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J A Phillips

Showing results (121-130 of 255) with videos related to

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Endocrine Journal|June 11, 2002
Screening for mutations in the GH-1 gene by dideoxy fingerprinting (ddF)I Miyata, Y Eto, T Kamijo, et al.
Clinical Endocrinology|August 1, 1987
Growth hormone blocking antibodies in a patient with deletion of the GH-N geneS Schwarz, P Berger, H Frisch, et al.
Gene Therapy|October 22, 2004
siRNA therapeutics: big potential from small RNAsR C C Ryther, A S Flynt, J A Phillips, et al.
Gene|October 27, 1995
Isolation, characterization and chromosomal localization of a human pseudogene for hexokinase IIH Ardehali, R L Printz, S Koch, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 1, 1988
Molecular basis of human growth hormone gene deletionsC L Vnencak-Jones, J A Phillips, E Y Chen, et al.
The Journal of Pharmacy and Pharmacology|September 1, 1985
Highly potent inhibition of prostaglandin 15-hydroxydehydrogenase in-vitro and of prostaglandin inactivation in perfused lung by the new azobenzene analogue, Ph CL 28AC N Berry, J R Hoult, J A Phillips, et al.
Biotechniques|September 1, 1992
Utility of internal markers to improve the accuracy of cystic fibrosis genotype analysisS Raskin, J A Phillips, C Vnencak-Jones, et al.
The Journal of Clinical Endocrinology and Metabolism|November 1, 1994
Familial growth hormone deficiency: a model of dominant and recessive mutations affecting a monomeric proteinJ D Cogan, J A Phillips, S S Schenkman, et al.
Chest|July 14, 2001
Idiopathic pulmonary fibrosis can be an autosomal dominant trait in some familiesA Marney, K B Lane, J A Phillips, et al.
American Journal of Medical Genetics|November 7, 1998
Familial growth hormone deficiency associated with MRI abnormalitiesJ Hamilton, D Chitayat, S Blaser, et al.
Pageof 26

Showing results (121-130 of 255) with videos related to

Sort By:
Pageof 26
Endocrine Journal|June 11, 2002
Screening for mutations in the GH-1 gene by dideoxy fingerprinting (ddF)I Miyata, Y Eto, T Kamijo, et al.
Clinical Endocrinology|August 1, 1987
Growth hormone blocking antibodies in a patient with deletion of the GH-N geneS Schwarz, P Berger, H Frisch, et al.
Gene Therapy|October 22, 2004
siRNA therapeutics: big potential from small RNAsR C C Ryther, A S Flynt, J A Phillips, et al.
Gene|October 27, 1995
Isolation, characterization and chromosomal localization of a human pseudogene for hexokinase IIH Ardehali, R L Printz, S Koch, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 1, 1988
Molecular basis of human growth hormone gene deletionsC L Vnencak-Jones, J A Phillips, E Y Chen, et al.
The Journal of Pharmacy and Pharmacology|September 1, 1985
Highly potent inhibition of prostaglandin 15-hydroxydehydrogenase in-vitro and of prostaglandin inactivation in perfused lung by the new azobenzene analogue, Ph CL 28AC N Berry, J R Hoult, J A Phillips, et al.
Biotechniques|September 1, 1992
Utility of internal markers to improve the accuracy of cystic fibrosis genotype analysisS Raskin, J A Phillips, C Vnencak-Jones, et al.
The Journal of Clinical Endocrinology and Metabolism|November 1, 1994
Familial growth hormone deficiency: a model of dominant and recessive mutations affecting a monomeric proteinJ D Cogan, J A Phillips, S S Schenkman, et al.
Chest|July 14, 2001
Idiopathic pulmonary fibrosis can be an autosomal dominant trait in some familiesA Marney, K B Lane, J A Phillips, et al.
American Journal of Medical Genetics|November 7, 1998
Familial growth hormone deficiency associated with MRI abnormalitiesJ Hamilton, D Chitayat, S Blaser, et al.
Pageof 26