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Elisa A Ferrante

Showing results (1-10 of 16) with videos related to

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Seminars in Immunopathology|March 2, 2022
Development of vascular disease models to explore disease causation and pathomechanisms of rare vascular diseasesRebecca L Harper, Elisa A Ferrante, Manfred Boehm
Current Opinion in Hematology|March 12, 2019
CADASIL: new advances in basic science and clinical perspectivesElisa A Ferrante, Cornelia D Cudrici, Manfred Boehm
Investigative Radiology|September 3, 2010
An ultrasound contrast agent targeted to P-selectin detects activated platelets at supra-arterial shear flow conditionsFelix Guenther, Constantin von zur Muhlen, Elisa A Ferrante, et al.
Anesthesia and Analgesia|May 26, 2016
A Novel Device for the Evaluation of Hemostatic Function in Critical Care SettingsElisa A Ferrante, Kiev R Blasier, Thomas B Givens, et al.
Stem Cell Research|June 25, 2019
Generation of human induced pluripotent stem cells from individuals with a homozygous CCR5Δ32 mutationGuibin Chen, Hui Jin, Zhen Yu, et al.
Biology Open|June 26, 2020
STAT3 modulates reprogramming efficiency of human somatic cells; insights from autosomal dominant Hyper IgE syndrome caused by STAT3 mutationsZhen Yu, Natalia I Dmitrieva, Avram D Walts, et al.
Vascular Medicine (London, England)|December 22, 2023
Images in Vascular Medicine: High-resolution CT imaging of arterial calcification in the hands and legs of patients with CD73 deficiencyAneesha Baral, Farah F Hussaini, Simone C Lee, et al.
Stem Cell Research|April 29, 2020
Generation of human induced pluripotent stem cells (NIHTVBi004-A, NIHTVBi005-A, NIHTVBi006-A, NIHTVBi007-A, NIHTVBi008-A) from 5 CADASIL patients with NOTCH3 mutationGuibin Chen, Zhongwen Li, Yangtengyu Liu, et al.
Stem Cell Research|November 11, 2019
Generation of human induced pluripotent stem cell lines (NIHTVBi011-A, NIHTVBi012-A, NIHTVBi013-A) from autosomal dominant Hyper IgE syndrome (AD-HIES) patients carrying STAT3 mutationHui Jin, Zhen Yu, Keron Navarengom, et al.
Radiology Case Reports|September 3, 2020
Morphology and chemical identity of periarticular and vascular calcification in a patient with the rare genetic disease of arterial calcification due to deficiency of CD73 (ACDC)Deepak R Lakshmipathy, Cornelia D Cudrici, Frederick Dyda, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Seminars in Immunopathology|March 2, 2022
Development of vascular disease models to explore disease causation and pathomechanisms of rare vascular diseasesRebecca L Harper, Elisa A Ferrante, Manfred Boehm
Current Opinion in Hematology|March 12, 2019
CADASIL: new advances in basic science and clinical perspectivesElisa A Ferrante, Cornelia D Cudrici, Manfred Boehm
Investigative Radiology|September 3, 2010
An ultrasound contrast agent targeted to P-selectin detects activated platelets at supra-arterial shear flow conditionsFelix Guenther, Constantin von zur Muhlen, Elisa A Ferrante, et al.
Anesthesia and Analgesia|May 26, 2016
A Novel Device for the Evaluation of Hemostatic Function in Critical Care SettingsElisa A Ferrante, Kiev R Blasier, Thomas B Givens, et al.
Stem Cell Research|June 25, 2019
Generation of human induced pluripotent stem cells from individuals with a homozygous CCR5Δ32 mutationGuibin Chen, Hui Jin, Zhen Yu, et al.
Biology Open|June 26, 2020
STAT3 modulates reprogramming efficiency of human somatic cells; insights from autosomal dominant Hyper IgE syndrome caused by STAT3 mutationsZhen Yu, Natalia I Dmitrieva, Avram D Walts, et al.
Vascular Medicine (London, England)|December 22, 2023
Images in Vascular Medicine: High-resolution CT imaging of arterial calcification in the hands and legs of patients with CD73 deficiencyAneesha Baral, Farah F Hussaini, Simone C Lee, et al.
Stem Cell Research|April 29, 2020
Generation of human induced pluripotent stem cells (NIHTVBi004-A, NIHTVBi005-A, NIHTVBi006-A, NIHTVBi007-A, NIHTVBi008-A) from 5 CADASIL patients with NOTCH3 mutationGuibin Chen, Zhongwen Li, Yangtengyu Liu, et al.
Stem Cell Research|November 11, 2019
Generation of human induced pluripotent stem cell lines (NIHTVBi011-A, NIHTVBi012-A, NIHTVBi013-A) from autosomal dominant Hyper IgE syndrome (AD-HIES) patients carrying STAT3 mutationHui Jin, Zhen Yu, Keron Navarengom, et al.
Radiology Case Reports|September 3, 2020
Morphology and chemical identity of periarticular and vascular calcification in a patient with the rare genetic disease of arterial calcification due to deficiency of CD73 (ACDC)Deepak R Lakshmipathy, Cornelia D Cudrici, Frederick Dyda, et al.
Pageof 2