Richard D Emes
Richard D Emes
PVC Research and International, Nottingham Trent University
E-mail megerősítve itt: ntu.ac.uk - Kezdőlap
Hivatkozott rá
Hivatkozott rá
Initial sequencing and comparative analysis of the mouse genome
European Bioinformatics Institute: Birney Ewan 3 Goldman Nick 3 Kasprzyk ...
Nature 420 (6915), 520-562, 2002
Genome sequence of the Brown Norway rat yields insights into mammalian evolution
University of Utah Weiss Robert B. 14 Dunn Diane M. 14, ...
Nature 428 (6982), 493-521, 2004
Mutations in radial spoke head protein genes RSPH9 and RSPH4A cause primary ciliary dyskinesia with central-microtubular-pair abnormalities
VH Castleman, L Romio, R Chodhari, RA Hirst, SCP de Castro, KA Parker, ...
The American Journal of Human Genetics 84 (2), 197-209, 2009
TP53 copy number expansion is associated with the evolution of increased body size and an enhanced DNA damage response in elephants
M Sulak, L Fong, K Mika, S Chigurupati, L Yon, NP Mongan, RD Emes, ...
elife 5, e11994, 2016
Synaptic scaffold evolution generated components of vertebrate cognitive complexity
J Nithianantharajah, NH Komiyama, A McKechanie, M Johnstone, ...
Nature neuroscience 16 (1), 16-24, 2013
A new sequence motif linking lissencephaly, Treacher Collins and oral–facial–digital type 1 syndromes, microtubule dynamics and cell migration
RD Emes, CP Ponting
Human molecular genetics 10 (24), 2813-2820, 2001
Comparison of the genomes of human and mouse lays the foundation of genome zoology
RD Emes, L Goodstadt, EE Winter, CP Ponting
Human molecular genetics 12 (7), 701-709, 2003
Evolutionary expansion and anatomical specialization of synapse proteome complexity
RD Emes, AJ Pocklington, CNG Anderson, A Bayes, MO Collins, ...
Nature neuroscience 11 (7), 799-806, 2008
Paternal diet programs offspring health through sperm-and seminal plasma-specific pathways in mice
AJ Watkins, I Dias, H Tsuro, D Allen, RD Emes, J Moreton, R Wilson, ...
Proceedings of the National Academy of Sciences 115 (40), 10064-10069, 2018
Splice-site mutations in the axonemal outer dynein arm docking complex gene CCDC114 cause primary ciliary dyskinesia
A Onoufriadis, T Paff, D Antony, A Shoemark, D Micha, B Kuyt, ...
The American Journal of Human Genetics 92 (1), 88-98, 2013
Mutations in CCDC39 and CCDC40 are the Major Cause of Primary Ciliary Dyskinesia with Axonemal Disorganization and Absent Inner Dynein Arms
D Antony, A Becker‐Heck, MA Zariwala, M Schmidts, A Onoufriadis, ...
Human mutation 34 (3), 462-472, 2013
N6-methyladenosine regulates the stability of RNA:DNA hybrids in human cells
A Abakir, TC Giles, A Cristini, JM Foster, N Dai, M Starczak, ...
Nature genetics 52 (1), 48-55, 2020
Evolution of Synapse Complexity and Diversity
RD Emes, SGN Grant
Annual Reviews in Neuroscience 35, 111-131, 2012
Mutations in ZMYND10, a gene essential for proper axonemal assembly of inner and outer dynein arms in humans and flies, cause primary ciliary dyskinesia
DJ Moore, A Onoufriadis, A Shoemark, MA Simpson, PI Zur Lage, ...
The American Journal of Human Genetics 93 (2), 346-356, 2013
Quantitative, high-resolution epigenetic profiling of CpG loci identifies associations with cord blood plasma homocysteine and birth weight in humans
AA Fryer, RD Emes, KMK Ismail, KE Haworth, C Mein, WD Carroll, ...
Epigenetics 6 (1), 86-94, 2011
Exome sequencing identifies DYNC2H1 mutations as a common cause of asphyxiating thoracic dystrophy (Jeune syndrome) without major polydactyly, renal or retinal involvement
M Schmidts, HH Arts, EMHF Bongers, Z Yap, MM Oud, D Antony, ...
Journal of medical genetics 50 (5), 309-323, 2013
X-linked primary ciliary dyskinesia due to mutations in the cytoplasmic axonemal dynein assembly factor PIH1D3
C Olcese, MP Patel, A Shoemark, S Kiviluoto, M Legendre, HJ Williams, ...
Nature communications 8 (1), 14279, 2017
Evolution of NMDA receptor cytoplasmic interaction domains: implications for organisation of synaptic signalling complexes
TJ Ryan, RD Emes, SGN Grant, NH Komiyama
BMC neuroscience 9, 1-14, 2008
Sexual selection and the adaptive evolution of mammalian ejaculate proteins
SA Ramm, PL Oliver, CP Ponting, P Stockley, RD Emes
Molecular biology and evolution 25 (1), 207-219, 2008
Mutations in the gene encoding IFT dynein complex component WDR34 cause Jeune asphyxiating thoracic dystrophy
M Schmidts, J Vodopiutz, S Christou-Savina, CR Cortés, ...
The American Journal of Human Genetics 93 (5), 932-944, 2013
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