Prevalence and antibiotic susceptibility of the common bacterial uropathogen among UTI patients in French Medical Institute for Children

M Joya, AK Aalemi, AT Baryali - Infection and drug resistance, 2022 - Taylor & Francis
Background Urinary tract infections (UTIs) are the most prevalent infections, with a variety of
etiologic agents, a high number of occurrences, relapses, and complications; also, antibiotic …

An International Project for Curriculum and Faculty Professional Development in Medical Laboratory Science

…, J Conway-Klaassen, M Joya… - American Society for …, 2018 - clsjournal.ascls.org
The Kabul University of Medical Science (KUMS) in Kabul, Afghanistan began a Medical
Laboratory Technology program in 2016. The program has struggled to achieve expected …

Enhanced Selection Combining by Choosing Independently the Strongest Real Component and the Strongest Imaginary Component of all Channels

…, R Kuroda, S Nag, T Al-Mahdawi… - IEEE transactions on …, 2014 - ieeexplore.ieee.org
Conventional selection combining (SC) selects the antenna with the largest channel envelope.
In this paper, we propose to select the largest real part and largest imaginary part of the …

[HTML][HTML] A drug combination rescues frataxin-dependent neural and cardiac pathophysiology in FA models

R Abeti, M Jasoliya, S Al-Mahdawi, M Pook… - Frontiers in Molecular …, 2022 - frontiersin.org
Friedreich's ataxia (FA) is an inherited multisystemic neuro- and cardio-degenerative disorder.
Seventy-four clinical trials are listed for FA (including past and present), but none are …

Generation and characterization of CD19 CAR T cells with CTLA-4/CD28 fusion receptor

J Mahdawi - 2023 - edoc.ub.uni-muenchen.de
Acute lymphoblastic leukemia (ALL) is the most common malignant disease in childhood
and the most frequent cause of death from cancer under 20 years of age1. The malignant …

[HTML][HTML] Transcriptional profiling of isogenic Friedreich ataxia neurons and effect of an HDAC inhibitor on disease signatures

JI Lai, D Nachun, L Petrosyan, B Throesch… - Journal of Biological …, 2019 - ASBMB
Friedreich ataxia (FRDA) is a neurodegenerative disorder caused by transcriptional silencing
of the frataxin (FXN) gene, resulting in loss of the essential mitochondrial protein frataxin. …

Epigenetic therapy for F riedreich ataxia

E Soragni, W Miao, M Iudicello, D Jacoby… - Annals of …, 2014 - Wiley Online Library
Objective To investigate whether a histone deacetylase inhibitor (HDACi) would be effective
in an in vitro model for the neurodegenerative disease Friedreich ataxia (FRDA) and to …

Long intronic GAA• TTC repeats induce epigenetic changes and reporter gene silencing in a molecular model of Friedreich ataxia

E Soragni, D Herman, SYR Dent… - Nucleic acids …, 2008 - academic.oup.com
Friedreich ataxia (FRDA) is caused by hyperexpansion of GAA•TTC repeats located in the
first intron of the FXN gene, which inhibits transcription leading to the deficiency of frataxin. …

Familial hypertrophic cardiomyopathy associated with a novel missense mutation affecting the ATP-binding region of the cardiac beta-myosin heavy chain

H Bundgaard, O Havndrup, PS Andersen… - Journal of molecular and …, 1999 - Elsevier
… regions in the MYH7 gene a specific analysis, chromosomal DNA was PCR-amplified mutation
seems to be of major importance for using Cloned Pfu Polymerase (Stratagene, La Jolla, …

[HTML][HTML] Role of mismatch repair enzymes in GAA· TTC triplet-repeat expansion in Friedreich ataxia induced pluripotent stem cells

J Du, E Campau, E Soragni, S Ku, JW Puckett… - Journal of Biological …, 2012 - ASBMB
The genetic mutation in Friedreich ataxia (FRDA) is a hyperexpansion of the triplet-repeat
sequence GAA·TTC within the first intron of the FXN gene. Although yeast and reporter …