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Blood
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July 1, 1995
cDNA structure, tissue-specific expression, and chromosomal localization of the murine band 7.2b gene
P 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 disease
G 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 hybridization
N 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 neonate
M 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 promoter
P 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 channels
D 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 triathlon
D 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 hybridization
M 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 ankyrin
P 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 spherocytosis
P G Gallagher, J D Ferreira, F F Costa, et al.
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Search research articles
Search
Showing results (51-60 of 94) with videos related to
Sort By:
Page
of 10
Blood
|
July 1, 1995
cDNA structure, tissue-specific expression, and chromosomal localization of the murine band 7.2b gene
P 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 disease
G 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 hybridization
N 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 neonate
M 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 promoter
P 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 channels
D 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 triathlon
D 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 hybridization
M 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 ankyrin
P 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 spherocytosis
P G Gallagher, J D Ferreira, F F Costa, et al.
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of 10