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Vincent P Schulz

Showing results (1-10 of 40) with videos related to

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Current Opinion in Hematology|February 27, 2015
Human and murine erythropoiesisXiuli An, Vincent P Schulz, Narla Mohandas, et al.
Hemoglobin|November 9, 2016
Mutation in a Highly Conserved COOH-Terminal Residue of Krüppel-Like Factor 1 Associated with Elevated Hb F in a Compound Heterozygous β-Thalassemia Patient with a Nontransfusion-Dependent Thalassemia PhenotypePatrick G Gallagher, Yelena Maksimova, Vincent P Schulz, 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.
The Journal of Biological Chemistry|September 23, 2011
Patterns of histone H3 lysine 27 monomethylation and erythroid cell type-specific gene expressionLaurie A Steiner, Vincent P Schulz, Yelena Maksimova, et al.
Pediatric Blood & Cancer|January 26, 2017
Hemoglobin C trait accentuates erythrocyte dehydration in hereditary xerocytosisElizabeth Yang, Erin B Voelkel, Kimberly Lezon-Geyda, et al.
Molecular Cytogenetics|January 14, 2014
Cytogenomic mapping and bioinformatic mining reveal interacting brain expressed genes for intellectual disabilityFang Xu, Lun Li, Vincent P Schulz, et al.
Molecular Biology of the Cell|June 12, 2002
Schizosaccharomyces pombe pfh1+ encodes an essential 5' to 3' DNA helicase that is a member of the PIF1 subfamily of DNA helicasesJin-Qiu Zhou, Haiyan Qi, Vincent P Schulz, et al.
Haematologica|June 5, 2014
Severe nondominant hereditary spherocytosis due to uniparental isodisomy at the SPTA1 locusHannah Bogardus, Vincent P Schulz, Yelena Maksimova, et al.
The Journal of Biological Chemistry|January 24, 2013
Identification of biologically relevant enhancers in human erythroid cellsMack Y Su, Laurie A Steiner, Hannah Bogardus, et al.
Cell Reports|September 12, 2019
A Unique Epigenomic Landscape Defines Human ErythropoiesisVincent P Schulz, Hongxia Yan, Kimberly Lezon-Geyda, et al.
Pageof 4

Showing results (1-10 of 40) with videos related to

Sort By:
Pageof 4
Current Opinion in Hematology|February 27, 2015
Human and murine erythropoiesisXiuli An, Vincent P Schulz, Narla Mohandas, et al.
Hemoglobin|November 9, 2016
Mutation in a Highly Conserved COOH-Terminal Residue of Krüppel-Like Factor 1 Associated with Elevated Hb F in a Compound Heterozygous β-Thalassemia Patient with a Nontransfusion-Dependent Thalassemia PhenotypePatrick G Gallagher, Yelena Maksimova, Vincent P Schulz, 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.
The Journal of Biological Chemistry|September 23, 2011
Patterns of histone H3 lysine 27 monomethylation and erythroid cell type-specific gene expressionLaurie A Steiner, Vincent P Schulz, Yelena Maksimova, et al.
Pediatric Blood & Cancer|January 26, 2017
Hemoglobin C trait accentuates erythrocyte dehydration in hereditary xerocytosisElizabeth Yang, Erin B Voelkel, Kimberly Lezon-Geyda, et al.
Molecular Cytogenetics|January 14, 2014
Cytogenomic mapping and bioinformatic mining reveal interacting brain expressed genes for intellectual disabilityFang Xu, Lun Li, Vincent P Schulz, et al.
Molecular Biology of the Cell|June 12, 2002
Schizosaccharomyces pombe pfh1+ encodes an essential 5' to 3' DNA helicase that is a member of the PIF1 subfamily of DNA helicasesJin-Qiu Zhou, Haiyan Qi, Vincent P Schulz, et al.
Haematologica|June 5, 2014
Severe nondominant hereditary spherocytosis due to uniparental isodisomy at the SPTA1 locusHannah Bogardus, Vincent P Schulz, Yelena Maksimova, et al.
The Journal of Biological Chemistry|January 24, 2013
Identification of biologically relevant enhancers in human erythroid cellsMack Y Su, Laurie A Steiner, Hannah Bogardus, et al.
Cell Reports|September 12, 2019
A Unique Epigenomic Landscape Defines Human ErythropoiesisVincent P Schulz, Hongxia Yan, Kimberly Lezon-Geyda, et al.
Pageof 4