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P G Gallagher

Showing results (51-60 of 94) with videos related to

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Blood|July 1, 1995
cDNA structure, tissue-specific expression, and chromosomal localization of the murine band 7.2b geneP G Gallagher, M Romana, J H Lieman, et al.
Blood Cells, Molecules & Diseases|May 19, 2001
Modification of erythrocyte hydration in the treatment of sickle cell diseaseG P Zhou, K P Anderson, C H Joiner, et al.
Cytogenetics and Cell Genetics|November 27, 1999
Assignment of the 2P domain, acid-sensitive potassium channel OAT1 gene KCNK3 to human chromosome bands 2p24.1-->p23.3 and murine 5B by in situ hybridizationN A Manjunath, P Bray-Ward, S A Goldstein, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|August 30, 2013
Late-onset Leclercia adecarboxylata sepsis in a premature neonateM U Nelson, Y Maksimova, V Schulz, et al.
Blood|July 27, 2000
The human ankyrin-1 gene is selectively transcribed in erythroid cell lines despite the presence of a housekeeping-like promoterP G Gallagher, M Romana, W T Tse, et al.
Gene|February 13, 2001
Genomic organization and chromosomal localization of the murine 2 P domain potassium channel gene Kcnk8: conservation of gene structure in 2 P domain potassium channelsD Bockenhauer, M A Nimmakayalu, D C Ward, et al.
Clinical Journal of Sport Medicine : Official Journal of the Canadian Academy of Sport Medicine|July 1, 1997
Hyponatremia and weight changes in an ultradistance triathlonD B Speedy, J G Faris, M Hamlin, et al.
Cytogenetics and Cell Genetics|January 1, 1994
Localization of the human alpha-fodrin gene (SPTAN1) to 9q33-->q34 by fluorescence in situ hybridizationM Upender, P G Gallagher, R T Moon, et al.
Transactions of the Association of American Physicians|January 1, 1992
Large numbers of alternatively spliced isoforms of the regulatory region of human erythrocyte ankyrinP G Gallagher, W T Tse, A L Scarpa, et al.
British Journal of Haematology|February 13, 2001
A recurrent frameshift mutation of the ankyrin gene associated with severe hereditary spherocytosisP G Gallagher, J D Ferreira, F F Costa, et al.
Pageof 10

Showing results (51-60 of 94) with videos related to

Sort By:
Pageof 10
Blood|July 1, 1995
cDNA structure, tissue-specific expression, and chromosomal localization of the murine band 7.2b geneP G Gallagher, M Romana, J H Lieman, et al.
Blood Cells, Molecules & Diseases|May 19, 2001
Modification of erythrocyte hydration in the treatment of sickle cell diseaseG P Zhou, K P Anderson, C H Joiner, et al.
Cytogenetics and Cell Genetics|November 27, 1999
Assignment of the 2P domain, acid-sensitive potassium channel OAT1 gene KCNK3 to human chromosome bands 2p24.1-->p23.3 and murine 5B by in situ hybridizationN A Manjunath, P Bray-Ward, S A Goldstein, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|August 30, 2013
Late-onset Leclercia adecarboxylata sepsis in a premature neonateM U Nelson, Y Maksimova, V Schulz, et al.
Blood|July 27, 2000
The human ankyrin-1 gene is selectively transcribed in erythroid cell lines despite the presence of a housekeeping-like promoterP G Gallagher, M Romana, W T Tse, et al.
Gene|February 13, 2001
Genomic organization and chromosomal localization of the murine 2 P domain potassium channel gene Kcnk8: conservation of gene structure in 2 P domain potassium channelsD Bockenhauer, M A Nimmakayalu, D C Ward, et al.
Clinical Journal of Sport Medicine : Official Journal of the Canadian Academy of Sport Medicine|July 1, 1997
Hyponatremia and weight changes in an ultradistance triathlonD B Speedy, J G Faris, M Hamlin, et al.
Cytogenetics and Cell Genetics|January 1, 1994
Localization of the human alpha-fodrin gene (SPTAN1) to 9q33-->q34 by fluorescence in situ hybridizationM Upender, P G Gallagher, R T Moon, et al.
Transactions of the Association of American Physicians|January 1, 1992
Large numbers of alternatively spliced isoforms of the regulatory region of human erythrocyte ankyrinP G Gallagher, W T Tse, A L Scarpa, et al.
British Journal of Haematology|February 13, 2001
A recurrent frameshift mutation of the ankyrin gene associated with severe hereditary spherocytosisP G Gallagher, J D Ferreira, F F Costa, et al.
Pageof 10