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C B Whitley

Showing results (21-30 of 58) with videos related to

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The Journal of Pediatrics|April 1, 1983
Warburg syndrome: lethal neurodysplasia with autosomal recessive inheritanceC B Whitley, T R Thompson, A R Mastri, et al.
American Journal of Human Genetics|March 1, 1995
Molecular diagnosis of mucopolysaccharidosis type II (Hunter syndrome) by automated sequencing and computer-assisted interpretation: toward mutation mapping of the iduronate-2-sulfatase geneJ J Jonsson, E L Aronovich, S E Braun, et al.
Human Molecular Genetics|December 1, 1992
Mutation R468W of the iduronate-2-sulfatase gene in mild Hunter syndrome (mucopolysaccharidosis type II) confirmed by in vitro mutagenesis and expressionP L Crotty, S E Braun, R A Anderson, et al.
Genomics|June 21, 2001
Molecular basis of mucopolysaccharidosis type IIIB in emu (Dromaius novaehollandiae): an avian model of Sanfilippo syndrome type BE L Aronovich, J M Johnston, P Wang, et al.
Molecular Genetics and Metabolism Reports|February 15, 2020
Response to: Investigating the neurobehavioral symptoms of neuronopathic Hunter syndromeJ B Eisengart, K E King, E Shapiro, et al.
Transfusion|July 1, 1997
Retroviral transduction of peripheral blood leukocytes in a hollow-fiber bioreactorR Shankar, C B Whitley, D Pan, et al.
Molecular Genetics and Metabolism|August 5, 2000
"Supercharged Cells" for delivery of recombinant human iduronate-2-sulfataseD Pan, J J Jonsson, S E Braun, et al.
Human Pathology|March 1, 1994
Light and electron microscopic features of the liver in mucopolysaccharidosisJ M Resnick, C B Whitley, A S Leonard, et al.
Cornea|May 1, 1994
Dense peripheral corneal clouding in Scheie syndromeC G Summers, C B Whitley, E J Holland, et al.
Molecular Genetics and Metabolism Reports|January 1, 2020
The nature and impact of neurobehavioral symptoms in neuronopathic Hunter syndromeJ B Eisengart, K E King, E G Shapiro, et al.
Pageof 6

Showing results (21-30 of 58) with videos related to

Sort By:
Pageof 6
The Journal of Pediatrics|April 1, 1983
Warburg syndrome: lethal neurodysplasia with autosomal recessive inheritanceC B Whitley, T R Thompson, A R Mastri, et al.
American Journal of Human Genetics|March 1, 1995
Molecular diagnosis of mucopolysaccharidosis type II (Hunter syndrome) by automated sequencing and computer-assisted interpretation: toward mutation mapping of the iduronate-2-sulfatase geneJ J Jonsson, E L Aronovich, S E Braun, et al.
Human Molecular Genetics|December 1, 1992
Mutation R468W of the iduronate-2-sulfatase gene in mild Hunter syndrome (mucopolysaccharidosis type II) confirmed by in vitro mutagenesis and expressionP L Crotty, S E Braun, R A Anderson, et al.
Genomics|June 21, 2001
Molecular basis of mucopolysaccharidosis type IIIB in emu (Dromaius novaehollandiae): an avian model of Sanfilippo syndrome type BE L Aronovich, J M Johnston, P Wang, et al.
Molecular Genetics and Metabolism Reports|February 15, 2020
Response to: Investigating the neurobehavioral symptoms of neuronopathic Hunter syndromeJ B Eisengart, K E King, E Shapiro, et al.
Transfusion|July 1, 1997
Retroviral transduction of peripheral blood leukocytes in a hollow-fiber bioreactorR Shankar, C B Whitley, D Pan, et al.
Molecular Genetics and Metabolism|August 5, 2000
"Supercharged Cells" for delivery of recombinant human iduronate-2-sulfataseD Pan, J J Jonsson, S E Braun, et al.
Human Pathology|March 1, 1994
Light and electron microscopic features of the liver in mucopolysaccharidosisJ M Resnick, C B Whitley, A S Leonard, et al.
Cornea|May 1, 1994
Dense peripheral corneal clouding in Scheie syndromeC G Summers, C B Whitley, E J Holland, et al.
Molecular Genetics and Metabolism Reports|January 1, 2020
The nature and impact of neurobehavioral symptoms in neuronopathic Hunter syndromeJ B Eisengart, K E King, E G Shapiro, et al.
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