Detalhe da pesquisa
1.
Heterozygous Variants in the Mechanosensitive Ion Channel TMEM63A Result in Transient Hypomyelination during Infancy.
Am J Hum Genet
; 105(5): 996-1004, 2019 11 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31587869
2.
Assessing DNA for fish identifications from reference collections: the good, bad and ugly shed light on formalin fixation and sequencing approaches.
J Fish Biol
; 98(5): 1421-1432, 2021 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-33484178
3.
A recurrent de novo mutation in TMEM106B causes hypomyelinating leukodystrophy.
Brain
; 140(12): 3105-3111, 2017 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29186371
4.
Placental transcriptome co-expression analysis reveals conserved regulatory programs across gestation.
BMC Genomics
; 18(1): 10, 2017 01 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-28049421
5.
X-linked hypomyelination with spondylometaphyseal dysplasia (H-SMD) associated with mutations in AIFM1.
Neurogenetics
; 18(4): 185-194, 2017 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-28842795
6.
Genomic Comparison of Two O111:H- Enterohemorrhagic Escherichia coli Isolates from a Historic Hemolytic-Uremic Syndrome Outbreak in Australia.
Infect Immun
; 84(3): 775-81, 2016 Jan 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-26729762
7.
A genetic screen reveals a periplasmic copper chaperone required for nitrite reductase activity in pathogenic Neisseria.
FASEB J
; 29(9): 3828-38, 2015 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-26031293
8.
Whole genome capture of vector-borne pathogens from mixed DNA samples: a case study of Borrelia burgdorferi.
BMC Genomics
; 16: 434, 2015 Jun 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-26048573
9.
massiR: a method for predicting the sex of samples in gene expression microarray datasets.
Bioinformatics
; 30(14): 2084-5, 2014 Jul 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24659105
10.
Borrelia burgdorferi sensu stricto and Borrelia afzelii: Population structure and differential pathogenicity.
Int J Med Microbiol
; 305(7): 673-81, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-26341331
11.
Monitoring human babesiosis emergence through vector surveillance New England, USA.
Emerg Infect Dis
; 20(2): 225-31, 2014 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-24447577
12.
Integrative transcriptome meta-analysis reveals widespread sex-biased gene expression at the human fetal-maternal interface.
Mol Hum Reprod
; 20(8): 810-9, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-24867328
13.
There is a specific response to pH by isolates of Haemophilus influenzae and this has a direct influence on biofilm formation.
BMC Microbiol
; 14: 47, 2014 Feb 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-24555828
14.
Identification of Borrelia burgdorferi ospC genotypes in host tissue and feeding ticks by terminal restriction fragment length polymorphisms.
Appl Environ Microbiol
; 79(3): 958-64, 2013 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-23183976
15.
Phylogeography of Borrelia burgdorferi in the eastern United States reflects multiple independent Lyme disease emergence events.
Proc Natl Acad Sci U S A
; 106(35): 15013-8, 2009 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-19706476
16.
Evolutionary Relationships and Range Evolution of Greenhood Orchids (Subtribe Pterostylidinae): Insights From Plastid Phylogenomics.
Front Plant Sci
; 13: 912089, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35845679
17.
Loop analysis for pathogens: niche partitioning in the transmission graph for pathogens of the North American tick Ixodes scapularis.
J Theor Biol
; 269(1): 96-103, 2011 Jan 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-20950628
18.
Regional variation in immature Ixodes scapularis parasitism on North American songbirds: implications for transmission of the Lyme pathogen, Borrelia burgdorferi.
J Med Entomol
; 48(2): 422-8, 2011 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-21485384
19.
Genotypic diversity of Borrelia burgdorferi strains detected in Ixodes scapularis larvae collected from North American songbirds.
Appl Environ Microbiol
; 76(24): 8265-8, 2010 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-20971869
20.
Genome sequencing in persistently unsolved white matter disorders.
Ann Clin Transl Neurol
; 7(1): 144-152, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31912665