Search Results - "Hansen, N. T."
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Generating Genome-Scale Candidate Gene Lists for Pharmacogenomics
Published in Clinical pharmacology and therapeutics (01-08-2009)“…A critical task in pharmacogenomics is identifying genes that may be important modulators of drug response. High‐throughput experimental methods are often…”
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X linked cone-rod dystrophy, CORDX3, is caused by a mutation in the CACNA1F gene
Published in Journal of medical genetics (01-08-2006)“…Background: X linked cone-rod dystrophy (CORDX) is a recessive retinal disease characterised by progressive dysfunction of photoreceptors. It is genetically…”
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3
Atomic-Scale Visualization of Inertial Dynamics
Published in Science (American Association for the Advancement of Science) (15-04-2005)“…The motion of atoms on interatomic potential energy surfaces is fundamental to the dynamics of liquids and solids. An accelerator-based source of femtosecond…”
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4
Management of trees in northern Ghana—when the approach of development organizations contradicts local practices
Published in Forests, trees and livelihoods (01-12-2012)“…This study documents the local use and management of trees in two communities in northern Ghana and compares this with development strategies. Information…”
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Channeling Vision: CaV1.4—A Critical Link in Retinal Signal Transmission
Published in BioMed research international (2018)“…Voltage-gated calcium channels (VGCC) are key to many biological functions. Entry of Ca2+ into cells is essential for initiating or modulating important…”
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Angular distribution of electron temperature and density in a laser-ablation plume
Published in Physical review letters (24-04-2000)“…The angular distribution of electron temperature and density in a laser-ablation plume has been studied for the first time. The electron temperature ranges…”
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Studies of resolidification of non-thermally molten InSb using time-resolved X-ray diffraction
Published in Applied physics. A, Materials science & processing (01-10-2005)“…We have used time-resolved X-ray diffraction to monitor the resolidification process of molten InSb. Melting was induced by an ultra-short laser pulse and the…”
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Observation of structural anisotropy and the onset of liquidlike motion during the nonthermal melting of InSb
Published in Physical review letters (16-09-2005)“…The melting dynamics of laser excited InSb have been studied with femtosecond x-ray diffraction. These measurements observe the delayed onset of diffusive…”
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Antifreeze Protein Modulates Cell Survival During Cryopreservation: Mediation through Influence on Ice Crystal Growth
Published in Proceedings of the National Academy of Sciences - PNAS (01-10-1992)“…Antifreeze proteins (AFPs) are extremely efficient at inhibiting ice recrystallization in frozen solutions. Knight and Duman [Knight, C. A. \& Duman, J. G…”
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Rapid Detection of Microorganisms in Blood Cultures of Newborn Infants Utilizing an Automated Blood Culture System
Published in Pediatrics (Evanston) (01-03-2000)“…Neonatal sepsis is a low incidence, high-risk disease with many sepsis work-ups performed to detect a single case. Seventy-two hours of antibiotic therapy have…”
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Antenatal steroids are associated with less need for blood pressure support in extremely premature infants
Published in Pediatrics (Evanston) (01-06-1995)“…To determine if antenatal steroids decrease the amount of blood pressure support required by extremely premature infants between 23 and 27 weeks' gestation…”
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Cone dystrophy and ectopic synaptogenesis in a Cacna1f loss of function model of congenital stationary night blindness (CSNB2A)
Published in Channels (Austin, Tex.) (01-01-2018)“…Congenital stationary night blindness 2A (CSNB2A) is an X-linked retinal disorder, characterized by phenotypically variable signs and symptoms of impaired…”
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A summary of 20 CACNA1F mutations identified in 36 families with incomplete X-linked congenital stationary night blindness, and characterization of splice variants
Published in Human genetics (01-02-2001)“…Incomplete X-linked congenital stationary night blindness (CSNB) is a recessive, non-progressive eye disorder characterized by abnormal electroretinogram and…”
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Is chronic lung disease in low birth weight infants preventable? A survey of eight centers
Published in Pediatrics (Evanston) (1987)“…Chronic lung disease in prematurely born infants, defined as the need for increased inspired oxygen at 28 days of age, was thought to be more common in some…”
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Localization of a gene for incomplete X-linked congenital stationary night blindness to the interval between DXS6849 and DXS8023 in Xp11.23
Published in Human genetics (01-08-1998)“…Congenital stationary night blindness (CSNB) is a nonprogressive retinal disorder characterized by night blindness, nystagmus, myopia, a variable decrease in…”
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Evolution of the plasma parameters in the expanding laser ablation plume of silver
Published in Applied surface science (28-01-2002)“…The angular and radial variation of the ion density and electron temperature in the plasma plume produced by laser ablation of silver at fluences of 0.8–1.3 J…”
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Increases in lung tissue expression of intercellular adhesion molecule-1 are associated with hyperoxic lung injury and inflammation in mice
Published in American journal of respiratory cell and molecular biology (01-10-1993)“…Lung injury caused by breathing enriched oxygen continues to be a major problem in clinical medicine. Experimentally, hyperoxic lung injury is characterized by…”
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Evidence for Genetic Heterogeneity in X-Linked Congenital Stationary Night Blindness
Published in American journal of human genetics (01-04-1998)“…X-linked congenital stationary night blindness (CSNB) is a nonprogressive retinal disorder characterized by disturbed or absent night vision; its clinical…”
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Oxidant stress responses in premature infants during exposure to hyperoxia
Published in Pediatric research (01-09-1993)“…To assess oxidant stress responses in newborn infants treated with elevated concentrations of oxygen, we measured plasma concentrations of glutathione (GSH)…”
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Congenital stationary night blindness in mice - a tale of two Cacna1f mutants
Published in Advances in experimental medicine and biology (01-01-2010)“…Mutations in CACNA1F, which encodes the Ca(v)1.4 subunit of a voltage-gated L-type calcium channel, cause X-linked incomplete congenital stationary night…”
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