Detalhe da pesquisa
1.
Effects of Porphyromonas gingivalis and Aggregatibacter actinomycetemcomitans on Modeling Subgingival Microbiome and Impairment of Oral Epithelial Barrier.
J Infect Dis
; 229(1): 262-272, 2024 Jan 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-37855446
2.
A Study on the Incidence and Prevalence of 5q Spinal Muscular Atrophy in Canada Using Multiple Data Sources.
Can J Neurol Sci
; : 1-12, 2024 Jan 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-38178730
3.
Bridging clinical care and research in Ontario, Canada: Maximizing diagnoses from reanalysis of clinical exome sequencing data.
Clin Genet
; 103(3): 288-300, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36353900
4.
The implementation of an enhanced clinical model to improve the diagnostic yield of exome sequencing for patients with a rare genetic disease: A Canadian experience.
Am J Med Genet A
; 191(2): 338-347, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36331261
5.
Study on Removal Mechanism for Copper Cyanide Complex Ions in Water: Ion Species Differences and Evolution Process.
Int J Mol Sci
; 24(6)2023 Mar 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-36982143
6.
Hydrogels for Oral Tissue Engineering: Challenges and Opportunities.
Molecules
; 28(9)2023 May 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37175356
7.
Clinical and functional characterization of recurrent missense variants implicated in THOC6-related intellectual disability.
Hum Mol Genet
; 28(6): 952-960, 2019 03 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-30476144
8.
Interplay between probe design and test performance: overlap between genomic regions of interest, capture regions and high quality reference calls influence performance of WES-based assays.
Hum Genet
; 140(2): 289-297, 2021 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-32627054
9.
Biallelic Mutations in LRRC56, Encoding a Protein Associated with Intraflagellar Transport, Cause Mucociliary Clearance and Laterality Defects.
Am J Hum Genet
; 103(5): 727-739, 2018 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30388400
10.
Multi-Aspect SAR Target Recognition Based on Prototypical Network with a Small Number of Training Samples.
Sensors (Basel)
; 21(13)2021 Jun 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-34202766
11.
Renpenning syndrome in a female.
Am J Med Genet A
; 182(3): 498-503, 2020 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31840929
12.
Compound heterozygous mutations in the gene PIGP are associated with early infantile epileptic encephalopathy.
Hum Mol Genet
; 26(9): 1706-1715, 2017 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28334793
13.
An Improved Imaging Algorithm for High-Resolution Spotlight SAR with Continuous PRI Variation Based on Modified Sinc Interpolation.
Sensors (Basel)
; 19(2)2019 Jan 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-30669345
14.
Analysis of the Azimuth Ambiguity and Imaging Area Restriction for Circular SAR Based on the Back-Projection Algorithm.
Sensors (Basel)
; 19(22)2019 Nov 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31726674
15.
Effects of bacterial physiological states and bacterial species on host-microbe interactions.
Biofouling
; 34(8): 870-879, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30326724
16.
An Improved BAQ Encoding and Decoding Method for Improving the Quantized SNR of SAR Raw Data.
Sensors (Basel)
; 18(12)2018 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30513763
17.
A High-Resolution SAR Focusing Experiment Based on GF-3 Staring Data.
Sensors (Basel)
; 18(4)2018 Mar 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-29565316
18.
Matchmaking facilitates the diagnosis of an autosomal-recessive mitochondrial disease caused by biallelic mutation of the tRNA isopentenyltransferase (TRIT1) gene.
Hum Mutat
; 38(5): 511-516, 2017 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-28185376
19.
A novel multisystem disease associated with recessive mutations in the tyrosyl-tRNA synthetase (YARS) gene.
Am J Med Genet A
; 173(1): 126-134, 2017 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-27633801
20.
Mandibulofacial Dysostosis with Microcephaly: Mutation and Database Update.
Hum Mutat
; 37(2): 148-54, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26507355