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Reiner Siebert

Showing results (81-90 of 547) with videos related to

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Human Mutation|January 15, 2004
Screening 500 unselected neurofibromatosis 1 patients for deletions of the NF1 geneLan Kluwe, Reiner Siebert, Stefan Gesk, et al.
Epigenomics|November 7, 2015
The differentially methylated region of MEG8 is hypermethylated in patients with Temple syndromeSusanne Bens, Julia Kolarova, Gabriele Gillessen-Kaesbach, et al.
Blood|September 24, 2011
A unique case of follicular lymphoma provides insights to the clonal evolution from follicular lymphoma in situ to manifest follicular lymphomaIrina Bonzheim, Itziar Salaverria, Andrea Haake, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 11, 2022
Congenital generalized lipodystrophy type 4 due to a novel PTRF/CAVIN1 pathogenic variant in a child: effects of metreleptin substitutionSuleyman Cem Adiyaman, Julia V Schnurbein, Jan De Laffolie, et al.
The American Journal of Pathology|August 1, 2006
Aberrant expression of ID2, a suppressor of B-cell-specific gene expression, in Hodgkin's lymphomaChristoph Renné, Jose Ignacio Martin-Subero, Maren Eickernjäger, et al.
Cellular & Molecular Immunology|August 22, 2020
DNA methylation profile of a hepatosplenic gamma/delta T-cell lymphoma patient associated with response to interferon-α therapyJaydeep Bhat, Anke K Bergmann, Silvio Waschina, et al.
Molecular and Cellular Pediatrics|April 10, 2026
The conundrum in diagnosing Maturity-Onset Diabetes of the Young (MODY) in a large German pedigree with early-onset diabetes and a novel HNF1A variantEleni Z Giannopoulou, Abubakar Moawia, Josef Högel, et al.
Clinical Epigenetics|September 8, 2023
A quantum physics layer of epigenetics: a hypothesis deduced from charge transfer and chirality-induced spin selectivity of DNAReiner Siebert, Ole Ammerpohl, Mirko Rossini, et al.
European Journal of Medical Genetics|June 25, 2011
A de novo 1.1Mb microdeletion of chromosome 19p13.11 provides indirect evidence for EPS15L1 to be a strong candidate for split hand split foot malformationSusanne Bens, Andrea Haake, Holger Tönnies, et al.
Cancer Genetics|September 29, 2014
Synchronous congenital malignant rhabdoid tumor of the orbit and atypical teratoid/rhabdoid tumor--feasibility and efficacy of multimodal therapy in a long-term survivorAngela Seeringer, Harald Reinhard, Martin Hasselblatt, et al.
Pageof 55

Showing results (81-90 of 547) with videos related to

Sort By:
Pageof 55
Human Mutation|January 15, 2004
Screening 500 unselected neurofibromatosis 1 patients for deletions of the NF1 geneLan Kluwe, Reiner Siebert, Stefan Gesk, et al.
Epigenomics|November 7, 2015
The differentially methylated region of MEG8 is hypermethylated in patients with Temple syndromeSusanne Bens, Julia Kolarova, Gabriele Gillessen-Kaesbach, et al.
Blood|September 24, 2011
A unique case of follicular lymphoma provides insights to the clonal evolution from follicular lymphoma in situ to manifest follicular lymphomaIrina Bonzheim, Itziar Salaverria, Andrea Haake, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 11, 2022
Congenital generalized lipodystrophy type 4 due to a novel PTRF/CAVIN1 pathogenic variant in a child: effects of metreleptin substitutionSuleyman Cem Adiyaman, Julia V Schnurbein, Jan De Laffolie, et al.
The American Journal of Pathology|August 1, 2006
Aberrant expression of ID2, a suppressor of B-cell-specific gene expression, in Hodgkin's lymphomaChristoph Renné, Jose Ignacio Martin-Subero, Maren Eickernjäger, et al.
Cellular & Molecular Immunology|August 22, 2020
DNA methylation profile of a hepatosplenic gamma/delta T-cell lymphoma patient associated with response to interferon-α therapyJaydeep Bhat, Anke K Bergmann, Silvio Waschina, et al.
Molecular and Cellular Pediatrics|April 10, 2026
The conundrum in diagnosing Maturity-Onset Diabetes of the Young (MODY) in a large German pedigree with early-onset diabetes and a novel HNF1A variantEleni Z Giannopoulou, Abubakar Moawia, Josef Högel, et al.
Clinical Epigenetics|September 8, 2023
A quantum physics layer of epigenetics: a hypothesis deduced from charge transfer and chirality-induced spin selectivity of DNAReiner Siebert, Ole Ammerpohl, Mirko Rossini, et al.
European Journal of Medical Genetics|June 25, 2011
A de novo 1.1Mb microdeletion of chromosome 19p13.11 provides indirect evidence for EPS15L1 to be a strong candidate for split hand split foot malformationSusanne Bens, Andrea Haake, Holger Tönnies, et al.
Cancer Genetics|September 29, 2014
Synchronous congenital malignant rhabdoid tumor of the orbit and atypical teratoid/rhabdoid tumor--feasibility and efficacy of multimodal therapy in a long-term survivorAngela Seeringer, Harald Reinhard, Martin Hasselblatt, et al.
Pageof 55