Dorothy L. Guilbride
Heidelberg, BW 69120, Germany
Last Updated: 09/26/2026
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Found 13 publications
Congenital coenzyme Q5-linked pathology: causal genetic association, core phenotype, and molecular mechanism.
Journal: Journal of applied genetics
Published: April 29, 2023
A Zebrafish/Drosophila Dual System Model for Investigating Human Microcephaly.
Journal: Cells
Published: August 14, 2022
De Novo ACTG1 Variant Expands the Phenotype and Genotype of Partial Deafness and Baraitser-Winter Syndrome.
Journal: International journal of molecular sciences
Published: December 01, 2021
A Patient with Berardinelli-Seip Syndrome, Novel AGPAT2 Splicesite Mutation and Concomitant Development of Non-diabetic Polyneuropathy
Journal: Journal of clinical research in pediatric endocrinology
Published: December 20, 2018
Phenotype expansion and development in Kosaki overgrowth syndrome.
Journal: Clinical genetics
Published: August 21, 2017
Operon structure and cotranslational subunit association direct protein assembly in bacteria.
Journal: Science (New York, N.Y.)
Published: June 17, 2015
Human Hsp70 Disaggregase Reverses Parkinson's-Linked α-Synuclein Amyloid Fibrils.
Journal: Molecular cell
Published: May 26, 2015
Cell Biology. Finding nascent proteins the right home.
Journal: Science (New York, N.Y.)
Published: April 11, 2015
Compartment-specific aggregases direct distinct nuclear and cytoplasmic aggregate deposition.
Journal: The EMBO journal
Published: February 13, 2015
Crucial HSP70 co-chaperone complex unlocks metazoan protein disaggregation.
Journal: Nature
Published: October 25, 2014
Last Updated: 09/26/2026