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Patrick G Gallagher

Blood

Showing results (1-10 of 35) with videos related to

Pageof 4
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Blood|October 21, 2017
Disorders of erythrocyte hydrationPatrick G Gallagher
Blood|February 25, 2022
Anemia in the pediatric patientPatrick G Gallagher
Blood|January 25, 2014
Long noncoding RNAs in erythropoiesisPatrick G Gallagher
Blood|November 8, 2008
Red cell membrane: past, present, and futureNarla Mohandas, Patrick G Gallagher
Blood|September 12, 2013
Applications of high-throughput DNA sequencing to benign hematologyVijay G Sankaran, Patrick G Gallagher
Blood|September 10, 2005
A novel splicing mutation of the alpha-spectrin gene in the original hereditary pyropoikilocytosis kindredDaniel B Costa, Larisa Lozovatsky, Patrick G Gallagher, et al.
Blood|January 26, 2008
Structural and functional effects of hereditary hemolytic anemia-associated point mutations in the alpha spectrin tetramer siteMassimiliano Gaetani, Sara Mootien, Sandra Harper, et al.
Blood|March 1, 2007
A complex splicing defect associated with homozygous ankyrin-deficient hereditary spherocytosisE Jennifer Edelman, Yelena Maksimova, Feride Duru, et al.
Blood|July 23, 2015
Mutations in the Gardos channel (KCNN4) are associated with hereditary xerocytosisEdyta Glogowska, Kimberly Lezon-Geyda, Yelena Maksimova, et al.
Blood|February 21, 2004
Human potassium chloride cotransporter 1 (SLC12A4) promoter is regulated by AP-2 and contains a functional downstream promoter elementGuo-Ping Zhou, Clara Wong, Robert Su, et al.
Pageof 4

Showing results (1-10 of 35) with videos related to

Sort By:
Pageof 4
Blood|October 21, 2017
Disorders of erythrocyte hydrationPatrick G Gallagher
Blood|February 25, 2022
Anemia in the pediatric patientPatrick G Gallagher
Blood|January 25, 2014
Long noncoding RNAs in erythropoiesisPatrick G Gallagher
Blood|November 8, 2008
Red cell membrane: past, present, and futureNarla Mohandas, Patrick G Gallagher
Blood|September 12, 2013
Applications of high-throughput DNA sequencing to benign hematologyVijay G Sankaran, Patrick G Gallagher
Blood|September 10, 2005
A novel splicing mutation of the alpha-spectrin gene in the original hereditary pyropoikilocytosis kindredDaniel B Costa, Larisa Lozovatsky, Patrick G Gallagher, et al.
Blood|January 26, 2008
Structural and functional effects of hereditary hemolytic anemia-associated point mutations in the alpha spectrin tetramer siteMassimiliano Gaetani, Sara Mootien, Sandra Harper, et al.
Blood|March 1, 2007
A complex splicing defect associated with homozygous ankyrin-deficient hereditary spherocytosisE Jennifer Edelman, Yelena Maksimova, Feride Duru, et al.
Blood|July 23, 2015
Mutations in the Gardos channel (KCNN4) are associated with hereditary xerocytosisEdyta Glogowska, Kimberly Lezon-Geyda, Yelena Maksimova, et al.
Blood|February 21, 2004
Human potassium chloride cotransporter 1 (SLC12A4) promoter is regulated by AP-2 and contains a functional downstream promoter elementGuo-Ping Zhou, Clara Wong, Robert Su, et al.
Pageof 4