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Patrick G Gallagher

Showing results (101-110 of 172) with videos related to

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Molecular and Cellular Biology|August 19, 2009
Chromatin architecture and transcription factor binding regulate expression of erythrocyte membrane protein genesLaurie A Steiner, Yelena Maksimova, Vincent Schulz, et al.
Blood Advances|October 6, 2025
A novel isoform of tensin-1 promotes actin filament assembly for efficient erythroblast enucleationArit Ghosh, Megan Coffin, Dimitri M Diaz, et al.
Human Molecular Genetics|July 23, 2005
A dinucleotide deletion in the ankyrin promoter alters gene expression, transcription initiation and TFIID complex formation in hereditary spherocytosisPatrick G Gallagher, Douglas G Nilson, Clara Wong, et al.
Blood|February 1, 2003
Altered erythrocyte endothelial adherence and membrane phospholipid asymmetry in hereditary hydrocytosisPatrick G Gallagher, Seon Hee Chang, Michael P Rettig, et al.
Pediatric Blood & Cancer|May 12, 2018
Hb Adana (HBA2 or HBA1: c.179G > A) and alpha thalassemia: Genotype-phenotype correlationSharon A Singh, Susmita Sarangi, Abena Appiah-Kubi, et al.
Blood|October 22, 2014
Global transcriptome analysis and enhancer landscape of human primary T follicular helper and T effector lymphocytesJason S Weinstein, Kimberly Lezon-Geyda, Yelena Maksimova, et al.
Blood Cells, Molecules & Diseases|September 11, 2024
Phenotypic and genotypic evaluation of bleeding diagnostic dilemmas: Two case studiesSean X Gu, Ayesha Butt, Vincent P Schulz, et al.
Veterinary Clinical Pathology|February 21, 2009
Canine elliptocytosis due to a mutant beta-spectrinRoberta Di Terlizzi, Patrick G Gallagher, Narla Mohandas, et al.
American Journal of Hematology|December 7, 2017
Hereditary xerocytosis: Diagnostic considerationsMary Risinger, Edyta Glogowska, Satheesh Chonat, et al.
Blood|February 28, 2018
A Ser725Arg mutation in Band 3 abolishes transport function and leads to anemia and renal tubular acidosisElizabeth Yang, Patricia Seo-Mayer, Kimberly Lezon-Geyda, et al.
Pageof 18

Showing results (101-110 of 172) with videos related to

Sort By:
Pageof 18
Molecular and Cellular Biology|August 19, 2009
Chromatin architecture and transcription factor binding regulate expression of erythrocyte membrane protein genesLaurie A Steiner, Yelena Maksimova, Vincent Schulz, et al.
Blood Advances|October 6, 2025
A novel isoform of tensin-1 promotes actin filament assembly for efficient erythroblast enucleationArit Ghosh, Megan Coffin, Dimitri M Diaz, et al.
Human Molecular Genetics|July 23, 2005
A dinucleotide deletion in the ankyrin promoter alters gene expression, transcription initiation and TFIID complex formation in hereditary spherocytosisPatrick G Gallagher, Douglas G Nilson, Clara Wong, et al.
Blood|February 1, 2003
Altered erythrocyte endothelial adherence and membrane phospholipid asymmetry in hereditary hydrocytosisPatrick G Gallagher, Seon Hee Chang, Michael P Rettig, et al.
Pediatric Blood & Cancer|May 12, 2018
Hb Adana (HBA2 or HBA1: c.179G > A) and alpha thalassemia: Genotype-phenotype correlationSharon A Singh, Susmita Sarangi, Abena Appiah-Kubi, et al.
Blood|October 22, 2014
Global transcriptome analysis and enhancer landscape of human primary T follicular helper and T effector lymphocytesJason S Weinstein, Kimberly Lezon-Geyda, Yelena Maksimova, et al.
Blood Cells, Molecules & Diseases|September 11, 2024
Phenotypic and genotypic evaluation of bleeding diagnostic dilemmas: Two case studiesSean X Gu, Ayesha Butt, Vincent P Schulz, et al.
Veterinary Clinical Pathology|February 21, 2009
Canine elliptocytosis due to a mutant beta-spectrinRoberta Di Terlizzi, Patrick G Gallagher, Narla Mohandas, et al.
American Journal of Hematology|December 7, 2017
Hereditary xerocytosis: Diagnostic considerationsMary Risinger, Edyta Glogowska, Satheesh Chonat, et al.
Blood|February 28, 2018
A Ser725Arg mutation in Band 3 abolishes transport function and leads to anemia and renal tubular acidosisElizabeth Yang, Patricia Seo-Mayer, Kimberly Lezon-Geyda, et al.
Pageof 18