Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Nada A, Al Tassan"'
Autor:
Abeer A. Alabdullah, Basma Al-Abdulaziz, Hanan Alsalem, Amna Magrashi, Subramanian M. Pulicat, Amer A. Almzroua, Falah Almohanna, Abdullah Mohamed Assiri, Nada A. Al Tassan, Bashayer R. Al-Mubarak
Publikováno v:
BMC Research Notes, Vol 12, Iss 1, Pp 1-7 (2019)
Abstract Objective Delivery of constructs for silencing or over-expressing genes or their modified versions is a crucial step for studying neuronal cell biology. Therefore, efficient transfection is important for the success of these experimental tec
Externí odkaz:
https://doaj.org/article/eead3479070b41148e82426a27eddf8e
Autor:
Christopher Wills, Katie Watts, Timothy S. Maughan, David Fisher, Nada A. Al‐Tassan, Richard S. Houlston, Valentina Escott‐Price, Jeremy P. Cheadle
Publikováno v:
Genes, Chromosomes and Cancer. 62:332-341
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::faac11a1adb2cff0078e18d2bf2ca088
https://doi.org/10.1002/gcc.23133
https://doi.org/10.1002/gcc.23133
Autor:
Faris M. Abomelha, Hesham AlDhalaan, Mohammad Ghaziuddin, Nada A. Al-Tassan, Bashayer R. Al-Mubarak
Publikováno v:
Genes. 13(9)
Even in the era of information “prosperity” in the form of databases and registries that compile a wealth of data, information about ASD and ADHD remains scattered and disconnected. These data systems are powerful tools that can inform decision-m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7d632e5b00a57575d278047cb5a0378
https://pubmed.ncbi.nlm.nih.gov/36140719
https://pubmed.ncbi.nlm.nih.gov/36140719
Autor:
Katie Watts, Christopher Wills, Ayman Madi, Claire Palles, Timothy S. Maughan, Richard Kaplan, Nada A. Al‐Tassan, Rachel Kerr, David J. Kerr, Richard S. Houlston, Valentina Escott‐Price, Jeremy P. Cheadle
Publikováno v:
International journal of cancer. 151(6)
Cancer patients treated with capecitabine and oxaliplatin (XELOX) often develop hand-foot syndrome (HFS) or palmar-plantar erythrodysesthesia. Genetic variation in ST6GAL1 is a risk factor for type-2 diabetes (T2D), a disease also associated with HFS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03f563aea901cfc69f478041c1ff121e
https://pubmed.ncbi.nlm.nih.gov/35467766
https://pubmed.ncbi.nlm.nih.gov/35467766
Autor:
Bashayer R Al-Mubarak, Saeed A Bohlega, Thamer S Alkhairallah, Amna I Magrashi, Maha I AlTurki, Dania S Khalil, Basma S AlAbdulaziz, Hussam Abou Al-Shaar, Abeer E Mustafa, Eman A Alyemni, Bashayer A Alsaffar, Asma I Tahir, Nada A Al Tassan
Publikováno v:
PLoS ONE, Vol 10, Iss 8, p e0135950 (2015)
Parkinson's disease (PD) is one of the major causes of parkinsonism syndrome. Its characteristic motor symptoms are attributable to dopaminergic neurons loss in the midbrain. Genetic advances have highlighted underlying molecular mechanisms and provi
Externí odkaz:
https://doaj.org/article/f62aea7f0947470ea1bff78fbff8926b
Autor:
Bashayer R. Al-Mubarak, Amer A. Almzroua, Nada A. Al Tassan, Abdullah Mohamed Assiri, Falah Al-Mohanna, Abeer A. Alabdullah, Hanan Alsalem, Basma S. AlAbdulaziz, Amna Magrashi, Subramanian M. Pulicat
Publikováno v:
BMC Research Notes, Vol 12, Iss 1, Pp 1-7 (2019)
BMC Research Notes
BMC Research Notes
Objective Delivery of constructs for silencing or over-expressing genes or their modified versions is a crucial step for studying neuronal cell biology. Therefore, efficient transfection is important for the success of these experimental techniques e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76c819f393e00362b6cd5e86ab959fd0
https://doi.org/10.1186/s13104-019-4249-5
https://doi.org/10.1186/s13104-019-4249-5
Autor:
Abeer E, Mustafa, Tariq, Faquih, Batoul, Baz, Rana, Kattan, Abdulelah, Al-Issa, Asma I, Tahir, Faiqa, Imtiaz, Khushnooda, Ramzan, Moeenaldeen, Al-Sayed, Mohammed, Alowain, Zuhair, Al-Hassnan, Hamad, Al-Zaidan, Mohamed, Abouelhoda, Bashayer R, Al-Mubarak, Nada A, Al Tassan
Publikováno v:
Genes
Quick and accurate molecular testing is necessary for the better management of many inherited diseases. Recent technological advances in various next generation sequencing (NGS) platforms, such as target panel-based sequencing, has enabled comprehens
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a9c3ecec698ab3c70d0f4ef00ced60e7
https://pubmed.ncbi.nlm.nih.gov/29789446
https://pubmed.ncbi.nlm.nih.gov/29789446
Autor:
Arif O, Khan, Jameela, Shinwari, Latifa, Al Sharif, Dania, Khalil, Saeed, Al-Gehedan, Nada A Al, Tassan
Publikováno v:
Molecular Vision
Purpose To describe phenotyping and linkage analysis results for available members from a consanguineous nuclear family with hereditary congenital strabismus. Methods Both parents and all 12 children underwent clinical examination. Available affected
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7ffe8928fdca3238baa0b30490966e8a
https://pubmed.ncbi.nlm.nih.gov/21850174
https://pubmed.ncbi.nlm.nih.gov/21850174