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Genes
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May 10, 2020
Efficient Generation and Correction of Mutations in Human iPS Cells Utilizing mRNAs of CRISPR Base Editors and Prime Editors
Duran Sürün, Aksana Schneider, Jovan Mircetic, et al.
Clinical Rheumatology
|
June 11, 2008
Chilblain lupus erythematosus--a review of literature
C M Hedrich, B Fiebig, F H Hauck, et al.
American Journal of Human Genetics
|
September 9, 2006
Familial chilblain lupus, a monogenic form of cutaneous lupus erythematosus, maps to chromosome 3p
Min Ae Lee-Kirsch, Maolian Gong, Herbert Schulz, et al.
Human Molecular Genetics
|
July 3, 2014
Altered spatio-temporal dynamics of RNase H2 complex assembly at replication and repair sites in Aicardi-Goutières syndrome
Barbara Kind, Britta Muster, Wolfgang Staroske, et al.
Nature Immunology
|
November 20, 2012
Trex1 regulates lysosomal biogenesis and interferon-independent activation of antiviral genes
Maroof Hasan, James Koch, Dinesh Rakheja, et al.
Journal of Molecular Medicine (Berlin, Germany)
|
February 2, 2013
Single-stranded nucleic acids promote SAMHD1 complex formation
Victoria Tüngler, Wolfgang Staroske, Barbara Kind, et al.
Brain & Development
|
March 1, 2016
Variable clinical course in acute necrotizing encephalopathy and identification of a novel RANBP2 mutation
Katharina Sell, Katja Storch, Gabriele Hahn, et al.
Frontiers in Pediatrics
|
January 22, 2025
SOCS1 deficiency-crossroads of autoimmunity and autoinflammation-two case reports
Kajetan Trojovsky, Maximilian Seidl, Florian Babor, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
December 10, 2017
Variable clinical phenotype in two siblings with Aicardi-Goutières syndrome type 6 and a novel mutation in the ADAR gene
Lisa Schmelzer, Martin Smitka, Christine Wolf, et al.
Orphanet Journal of Rare Diseases
|
November 13, 2021
An Integrated clinical pathway for diagnosis, treatment and care of rare diseases: model, operating procedures, and results of the project TRANSLATE-NAMSE funded by the German Federal Joint Committee
Daniela Choukair, Fabian Hauck, Markus Bettendorf, et al.
Page
of 9
Search research articles
Search
Showing results (31-40 of 86) with videos related to
Sort By:
Page
of 9
Genes
|
May 10, 2020
Efficient Generation and Correction of Mutations in Human iPS Cells Utilizing mRNAs of CRISPR Base Editors and Prime Editors
Duran Sürün, Aksana Schneider, Jovan Mircetic, et al.
Clinical Rheumatology
|
June 11, 2008
Chilblain lupus erythematosus--a review of literature
C M Hedrich, B Fiebig, F H Hauck, et al.
American Journal of Human Genetics
|
September 9, 2006
Familial chilblain lupus, a monogenic form of cutaneous lupus erythematosus, maps to chromosome 3p
Min Ae Lee-Kirsch, Maolian Gong, Herbert Schulz, et al.
Human Molecular Genetics
|
July 3, 2014
Altered spatio-temporal dynamics of RNase H2 complex assembly at replication and repair sites in Aicardi-Goutières syndrome
Barbara Kind, Britta Muster, Wolfgang Staroske, et al.
Nature Immunology
|
November 20, 2012
Trex1 regulates lysosomal biogenesis and interferon-independent activation of antiviral genes
Maroof Hasan, James Koch, Dinesh Rakheja, et al.
Journal of Molecular Medicine (Berlin, Germany)
|
February 2, 2013
Single-stranded nucleic acids promote SAMHD1 complex formation
Victoria Tüngler, Wolfgang Staroske, Barbara Kind, et al.
Brain & Development
|
March 1, 2016
Variable clinical course in acute necrotizing encephalopathy and identification of a novel RANBP2 mutation
Katharina Sell, Katja Storch, Gabriele Hahn, et al.
Frontiers in Pediatrics
|
January 22, 2025
SOCS1 deficiency-crossroads of autoimmunity and autoinflammation-two case reports
Kajetan Trojovsky, Maximilian Seidl, Florian Babor, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
December 10, 2017
Variable clinical phenotype in two siblings with Aicardi-Goutières syndrome type 6 and a novel mutation in the ADAR gene
Lisa Schmelzer, Martin Smitka, Christine Wolf, et al.
Orphanet Journal of Rare Diseases
|
November 13, 2021
An Integrated clinical pathway for diagnosis, treatment and care of rare diseases: model, operating procedures, and results of the project TRANSLATE-NAMSE funded by the German Federal Joint Committee
Daniela Choukair, Fabian Hauck, Markus Bettendorf, et al.
Page
of 9