar, Nazish Rafique Ahmed, Neda Z. Ghanem
Publikováno v:
Archives of Medical Science, Vol 16, Iss 2, Pp 453-459 (2019)
Archives of Medical Science : AMS
Archives of Medical Science : AMS
Introduction: Abnormality in HBB results in an inherited recessive blood disorder, which can be caused by variants at the transcriptional or translational level affecting the stability and the production of the HBB chain. The severity of the disease
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0953cc83b9022011c4d884f8199f2814
https://www.termedia.pl/Identification-of-seven-novel-variants-in-the-globin-gene-in-transfusion-dependent-and-normal-patients,19,36521,1,1.html
https://www.termedia.pl/Identification-of-seven-novel-variants-in-the-globin-gene-in-transfusion-dependent-and-normal-patients,19,36521,1,1.html
Autor:
Sayed AbdulAzeez, Noor B. Almandil, Zaki A. Naserullah, Mohammed Shakil Akhtar, Amani M. Al-Amodi, Neda Z. Ghanem, Nazish Rafique Ahmed, Sana Al-Jarrash, Lubna Ibrahim Al Asoom, Amein K. Al-Ali, Sumayh A Aldakeel, J. Francis Borgio
Publikováno v:
Current Medical Research and Opinion. 34:945-951
Introduction: Detection of β-thalassemia trait or carriers (β-TT) depends significantly on an increase in Hemoglobin A2 (HbA2) levels, which is found at low levels (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b014a04cf61ad60e66bcd9c7434eab8f
https://doi.org/10.1080/03007995.2018.1435520
https://doi.org/10.1080/03007995.2018.1435520
Autor:
Sayed AbdulAzeez, Antonino Giambona, Amani M. Al-Amodi, B. Rabindran Jermy, Nourah H. Al Qahtani, Hatoon Ahmed Al Taifi, Quds Abdulhakeem AlQattan, Vinoth Raman, Noor B. Almandil, Norah Fahad Alhur, Neda Z. Ghanem, Abdulrahman Abdulaziz Alghamdi, Ameen AlTurki, J. Francis Borgio, Halah Egal Aljofi, Deem N. Alkuroud, Aurelio Maggio, Sumayh A Aldakeel
Publikováno v:
Scientific Reports
Scientific Reports, Vol 9, Iss 1, Pp 1-8 (2019)
Scientific Reports, Vol 9, Iss 1, Pp 1-8 (2019)
The prevalence of consanguineous marriage and genetic disorders are high in Saudi Arabia. There were records on the practices of Saudis toward prenatal diagnosis (PND) and termination of pregnancy (TOP), however the sample sizes are small. This study
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63b172d2c4f60250c85af92c90ec5d6f
https://doi.org/10.1038/s41598-019-53655-8
https://doi.org/10.1038/s41598-019-53655-8
Publikováno v:
Exp Cell Res
Telomerase-deficient cells of the budding yeast S. cerevisiae experience progressive telomere shortening and undergo senescence in a manner similar to that seen in cultured human fibroblasts. The cells exhibit a DNA damage checkpoint-like stress resp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f96defb0b8e3c13dcb106dd97bb1977f
https://pubmed.ncbi.nlm.nih.gov/31075257
https://pubmed.ncbi.nlm.nih.gov/31075257
Autor:
Amani M, Al-Amodi, Neda Z, Ghanem, Sumayh A, Aldakeel, Lubna, Ibrahim Al Asoom, Nazish, Rafique Ahmed, Noor B, Almandil, Zaki A, Naserullah, Sana, Al-Jarrash, Mohammed, Shakil Akhtar, Sayed, AbdulAzeez, Amein K, Al-Ali, J Francis, Borgio
Publikováno v:
Current medical research and opinion. 34(5)
Detection of β-thalassemia trait or carriers (β-TT) depends significantly on an increase in Hemoglobin AThe widely used high performance liquid chromatography (Variant II Bio-Rad) was used to measure HbAOut of 288 samples, 96 had HBB gene mutations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f726f703f11018fbf837f3d2f5f4e097
https://pubmed.ncbi.nlm.nih.gov/29383950
https://pubmed.ncbi.nlm.nih.gov/29383950