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69篇 您的检索式:作者名="Ophoff"
    题名 作者 年代 出处 被引量
1A new approach for fuel injection into a solar receiver/ reactor:Numerical and experimental investigation显示文摘An innovative and efficient design of solar receivers/reactors can enhance the production of clean fuels via concentrated solar energy.This study presents a new jet-type burner nozzle for gaseous feedstock injection into a cavity solar receiver inspired from the combustion technology.The nozzle design was adapted from a combustion burner and successfully implemented into a solar receiver and studied the influence of the nozzle design on the fluid mixing and temperature distribution inside the solar receiver using a 7 kW solar simulator and nitrogen as working fluid.Finally,a thorough computational fluid dynamics (CFD) analysis was performed and validated against the experimental results.The CFD results showed a variation of the gas flow pattern and gas mixing after the burner nozzle adaptation,which resulted an intense effect on the heat transfer inside the solar receiver.M Helal Uddin Nesrin Ozalp Jens Heylen Cedric Ophoff 2018Frontiers of Chemical Science and Engineering2018,12,4:2
2A modified four- vessel occlusion model for inducing in complete forebrain ischemia in rats 显示文摘Schmidt-Kastner R Paschen W Ophoff B G 1989Stroke1989,20,7:1
3Common variants confer- ring risk of schizophrenia 显示文摘Stefansson H Ophoff RA Stacy S 2009Nature2009,460,7256:1
4Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+channel gene CACNL1A4显示文摘Ophoff RA Terwindt GM Vergouwe MN 1996Cell1996,87,3:1
5Common variants con- ferring risk of schizophrenia 显示文摘Stefansson H Ophoff RA Steinberg S 2009Nature2009,460,7256:1
6Familial hemilegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNLI A4显示文摘 Terwindt GM Vergouwe MN 1996Cell1996,57,:1
7Sex steroids during bone growth:a comparative study between mouse models for hypogonadal and senile osteoporosis显示文摘Ophoff J Venken K Callewaert F 0,,10:1
8A modified fourvessel occlusion model fur inducing incomplete furebrain ischemia in rats显示文摘Schmidt-Kastner R Paschen W Ophoff BG 1989Stroke1989,20,7:1
9Common variants conferring risk of schizophrenia 显示文摘Stefansson H Ophoff RA Steinberg S 2009Nature2009,460,7256:1
10A modifi- ed four-vessel occlusion model for inducing incomplete forebrain ischemia in rats显示文摘Schmidt-Kastner R Paschen W Ophoff B G 1989Stroke1989,20,7:1
11Familial bemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2 + channel gene CACNL1A4显示文摘Ophoff RA 1996Cell1996,87,3:1
12Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2~ channel gene CACNL1A4显示文摘Ophoff RA Terwindt GM Vergouwe MN 1996Cell1996,87,3:1
13A modified four - vesselocclusion model for inducing in complete forebrain ischemia in- rats显示文摘Schmidt - Kastner R Paschen W Ophoff BG 1989Stroke1989,20,7:1
14A modified four-vessel occlusion model for indu-cing in complete forebrain ischemia in rats显示文摘SCHMIDT-KASTNER R PASCHEN W OPHOFF B G 1989Stroke1989,20,:1
15Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca^2+ channel gene显示文摘Ophoff RA Terwindt GM Vergouwe MN 1996CACNLIA4 Ce111996,87,3:1
16Common variants conferring risk of schizophrenia显示文摘Stefansson H Ophoff R A Steinberg S 2009Nature2009,460,7256:1
17Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca^2+ channel gene CACNL1A4显示文摘Ophoff RA Terwindt GM Vergouwe MN 1996Cell1996,87,3:1
18Clinical and genetic analysis of a large Dutch family with autosomal dominant vascular retinopathy,migraine and Raynaud's phenomenon显示文摘GM Terwindt J Haan RA Ophoff SM Groenen CW Storimans JB Lanser RA Roos EM Bleeker-Wagemakers RR Frants and MD Ferrari 1998Brain Vol 121 Issue 2:303-3161998,,:1
19Elektronikschrott-Anforderungen an eine Entsorgung im Sinne der Schliessung von Stoffkreisl? ufen (electronics scrap-requirements of disposal in a sense of a closed-loop life circle) 显示文摘 Gruber M F 1995Abfallwirtschafts Journal1995,12,:1
20Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutation in the Ca2 + channel' gene CACNA1A 显示文摘Ophoff R A Terwindt G M Vergouwe M N 1996Cell1996,87,3:1
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