Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Reham M. Milhem"'
Autor:
Reham M. Milhem, Bassam R. Ali
Publikováno v:
Molecular Medicine, Vol 26, Iss 1, Pp 1-18 (2019)
Abstract The ER is hub for protein folding. Proteins that harbor a Frizzled cysteine-rich domain (FZ-CRD) possess 10 conserved cysteine motifs held by a unique disulfide bridge pattern which attains a correct fold in the ER. Little is known about imp
Externí odkaz:
https://doaj.org/article/d84f1268e94f4af6a4938749558447cf
Autor:
Bassam R Ali, Imen Ben-Rebeh, Anne John, Nadia A Akawi, Reham M Milhem, Nouf A Al-Shehhi, Mouza M Al-Ameri, Shamma A Al-Shamisi, Lihadh Al-Gazali
Publikováno v:
PLoS ONE, Vol 6, Iss 10, p e26206 (2011)
Hereditary haemorrhagic telangiectasia (HHT) is an autosomal dominant genetic condition affecting the vascular system and is characterised by epistaxis, arteriovenous malformations and mucocutaneous and gastrointestinal telangiectases. This disorder
Externí odkaz:
https://doaj.org/article/0c1361e492a343028561c1a1d16335c9
Autor:
Bassam R. Ali, Reham M. Milhem
Publikováno v:
Molecular Medicine
Molecular Medicine, Vol 26, Iss 1, Pp 1-18 (2019)
Molecular Medicine, Vol 26, Iss 1, Pp 1-18 (2019)
The ER is hub for protein folding. Proteins that harbor a Frizzled cysteine-rich domain (FZ-CRD) possess 10 conserved cysteine motifs held by a unique disulfide bridge pattern which attains a correct fold in the ER. Little is known about implications
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e71793130d50e2e27cda223acfac452e
https://doi.org/10.1186/s10020-019-0129-7
https://doi.org/10.1186/s10020-019-0129-7
Publikováno v:
The International Journal of Biochemistry & Cell Biology. 60:119-129
Muscle, skeletal, receptor tyrosine kinase (MuSK) is a key organizer at the postsynaptic membrane and critical for proper development and maintenance of the neuromuscular junction. Mutations in MUSK result in congenital myasthenic syndrome (CMS). We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f413ee4913e4786fde12af563eb1e88
https://doi.org/10.1016/j.biocel.2014.12.015
https://doi.org/10.1016/j.biocel.2014.12.015
Autor:
Hussein N. Matlik, Hayat Aljaibeji, Reham M. Milhem, Lihadh Al-Gazali, Bassam R. Ali, Imad Y. Saadeldin
Publikováno v:
Pediatric Neurology. 51:165-169
Background Congenital myasthenic syndromes with end-plate acetylcholinesterase deficiency are rare autosomal recessive disorders characterized by onset of the disease in early childhood, general weakness exacerbated by exertion, ophthalmoplegia, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76056dcf99c153fe55228daf7fb95b27
https://doi.org/10.1016/j.pediatrneurol.2014.03.012
https://doi.org/10.1016/j.pediatrneurol.2014.03.012
Publikováno v:
Scientific Reports
Integrated DNA-based nanoscale electronic devices will enable the continued realization of Moore’s Law at the level of functional devices and systems. In this work, the electrical characterization of single and complementary base paired DNA has bee
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::590bc32444899d8ce1e2f86b5c97a479
https://doi.org/10.1038/srep29089
https://doi.org/10.1038/srep29089
Publikováno v:
Investigative Opthalmology & Visual Science. 55:3423
Purpose Fifteen missense mutations in the frizzled family receptor 4 (FZD4) reported to cause familial exudative vitreoretinopathy (FEVR) were evaluated to establish the pathological cellular mechanism of disease and to explore novel therapeutic stra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20bd4c66e69b09f89a107f18f70f72ef
https://doi.org/10.1167/iovs.14-13885
https://doi.org/10.1167/iovs.14-13885
Autor:
Nadia Akawi, Imen Ben-Rebeh, Shamma A. Al-Shamisi, Bassam R. Ali, Anne John, Reham M. Milhem, Mouza M. Al-Ameri, Nouf Ahmed Alshehhi, Lihadh Al-Gazali
Publikováno v:
PLoS ONE
PLoS ONE, Vol 6, Iss 10, p e26206 (2011)
PLoS ONE, Vol 6, Iss 10, p e26206 (2011)
Hereditary haemorrhagic telangiectasia (HHT) is an autosomal dominant genetic condition affecting the vascular system and is characterised by epistaxis, arteriovenous malformations and mucocutaneous and gastrointestinal telangiectases. This disorder
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f47a53089e63c9fa74696c5967d36bf
https://doi.org/10.1371/journal.pone.0026206
https://doi.org/10.1371/journal.pone.0026206