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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 markers
S 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 limitation
R 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 dystrophy
P 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 kidney
Luise A Cullen-McEwen, Richard J Young, Gabriel Fricout, et al.
IEEE Transactions on Bio-Medical Engineering
|
January 22, 2015
A Device for Human Ultrasonic Echolocation
Jascha 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-sulphatase
D 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, huntingtin
J 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 dystrophy
P W Lunt, P E Jardine, M Koch, et al.
Page
of 123
Search research articles
Search
Showing results (631-640 of 1,225) with videos related to
Sort By:
Page
of 123
Annals of the New York Academy of Sciences
|
January 1, 1986
Evidence against linkage of von Recklinghausen neurofibromatosis and chromosome 19 markers
S 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 limitation
R 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 dystrophy
P 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 kidney
Luise A Cullen-McEwen, Richard J Young, Gabriel Fricout, et al.
IEEE Transactions on Bio-Medical Engineering
|
January 22, 2015
A Device for Human Ultrasonic Echolocation
Jascha 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-sulphatase
D 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, huntingtin
J 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 dystrophy
P W Lunt, P E Jardine, M Koch, et al.
Page
of 123