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P Clayton

Showing results (71-80 of 189) with videos related to

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Journal of Inherited Metabolic Disease|January 14, 1998
A case of the carbohydrate-deficient glycoprotein syndrome type 1 (CDGS type 1) with normal phosphomannomutase activityJ Charlwood, P Clayton, A Johnson, et al.
The Journal of Nervous and Mental Disease|May 1, 1983
Facial electromyography and reactivity in depressionR M Carney, B A Hong, J Brim, et al.
Modern Veterinary Practice|September 1, 1984
Slaughter weight loss attributable to pregnancy in feedlot heifersB W Bennett, R P Clayton, R L Cravens, et al.
Human Immunology|April 25, 2020
Development of de novo HLA donor specific antibodies (HLA-DSA), HLA antibodies (HLA-Ab) and allograft rejection post blood transfusion in kidney transplant recipientsM Jalalonmuhali, R P Carroll, E Tsiopelas, et al.
The Biochemical Journal|October 5, 2001
Congenital disorders of glycosylation type I leads to altered processing of N-linked glycans, as well as underglycosylationP Mills, K Mills, P Clayton, et al.
Proceedings. Symposium on Computer Applications in Medical Care|January 1, 1995
Using intermediate states to improve the ability of the Arden Syntax to implement care plans and reuse knowledgeE H Sherman, G Hripcsak, J Starren, et al.
Experimental Cell Research|April 1, 1975
Chromosomal localisation of DNA sequences in condensed and dispersed human chromatinJ R Gosden, R A Buckland, R P Clayton, et al.
Meat Science|November 9, 2011
The vital role of science in global policy decision-making: An analysis of past, current, and forecasted trends and issues in global red meat trade and policyK R Smith, P Clayton, B Stuart, et al.
Prenatal Diagnosis|August 26, 1998
Prenatal diagnosis of the carbohydrate-deficient glycoprotein syndrome type 1A (CDG1A) by a combination of enzymology and genetic linkage analysis after amniocentesis or chorionic villus samplingJ Charlwood, P Clayton, G Keir, et al.
Lancet (London, England)|April 10, 1993
Carbohydrate-deficient glycoprotein syndrome: normal glycosylation in the fetusP Clayton, B Winchester, E Di Tomaso, et al.
Pageof 19

Showing results (71-80 of 189) with videos related to

Sort By:
Pageof 19
Journal of Inherited Metabolic Disease|January 14, 1998
A case of the carbohydrate-deficient glycoprotein syndrome type 1 (CDGS type 1) with normal phosphomannomutase activityJ Charlwood, P Clayton, A Johnson, et al.
The Journal of Nervous and Mental Disease|May 1, 1983
Facial electromyography and reactivity in depressionR M Carney, B A Hong, J Brim, et al.
Modern Veterinary Practice|September 1, 1984
Slaughter weight loss attributable to pregnancy in feedlot heifersB W Bennett, R P Clayton, R L Cravens, et al.
Human Immunology|April 25, 2020
Development of de novo HLA donor specific antibodies (HLA-DSA), HLA antibodies (HLA-Ab) and allograft rejection post blood transfusion in kidney transplant recipientsM Jalalonmuhali, R P Carroll, E Tsiopelas, et al.
The Biochemical Journal|October 5, 2001
Congenital disorders of glycosylation type I leads to altered processing of N-linked glycans, as well as underglycosylationP Mills, K Mills, P Clayton, et al.
Proceedings. Symposium on Computer Applications in Medical Care|January 1, 1995
Using intermediate states to improve the ability of the Arden Syntax to implement care plans and reuse knowledgeE H Sherman, G Hripcsak, J Starren, et al.
Experimental Cell Research|April 1, 1975
Chromosomal localisation of DNA sequences in condensed and dispersed human chromatinJ R Gosden, R A Buckland, R P Clayton, et al.
Meat Science|November 9, 2011
The vital role of science in global policy decision-making: An analysis of past, current, and forecasted trends and issues in global red meat trade and policyK R Smith, P Clayton, B Stuart, et al.
Prenatal Diagnosis|August 26, 1998
Prenatal diagnosis of the carbohydrate-deficient glycoprotein syndrome type 1A (CDG1A) by a combination of enzymology and genetic linkage analysis after amniocentesis or chorionic villus samplingJ Charlwood, P Clayton, G Keir, et al.
Lancet (London, England)|April 10, 1993
Carbohydrate-deficient glycoprotein syndrome: normal glycosylation in the fetusP Clayton, B Winchester, E Di Tomaso, et al.
Pageof 19