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Showing results (631-640 of 1,225) with videos related to

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Annals of the New York Academy of Sciences|January 1, 1986
Evidence against linkage of von Recklinghausen neurofibromatosis and chromosome 19 markersS M Huson, A L Meredith, M Sarfarazi, et al.
Thorax|May 1, 1994
Effect of increasing doses of beta agonists on spirometric parameters, exercise capacity, and quality of life in patients with chronic airflow limitationR Jaeschke, G H Guyatt, A Willan, et al.
Archives of Disease in Childhood|September 1, 1994
De novo facioscapulohumeral muscular dystrophy defined by DNA probe p13E-11 (D4F104S1)P E Jardine, M C Koch, P W Lunt, et al.
Muscle & Nerve. Supplement|January 1, 1995
Phenotypic-genotypic correlation will assist genetic counseling in 4q35-facioscapulohumeral muscular dystrophyP W Lunt, P E Jardine, M Koch, et al.
Methods in Molecular Biology (Clifton, N.J.)|September 21, 2013
Imaging tools for analysis of the ureteric tree in the developing mouse kidneyLuise A Cullen-McEwen, Richard J Young, Gabriel Fricout, et al.
IEEE Transactions on Bio-Medical Engineering|January 22, 2015
A Device for Human Ultrasonic EcholocationJascha Sohl-Dickstein, Santani Teng, Benjamin M Gaub, et al.
The Biochemical Journal|June 15, 1992
Correction of human mucopolysaccharidosis type-VI fibroblasts with recombinant N-acetylgalactosamine-4-sulphataseD S Anson, J A Taylor, J Bielicki, et al.
Human Molecular Genetics|August 11, 1999
Aberrant interactions of transcriptional repressor proteins with the Huntington's disease gene product, huntingtinJ M Boutell, P Thomas, J W Neal, et al.
RNA Biology|August 22, 2019
The VEGF-A exon 8 splicing-sensitive fluorescent reporter mouse is a novel tool to assess the effects of splicing regulatory compounds <i>in vivo</i>M Stevens, E Star, M Lee, et al.
Muscle & Nerve. Supplement|April 12, 2013
Phenotypic-genotypic correlation will assist genetic counseling in 4q35-facioscapulohumeral muscular dystrophyP W Lunt, P E Jardine, M Koch, et al.
Pageof 123

Showing results (631-640 of 1,225) with videos related to

Sort By:
Pageof 123
Annals of the New York Academy of Sciences|January 1, 1986
Evidence against linkage of von Recklinghausen neurofibromatosis and chromosome 19 markersS M Huson, A L Meredith, M Sarfarazi, et al.
Thorax|May 1, 1994
Effect of increasing doses of beta agonists on spirometric parameters, exercise capacity, and quality of life in patients with chronic airflow limitationR Jaeschke, G H Guyatt, A Willan, et al.
Archives of Disease in Childhood|September 1, 1994
De novo facioscapulohumeral muscular dystrophy defined by DNA probe p13E-11 (D4F104S1)P E Jardine, M C Koch, P W Lunt, et al.
Muscle & Nerve. Supplement|January 1, 1995
Phenotypic-genotypic correlation will assist genetic counseling in 4q35-facioscapulohumeral muscular dystrophyP W Lunt, P E Jardine, M Koch, et al.
Methods in Molecular Biology (Clifton, N.J.)|September 21, 2013
Imaging tools for analysis of the ureteric tree in the developing mouse kidneyLuise A Cullen-McEwen, Richard J Young, Gabriel Fricout, et al.
IEEE Transactions on Bio-Medical Engineering|January 22, 2015
A Device for Human Ultrasonic EcholocationJascha Sohl-Dickstein, Santani Teng, Benjamin M Gaub, et al.
The Biochemical Journal|June 15, 1992
Correction of human mucopolysaccharidosis type-VI fibroblasts with recombinant N-acetylgalactosamine-4-sulphataseD S Anson, J A Taylor, J Bielicki, et al.
Human Molecular Genetics|August 11, 1999
Aberrant interactions of transcriptional repressor proteins with the Huntington's disease gene product, huntingtinJ M Boutell, P Thomas, J W Neal, et al.
RNA Biology|August 22, 2019
The VEGF-A exon 8 splicing-sensitive fluorescent reporter mouse is a novel tool to assess the effects of splicing regulatory compounds <i>in vivo</i>M Stevens, E Star, M Lee, et al.
Muscle & Nerve. Supplement|April 12, 2013
Phenotypic-genotypic correlation will assist genetic counseling in 4q35-facioscapulohumeral muscular dystrophyP W Lunt, P E Jardine, M Koch, et al.
Pageof 123