D e Cole - JoVE Visualize

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Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|March 1, 1990

Characterization of immunoglobulin and T-cell receptor gene patterns in B-cell precursor acute lymphoblastic leukemia of childhoodC A Felix, D G Poplack, G H Reaman, et al.

The Journal of Clinical Endocrinology and Metabolism|February 1, 1986

Secretory dysfunction in parathyroid cells from a neonate with severe primary hyperparathyroidismS J Marx, R D Lasker, E M Brown, et al.

American Journal of Medical Genetics|June 28, 1996

Heteroallelic missense mutations of the galactosamine-6-sulfate sulfatase (GALNS) gene in a mild form of Morquio disease (MPS IVA)D E Cole, S Fukuda, B A Gordon, et al.

Lancet (London, England)|February 19, 1999

A986S polymorphism of the calcium-sensing receptor and circulating calcium concentrationsD E Cole, V D Peltekova, L A Rubin, et al.

Cancer Research|February 1, 1989

Phase I and pharmacokinetic evaluation of thiotepa in the cerebrospinal fluid and plasma of pediatric patients: evidence for dose-dependent plasma clearance of thiotepaR L Heideman, D E Cole, F Balis, et al.

Cancer Research|March 1, 1993

Pediatric phase I trial and pharmacokinetic study of topotecan administered as a 24-hour continuous infusionS M Blaney, F M Balis, D E Cole, et al.

The Journal of Clinical Investigation|February 1, 1992

Hereditary and acquired p53 gene mutations in childhood acute lymphoblastic leukemiaC A Felix, M M Nau, T Takahashi, et al.

American Journal of Human Genetics|October 30, 1998

Founder BRCA1 and BRCA2 mutations in French Canadian breast and ovarian cancer familiesP N Tonin, A M Mes-Masson, P A Futreal, et al.

The Journal of Clinical Investigation|August 11, 1992

Absence of hereditary p53 mutations in 10 familial leukemia pedigreesC A Felix, D D'Amico, T Mitsudomi, et al.

The Journal of Pediatrics|November 1, 1989

Effect of high-dose vitamin D supplementation on radiographically detectable bone disease of very low birth weight infantsJ R Evans, A C Allen, D A Stinson, et al.

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Showing results (111-120 of 126) with videos related to

Sort By:

Pageof 13

Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|March 1, 1990

Characterization of immunoglobulin and T-cell receptor gene patterns in B-cell precursor acute lymphoblastic leukemia of childhoodC A Felix, D G Poplack, G H Reaman, et al.

The Journal of Clinical Endocrinology and Metabolism|February 1, 1986

Secretory dysfunction in parathyroid cells from a neonate with severe primary hyperparathyroidismS J Marx, R D Lasker, E M Brown, et al.

American Journal of Medical Genetics|June 28, 1996

Heteroallelic missense mutations of the galactosamine-6-sulfate sulfatase (GALNS) gene in a mild form of Morquio disease (MPS IVA)D E Cole, S Fukuda, B A Gordon, et al.

Lancet (London, England)|February 19, 1999

A986S polymorphism of the calcium-sensing receptor and circulating calcium concentrationsD E Cole, V D Peltekova, L A Rubin, et al.

Cancer Research|February 1, 1989

Phase I and pharmacokinetic evaluation of thiotepa in the cerebrospinal fluid and plasma of pediatric patients: evidence for dose-dependent plasma clearance of thiotepaR L Heideman, D E Cole, F Balis, et al.

Cancer Research|March 1, 1993

Pediatric phase I trial and pharmacokinetic study of topotecan administered as a 24-hour continuous infusionS M Blaney, F M Balis, D E Cole, et al.

The Journal of Clinical Investigation|February 1, 1992

Hereditary and acquired p53 gene mutations in childhood acute lymphoblastic leukemiaC A Felix, M M Nau, T Takahashi, et al.

American Journal of Human Genetics|October 30, 1998

Founder BRCA1 and BRCA2 mutations in French Canadian breast and ovarian cancer familiesP N Tonin, A M Mes-Masson, P A Futreal, et al.

The Journal of Clinical Investigation|August 11, 1992

Absence of hereditary p53 mutations in 10 familial leukemia pedigreesC A Felix, D D'Amico, T Mitsudomi, et al.

The Journal of Pediatrics|November 1, 1989

Effect of high-dose vitamin D supplementation on radiographically detectable bone disease of very low birth weight infantsJ R Evans, A C Allen, D A Stinson, et al.

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