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Lachlan De Hayr
Lachlan De Hayr
uq.edu.au üzerinde doğrulanmış e-posta adresine sahip
Başlık
Alıntı yapanlar
Alıntı yapanlar
Yıl
Density-dependent enhanced replication of a densovirus in Wolbachia-infected Aedes cells is associated with production of piRNAs and higher virus-derived siRNAs
R Parry, C Bishop, L De Hayr, S Asgari
Virology 528, 89-100, 2019
402019
others. 2022
CC Chen, KA Wilson, N Schaefer, L De Hayr, M Windsor, E Scalais
The data and metadata of this study are available in the Dryad data …, 1990
401990
Loss, gain and altered function of GlyR α2 subunit mutations in neurodevelopmental disorders
X Chen, KA Wilson, N Schaefer, L De Hayr, M Windsor, E Scalais, ...
Frontiers in molecular neuroscience 15, 886729, 2022
162022
Pharmacokinetic and pharmacodynamic considerations for treating sarcoptic mange with cross-relevance to Australian wildlife
K Takano, L De Hayr, S Carver, RJ Harvey, KE Mounsey
International Journal for Parasitology: Drugs and Drug Resistance 21, 97-113, 2023
152023
The flavivirus non-structural protein 5 (NS5): structure, functions, and targeting for development of vaccines and therapeutics
JZH Goh, L De Hayr, AA Khromykh, A Slonchak
Vaccines 12 (8), 865, 2024
112024
De Novo ZMYND8 variants result in an autosomal dominant neurodevelopmental disorder with cardiac malformations
KR Dias, CM Carlston, LER Blok, L De Hayr, U Nawaz, CA Evans, ...
Genetics in Medicine 24 (9), 1952-1966, 2022
102022
RNA activation in insects: The targeted activation of endogenous and exogenous genes
L De Hayr, S Asad, M Hussain, S Asgari
Insect biochemistry and molecular biology 119, 103325, 2020
82020
Dominant-negative variants in CBX1 cause a neurodevelopmental disorder
Y Kuroda, A Iwata-Otsubo, KR Dias, SEL Temple, K Nagao, L De Hayr, ...
Genetics in Medicine 25 (7), 100861, 2023
62023
Biallelic SLC13A1 loss-of-function variants result in impaired sulfate transport and skeletal phenotypes, including short stature, scoliosis, and skeletal dysplasia
CG Tise, K Ashton, L de Hayr, KD Lee, OL Patkar, E Krzesinski, ...
Genetics in Medicine Open 3, 101958, 2025
2025
Biallelic variants in GTF3C3 result in an autosomal recessive disorder with intellectual disability
L De Hayr, LER Blok, KR Dias, J Long, A Begemann, RD Moir, IM Willis, ...
Genetics in Medicine 27 (1), 101253, 2025
2025
Investigating the role of non-coding RNAs in Aedes aegypti biology
L De Hayr
2020
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