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B W Uhlendorf

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Cell Differentiation|August 1, 1985
The differentiation of L5/A10 myoblast cell line (a subclone of L5 line) is controlled by changes of culture conditionsS Scarpa, B W Uhlendorf, G L Cantoni
The Journal of Clinical Investigation|March 1, 1970
A defect in pyruvate decarboxylase in a child with an intermittent movement disorderJ P Blass, J Avigan, B W Uhlendorf
Science (New York, N.Y.)|April 9, 1971
Fabry's disease: antenatal detectionR O Brady, B W Uhlendorf, C B Jacobson
Pediatric Research|July 1, 1973
Homocystinuria: studies in tissue cultureB W Uhlendorf, E B Conerly, S H Mudd
Biochemical Medicine|November 1, 1970
Deranged B 12 metabolism: studies of fibroblasts grown in tissue cultureS H Mudd, B W Uhlendorf, K R Hinds
The American Journal of Medicine|October 1, 1971
Identification of heterozygous carriers of lipid storage diseases. Current status and clinical applicationsR O Brady, W G Johnson, B W Uhlendorf
Lancet (London, England)|June 19, 1971
Intermittent ataxia with pyruvate-decarboxylase deficiencyJ P Blass, D Lonsdale, B W Uhlendorf, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|January 6, 1975
Cystathioninuria and homocystinuriaH L Levy, S H Mudd, B W Uhlendorf, et al.
Biochemical and Biophysical Research Communications|July 16, 1971
Defective metabolism of vitamin B 12 in fibroblasts from children with methylmalonicaciduriaM J Mahoney, L E Rosenberg, S H Mudd, et al.
Pediatric Research|March 1, 1976
Cobalamins in fibroblasts cultured from normal control subjects and patients with methylmalonic aciduriaJ C Linnell, D M Matthews, S H Mudd, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Cell Differentiation|August 1, 1985
The differentiation of L5/A10 myoblast cell line (a subclone of L5 line) is controlled by changes of culture conditionsS Scarpa, B W Uhlendorf, G L Cantoni
The Journal of Clinical Investigation|March 1, 1970
A defect in pyruvate decarboxylase in a child with an intermittent movement disorderJ P Blass, J Avigan, B W Uhlendorf
Science (New York, N.Y.)|April 9, 1971
Fabry's disease: antenatal detectionR O Brady, B W Uhlendorf, C B Jacobson
Pediatric Research|July 1, 1973
Homocystinuria: studies in tissue cultureB W Uhlendorf, E B Conerly, S H Mudd
Biochemical Medicine|November 1, 1970
Deranged B 12 metabolism: studies of fibroblasts grown in tissue cultureS H Mudd, B W Uhlendorf, K R Hinds
The American Journal of Medicine|October 1, 1971
Identification of heterozygous carriers of lipid storage diseases. Current status and clinical applicationsR O Brady, W G Johnson, B W Uhlendorf
Lancet (London, England)|June 19, 1971
Intermittent ataxia with pyruvate-decarboxylase deficiencyJ P Blass, D Lonsdale, B W Uhlendorf, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|January 6, 1975
Cystathioninuria and homocystinuriaH L Levy, S H Mudd, B W Uhlendorf, et al.
Biochemical and Biophysical Research Communications|July 16, 1971
Defective metabolism of vitamin B 12 in fibroblasts from children with methylmalonicaciduriaM J Mahoney, L E Rosenberg, S H Mudd, et al.
Pediatric Research|March 1, 1976
Cobalamins in fibroblasts cultured from normal control subjects and patients with methylmalonic aciduriaJ C Linnell, D M Matthews, S H Mudd, et al.
Pageof 2