Results 111 to 120 of about 79,532 (296)
A Preliminary microRNA Analysis of non Syndromic Thoracic Aortic Aneurysms
Balkan Journal of Medical Genetics, 2012 The development of thoracic aortic aneurysms (TAAs) involves a multifactorial process resulting in alterations of the structure and composition of the extracellular matrix (ECM).
Patuzzo Cristina +6 more
doaj +1 more source
FEBS Open Bio, EarlyView.The cytoskeleton‐mediated transport of mitochondria via tunnelling nanotubes restores respiration, increases ATP production, rescues cells from apoptosis, activates the AKT/mTOR signalling pathway, promotes cell migration and invasiveness, contributes to cancer progression and treatment resistance.
Stanislava Martínková, Jan Trnka
wiley +1 more source
Molecular analysis of the TMPRSS3 gene in Moroccan families with non-syndromic hearing loss [PDF]
, 2012 Autosomal recessive non-syndromic hearing impairment (ARNSHI) is the most common type of inherited hearing impairment, accounting for approximately 80% of inherited prelingual hearing impairment.
R. Boulouiz +8 more
core +2 more sources
Delivery of DNA‐encoded vaccines and proteins in mice using cutaneous suction‐mediated transfection
FEBS Open Bio, EarlyView.Cutaneous suction‐mediated transfection in mice for delivery of DNA‐encoded vaccines and proteins. A critical limitation of DNA vaccines and other therapeutics is transfection in vivo to produce the encoded antigens or therapeutic proteins. Cutaneous suction‐based methods have demonstrated effectiveness in many animal models and have been successfully ...
Emran O. Lallow +12 more
wiley +1 more source
Proteomic investigations into non-syndromic aneurysms of the ascending aorta. [PDF]
, 2007 The results of proteomic investigations into non-syndromic aneurysms of the ascending aorta are preliminarily ...
DAL PRÀ, Ilaria Pierpaola +6 more
core
The management of craniosynostosis in Australia and New Zealand
Australasian Journal of Plastic Surgery, 2019 **Introduction**: The management of syndromic and non-syndromic craniosynostosis is controversial with different units performing various procedures at different points in time and for different reasons.
William A Ziaziaris, Damian D Marucci
doaj +1 more source
Non syndromic oligodontia: case report.
Ethiopian journal of health sciences, 2012 Oligodontia is a rare genetic disorder which represents the congenital absence of more than six teeth in primary, permanent or both dentitions. It is usually a part of a syndrome and seldom occurs as an isolated entity. Genes responsible for non syndromic oligodontia are found to be MSX1 and PAX9 genes.
Tangade, Pradeep, Batra, Manu
openaire +2 more sources
Non-Syndromic Multiple Odontomes
International Journal of Clinical & Medical Imaging, 2017 Clinical Image: A 10 year old male patient visited the department of oral medicine and radiology with a chief complaint of pain and swelling on right side of face (Figure 1). Patient gave history of swelling on right side of lower 1/3rd of face since 7-8 years with dull, intermittent pain which aggravates on taking food since 1 month.
Agarwal S, Garg A
openaire +1 more source
Mutant NPM1 in Acute Myeloid Leukemia Initiation and Maintenance
Aging and Cancer, EarlyView.NPM1 mutations drive acute myeloid leukemia by acting as neomorphic transcriptional regulators that cooperate with Menin–MLL and XPO1 to sustain HOX/MEIS1 expression and block differentiation. Targeting these mutant‐specific transcriptional dependencies provides a rational therapeutic strategy for NPM1‐mutated AML.
Yanan Jiang +3 more
wiley +1 more source
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Super‐Refractory Status Epilepticus (SRSE) is a rare, life‐threatening neurological emergency with unclear etiology in many cases. Mitochondrial dysfunction, often due to disease‐causing genetic variants, is increasingly recognized as a cause, with each gene producing distinct pathophysiological mechanisms.
Pouria Mohammadi +2 more
wiley +1 more source