Следене
Joshua D. Mast
Joshua D. Mast
Perlara PBC
Потвърден имейл адрес: perlara.com
Заглавие
Позовавания
Позовавания
Година
Multiplexed shotgun genotyping for rapid and efficient genetic mapping
P Andolfatto, D Davison, D Erezyilmaz, TT Hu, J Mast, T Sunayama-Morita, ...
Genome research 21 (4), 610-617, 2011
4852011
Evolved differences in larval social behavior mediated by novel pheromones
JD Mast, CM De Moraes, HT Alborn, LD Lavis, DL Stern
Elife 3, e04205, 2014
682014
Genetic and Transgenic Reagents for Drosophila simulans, D. mauritiana, D. yakuba, D. santomea, and D. virilis
DL Stern, J Crocker, Y Ding, N Frankel, G Kappes, E Kim, R Kuzmickas, ...
G3: Genes, Genomes, Genetics 7 (4), 1339-1347, 2017
632017
The mechanisms and molecules that connect photoreceptor axons to their targets in Drosophila
JD Mast, S Prakash, PL Chen, TR Clandinin
Seminars in cell & developmental biology 17 (1), 42-49, 2006
522006
Reactive oxygen species act remotely to cause synapse loss in a Drosophila model of developmental mitochondrial encephalopathy
JD Mast, KMH Tomalty, H Vogel, TR Clandinin
Oxford University Press for The Company of Biologists Limited 135 (15), 2669 …, 2008
432008
Defects in the Neuroendocrine Axis Contribute to Global Development Delay in a Drosophila Model of NGLY1 Deficiency
TP Rodriguez, JD Mast, T Hartl, T Lee, P Sand, EO Perlstein
G3: Genes, Genomes, Genetics 8 (7), 2193-2204, 2018
322018
Drug screens of NGLY1 deficiency in worm and fly models reveal catecholamine, NRF2 and anti-inflammatory-pathway activation as potential clinical approaches
S Iyer, JD Mast, H Tsang, TP Rodriguez, N DiPrimio, M Prangley, FS Sam, ...
Disease Models & Mechanisms 12 (11), dmm040576, 2019
262019
RNA-Seq following PCR-based sorting reveals rare cell transcriptional signatures
M Pellegrino, A Sciambi, JL Yates, JD Mast, C Silver, DJ Eastburn
BMC genomics 17, 1-12, 2016
232016
Yeast models of phosphomannomutase 2 deficiency, a congenital disorder of glycosylation
JP Lao, N DiPrimio, M Prangley, FS Sam, JD Mast, EO Perlstein
G3: Genes, Genomes, Genetics 9 (2), 413-423, 2019
172019
Glial control of sphingolipid levels sculpts diurnal remodeling in a circadian circuit
JP Vaughen, E Theisen, IM Rivas-Serna, AB Berger, P Kalakuntla, ...
Neuron 110 (19), 3186-3205. e7, 2022
142022
The cytoskeletal regulator Genghis khan is required for columnar target specificity in the Drosophila visual system
AC Gontang, JJ Hwa, JD Mast, T Schwabe, TR Clandinin
Development 138 (22), 4899-4909, 2011
92011
Methods for treating congenital disorders of glycosylation
EO Perlstein, J Lao, F Sam, N Diprimio, Z Parton, H Tsang, K Murthy, ...
US Patent 11,160,794, 2021
12021
Defects in the neuroendocrine axis cause global development delay in a Drosophila model of NGLY1 deficiency
TP Rodriguez, JD Mast, T Hartl, EO Perlstein
BioRxiv, 241653, 2018
12018
Genetic and Transgenic Reagents for Drosophila
DL Stern, J Crocker, Y Ding, N Frankel, G Kappes, E Kim, R Kuzmickas, ...
12017
Methods for treating congenital disorders of glycosylation
EO Perlstein, J Lao, F Sam, N Diprimio, Z Parton, H Tsang, K Murthy, ...
US Patent App. 17/489,149, 2022
2022
Multi-Species Phenotypic Screening across Disease Models of Mucolipidosis Type IV
A Hadjikyriacou, S Iyer, JD Mast, N DiPrimio, J Concannon, J Ketterman, ...
BioRxiv, 2021.03. 05.434120, 2021
2021
Defects in the Neuroendocrine Axis Contribute to Global Development Delay in a Drosophila Model of NGLY1 Deficiency (vol 8, pg 2193, 2018)
TP Rodriguez, JD Mast, T Hartl, T Lee, P Sand, EO Perlstein
G3-GENES GENOMES GENETICS 9 (1), 315-315, 2019
2019
Defects in the neuroendocrine axis cause global development delay in a
TP Rodriguez, JD Mast, T Hartl, EO Perlstein
Chem Lett 27, 2962-2966, 2017
2017
Mitochondrial Dysfunction Induces Neurodegeneration and Synapse Loss in the Drosophila Visual System
JD Mast
ProQuest, 2007
2007
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Статии 1–19