Genetic modifiers of abnormal organelle biogenesis in a Drosophila model of BLOC-1 deficiency

VT Cheli, RW Daniels, R Godoy… - Human molecular …, 2010 - academic.oup.com
Biogenesis of lysosome-related organelles complex 1 (BLOC-1) is a protein complex formed
by the products of eight distinct genes. Loss-of-function mutations in two of these genes …

Genetic analyses of fancy rat-derived mutations

T Kuramoto, M Yokoe, K Yagasaki… - Experimental …, 2010 - jstage.jst.go.jp
To collect rat mutations and increase the value of the rat model system, we introduced fancy-
derived mutations to the laboratory and carried out genetic analyses. Six fancy rats were …

Early origin of genes encoding subunits of biogenesis of lysosome‐related organelles complex‐1,‐2 and‐3

VT Cheli, EC Dell'Angelica - Traffic, 2010 - Wiley Online Library
Biogenesis of lysosome‐related organelles complex (BLOC)‐1,‐2 and‐3 are three multi‐
subunit protein complexes that are deficient in various forms of Hermansky‐Pudlak …

[PDF][PDF] Genetic quality control of the rat strains at the national bio resource project-rat

Y Lee, S Womens - IBC, 2010 - Citeseer
ABSTRACT The National Bio Resource Project-Rat (NBRP-Rat) comprises the largest bank
of laboratory rat (Rattus norvegicus) strains in the world. Its main focus is to develop …

Albinism: Ocular And Oculocutaneous Albinism and Hermansky–Pudlak Syndrome

RA King, CG Summers - Manag Genet Syndr, 2010 - books.google.com
The term albinism refers to a group of congenital genetic abnormalities resulting from an
inability of the pigment cell (melanocyte) to synthesize normal amounts of melanin pigment …

Inter-kingdom epigenetics: characterization of maize b1 tandem repeat-mediated silencing in Drosophila melanogaster

LA McEachern - 2010 - dalspace.library.dal.ca
Transgenic organisms are a valuable tool for studying epigenetics, as they provide
significant insight into the evolutionary conservation of epigenetic control sequences, the …

Hermansky–Pudlak Syndrome

LR Young, WA Gahl - Molecular Basis of Pulmonary Disease: Insights from …, 2010 - Springer
Hermansky–Pudlak syndrome (HPS) is a group of rare autosomal recessive disorders
characterized by albinism and platelet dysfunction. A subset of HPS patients also develop …