Zobrazeno 1 - 10
of 150
pro vyhledávání: '"G, Victoria"'
Autor:
Abdul K. Siraj, Rong Bu, Sandeep Kumar Parvathareddy, Kaleem Iqbal, Saud Azam, Zeeshan Qadri, Maha Al-Rasheed, Wael Haqawi, Mark Diaz, Ingrid G. Victoria, Ismail A. Al-Badawi, Asma Tulbah, Fouad Al-Dayel, Dahish Ajarim, Khawla S. Al-Kuraya
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-7 (2023)
Abstract The PALB2 gene is a breast cancer (BC) and ovarian cancer (OC) predisposition gene involved in the homologous recombination repair pathway. However, the prevalence and clinicopathological association of PALB2 pathogenic/likely pathogenic (PV
Externí odkaz:
https://doaj.org/article/0c97e2f47b824050854ac2fed92effc0
Autor:
Luisa Fernanda Ferro Valencia, Juliana Juliana Franco Maya, G. Victoria Izquierdo Cubillos, Luisa Fernanda González Suárez, Martha Juliana Villegas Moreno
Publikováno v:
Cuadernos Hispanoamericanos de Psicología, Vol 19, Iss 2, Pp 1-25 (2019)
La depresión es un problema de salud pública, con una prevalencia del 15,8% en niños y adolescentes entre 10 y 14 años; este trastorno está directamente relacionado con conductas autolesivas no suicidas. Diversas investigaciones han demostrado q
Externí odkaz:
https://doaj.org/article/b0f061c6569e47ff9b0ba55bcd05a724
Autor:
Rong Bu, Abdul K. Siraj, Tariq Masoodi, Sandeep Kumar Parvathareddy, Kaleem Iqbal, Maha Al-Rasheed, Wael Haqawi, Mark Diaz, Ingrid G. Victoria, Saud M. Aldughaither, Saif S. Al-Sobhi, Fouad Al-Dayel, Khawla S. Al-Kuraya
Publikováno v:
Frontiers in Oncology, Vol 11 (2021)
Mitogen-activated protein kinase kinase 1 (MAP2K1) is a dual specificity protein kinase that phosphorylates both threonine and tyrosine residues in ERK. MAP2K1 mutations have been identified in several cancers. However, their role in Middle Eastern p
Externí odkaz:
https://doaj.org/article/f157ad0be48f4d4493b2553807f46b9b
Autor:
Abdul K. Siraj, Rong Bu, Kaleem Iqbal, Sandeep K. Parvathareddy, Tariq Masoodi, Nabil Siraj, Maha Al‐Rasheed, Yan Kong, Saeeda O. Ahmed, Khadija A. S. Al‐Obaisi, Ingrid G. Victoria, Maham Arshad, Fouad Al‐Dayel, Alaa Abduljabbar, Luai H. Ashari, Khawla S. Al‐Kuraya
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 8, Pp n/a-n/a (2020)
Abstract Background Colorectal cancer (CRC) is a major contributor to morbidity and mortality related to cancer. Only ~5% of all CRCs occur as a result of pathogenic variants in well‐defined CRC predisposing genes. The frequency and effect of exonu
Externí odkaz:
https://doaj.org/article/b914458beafd4f359c0dd5f329bbe6c5
The purpose of this study was an attempt to examine the effect of using Flashcard and Blackboard in learning vocabulary among students with hearing impairment. The study was an experimental method using pre-test and post-test design. The sample of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1648::dc3851d1416f43d1c8546334dfa2726a
https://hdl.handle.net/10481/79688
https://hdl.handle.net/10481/79688
Akademický článek
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Akademický článek
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K zobrazení výsledku je třeba se přihlásit.
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Autor:
Rong Bu, Abdul K. Sira, Sandeep Parvathareddy, Kaleem Iqbal, Saud Azam, Zeeshan Qadri, Maha Al-Rasheed, Wael Haqawi, Mark Diaz, Ingrid G. Victoria, Khawla S. Al-Kuraya
Publikováno v:
Cancer Research. 83:6086-6086
Background: The PALB2 gene encoding protein is involved in the homologous recombination repair pathway and plays an important role in maintaining genomic integrity. PALB2 heterozygous pathological variants (PV) or likely pathogenic variants (LPV) are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa41194edff868aa3be5d7c619a67edc
https://doi.org/10.1158/1538-7445.am2023-6086
https://doi.org/10.1158/1538-7445.am2023-6086
Autor:
Bailey L Arruda, Paulo H Arruda, Drew R Magstadt, Kent J Schwartz, Tyler Dohlman, Jennifer A Schleining, Abby R Patterson, Callie A Visek, Joseph G Victoria
Publikováno v:
PLoS ONE, Vol 11, Iss 2, p e0150104 (2016)
Congenital tremors is a sporadic disease of neonatal pigs characterized by action-related repetitive myoclonus. A majority of outbreaks of congenital tremors have been attributed to an unidentified virus. The objectives of this project were to 1) det
Externí odkaz:
https://doaj.org/article/8c133bda68344167bb3bb7de69e0f910
Autor:
Dahish Ajarim, Khawla S. Al-Kuraya, Dionne Rae Rala, Shamayel Mohammed, Abdul K. Siraj, Mark Diaz, Allianah Benito, Fouad Al-Dayel, Kaleem Iqbal, Nabil Siraj, Malak Abedalthagafi, Ingrid G. Victoria, Turki Alhussain, Asma Tulbah, Khadija A.S. Al-Obaisi, Sandeep Kumar Parvathareddy, Sarah Siraj, Wael Al-Haqawi, Maha Al-Rasheed, Salma M. Wakil, Wafaa Al Balawy, Ismail A. Al-Badawi, Maria Angelita Sabido, Rong Bu
Publikováno v:
Genomics. 112:1746-1753
Sanger Sequencing and immunohistochemistry was employed to investigate the TERT promoter mutations and TERT protein expression with their association to clinicopathological characteristics in over 2200 samples of Middle Eastern origin from 13 differe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7898a223eb59d4227d7bdab228e4be51
https://doi.org/10.1016/j.ygeno.2019.09.017
https://doi.org/10.1016/j.ygeno.2019.09.017