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Julia Böck

Showing results (1-10 of 20) with videos related to

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International Journal of Molecular Sciences|June 18, 2020
Evolutionary Aspects of TRPMLs and TPCsDawid Jaślan, Julia Böck, Einar Krogsaeter, et al.
Cells|September 23, 2022
Neurodegenerative Lysosomal Storage Disorders: TPC2 Comes to the Rescue!Sandra Prat Castro, Veronika Kudrina, Dawid Jaślan, et al.
Plos One|April 9, 2013
Sterile alpha motif containing 7 (samd7) is a novel crx-regulated transcriptional repressor in the retinaJulia Hlawatsch, Marcus Karlstetter, Alexander Aslanidis, et al.
Plos Genetics|January 19, 2021
Human genome diversity data reveal that L564P is the predominant TPC2 variant and a prerequisite for the blond hair associated M484L gain-of-function effectJulia Böck, Einar Krogsaeter, Marcel Passon, et al.
Epigenomics|September 22, 2018
Allele-specific methylation of imprinted genes in fetal cord blood is influenced by cis-acting genetic variants and parental factorsRamya Potabattula, Marcus Dittrich, Julia Böck, et al.
Frontiers in Oncology|September 4, 2023
Targeted panel sequencing in the routine diagnosis of mature T- and NK-cell lymphomas: report of 128 cases from two German reference centersJulia Böck, Katja Maurus, Elena Gerhard-Hartmann, et al.
Gene|July 30, 2016
CpG sites with continuously increasing or decreasing methylation from early to late human fetal brain developmentEberhard Schneider, Marcus Dittrich, Julia Böck, 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.
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.
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.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
International Journal of Molecular Sciences|June 18, 2020
Evolutionary Aspects of TRPMLs and TPCsDawid Jaślan, Julia Böck, Einar Krogsaeter, et al.
Cells|September 23, 2022
Neurodegenerative Lysosomal Storage Disorders: TPC2 Comes to the Rescue!Sandra Prat Castro, Veronika Kudrina, Dawid Jaślan, et al.
Plos One|April 9, 2013
Sterile alpha motif containing 7 (samd7) is a novel crx-regulated transcriptional repressor in the retinaJulia Hlawatsch, Marcus Karlstetter, Alexander Aslanidis, et al.
Plos Genetics|January 19, 2021
Human genome diversity data reveal that L564P is the predominant TPC2 variant and a prerequisite for the blond hair associated M484L gain-of-function effectJulia Böck, Einar Krogsaeter, Marcel Passon, et al.
Epigenomics|September 22, 2018
Allele-specific methylation of imprinted genes in fetal cord blood is influenced by cis-acting genetic variants and parental factorsRamya Potabattula, Marcus Dittrich, Julia Böck, et al.
Frontiers in Oncology|September 4, 2023
Targeted panel sequencing in the routine diagnosis of mature T- and NK-cell lymphomas: report of 128 cases from two German reference centersJulia Böck, Katja Maurus, Elena Gerhard-Hartmann, et al.
Gene|July 30, 2016
CpG sites with continuously increasing or decreasing methylation from early to late human fetal brain developmentEberhard Schneider, Marcus Dittrich, Julia Böck, 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.
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.
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.
Pageof 2