about
Carcinoembryonic antigen-related cell adhesion molecule 16 interacts with alpha-tectorin and is mutated in autosomal dominant hearing loss (DFNA4).The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)Exome sequencing and analysis of induced pluripotent stem cells identify the cilia-related gene male germ cell-associated kinase (MAK) as a cause of retinitis pigmentosaA BBSome subunit links ciliogenesis, microtubule stability, and acetylationGeneration and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet-Biedl syndrome gene (BBS11)Insights into a dinoflagellate genome through expressed sequence tag analysis.A Mutation in LTBP2 Causes Congenital Glaucoma in Domestic Cats (Felis catus)RetFM-J, an ImageJ-based module for automated counting and quantifying features of nuclei in retinal whole-mountsAdvancing genetic testing for deafness with genomic technology.Prediction of cochlear implant performance by genetic mutation: the spiral ganglion hypothesisAn international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge.Cordova: web-based management of genetic variation data.Anopheles gambiae pilot gene discovery project: identification of mosquito innate immunity genes from expressed sequence tags generated from immune-competent cell linesEST-based gene discovery in pig: virtual expression patterns and comparative mapping to human.A comprehensive nonredundant expressed sequence tag collection for the developing Rattus norvegicus heart.Prioritization of retinal disease genes: an integrative approach1274 full-open reading frames of transcripts expressed in the developing mouse nervous system.Large-scale gene discovery in human airway epithelia reveals novel transcripts.High-throughput gene discovery in the rat.Identifying components of the NF-kappaB pathway in the beneficial Euprymna scolopes-Vibrio fischeri light organ symbiosis.An annotated cDNA library of juvenile Euprymna scolopes with and without colonization by the symbiont Vibrio fischeriDifferential gene expression in human conducting airway surface epithelia and submucosal glands.Construction of a medicinal leech transcriptome database and its application to the identification of leech homologs of neural and innate immune genes.Transcriptional patterns in both host and bacterium underlie a daily rhythm of anatomical and metabolic change in a beneficial symbiosis.Somatic mutagenesis with a Sleeping Beauty transposon system leads to solid tumor formation in zebrafish.Novel molecular and computational methods improve the accuracy of insertion site analysis in Sleeping Beauty-induced tumors.Comprehensive genetic testing for hereditary hearing loss using massively parallel sequencing.The air-liquid interface and use of primary cell cultures are important to recapitulate the transcriptional profile of in vivo airway epithelia.Genome-wide identification of pseudogenes capable of disease-causing gene conversion.A genome-wide association study for primary open angle glaucoma and macular degeneration reveals novel LociTranscriptomic analysis across nasal, temporal, and macular regions of human neural retina and RPE/choroid by RNA-SeqIdentification of rtl1, a retrotransposon-derived imprinted gene, as a novel driver of hepatocarcinogenesisAutomated quantification of inherited phenotypes from color images: a twin study of the variability of optic nerve head shape.Copy number variations on chromosome 12q14 in patients with normal tension glaucomaIntegration site choice of a feline immunodeficiency virus vector.Computational quantification of complex fundus phenotypes in age-related macular degeneration and Stargardt diseaseGenomics-based approaches to gene discovery in innate immunity.Characterization of Cav1.4 complexes (α11.4, β2, and α2δ4) in HEK293T cells and in the retinaRegulation of gene expression in the mammalian eye and its relevance to eye disease.
P50
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P50
description
onderzoeker
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researcher
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հետազոտող
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name
Todd E. Scheetz
@ast
Todd E. Scheetz
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Todd E. Scheetz
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Todd E. Scheetz
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Todd E. Scheetz
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type
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Todd E. Scheetz
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Todd E. Scheetz
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Todd E. Scheetz
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Todd E. Scheetz
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Todd E. Scheetz
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prefLabel
Todd E. Scheetz
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Todd E. Scheetz
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Todd E. Scheetz
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Todd E. Scheetz
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Todd E. Scheetz
@sl
P106
P1153
6603782802
P2456
P31
P496
0000-0002-1965-5811