Hasil Pencarian - Almuth Caliebe

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  1. 1
    Case Report: GNAQ- and SF3B1 Mutations in an Aggressive Case of Relapsing Uveal Ring Melanoma

    Case Report: GNAQ- and SF3B1 Mutations in an Aggressive Case of Relapsing Uveal Ring Melanoma oleh Michelle Prasuhn, Josephine Christin Freitag, Sabine Lüken, Vinodh Kakkassery, Hartmut Merz, Almuth Caliebe, Malte Spielmann, Mahdy Ranjbar, Felix Rommel

    Diterbitkan 2022-05-01
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  2. 2
    Correction: Deep Bisulfite Sequencing of Aberrantly Methylated Loci in a Patient with Multiple Methylation Defects.

    Correction: Deep Bisulfite Sequencing of Aberrantly Methylated Loci in a Patient with Multiple Methylation Defects. oleh Jasmin Beygo, Ole Ammerpohl, Daniela Gritzan, Melanie Heitmann, Katrin Rademacher, Julia Richter, Almuth Caliebe, Reiner Siebert, Bernhard Horsthemke, Karin Buiting

    Diterbitkan 2013-01-01
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  3. 3
    Deep bisulfite sequencing of aberrantly methylated loci in a patient with multiple methylation defects.

    Deep bisulfite sequencing of aberrantly methylated loci in a patient with multiple methylation defects. oleh Jasmin Beygo, Ole Ammerpohl, Daniela Gritzan, Melanie Heitmann, Katrin Rademacher, Julia Richter, Almuth Caliebe, Reiner Siebert, Bernhard Horsthemke, Karin Buiting

    Diterbitkan 2013-01-01
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  4. 4
    In vivo investigations of the effect of short- and long-term recombinant growth hormone treatment on DNA-methylation in humans.

    In vivo investigations of the effect of short- and long-term recombinant growth hormone treatment on DNA-methylation in humans. oleh Julia Kolarova, Ole Ammerpohl, Jana Gutwein, Maik Welzel, Inka Baus, Felix G Riepe, Thomas Eggermann, Almuth Caliebe, Paul-Martin Holterhus, Reiner Siebert, Susanne Bens

    Diterbitkan 2015-01-01
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  5. 5
    DNA-methylation profiling of fetal tissues reveals marked epigenetic differences between chorionic and amniotic samples.

    DNA-methylation profiling of fetal tissues reveals marked epigenetic differences between chorionic and amniotic samples. oleh Christel Eckmann-Scholz, Susanne Bens, Julia Kolarova, Sina Schneppenheim, Almuth Caliebe, Simone Heidemann, Constantin von Kaisenberg, Monika Kautza, Walter Jonat, Reiner Siebert, Ole Ammerpohl

    Diterbitkan 2012-01-01
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  6. 6
    LINE1-mediated epigenetic repression of androgen receptor transcription causes androgen insensitivity syndrome

    LINE1-mediated epigenetic repression of androgen receptor transcription causes androgen insensitivity syndrome oleh Jelena Pozojevic, Radhika Sivaprasad, Joshua Laß, Franziska Haarich, Joanne Trinh, Naseebullah Kakar, Kristin Schulz, Kristian Händler, Annemarie A. Verrijn Stuart, Jacques C. Giltay, Koen L. van Gassen, Almuth Caliebe, Paul-Martin Holterhus, Malte Spielmann, Nadine C. Hornig

    Diterbitkan 2024-07-01
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  7. 7
    Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease.

    Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease. oleh Enrique Audain, Anna Wilsdon, Jeroen Breckpot, Jose M G Izarzugaza, Tomas W Fitzgerald, Anne-Karin Kahlert, Alejandro Sifrim, Florian Wünnemann, Yasset Perez-Riverol, Hashim Abdul-Khaliq, Mads Bak, Anne S Bassett, D Woodrow Benson, Felix Berger, Ingo Daehnert, Koenraad Devriendt, Sven Dittrich, Piers Ef Daubeney, Vidu Garg, Karl Hackmann, Kirstin Hoff, Philipp Hofmann, Gregor Dombrowsky, Thomas Pickardt, Ulrike Bauer, Bernard D Keavney, Sabine Klaassen, Hans-Heiner Kramer, Christian R Marshall, Dianna M Milewicz, Scott Lemaire, Joseph S Coselli, Michael E Mitchell, Aoy Tomita-Mitchell, Siddharth K Prakash, Karl Stamm, Alexandre F R Stewart, Candice K Silversides, Reiner Siebert, Brigitte Stiller, Jill A Rosenfeld, Inga Vater, Alex V Postma, Almuth Caliebe, J David Brook, Gregor Andelfinger, Matthew E Hurles, Bernard Thienpont, Lars Allan Larsen, Marc-Phillip Hitz

    Diterbitkan 2021-07-01
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  8. 8
    Correction: Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease.

    Correction: Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease. oleh Enrique Audain, Anna Wilsdon, Jeroen Breckpot, Jose M G Izarzugaza, Tomas W Fitzgerald, Anne-Karin Kahlert, Alejandro Sifrim, Florian Wünnemann, Yasset Perez-Riverol, Hashim Abdul-Khaliq, Mads Bak, Anne S Bassett, D Woodrow Benson, Felix Berger, Ingo Daehnert, Koenraad Devriendt, Sven Dittrich, Piers Ef Daubeney, Vidu Garg, Karl Hackmann, Kirstin Hoff, Philipp Hofmann, Gregor Dombrowsky, Thomas Pickardt, Ulrike Bauer, Bernard D Keavney, Sabine Klaassen, Hans-Heiner Kramer, Christian R Marshall, Dianna M Milewicz, Scott Lemaire, Joseph S Coselli, Michael E Mitchell, Aoy Tomita-Mitchell, Siddharth K Prakash, Karl Stamm, Alexandre F R Stewart, Candice K Silversides, Reiner Siebert, Brigitte Stiller, Jill A Rosenfeld, Inga Vater, Alex V Postma, Almuth Caliebe, J David Brook, Gregor Andelfinger, Matthew E Hurles, Bernard Thienpont, Lars Allan Larsen, Marc-Phillip Hitz

    Diterbitkan 2021-09-01
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