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Y H Fu

Showing results (81-90 of 94) with videos related to

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Neurology|October 1, 1992
Anticipation in myotonic dystrophy. II. Complex relationships between clinical findings and structure of the GCT repeatT Ashizawa, J R Dubel, P W Dunne, et al.
American Journal of Medical Genetics|April 1, 1992
Intragenic probe used for diagnostics in fragile X familiesA J Verkerk, B B deVries, M F Niermeijer, et al.
Zhonghua Liu Xing Bing Xue Za Zhi = Zhonghua Liuxingbingxue Zazhi|May 6, 2023
[Forecasting the burden of disease from diabetes under the scenarios of specific risk factors control in China in 2030]Y H Fu, T L Xu, Z Z Rao, et al.
Science (New York, N.Y.)|April 12, 1996
Positional cloning of the Werner's syndrome geneC E Yu, J Oshima, Y H Fu, et al.
Human Molecular Genetics|April 6, 2000
Genetic localization of an autosomal dominant leukodystrophy mimicking chronic progressive multiple sclerosis to chromosome 5q31C M Coffeen, C E McKenna, A H Koeppen, et al.
European Review for Medical and Pharmacological Sciences|December 2, 2022
Predictive model for deep venous thrombosis caused by closed lower limb fracture after thromboprophylactic treatmentJ Xing, Y-H Fu, Z Song, et al.
Methods and Findings in Experimental and Clinical Pharmacology|October 3, 2009
A novel rat model of chronic heart failure following myocardial infarctionY-H Fu, Q-X Lin, X-H Li, et al.
Molecular Biology Reports|July 16, 2009
Comparison of approaches for efficient gene silencing induced by microRNA-based short hairpin RNA and indicator gene expressionZ X Shan, Q X Lin, C Y Deng, et al.
Neurology|June 11, 2003
PIP2 binding residues of Kir2.1 are common targets of mutations causing Andersen syndromeM R Donaldson, J L Jensen, M Tristani-Firouzi, et al.
Neurology|December 30, 2004
Clinical evaluation of idiopathic paroxysmal kinesigenic dyskinesia: new diagnostic criteriaM K Bruno, M Hallett, K Gwinn-Hardy, et al.
Pageof 10

Showing results (81-90 of 94) with videos related to

Sort By:
Pageof 10
Neurology|October 1, 1992
Anticipation in myotonic dystrophy. II. Complex relationships between clinical findings and structure of the GCT repeatT Ashizawa, J R Dubel, P W Dunne, et al.
American Journal of Medical Genetics|April 1, 1992
Intragenic probe used for diagnostics in fragile X familiesA J Verkerk, B B deVries, M F Niermeijer, et al.
Zhonghua Liu Xing Bing Xue Za Zhi = Zhonghua Liuxingbingxue Zazhi|May 6, 2023
[Forecasting the burden of disease from diabetes under the scenarios of specific risk factors control in China in 2030]Y H Fu, T L Xu, Z Z Rao, et al.
Science (New York, N.Y.)|April 12, 1996
Positional cloning of the Werner's syndrome geneC E Yu, J Oshima, Y H Fu, et al.
Human Molecular Genetics|April 6, 2000
Genetic localization of an autosomal dominant leukodystrophy mimicking chronic progressive multiple sclerosis to chromosome 5q31C M Coffeen, C E McKenna, A H Koeppen, et al.
European Review for Medical and Pharmacological Sciences|December 2, 2022
Predictive model for deep venous thrombosis caused by closed lower limb fracture after thromboprophylactic treatmentJ Xing, Y-H Fu, Z Song, et al.
Methods and Findings in Experimental and Clinical Pharmacology|October 3, 2009
A novel rat model of chronic heart failure following myocardial infarctionY-H Fu, Q-X Lin, X-H Li, et al.
Molecular Biology Reports|July 16, 2009
Comparison of approaches for efficient gene silencing induced by microRNA-based short hairpin RNA and indicator gene expressionZ X Shan, Q X Lin, C Y Deng, et al.
Neurology|June 11, 2003
PIP2 binding residues of Kir2.1 are common targets of mutations causing Andersen syndromeM R Donaldson, J L Jensen, M Tristani-Firouzi, et al.
Neurology|December 30, 2004
Clinical evaluation of idiopathic paroxysmal kinesigenic dyskinesia: new diagnostic criteriaM K Bruno, M Hallett, K Gwinn-Hardy, et al.
Pageof 10