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Thomas Haaf

Showing results (101-110 of 190) with videos related to

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European Journal of Human Genetics : EJHG|March 1, 2007
De novo t(12;17)(p13.3;q21.3) translocation with a breakpoint near the 5' end of the HOXB gene cluster in a patient with developmental delay and skeletal malformationsYing Yue, Ruxandra Farcas, Gundula Thiel, et al.
Frontiers in Molecular Biosciences|May 6, 2026
Functional and genomic characterization of LCN2-deficient PC-3 cells reveals insights into prostate cancer progressionKiara Gäberlein, Diandra T Keller, Sarah K Schröder-Lange, et al.
International Journal of Cancer|April 17, 2018
Single CpG hypermethylation, allele methylation errors, and decreased expression of multiple tumor suppressor genes in normal body cells of mutation-negative early-onset and high-risk breast cancer patientsJulia Böck, Silke Appenzeller, Larissa Haertle, et al.
BMC Medical Genomics|June 9, 2019
Unbalanced segregation of a paternal t(9;11)(p24.3;p15.4) translocation causing familial Beckwith-Wiedemann syndrome: a case reportCaroline Lekszas, Indrajit Nanda, Barbara Vona, et al.
Molecular Reproduction and Development|February 11, 2017
Gene expression and epigenetic aberrations in F1-placentas fathered by obese malesMegan Mitchell, Reiner Strick, Pamela L Strissel, et al.
Plos One|August 31, 2017
Hypermethylation of the non-imprinted maternal MEG3 and paternal MEST alleles is highly variable among normal individualsLarissa Haertle, Anna Maierhofer, Julia Böck, et al.
Cells|June 10, 2022
Genetic Characterization of Rat Hepatic Stellate Cell Line HSC-T6 for In Vitro Cell Line AuthenticationIndrajit Nanda, Claus Steinlein, Thomas Haaf, et al.
Elife|February 27, 2020
Biallelic <i>TANGO1</i> mutations cause a novel syndromal disease due to hampered cellular collagen secretionCaroline Lekszas, Ombretta Foresti, Ishier Raote, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 24, 2002
A duplicated copy of DMRT1 in the sex-determining region of the Y chromosome of the medaka, Oryzias latipesIndrajit Nanda, Mariko Kondo, Ute Hornung, et al.
Molecular Biology and Evolution|March 14, 2009
Differences in DNA methylation patterns and expression of the CCRK gene in human and nonhuman primate corticesRuxandra Farcas, Eberhard Schneider, Katrin Frauenknecht, et al.
Pageof 19

Showing results (101-110 of 190) with videos related to

Sort By:
Pageof 19
European Journal of Human Genetics : EJHG|March 1, 2007
De novo t(12;17)(p13.3;q21.3) translocation with a breakpoint near the 5' end of the HOXB gene cluster in a patient with developmental delay and skeletal malformationsYing Yue, Ruxandra Farcas, Gundula Thiel, et al.
Frontiers in Molecular Biosciences|May 6, 2026
Functional and genomic characterization of LCN2-deficient PC-3 cells reveals insights into prostate cancer progressionKiara Gäberlein, Diandra T Keller, Sarah K Schröder-Lange, et al.
International Journal of Cancer|April 17, 2018
Single CpG hypermethylation, allele methylation errors, and decreased expression of multiple tumor suppressor genes in normal body cells of mutation-negative early-onset and high-risk breast cancer patientsJulia Böck, Silke Appenzeller, Larissa Haertle, et al.
BMC Medical Genomics|June 9, 2019
Unbalanced segregation of a paternal t(9;11)(p24.3;p15.4) translocation causing familial Beckwith-Wiedemann syndrome: a case reportCaroline Lekszas, Indrajit Nanda, Barbara Vona, et al.
Molecular Reproduction and Development|February 11, 2017
Gene expression and epigenetic aberrations in F1-placentas fathered by obese malesMegan Mitchell, Reiner Strick, Pamela L Strissel, et al.
Plos One|August 31, 2017
Hypermethylation of the non-imprinted maternal MEG3 and paternal MEST alleles is highly variable among normal individualsLarissa Haertle, Anna Maierhofer, Julia Böck, et al.
Cells|June 10, 2022
Genetic Characterization of Rat Hepatic Stellate Cell Line HSC-T6 for In Vitro Cell Line AuthenticationIndrajit Nanda, Claus Steinlein, Thomas Haaf, et al.
Elife|February 27, 2020
Biallelic <i>TANGO1</i> mutations cause a novel syndromal disease due to hampered cellular collagen secretionCaroline Lekszas, Ombretta Foresti, Ishier Raote, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 24, 2002
A duplicated copy of DMRT1 in the sex-determining region of the Y chromosome of the medaka, Oryzias latipesIndrajit Nanda, Mariko Kondo, Ute Hornung, et al.
Molecular Biology and Evolution|March 14, 2009
Differences in DNA methylation patterns and expression of the CCRK gene in human and nonhuman primate corticesRuxandra Farcas, Eberhard Schneider, Katrin Frauenknecht, et al.
Pageof 19