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Michael Gertz

Showing results (81-90 of 91) with videos related to

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Journal of Medical Internet Research|September 6, 2024
Establishing Medical Intelligence-Leveraging Fast Healthcare Interoperability Resources to Improve Clinical Management: Retrospective Cohort and Clinical Implementation StudyAlexander Brehmer, Christopher Martin Sauer, Jayson Salazar Rodríguez, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|April 8, 2020
Single-Cell-Derived Primary Rectal Carcinoma Cell Lines Reflect Intratumor Heterogeneity Associated with Treatment ResponseRüdiger Braun, Lena Anthuber, Daniela Hirsch, et al.
Blood|April 23, 2014
Inherited biallelic CSF3R mutations in severe congenital neutropeniaAlexa Triot, Päivi M Järvinen, Juan I Arostegui, et al.
The New England Journal of Medicine|November 6, 2009
Inflammatory bowel disease and mutations affecting the interleukin-10 receptorErik-Oliver Glocker, Daniel Kotlarz, Kaan Boztug, et al.
The Journal of Experimental Medicine|February 27, 2013
Loss-of-function mutations in the IL-21 receptor gene cause a primary immunodeficiency syndromeDaniel Kotlarz, Natalia Ziętara, Gulbu Uzel, et al.
Biorxiv : the Preprint Server for Biology|September 15, 2025
Long-read sequencing of single cell-derived melanoma subclones reveals divergent and parallel genomic and epigenomic evolutionary trajectoriesYuelin Liu, Anton Goretsky, Ayse G Keskus, et al.
Gut|August 3, 2021
The tumour microenvironment shapes innate lymphoid cells in patients with hepatocellular carcinomaBernd Heinrich, E Michael Gertz, Alejandro A Schäffer, et al.
American Journal of Human Genetics|May 22, 2012
Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunityGabriela Lopez-Herrera, Giacomo Tampella, Qiang Pan-Hammarström, et al.
Blood|November 5, 2008
Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromesUlrich Salzer, Chiara Bacchelli, Sylvie Buckridge, et al.
Nature Genetics|August 18, 2014
JAGN1 deficiency causes aberrant myeloid cell homeostasis and congenital neutropeniaKaan Boztug, Päivi M Järvinen, Elisabeth Salzer, et al.
Pageof 10

Showing results (81-90 of 91) with videos related to

Sort By:
Pageof 10
Journal of Medical Internet Research|September 6, 2024
Establishing Medical Intelligence-Leveraging Fast Healthcare Interoperability Resources to Improve Clinical Management: Retrospective Cohort and Clinical Implementation StudyAlexander Brehmer, Christopher Martin Sauer, Jayson Salazar Rodríguez, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|April 8, 2020
Single-Cell-Derived Primary Rectal Carcinoma Cell Lines Reflect Intratumor Heterogeneity Associated with Treatment ResponseRüdiger Braun, Lena Anthuber, Daniela Hirsch, et al.
Blood|April 23, 2014
Inherited biallelic CSF3R mutations in severe congenital neutropeniaAlexa Triot, Päivi M Järvinen, Juan I Arostegui, et al.
The New England Journal of Medicine|November 6, 2009
Inflammatory bowel disease and mutations affecting the interleukin-10 receptorErik-Oliver Glocker, Daniel Kotlarz, Kaan Boztug, et al.
The Journal of Experimental Medicine|February 27, 2013
Loss-of-function mutations in the IL-21 receptor gene cause a primary immunodeficiency syndromeDaniel Kotlarz, Natalia Ziętara, Gulbu Uzel, et al.
Biorxiv : the Preprint Server for Biology|September 15, 2025
Long-read sequencing of single cell-derived melanoma subclones reveals divergent and parallel genomic and epigenomic evolutionary trajectoriesYuelin Liu, Anton Goretsky, Ayse G Keskus, et al.
Gut|August 3, 2021
The tumour microenvironment shapes innate lymphoid cells in patients with hepatocellular carcinomaBernd Heinrich, E Michael Gertz, Alejandro A Schäffer, et al.
American Journal of Human Genetics|May 22, 2012
Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunityGabriela Lopez-Herrera, Giacomo Tampella, Qiang Pan-Hammarström, et al.
Blood|November 5, 2008
Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromesUlrich Salzer, Chiara Bacchelli, Sylvie Buckridge, et al.
Nature Genetics|August 18, 2014
JAGN1 deficiency causes aberrant myeloid cell homeostasis and congenital neutropeniaKaan Boztug, Päivi M Järvinen, Elisabeth Salzer, et al.
Pageof 10