Search Results - "Love, DR"
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Emotional Eating: A Major Contributing Factor to Weight Regain Post Bariattric Surgery in African American Women over Age 40 Following a Five-Year Span?
Published 01-01-2022“…Obesity is a health issue that transcends all demographic lines, including age, sexual orientation, socioeconomic status, and social position. It has been…”
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Dissertation -
2
Genetic markers of repolarization and arrhythmic events after acute coronary syndromes: Genetics
Published in The American heart journal (01-04-2015)“…Background There is a genetic contribution to the risk of ventricular arrhythmias in survivors of acute coronary syndromes (ACS). We wished to explore the role…”
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Journal Article -
3
Visualization, characterization and modulation of calcium signaling during the development of slow muscle cells in intact zebrafish embryos
Published in The International journal of developmental biology (2011)“…Intact zebrafish embryos were used as an in vivo animal model to investigate the role of Ca2+ signaling during the differentiation of slow muscle cells (SMCs)…”
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Journal Article -
4
Direct Interaction between Emerin and Lamin A
Published in Biochemical and biophysical research communications (27-01-2000)“…Emerin is the protein of the inner nuclear membrane that is affected by mutation in X-linked Emery-Dreifuss muscular dystrophy. The autosomal dominant form of…”
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Journal Article -
5
A mutation in the gene TNFRSF11B encoding osteoprotegerin causes an idiopathic hyperphosphatasia phenotype
Published in Human molecular genetics (01-09-2002)“…Idiopathic hyperphosphatasia is an autosomal recessive bone disease characterized by deformities of long bones, kyphosis and acetabular protrusion, increasing…”
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Journal Article -
6
Chemical discovery and global gene expression analysis in zebrafish
Published in Nature biotechnology (01-08-2003)“…The zebrafish (Danio rerio) provides an excellent model for studying vertebrate development and human disease because of its ex utero, optically transparent…”
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Journal Article -
7
Genetic markers of repolarization and arrhythmic events after acute coronary syndromes
Published in The American heart journal (01-04-2015)“…Background There is a genetic contribution to the risk of ventricular arrhythmias in survivors of acute coronary syndromes (ACS). We wished to explore the role…”
Get full text
Journal Article -
8
Short interfering RNA-mediated gene targeting in the zebrafish
Published in FEBS letters (12-03-2004)“…Short interfering RNAs (siRNAs) have proved to be a useful tool in studying gene function in plants, invertebrates and mammalian systems. Here we report the…”
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Journal Article -
9
Identification of large gene deletions and duplications in KCNQ1 and KCNH2 in patients with long QT syndrome
Published in Heart rhythm (01-09-2008)“…Background Sequencing or denaturing high-performance liquid chromatography (dHPLC) analysis of the known genes associated with the long QT syndrome (LQTS)…”
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Journal Article -
10
Technology for high-throughput screens: the present and future using zebrafish
Published in Current opinion in biotechnology (01-12-2004)“…The zebrafish is a popular vertebrate model organism with similar organ systems and gene sequences to humans. Zebrafish embryos are optically transparent…”
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Journal Article -
11
Novel mutation in the TMEM127 gene associated with phaeochromocytoma
Published in Internal medicine journal (01-04-2013)“…Phaeochromocytomas and paragangliomas are rare neuroendocrine tumours that arise from the adrenal glands or paraganglia (paragangliomas) within the abdomen,…”
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Journal Article -
12
Zebrafish : bridging the gap between development and disease
Published in Human molecular genetics (01-10-2000)“…The zebrafish has been the model of choice amongst developmental biologists for many years. This small freshwater species offers many advantages to the study…”
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Journal Article -
13
13q33.2 deletion: a rare cause of ambiguous genitalia in a male newborn with growth restriction
Published in Acta Paediatrica (01-05-2010)“…13q deletion is a rare cause of ambiguous genitalia in the male newborn, and can be associated with mental retardation of varying degree, retinoblastoma, and…”
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Journal Article -
14
Inhibin: a candidate gene for premature ovarian failure
Published in Human reproduction (Oxford) (01-12-2000)“…Premature ovarian failure (POF) occurs in 1% of all women, and in 0.1% of women under the age of 30 years. The mechanisms that give rise to POF are largely…”
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Journal Article -
15
Spectrum of MODY in the south of New Zealand – including two novel mutations
Published in International journal of pediatric endocrinology (03-10-2013)Get full text
Journal Article -
16
Developing Health-Based Pre-Planning Clearance Goals for Airport Remediation Following Chemical Terrorist Attack: Introduction and Key Assessment Considerations
Published in Human and ecological risk assessment (01-01-2011)“…In the event of a chemical terrorist attack on a transportation hub, post-event remediation and restoration activities necessary to attain unrestricted…”
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Journal Article -
17
Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A
Published in Nature (London) (03-06-1993)“…Multiple endocrine neoplasia type 2A (MEN 2A) is a dominantly inherited cancer syndrome that affects tissues derived from neural ectoderm. It is characterized…”
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Journal Article -
18
G.P.46 Screening for deletion and duplication mutations in genes implicated in LGMD
Published in Neuromuscular disorders : NMD (01-10-2012)“…Abstract LGMD is predominantly inherited in an autosomal recessive manner; however autosomal dominant and X-linked subtypes have also been described. To date,…”
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Journal Article -
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Developing Health-Based Pre-Planning Clearance Goals for Airport Remediation Following a Chemical Terrorist Attack: Decision Criteria for Multipathway Exposure Routes
Published in Human and ecological risk assessment (01-01-2011)“…In the event of a chemical terrorist attack on a transportation hub, post-event remediation and restoration activities necessary to attain unrestricted…”
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Journal Article -
20
Automation of a primer design and evaluation pipeline for subsequent sequencing of the coding regions of all human Refseq genes
Published in Bioinformation (01-01-2012)“…Screening for mutations in human disease-causing genes in a molecular diagnostic environment demands simplicity with a view to allowing high throughput…”
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Journal Article