There he pioneered the development of
a novel gene identification technique of mapping by admixture linkage disequilibrium.
Not exact matches
Identification of
novel polymorphisms in the glucokinase and glucose -6-phosphatase
genes in infants who died suddenly and unexpectedly
It has been estimated that 5 % to 10 % of infants who die from SIDS have
novel mutations in the cardiac sodium or potassium channel
genes that result in long QT syndrome as well as in other
genes that regulate channel function.44 A recent report described important new molecular and functional evidence that implicates specific SCN5A (sodium channel
gene) β subunits in SIDS pathogenesis.47 The
identification of polymorphisms in
genes pertinent to the embryologic origin of the autonomic nervous system in SIDS cases also lends support to the hypothesis that a genetic predisposition contributes to the etiology of SIDS.
M. J. Bertram et al.,
Identification of a
gene that reverses the immortal phenotype of a subset of cells and is a member of a
novel family of transcription factor - like
genes.
His current specific interest is the elucidation of
novel mechanisms of drug resistance through the discovery /
identification of
novel gene function (s) and phenotypes using RNAi - mediated
gene silencing or cDNA overexpression.
Collaborative research in Japan, under the guidance of the principle investigators from Fujita Health University and RIKEN, led to the
identification of a
novel risk
gene (FADS1 and FADS2) for bipolar disorder via GWAS performed using samples collected in Japan (2,964 cases and 61,887 comparison subjects).
Conventional methods for
identification of both RP mutations and
novel RP
genes involve the screening of DNA coding sequences.
Genome - scale metabolic models as platforms for
identification of
novel genes as antimicrobial drug targets — Bashir Sajo Mienda — Future Medicine
The transcriptomics and phosphoproteomics data generated by this project will allow the
identification of
novel host and parasite
genes and pathways that play a key role during infection.
We are focusing on a few key molecular pathways including; 1) Polycomb - mediated epigenetic
gene silencing in the tumor initiation, maintenance, and invasion, 2) c - Met (receptor tyrosine kinase) signal transduction pathways in stemness and migration of these tumor cells, 3)
Novel mitogenic signaling pathways that are specific to GSCs, and 4)
Identification of radio - and chemo - sensitizing pathway to maximize therapeutic efficacy.
Identification of
novel Regulatory Factor X (RFX) target
genes by Comparative Genomics in Drosophila species.
More recently, in a joint initiative with the BBMRI - LPC project (Biobanking and Biomolecular Resources Research Infrastructure — Large Prospective Cohorts) and the Wellcome Trust Sanger Institute, the CNAG - CRG launched a call to promote the use of sequencing technologies for the
identification of
novel causative variants and
genes and to molecularly diagnose rare disease patients.
Identification of patients sharing variants in a given
gene and having phenotypic features in common leads to greater certainty in the pathogenic nature of the
gene and enables to the role of
novel genes in development and disease to be defined.
He has made several important contributions in this area including identifying a new strain of CHIKV virus,
identification of host cellular targets of HIV accessory
genes, new
novel DNA vaccine approaches for HIV, CHIKV, RSV, Dengue, MERS and Zika among others.
Identification of
novel NRF2 - regulated
genes by ChIPSeq: influence on retinoid X receptor alpha.
Identification of a
novel sequence element in the common promoter region of human collagen type IV
genes, involved in the regulation of divergent transcription
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Identification of RCBTB1 as
novel disease
gene for retinal ciliopathy.
Identification of
novel mutations in the ENPP1
gene in eight patients with hypopigmented and hyperpigmented lesions and punctate palmoplantar keratosis led Radiocarbon dating is a popular dating method the general public is fairly familiar with.