D e Cole - JoVE Visualize

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Connective Tissue Research|January 1, 1989

First identification of a gene defect for hypophosphatasia: evidence that alkaline phosphatase acts in skeletal mineralizationM J Weiss, D E Cole, K Ray, et al.

Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|November 9, 2000

Low glucocorticoid receptor alpha/beta ratio in T-cell lymphoblastic leukemiaC A Longui, A Vottero, P C Adamson, et al.

Pediatric Research|March 1, 1987

Clearance of osteocalcin by peritoneal dialysis in children with end-stage renal diseaseC M Gundberg, R M Hanning, Y A Liu, et al.

Proceedings of the National Academy of Sciences of the United States of America|October 1, 1988

A missense mutation in the human liver/bone/kidney alkaline phosphatase gene causing a lethal form of hypophosphatasiaM J Weiss, D E Cole, K Ray, et al.

American Journal of Human Genetics|March 1, 1995

Mutations in the X-linked E1 alpha subunit of pyruvate dehydrogenase: exon skipping, insertion of duplicate sequence, and missense mutations leading to the deficiency of the pyruvate dehydrogenase complexK Chun, N MacKay, R Petrova-Benedict, et al.

Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.)|January 8, 1998

A cartilage matrix deficiency experimentally induced by vitamin B6 deficiencyP G Massé, I Ziv, D E Cole, et al.

Scandinavian Journal of Clinical and Laboratory Investigation. Supplementum|January 1, 1997

Calcium sensing receptor gene: analysis of polymorphism frequencyL A Rubin, V Peltekova, N Janicic, et al.

Blood|September 1, 1989

Expression of the mdr-1/P-170 gene in patients with acute lymphoblastic leukemiaM L Rothenberg, L A Mickley, D E Cole, et al.

Cancer Chemotherapy and Pharmacology|April 29, 1998

Plasma and cerebrospinal fluid pharmacokinetics of 9-aminocamptothecin (9-AC), irinotecan (CPT-11), and SN-38 in nonhuman primatesS M Blaney, C Takimoto, D J Murry, et al.

Journal of Medical Genetics|June 1, 1997

Metachromatic leucodystrophy in three families from Nova Scotia, Canada: a recurring mutation in the arylsulphatase A geneM B Coulter-Mackie, L Gagnier, M J Beis, et al.

Pageof 13

Showing results (91-100 of 126) with videos related to

Sort By:

Pageof 13

Connective Tissue Research|January 1, 1989

First identification of a gene defect for hypophosphatasia: evidence that alkaline phosphatase acts in skeletal mineralizationM J Weiss, D E Cole, K Ray, et al.

Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|November 9, 2000

Low glucocorticoid receptor alpha/beta ratio in T-cell lymphoblastic leukemiaC A Longui, A Vottero, P C Adamson, et al.

Pediatric Research|March 1, 1987

Clearance of osteocalcin by peritoneal dialysis in children with end-stage renal diseaseC M Gundberg, R M Hanning, Y A Liu, et al.

Proceedings of the National Academy of Sciences of the United States of America|October 1, 1988

A missense mutation in the human liver/bone/kidney alkaline phosphatase gene causing a lethal form of hypophosphatasiaM J Weiss, D E Cole, K Ray, et al.

American Journal of Human Genetics|March 1, 1995

Mutations in the X-linked E1 alpha subunit of pyruvate dehydrogenase: exon skipping, insertion of duplicate sequence, and missense mutations leading to the deficiency of the pyruvate dehydrogenase complexK Chun, N MacKay, R Petrova-Benedict, et al.

Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.)|January 8, 1998

A cartilage matrix deficiency experimentally induced by vitamin B6 deficiencyP G Massé, I Ziv, D E Cole, et al.

Scandinavian Journal of Clinical and Laboratory Investigation. Supplementum|January 1, 1997

Calcium sensing receptor gene: analysis of polymorphism frequencyL A Rubin, V Peltekova, N Janicic, et al.

Blood|September 1, 1989

Expression of the mdr-1/P-170 gene in patients with acute lymphoblastic leukemiaM L Rothenberg, L A Mickley, D E Cole, et al.

Cancer Chemotherapy and Pharmacology|April 29, 1998

Plasma and cerebrospinal fluid pharmacokinetics of 9-aminocamptothecin (9-AC), irinotecan (CPT-11), and SN-38 in nonhuman primatesS M Blaney, C Takimoto, D J Murry, et al.

Journal of Medical Genetics|June 1, 1997

Metachromatic leucodystrophy in three families from Nova Scotia, Canada: a recurring mutation in the arylsulphatase A geneM B Coulter-Mackie, L Gagnier, M J Beis, et al.

Pageof 13