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D E Cole

Showing results (121-130 of 162) with videos related to

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Genetics|July 2, 1999
Spatial and temporal distribution of the neutral polymorphisms in the last ZFX intron: analysis of the haplotype structure and genealogyJ Jaruzelska, E Zietkiewicz, M Batzer, et al.
The New England Journal of Medicine|April 10, 1986
Increased serum pyridoxal-5'-phosphate in pseudohypophosphatasiaD E Cole, S R Salisbury, R A Stinson, et al.
The Journal of Clinical Investigation|April 15, 1997
Markedly reduced activity of mutant calcium-sensing receptor with an inserted Alu element from a kindred with familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidismM Bai, N Janicic, S Trivedi, et al.
Kidney International|March 1, 1990
Glucocorticoid-induced polycystic kidney disease--a threshold traitA T McDonald, J F Crocker, S C Digout, et al.
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.
Journal of the American Society of Nephrology : JASN|April 1, 1996
Thyroid hormone modulation of glucocorticoid-induced polycystic kidney diseaseJ F Crocker, M E Schenk, D A Hamilton, 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.
Pageof 17

Showing results (121-130 of 162) with videos related to

Sort By:
Pageof 17
Genetics|July 2, 1999
Spatial and temporal distribution of the neutral polymorphisms in the last ZFX intron: analysis of the haplotype structure and genealogyJ Jaruzelska, E Zietkiewicz, M Batzer, et al.
The New England Journal of Medicine|April 10, 1986
Increased serum pyridoxal-5'-phosphate in pseudohypophosphatasiaD E Cole, S R Salisbury, R A Stinson, et al.
The Journal of Clinical Investigation|April 15, 1997
Markedly reduced activity of mutant calcium-sensing receptor with an inserted Alu element from a kindred with familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidismM Bai, N Janicic, S Trivedi, et al.
Kidney International|March 1, 1990
Glucocorticoid-induced polycystic kidney disease--a threshold traitA T McDonald, J F Crocker, S C Digout, et al.
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.
Journal of the American Society of Nephrology : JASN|April 1, 1996
Thyroid hormone modulation of glucocorticoid-induced polycystic kidney diseaseJ F Crocker, M E Schenk, D A Hamilton, 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.
Pageof 17