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Irina Kondratenko

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Advances in Experimental Medicine and Biology|August 24, 2007
Mycobacterial infections in primary immunodeficiency patientsElizaveta Galkina, Irina Kondratenko, Andrey Bologov
Advances in Experimental Medicine and Biology|August 24, 2007
Nijmegen breakage syndromeIrina Kondratenko, Olga Paschenko, Alexandr Polyakov, et al.
European Journal of Medical Genetics|February 18, 2019
ATM mutation spectrum in Russian children with ataxia-telangiectasiaEvgeny Suspitsin, Anna Sokolenko, Ilya Bizin, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|January 12, 2020
Mitochondrial permeability transition pore is involved in oxidative burst and NETosis of human neutrophilsNina Vorobjeva, Ivan Galkin, Olga Pletjushkina, et al.
The Journal of Pediatrics|April 16, 2002
Nijmegen breakage syndrome: clinical characteristics and mutation analysis in eight unrelated Russian familiesIgor B Resnick, Irina Kondratenko, Oleg Togoev, et al.
American Journal of Medical Genetics. Part A|July 2, 2003
657del5 mutation in the gene for Nijmegen breakage syndrome (NBS1) in a cohort of Russian children with lymphoid tissue malignancies and controlsIgor B Resnick, Irina Kondratenko, Eugeni Pashanov, et al.
Journal of Clinical Immunology|April 3, 2023
Allogeneic Hematopoietic Stem Cell Transplantation Activity in Inborn Errors of Immunity in Russian FederationAlexandra Laberko, Anna Mukhinа, Elena Machneva, et al.
American Journal of Human Genetics|February 7, 2008
Gross deletions involving IGHM, BTK, or Artemis: a model for genomic lesions mediated by transposable elementsMenno C van Zelm, Corinne Geertsema, Nicole Nieuwenhuis, et al.
Molecular Immunology|December 28, 2010
Genetic characteristics of eighty-seven patients with the Wiskott-Aldrich syndromeVera Gulácsy, Tomas Freiberger, Anna Shcherbina, et al.
The New England Journal of Medicine|November 12, 2010
Stem-cell gene therapy for the Wiskott-Aldrich syndromeKaan Boztug, Manfred Schmidt, Adrian Schwarzer, et al.
Pageof 2

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

Sort By:
Pageof 2
Advances in Experimental Medicine and Biology|August 24, 2007
Mycobacterial infections in primary immunodeficiency patientsElizaveta Galkina, Irina Kondratenko, Andrey Bologov
Advances in Experimental Medicine and Biology|August 24, 2007
Nijmegen breakage syndromeIrina Kondratenko, Olga Paschenko, Alexandr Polyakov, et al.
European Journal of Medical Genetics|February 18, 2019
ATM mutation spectrum in Russian children with ataxia-telangiectasiaEvgeny Suspitsin, Anna Sokolenko, Ilya Bizin, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|January 12, 2020
Mitochondrial permeability transition pore is involved in oxidative burst and NETosis of human neutrophilsNina Vorobjeva, Ivan Galkin, Olga Pletjushkina, et al.
The Journal of Pediatrics|April 16, 2002
Nijmegen breakage syndrome: clinical characteristics and mutation analysis in eight unrelated Russian familiesIgor B Resnick, Irina Kondratenko, Oleg Togoev, et al.
American Journal of Medical Genetics. Part A|July 2, 2003
657del5 mutation in the gene for Nijmegen breakage syndrome (NBS1) in a cohort of Russian children with lymphoid tissue malignancies and controlsIgor B Resnick, Irina Kondratenko, Eugeni Pashanov, et al.
Journal of Clinical Immunology|April 3, 2023
Allogeneic Hematopoietic Stem Cell Transplantation Activity in Inborn Errors of Immunity in Russian FederationAlexandra Laberko, Anna Mukhinа, Elena Machneva, et al.
American Journal of Human Genetics|February 7, 2008
Gross deletions involving IGHM, BTK, or Artemis: a model for genomic lesions mediated by transposable elementsMenno C van Zelm, Corinne Geertsema, Nicole Nieuwenhuis, et al.
Molecular Immunology|December 28, 2010
Genetic characteristics of eighty-seven patients with the Wiskott-Aldrich syndromeVera Gulácsy, Tomas Freiberger, Anna Shcherbina, et al.
The New England Journal of Medicine|November 12, 2010
Stem-cell gene therapy for the Wiskott-Aldrich syndromeKaan Boztug, Manfred Schmidt, Adrian Schwarzer, et al.
Pageof 2