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Clinica Chimica Acta; International Journal of Clinical Chemistry
|
June 15, 1992
Abnormal lysosomal cathepsin activities in leukocytes and cultured skin fibroblasts in late infantile, but not in juvenile neuronal ceroid-lipofuscinosis (Batten disease)
M J Bennett, L Chern, K H Carpenter, et al.
Gene Therapy
|
October 11, 2013
AAV-encoded OTC activity persisting to adulthood following delivery to newborn spf(ash) mice is insufficient to prevent shRNA-induced hyperammonaemia
S C Cunningham, C Y Kok, A Spinoulas, et al.
Biochemical Society Transactions
|
December 1, 1990
Ceroid, macrophages and atherosclerosis
M J Mitchinson, R Y Ball, K H Carpenter, et al.
The Journal of Pediatrics
|
December 1, 1992
A fatal neonatal case of medium-chain acyl-coenzyme A dehydrogenase deficiency with homozygous A-->G985 transition
K C Leung, J W Hammond, S Chabra, et al.
Gene Therapy
|
April 10, 2009
In vivo assessment of mutations in OTC for dominant-negative effects following rAAV2/8-mediated gene delivery to the mouse liver
S L Ginn, S C Cunningham, M Zheng, et al.
Pediatric Research
|
July 1, 1990
D(+)-glyceric aciduria: etiology and clinical consequences
J R Bonham, T J Stephenson, K H Carpenter, et al.
Annals of Clinical Biochemistry
|
March 1, 1994
Quality assessment of urinary organic acid analysis
J R Bonham, M Downing, R J Pollitt, et al.
Prenatal Diagnosis
|
June 1, 1994
Prenatal diagnosis of glutathione synthase deficiency
N J Manning, N P Davies, S E Olpin, et al.
Brain & Development
|
January 1, 1990
Abnormalities of carbohydrate metabolism and of OCT gene function in the Rett syndrome
A Clarke, D Gardner-Medwin, J Richardson, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 19) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 19 results.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
June 15, 1992
Abnormal lysosomal cathepsin activities in leukocytes and cultured skin fibroblasts in late infantile, but not in juvenile neuronal ceroid-lipofuscinosis (Batten disease)
M J Bennett, L Chern, K H Carpenter, et al.
Gene Therapy
|
October 11, 2013
AAV-encoded OTC activity persisting to adulthood following delivery to newborn spf(ash) mice is insufficient to prevent shRNA-induced hyperammonaemia
S C Cunningham, C Y Kok, A Spinoulas, et al.
Biochemical Society Transactions
|
December 1, 1990
Ceroid, macrophages and atherosclerosis
M J Mitchinson, R Y Ball, K H Carpenter, et al.
The Journal of Pediatrics
|
December 1, 1992
A fatal neonatal case of medium-chain acyl-coenzyme A dehydrogenase deficiency with homozygous A-->G985 transition
K C Leung, J W Hammond, S Chabra, et al.
Gene Therapy
|
April 10, 2009
In vivo assessment of mutations in OTC for dominant-negative effects following rAAV2/8-mediated gene delivery to the mouse liver
S L Ginn, S C Cunningham, M Zheng, et al.
Pediatric Research
|
July 1, 1990
D(+)-glyceric aciduria: etiology and clinical consequences
J R Bonham, T J Stephenson, K H Carpenter, et al.
Annals of Clinical Biochemistry
|
March 1, 1994
Quality assessment of urinary organic acid analysis
J R Bonham, M Downing, R J Pollitt, et al.
Prenatal Diagnosis
|
June 1, 1994
Prenatal diagnosis of glutathione synthase deficiency
N J Manning, N P Davies, S E Olpin, et al.
Brain & Development
|
January 1, 1990
Abnormalities of carbohydrate metabolism and of OCT gene function in the Rett syndrome
A Clarke, D Gardner-Medwin, J Richardson, et al.
Page
of 2