Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Andrea Tyrer"'
Autor:
Lily Van, Tracy Heung, Sarah L. Malecki, Christian Fenn, Andrea Tyrer, Marcos Sanches, Eva W.C. Chow, Erik Boot, Maria Corral, Satya Dash, Susan R. George, Anne S. Bassett
Publikováno v:
EClinicalMedicine, Vol 26, Iss , Pp 100528- (2020)
Background: The 22q11.2 microdeletion is the pathogenic copy number variation (CNV) associated with 22q11.2 deletion syndrome (22q11.2DS, formerly known as DiGeorge syndrome). Familiar endocrinological manifestations include hypoparathyroidism and hy
Externí odkaz:
https://doaj.org/article/c77059ec52e54db79f5bf6dcc86a5cd2
Autor:
Erik Boot, Andrea Tyrer, Lily Van, Tracy Heung, Christian Fenn, Anne S. Bassett, Eva W.C. Chow, Sarah L. Malecki, Marcos Sanches, Maria Corral, Susan R. George, Satya Dash
Publikováno v:
EClinicalMedicine
EClinicalMedicine, Vol 26, Iss, Pp 100528-(2020)
EClinicalMedicine, Vol 26, Iss, Pp 100528-(2020)
Background: The 22q11.2 microdeletion is the pathogenic copy number variation (CNV) associated with 22q11.2 deletion syndrome (22q11.2DS, formerly known as DiGeorge syndrome). Familiar endocrinological manifestations include hypoparathyroidism and hy
Autor:
Stephen H. Pasternak, Andrea Tyrer, Sean P. Cregan, Susan O. Meakin, Justin Chiu, Joshua H. K. Tam, Weihao Tang, Claudia Seah
Publikováno v:
Paediatrics Publications
Molecular Brain
Molecular Brain
Alzheimer’s disease (AD) is characterized by the deposition of Beta-Amyloid (Aβ) peptides in the brain. Aβ peptides are generated by cleavage of the Amyloid Precursor Protein (APP) by the β − and γ − secretase enzymes. Although this process
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d17848c203fb3f1b4b21a83ae4b89df5
https://ir.lib.uwo.ca/paedpub/1568
https://ir.lib.uwo.ca/paedpub/1568
Publikováno v:
Scopus-Elsevier