Reham M. Milhem
Reham M. Milhem
MedComms | Research
Η διεύθυνση ηλεκτρονικού ταχυδρομείου έχει επαληθευτεί στον τομέα uaeu.ac.ae
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Identification of the cellular mechanisms that modulate trafficking of frizzled family receptor 4 (FZD4) missense mutants associated with familial exudative vitreoretinopathy
RM Milhem, S Ben-Salem, L Al-Gazali, BR Ali
Investigative ophthalmology & visual science 55 (6), 3423-3431, 2014
292014
Endoplasmic reticulum quality control is involved in the mechanism of endoglin-mediated hereditary haemorrhagic telangiectasia
BR Ali, I Ben-Rebeh, A John, NA Akawi, RM Milhem, NA Al-Shehhi, ...
PLoS One 6 (10), e26206, 2011
282011
Novel KCNQ2 mutation in a large Emirati family with benign familial neonatal seizures
IY Saadeldin, RM Milhem, L Al-Gazali, BR Ali
Pediatric neurology 48 (1), 63-66, 2013
92013
Clinical and molecular analysis of a novel COLQ missense mutation causing congenital myasthenic syndrome in a Syrian family
HN Matlik, RM Milhem, IY Saadeldin, HS Al-Jaibeji, L Al-Gazali, BR Ali
Pediatric neurology 51 (1), 165-169, 2014
82014
Electrical characterization of DNA supported on nitrocellulose membranes
M Al Ahmad, RM Milhem, NG Panicker, TA Rizvi, F Mustafa
Scientific reports 6 (1), 1-9, 2016
52016
Improved plasma membrane expression of the trafficking defective P344R mutant of muscle, skeletal, receptor tyrosine kinase (MuSK) causing congenital myasthenic syndrome
RM Milhem, L Al-Gazali, BR Ali
The international journal of biochemistry & cell biology 60, 119-129, 2015
42015
Disorders of FZ-CRD; insights towards FZ-CRD folding and therapeutic landscape
RM Milhem
Molecular Medicine 26, 2019
22019
ELUCIDATION OF THE CELLULAR AND MOLECULAR MECHANISMS OF MISSENSE MUTATIONS ASSOCIATED WITH FAMILIAL EXUDATIVE VITREORETINOPATHY AND CONGENITAL MYASTHENIC SYNDROME
RMM Milhem
United Arab Emirates University, 2015
12015
Cover Image
RMM Salma Ben-Salem, Lihadh Al-Gazali, Bassam R Ali
Investigative ophthalmology & visual science 55 (6), 2014
2014
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