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Almuth Caliebe

Showing results (31-40 of 81) with videos related to

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American Journal of Medical Genetics. Part A|February 14, 2006
Characterization of two supernumerary marker chromosomes in a patient with signs of Klinefelter syndrome, mild facial anomalies, and severe speech delayJörg Weimer, Simone Metzke-Heidemann, Hansjörg Plendl, et al.
European Journal of Medical Genetics|May 25, 2015
Array-based DNA methylation analysis in individuals with developmental delay/intellectual disability and normal molecular karyotypeJulia Kolarova, Imke Tangen, Susanne Bens, et al.
Journal of Medical Genetics|August 21, 2020
Telangiectasia-ectodermal dysplasia-brachydactyly-cardiac anomaly syndrome is caused by de novo mutations in <i>protein kinase D1</i>Svenja Alter, Andreas David Zimmer, Misun Park, et al.
European Journal of Medical Genetics|July 9, 2011
A 2 Mb deletion in 14q13 associated with severe developmental delay and hemophagocytic lymphohistiocytosisAlmuth Caliebe, Jose I Martin Subero, Hiltrud Muhle, et al.
Nature|March 27, 2023
Formin-mediated nuclear actin at androgen receptors promotes transcriptionJulian Knerr, Ralf Werner, Carsten Schwan, et al.
Plos One|March 19, 2015
In vivo investigations of the effect of short- and long-term recombinant growth hormone treatment on DNA-methylation in humansJulia Kolarova, Ole Ammerpohl, Jana Gutwein, et al.
Breast Care (Basel, Switzerland)|March 15, 2021
A Giant Mammary Hamartoma in a Young Breast Cancer PatientAnna-Lena Rumpf, Micaela Mathiak, Fritz K Schäfer, et al.
Plos One|June 23, 2012
DNA-methylation profiling of fetal tissues reveals marked epigenetic differences between chorionic and amniotic samplesChristel Eckmann-Scholz, Susanne Bens, Julia Kolarova, et al.
Blood Advances|September 9, 2021
Aggressive B-cell lymphoma cases with 11q aberration patterns indicate a spectrum beyond Burkitt-like lymphomaNiklas Gebauer, Hanno M Witte, Hartmut Merz, et al.
Human Mutation|October 23, 2009
A specific mutation in the distant sonic hedgehog (SHH) cis-regulator (ZRS) causes Werner mesomelic syndrome (WMS) while complete ZRS duplications underlie Haas type polysyndactyly and preaxial polydactyly (PPD) with or without triphalangeal thumbDagmar Wieczorek, Barbara Pawlik, Yun Li, et al.
Pageof 9

Showing results (31-40 of 81) with videos related to

Sort By:
Pageof 9
American Journal of Medical Genetics. Part A|February 14, 2006
Characterization of two supernumerary marker chromosomes in a patient with signs of Klinefelter syndrome, mild facial anomalies, and severe speech delayJörg Weimer, Simone Metzke-Heidemann, Hansjörg Plendl, et al.
European Journal of Medical Genetics|May 25, 2015
Array-based DNA methylation analysis in individuals with developmental delay/intellectual disability and normal molecular karyotypeJulia Kolarova, Imke Tangen, Susanne Bens, et al.
Journal of Medical Genetics|August 21, 2020
Telangiectasia-ectodermal dysplasia-brachydactyly-cardiac anomaly syndrome is caused by de novo mutations in <i>protein kinase D1</i>Svenja Alter, Andreas David Zimmer, Misun Park, et al.
European Journal of Medical Genetics|July 9, 2011
A 2 Mb deletion in 14q13 associated with severe developmental delay and hemophagocytic lymphohistiocytosisAlmuth Caliebe, Jose I Martin Subero, Hiltrud Muhle, et al.
Nature|March 27, 2023
Formin-mediated nuclear actin at androgen receptors promotes transcriptionJulian Knerr, Ralf Werner, Carsten Schwan, et al.
Plos One|March 19, 2015
In vivo investigations of the effect of short- and long-term recombinant growth hormone treatment on DNA-methylation in humansJulia Kolarova, Ole Ammerpohl, Jana Gutwein, et al.
Breast Care (Basel, Switzerland)|March 15, 2021
A Giant Mammary Hamartoma in a Young Breast Cancer PatientAnna-Lena Rumpf, Micaela Mathiak, Fritz K Schäfer, et al.
Plos One|June 23, 2012
DNA-methylation profiling of fetal tissues reveals marked epigenetic differences between chorionic and amniotic samplesChristel Eckmann-Scholz, Susanne Bens, Julia Kolarova, et al.
Blood Advances|September 9, 2021
Aggressive B-cell lymphoma cases with 11q aberration patterns indicate a spectrum beyond Burkitt-like lymphomaNiklas Gebauer, Hanno M Witte, Hartmut Merz, et al.
Human Mutation|October 23, 2009
A specific mutation in the distant sonic hedgehog (SHH) cis-regulator (ZRS) causes Werner mesomelic syndrome (WMS) while complete ZRS duplications underlie Haas type polysyndactyly and preaxial polydactyly (PPD) with or without triphalangeal thumbDagmar Wieczorek, Barbara Pawlik, Yun Li, et al.
Pageof 9