Blerida Banushi

Blerida Banushi

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Blerida Banushi

Blerida Banushi

Publications by authors named "Blerida Banushi"

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12Publications

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Free urinary glycosylated hydroxylysine as an indicator of altered collagen degradation in the mucopolysaccharidoses.

J Inherit Metab Dis 2019 Aug 26. Epub 2019 Aug 26.

Inborn Errors of Metabolism Section, Genetics & Genomic Medicine Unit, Great Ormond Street Institute of Child Health, University College London, London, UK.

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http://dx.doi.org/10.1002/jimd.12166DOI Listing
August 2019

An Ex Vivo Human Tumor Assay Shows Distinct Patterns of EGFR Trafficking in Squamous Cell Carcinoma Correlating to Therapeutic Outcomes.

J Invest Dermatol 2019 Jan 2;139(1):213-223. Epub 2018 Aug 2.

The University of Queensland Diamantina Institute, Faculty of Medicine, The University of Queensland, Translational Research Institute, Woolloongabba, Queensland, Australia. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S0022202X183245
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http://dx.doi.org/10.1016/j.jid.2018.06.190DOI Listing
January 2019

Molecular architecture of the multifunctional collagen lysyl hydroxylase and glycosyltransferase LH3.

Nat Commun 2018 08 8;9(1):3163. Epub 2018 Aug 8.

The Armenise-Harvard Laboratory of Structural Biology, Department of Biology and Biotechnology, University of Pavia, Via Ferrata 9/A, 27100, Pavia, Italy.

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http://dx.doi.org/10.1038/s41467-018-05631-5DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6082870PMC
August 2018

Vps33b is crucial for structural and functional hepatocyte polarity.

J Hepatol 2017 05 9;66(5):1001-1011. Epub 2017 Jan 9.

UCL Institute of Child Health, University College London, London WC1N 1EH, UK; MRC Laboratory for Molecular Cell Biology, University College London, London WC1E 6BT, UK; Inherited Metabolic Disease Unit, Great Ormond Street Hospital for Children NHS Trust, London WC1N 3JH, UK. Electronic address:

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http://dx.doi.org/10.1016/j.jhep.2017.01.001DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5387182PMC
May 2017

Autosomal Recessive Keratoderma-Ichthyosis-Deafness (ARKID) Syndrome Is Caused by VPS33B Mutations Affecting Rab Protein Interaction and Collagen Modification.

J Invest Dermatol 2017 04 23;137(4):845-854. Epub 2016 Dec 23.

MRC Laboratory for Molecular Cell Biology, University College London, London, UK; Institute of Child Health, University College London, London, UK; Inherited Metabolic Diseases Unit, Great Ormond Street Hospital, London, UK. Electronic address:

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http://dx.doi.org/10.1016/j.jid.2016.12.010DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5358661PMC
April 2017

VPS33B regulates protein sorting into and maturation of α-granule progenitor organelles in mouse megakaryocytes.

Blood 2015 Jul 6;126(2):133-43. Epub 2015 May 6.

Medical Research Council, Laboratory for Molecular Cell Biology, University College London, London, United Kingdom; Inherited Metabolic Diseases, Great Ormond Street Hospital, London, United Kingdom.

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http://dx.doi.org/10.1182/blood-2014-12-614677DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4497959PMC
July 2015