受强制性开放获取政策约束的文章 - Joanna Crawford了解详情
无法在其他位置公开访问的文章：2 篇
A novel X-linked trichothiodystrophy associated with a nonsense mutation in RNF113A
MA Corbett, T Dudding-Byth, PA Crock, E Botta, LM Christie, T Nardo, ...
Journal of medical genetics 52 (4), 269-274, 2015
强制性开放获取政策： National Health and Medical Research Council, Australia
Apicomplexan parasite adhesins: novel strategies for targeting host cell carbohydrates
MJ Boulanger, ML Tonkin, J Crawford
Current opinion in structural biology 20 (5), 551-559, 2010
强制性开放获取政策： Canadian Institutes of Health Research
可在其他位置公开访问的文章：40 篇
The human mitochondrial transcriptome
TR Mercer, S Neph, ME Dinger, J Crawford, MA Smith, AMJ Shearwood, ...
Cell 146 (4), 645-658, 2011
强制性开放获取政策： US National Institutes of Health
Targeted RNA sequencing reveals the deep complexity of the human transcriptome
TR Mercer, DJ Gerhardt, ME Dinger, J Crawford, C Trapnell, JA Jeddeloh, ...
Nature biotechnology 30 (1), 99-104, 2012
强制性开放获取政策： US National Institutes of Health
Genome-wide discovery of human splicing branchpoints
TR Mercer, MB Clark, SB Andersen, ME Brunck, W Haerty, J Crawford, ...
Genome research 25 (2), 290-303, 2015
强制性开放获取政策： Australian Research Council, National Health and Medical Research Council …
Host cell invasion by apicomplexan parasites: insights from the co-structure of AMA1 with a RON2 peptide
ML Tonkin, M Roques, MH Lamarque, M Pugnière, D Douguet, ...
Science 333 (6041), 463-467, 2011
强制性开放获取政策： Canadian Institutes of Health Research
A de novo mutation in the β-tubulin gene TUBB4A results in the leukoencephalopathy hypomyelination with atrophy of the basal ganglia and cerebellum
C Simons, NI Wolf, N McNeil, L Caldovic, JM Devaney, A Takanohashi, ...
The American Journal of Human Genetics 92 (5), 767-773, 2013
强制性开放获取政策： US National Institutes of Health, Australian Research Council
Mutations in DARS cause hypomyelination with brain stem and spinal cord involvement and leg spasticity
RJ Taft, A Vanderver, RJ Leventer, SA Damiani, C Simons, SM Grimmond, ...
The American Journal of Human Genetics 92 (5), 774-780, 2013
强制性开放获取政策： US National Institutes of Health, Australian Research Council
Patient-iPSC-derived kidney organoids show functional validation of a ciliopathic renal phenotype and reveal underlying pathogenetic mechanisms
TA Forbes, SE Howden, K Lawlor, B Phipson, J Maksimovic, L Hale, ...
The American Journal of Human Genetics 102 (5), 816-831, 2018
强制性开放获取政策： National Health and Medical Research Council, Australia
Targeted sequencing for gene discovery and quantification using RNA CaptureSeq
TR Mercer, MB Clark, J Crawford, ME Brunck, DJ Gerhardt, RJ Taft, ...
Nature protocols 9 (5), 989-1009, 2014
强制性开放获取政策： National Health and Medical Research Council, Australia
Quantitative gene profiling of long noncoding RNAs with targeted RNA sequencing
MB Clark, TR Mercer, G Bussotti, T Leonardi, KR Haynes, J Crawford, ...
Nature methods 12 (4), 339-342, 2015
强制性开放获取政策： National Health and Medical Research Council, Australia, UK Biotechnology …
Mutations in the voltage-gated potassium channel gene KCNH1 cause Temple-Baraitser syndrome and epilepsy
C Simons, LD Rash, J Crawford, L Ma, B Cristofori-Armstrong, D Miller, ...
Nature genetics 47 (1), 73-77, 2015
强制性开放获取政策： Australian Research Council, National Health and Medical Research Council …
Whole exome sequencing in patients with white matter abnormalities
A Vanderver, C Simons, G Helman, J Crawford, NI Wolf, G Bernard, ...
Annals of neurology 79 (6), 1031-1037, 2016
强制性开放获取政策： US National Institutes of Health, Australian Research Council, National …
Universal alternative splicing of noncoding exons
IW Deveson, ME Brunck, J Blackburn, E Tseng, T Hon, TA Clark, MB Clark, ...
Cell Systems 6 (2), 245-255. e5, 2018
强制性开放获取政策： Australian Research Council, National Health and Medical Research Council …
Loss-of-function alanyl-tRNA synthetase mutations cause an autosomal-recessive early-onset epileptic encephalopathy with persistent myelination defect
C Simons, LB Griffin, G Helman, G Golas, A Pizzino, M Bloom, ...
The American Journal of Human Genetics 96 (4), 675-681, 2015
强制性开放获取政策： US National Institutes of Health, Australian Research Council, National …
Long noncoding RNAs CUPID1 and CUPID2 mediate breast cancer risk at 11q13 by modulating the response to DNA damage
JA Betts, MM Marjaneh, F Al-Ejeh, YC Lim, W Shi, H Sivakumaran, ...
The American Journal of Human Genetics 101 (2), 255-266, 2017
强制性开放获取政策： Australian Research Council, National Health and Medical Research Council …
Genotype-free demultiplexing of pooled single-cell RNA-seq
J Xu, C Falconer, Q Nguyen, J Crawford, BD McKinnon, S Mortlock, ...
Genome biology 20, 1-12, 2019
强制性开放获取政策： Australian Research Council, National Health and Medical Research Council …
A recurrent de novo mutation in TMEM106B causes hypomyelinating leukodystrophy
C Simons, D Dyment, SJ Bent, J Crawford, M D’Hooghe, A Kohlschütter, ...
Brain 140 (12), 3105-3111, 2017
强制性开放获取政策： National Health and Medical Research Council, Australia, Canadian Institutes …
Structural characterization of apical membrane antigen 1 (AMA1) from Toxoplasma gondii
J Crawford, ML Tonkin, O Grujic, MJ Boulanger
Journal of Biological Chemistry 285 (20), 15644-15652, 2010
强制性开放获取政策： Canadian Institutes of Health Research
Heterozygous variants in the mechanosensitive ion channel TMEM63A result in transient hypomyelination during infancy
H Yan, G Helman, SE Murthy, H Ji, J Crawford, T Kubisiak, SJ Bent, J Xiao, ...
The American Journal of Human Genetics 105 (5), 996-1004, 2019
强制性开放获取政策： National Health and Medical Research Council, Australia, 国家自然科学基金委员会
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