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K D Smith

Showing results (171-180 of 211) with videos related to

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British Journal of Haematology|September 21, 2001
The role of heterocellular hereditary persistence of fetal haemoglobin in beta(0)-thalassaemia intermediaY P Chang, R Littera, R Garau, et al.
Cancer Gene Therapy|August 6, 2005
Ionizing radiation: a genetic switch for cancer therapyJ J Mezhir, K D Smith, M C Posner, et al.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|July 15, 2004
Utilization of commercial laboratory results in management of hyperandrogenism in womenE Steinberger, C Ayala, B Hsi, et al.
American Journal of Human Genetics|January 1, 1981
The molecular basis of hemoglobin GradyA F Scott, J A Phillips, K E Young, et al.
Blood|August 1, 1992
Fetal hemoglobin levels in sickle cell disease and normal individuals are partially controlled by an X-linked gene located at Xp22.2G J Dover, K D Smith, Y C Chang, et al.
Research in Veterinary Science|September 16, 2020
Investigation of fibrillin microfibrils in the canine cruciate ligament in dogs with different predispositions to ligament ruptureT Cox, E J Comerford, M Wegg, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 30, 2000
The repertoire for pattern recognition of pathogens by the innate immune system is defined by cooperation between toll-like receptorsA Ozinsky, D M Underhill, J D Fontenot, et al.
Blood|December 1, 1979
A molecular basis for hemoglobin-H disease in American blacksJ A Phillips, A F Scott, K D Smith, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 19, 1997
A mouse model for X-linked adrenoleukodystrophyJ F Lu, A M Lawler, P A Watkins, et al.
American Journal of Human Genetics|January 1, 1981
Population heterogeneity of the Hpa I restriction site associated with the beta globin gene: implications for prenatal diagnosisS R Panny, A F Scott, K D Smith, et al.
Pageof 22

Showing results (171-180 of 211) with videos related to

Sort By:
Pageof 22
British Journal of Haematology|September 21, 2001
The role of heterocellular hereditary persistence of fetal haemoglobin in beta(0)-thalassaemia intermediaY P Chang, R Littera, R Garau, et al.
Cancer Gene Therapy|August 6, 2005
Ionizing radiation: a genetic switch for cancer therapyJ J Mezhir, K D Smith, M C Posner, et al.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|July 15, 2004
Utilization of commercial laboratory results in management of hyperandrogenism in womenE Steinberger, C Ayala, B Hsi, et al.
American Journal of Human Genetics|January 1, 1981
The molecular basis of hemoglobin GradyA F Scott, J A Phillips, K E Young, et al.
Blood|August 1, 1992
Fetal hemoglobin levels in sickle cell disease and normal individuals are partially controlled by an X-linked gene located at Xp22.2G J Dover, K D Smith, Y C Chang, et al.
Research in Veterinary Science|September 16, 2020
Investigation of fibrillin microfibrils in the canine cruciate ligament in dogs with different predispositions to ligament ruptureT Cox, E J Comerford, M Wegg, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 30, 2000
The repertoire for pattern recognition of pathogens by the innate immune system is defined by cooperation between toll-like receptorsA Ozinsky, D M Underhill, J D Fontenot, et al.
Blood|December 1, 1979
A molecular basis for hemoglobin-H disease in American blacksJ A Phillips, A F Scott, K D Smith, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 19, 1997
A mouse model for X-linked adrenoleukodystrophyJ F Lu, A M Lawler, P A Watkins, et al.
American Journal of Human Genetics|January 1, 1981
Population heterogeneity of the Hpa I restriction site associated with the beta globin gene: implications for prenatal diagnosisS R Panny, A F Scott, K D Smith, et al.
Pageof 22