受强制性开放获取政策约束的文章 - Allison Cox了解详情
无法在其他位置公开访问的文章：1 篇
Update on the genetics of nonbacterial osteomyelitis in humans
AJ Cox, PJ Ferguson
Current opinion in rheumatology 30 (5), 521-525, 2018
强制性开放获取政策： US National Institutes of Health
可在其他位置公开访问的文章：18 篇
A new standard genetic map for the laboratory mouse
A Cox, CL Ackert-Bicknell, BL Dumont, Y Ding, JT Bell, GA Brockmann, ...
Genetics 182 (4), 1335-1344, 2009
强制性开放获取政策： US National Institutes of Health
Seizures are regulated by ubiquitin-specific peptidase 9 X-linked (USP9X), a de-ubiquitinase
L Paemka, VB Mahajan, SN Ehaideb, JM Skeie, MC Tan, S Wu, AJ Cox, ...
PLoS genetics 11 (3), e1005022, 2015
强制性开放获取政策： US National Institutes of Health, National Health and Medical Research …
Recessive coding and regulatory mutations in FBLIM1 underlie the pathogenesis of chronic recurrent multifocal osteomyelitis (CRMO)
AJ Cox, BW Darbro, RM Laxer, G Velez, X Bing, AL Finer, A Erives, ...
PloS one 12 (3), e0169687, 2017
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A missense mutation in the MLKL brace region promotes lethal neonatal inflammation and hematopoietic dysfunction
JM Hildebrand, M Kauppi, IJ Majewski, Z Liu, AJ Cox, S Miyake, EJ Petrie, ...
Nature communications 11 (1), 3150, 2020
强制性开放获取政策： US National Institutes of Health, Howard Hughes Medical Institute, National …
Practical applications of the bioinformatics toolbox for narrowing quantitative trait loci
SL Burgess-Herbert, A Cox, SW Tsaih, B Paigen
Genetics 180 (4), 2227-2235, 2008
强制性开放获取政策： US National Institutes of Health
Gain-of-function mutations in a member of the Src family kinases cause autoinflammatory bone disease in mice and humans
K Abe, A Cox, N Takamatsu, G Velez, RM Laxer, SML Tse, VB Mahajan, ...
Proceedings of the National Academy of Sciences 116 (24), 11872-11877, 2019
强制性开放获取政策： US National Institutes of Health, Doris Duke Charitable Foundation, Federal …
Calpain-5 expression in the retina localizes to photoreceptor synapses
KA Schaefer, MA Toral, G Velez, AJ Cox, SA Baker, NC Borcherding, ...
Investigative ophthalmology & visual science 57 (6), 2509-2521, 2016
强制性开放获取政策： US National Institutes of Health, Doris Duke Charitable Foundation
The mouse QTL map helps interpret human genome-wide association studies for HDL cholesterol [S]
MS Leduc, M Lyons, K Darvishi, K Walsh, S Sheehan, S Amend, A Cox, ...
Journal of lipid research 52 (6), 1139-1149, 2011
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Genetic basis of HDL variation in 129/SvImJ and C57BL/6J mice: importance of testing candidate genes in targeted mutant mice* s⃞
Z Su, X Wang, SW Tsaih, A Zhang, A Cox, S Sheehan, B Paigen
Journal of lipid research 50 (1), 116-125, 2009
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Farp2 and Stk25 Are Candidate Genes for the HDL Cholesterol Locus on Mouse Chromosome 1
Z Su, A Cox, Y Shen, IM Stylianou, B Paigen
Arteriosclerosis, thrombosis, and vascular biology 29 (1), 107-113, 2009
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An experimental assessment of in silico haplotype association mapping in laboratory mice
SL Burgess-Herbert, SW Tsaih, IM Stylianou, K Walsh, AJ Cox, B Paigen
BMC genetics 10, 1-12, 2009
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Biallelic SCN10A mutations in neuromuscular disease and epileptic encephalopathy
M Kambouris, J Thevenon, A Soldatos, A Cox, J Stephen, T Ben‐Omran, ...
Annals of clinical and translational neurology 4 (1), 26-35, 2017
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D‐bifunctional protein deficiency caused by splicing variants in a neonate with severe peroxisomal dysfunction and persistent hypoglycemia
KM Werner, AJ Cox, E Qian, P Jain, W Ji, I Tikhonova, C Castaldi, ...
American Journal of Medical Genetics Part A 188 (1), 357-363, 2022
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Combining QTL data for HDL cholesterol levels from two different species leads to smaller confidence intervals
A Cox, SM Sheehan, I Klöting, B Paigen, R Korstanje
Heredity 105 (5), 426-432, 2010
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In trans variant calling reveals enrichment for compound heterozygous variants in genes involved in neuronal development and growth.
AJ Cox, F Grady, G Velez, VB Mahajan, PJ Ferguson, A Kitchen, ...
Genetics research 101, e8, 2019
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P2RX7 gene variants associate with altered inflammasome assembly and reduced pyroptosis in chronic nonbacterial osteomyelitis (CNO)
A Charras, SR Hofmann, A Cox, F Schulze, S Russ, S Northey, X Liu, ...
Journal of autoimmunity 144, 103183, 2024
强制性开放获取政策： Versus Arthritis, UK
Missense mutations in the MLKL ‘brace’region lead to lethal neonatal inflammation in mice and are present in high frequency in humans
JM Hildebrand, M Kauppi, IJ Majewski, Z Liu, A Cox, S Miyake, EJ Petrie, ...
bioRxiv, 628370, 2019
强制性开放获取政策： US National Institutes of Health, Howard Hughes Medical Institute, National …
FKBP14 kyphoscoliotic Ehlers–Danlos syndrome misdiagnosed as Larsen syndrome: a case report
A Wiegand, R Kastury, A Neogi, A Mani, A Bale, A Cox
Molecular Case Studies 9 (3), a006281, 2023
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