Results 251 to 260 of about 5,995,584 (403)

Interactions between dorsal and helix-loop-helix proteins initiate the differentiation of the embryonic mesoderm and neuroectoderm in Drosophila. [PDF]

, 1993
Sergio González‐Crespo, Michael Levine   +1 more
openalex   +1 more source

Neurodegenerative and Neurodevelopmental Roles for Bulk Lipid Transporters VPS13A and BLTP2

Movement Disorders, EarlyView.
Abstract Background Bridge‐like lipid transfer proteins (BLTPs) mediate bulk lipid transport at membrane contact sites. Mutations in BLTPs are linked to both early‐onset neurodevelopmental and later‐onset neurodegenerative diseases, including movement disorders.
Sarah D. Neuman, Rajan S. Thakur, Scott J. Gratz, Kate M. O'Connor‐Giles, Arash Bashirullah   +4 more
wiley   +1 more source

Inwardly rectifying potassium channels: Critical insights for insect species and Apis mellifera. [PDF]

Channels (Austin)
Sourisseau F, Doupnik CA, Charnet P, Chahine M.   +3 more
europepmc   +1 more source

The Drosophila l(2)35Ba/nocA gene encodes a putative Zn finger protein involved in the development of the embryonic brain and the adult ocellar structures. [PDF]

, 1994
P Y Cheah, Y B Meng, Xiujunan Yang, D Kimbrell, M Ashburner, W Chia   +5 more
openalex   +1 more source

Disruption of Axonal Transport by Loss of Huntingtin or Expression of Pathogenic PolyQ Proteins in Drosophila

Neuron, 2003
S. Gunawardena, L. Her, R. Brusch, R. A. Laymon, I. Niesman, B. Gordesky-Gold, L. Sintasath, N. Bonini, L. Goldstein   +8 more
semanticscholar   +1 more source

Treatment Selection and Prioritization for the EJS ACT‐PD MAMS Trial Platform

Movement Disorders, EarlyView.
Abstract Background There are currently no disease‐modifying therapies (DMTs) registered for Parkinson's disease (PD). The Edmond J. Safra Accelerating Clinical Trials in Parkinson Disease (EJS ACT‐PD) initiative will expedite clinical assessment of putative DMTs through a multi‐arm multistage (MAMS) trial, testing several treatments against a common ...
Cristina Gonzalez‐Robles, Dilan Athauda, Thomas R. Barber, Roger A. Barker, David T. Dexter, Susan Duty, Romy Ellis‐Doyle, Sonia Gandhi, Joel Handley, Edwin Jabbari, Keith Martin, Kevin McFarthing, Georgia Mills, Heather Mortiboys, Stephen Mullin, Rebecca Petty, Esther Sammler, Paula Scurfield, Simon R.W. Stott, George K. Tofaris, Li Wei, Caroline H. Williams‐Gray, Alan Wong, Marie‐Louise Zeissler, Richard K. Wyse, Camille B. Carroll, Thomas Foltynie, Oliver Bandmann, Anthony H.V. Schapira, on behalf of the EJS ACT‐PD Consortium   +29 more
wiley   +1 more source

Higher resolution pooled genome-wide CRISPR knockout screening in Drosophila cells using integration and anti-CRISPR (IntAC). [PDF]

Nat Commun
Viswanatha R, Entwisle S, Hu Y, Kim AR, Reap K, Butnaru M, Qadiri M, Mohr SE, Perrimon N.   +8 more
europepmc   +1 more source

Genetic investigation of cAMP-dependent protein kinase function in Drosophila development. [PDF]

, 1993
Mary Ellen Lane, Daniel Kalderon
openalex   +1 more source

Evolutionary EST analysis identifies rapidly evolving male reproductive proteins in Drosophila

Proceedings of the National Academy of Sciences of the United States of America, 2001
W. Swanson, A. Clark, Heidi M. Waldrip-Dail, M. Wolfner, C. Aquadro   +4 more
semanticscholar   +1 more source

EFNB3 Frameshift Variant in Weimaraner Dogs with a Condition Resembling a Congenital Mirror Movement Disorder

Movement Disorders, EarlyView.
ABSTRACT Background Congenital mirror movement disorders (CMMs) are clinically and genetically heterogeneous in human patients. CMMs have not been documented to occur spontaneously in animals. Objective The objective of this work was to document the first case of CMMs spontaneously occurring in Weimaraner dogs and to identify the underlying genetic ...
Cleo Schwarz, Florian Bartenschlager, Olivia Kershaw, Judith Braun, Julien Guevar, Vidhya Jagannathan, Jörg T. Epplen, Wencke Reineking, Wolfgang Baumgärtner, Kailash P. Bhatia, Achim D. Gruber, Tosso Leeb   +11 more
wiley   +1 more source