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K Delgrosso

Showing results (11-20 of 16) with videos related to

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Physiological Genomics|August 31, 2006
Transcriptional regulatory network analysis of developing human erythroid progenitors reveals patterns of coregulation and potential transcriptional regulatorsM A Keller, S Addya, R Vadigepalli, et al.
Biochemistry|February 6, 1990
Organization of the gene for platelet glycoprotein IIbR Heidenreich, R Eisman, S Surrey, et al.
European Journal of Human Genetics : EJHG|November 28, 2000
Simple two-color array-based approach for mutation detectionP Fortina, K Delgrosso, T Sakazume, et al.
Blood|June 1, 1994
Interaction of rare illegitimate recombination event and a poly A addition site mutation resulting in a severe form of alpha thalassemiaP Fortina, T Parrella, M Sartore, et al.
Blood|February 1, 1990
The -175T----C mutation increases promoter strength in erythroid cells: correlation with evolutionary conservation of binding sites for two trans-acting factorsD L Gumucio, W K Lockwood, J L Weber, et al.
Human Molecular Genetics|September 1, 1997
Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in MediterraneansL Zelante, P Gasparini, X Estivill, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
Physiological Genomics|August 31, 2006
Transcriptional regulatory network analysis of developing human erythroid progenitors reveals patterns of coregulation and potential transcriptional regulatorsM A Keller, S Addya, R Vadigepalli, et al.
Biochemistry|February 6, 1990
Organization of the gene for platelet glycoprotein IIbR Heidenreich, R Eisman, S Surrey, et al.
European Journal of Human Genetics : EJHG|November 28, 2000
Simple two-color array-based approach for mutation detectionP Fortina, K Delgrosso, T Sakazume, et al.
Blood|June 1, 1994
Interaction of rare illegitimate recombination event and a poly A addition site mutation resulting in a severe form of alpha thalassemiaP Fortina, T Parrella, M Sartore, et al.
Blood|February 1, 1990
The -175T----C mutation increases promoter strength in erythroid cells: correlation with evolutionary conservation of binding sites for two trans-acting factorsD L Gumucio, W K Lockwood, J L Weber, et al.
Human Molecular Genetics|September 1, 1997
Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in MediterraneansL Zelante, P Gasparini, X Estivill, et al.
Pageof 2