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Janine Altmüller

Showing results (11-20 of 326) with videos related to

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Cold Spring Harbor Molecular Case Studies|December 21, 2017
Late diagnosis of a truncating <i>WISP3</i> mutation entails a severe phenotype of progressive pseudorheumatoid dysplasiaSalem Alawbathani, Amit Kawalia, Mert Karakaya, et al.
Journal of Biomolecular Structure & Dynamics|June 19, 2012
Apoptotic cleavage of DNA in human lymphocyte chromatin shows high sequence specificityThomas Bettecken, Zakharia M Frenkel, Janine Altmüller, et al.
Plant Methods|January 1, 2020
A protocol for laser microdissection (LMD) followed by transcriptome analysis of plant reproductive tissue in phylogenetically distant angiospermsKimmo Kivivirta, Denise Herbert, Matthias Lange, et al.
Molecular and Cellular Probes|July 18, 2015
Exome sequencing identifies a novel heterozygous TGFB3 mutation in a disorder overlapping with Marfan and Loeys-Dietz syndromeAlma Kuechler, Janine Altmüller, Peter Nürnberg, et al.
Genome Biology|May 16, 2022
RNA modification mapping with JACUSA2Michael Piechotta, Isabel S Naarmann-de Vries, Qi Wang, et al.
Respiratory Research|April 8, 2006
Asthma families show transmission disequilibrium of gene variants in the vitamin D metabolism and signalling pathwayMatthias Wjst, Janine Altmüller, Theresia Faus-Kessler, et al.
Biological Chemistry|March 30, 2016
A systematic comparison of two new releases of exome sequencing products: the aim of use determines the choice of productJanine Altmüller, Susanne Motameny, Christian Becker, et al.
Plos One|June 13, 2015
RNA-Seq Analysis of Human Trigeminal and Dorsal Root Ganglia with a Focus on ChemoreceptorsCaroline Flegel, Nicole Schöbel, Janine Altmüller, et al.
Molecular Medicine Reports|December 20, 2017
Whole exome sequencing identifies a mutation in EYA1 and GLI3 in a patient with branchio‑otic syndrome and esophageal atresia: Coincidence or a digenic mode of inheritance?Franziska Kause, Heiko Reutter, Florian Marsch, et al.
Archives of Biochemistry and Biophysics|March 22, 2018
OR2H2 regulates the differentiation of human myoblast cells by its ligand aldehyde 13-13Benjamin Kalbe, Markus Osterloh, Viola M Schulz, et al.
Pageof 33

Showing results (11-20 of 326) with videos related to

Sort By:
Pageof 33
Cold Spring Harbor Molecular Case Studies|December 21, 2017
Late diagnosis of a truncating <i>WISP3</i> mutation entails a severe phenotype of progressive pseudorheumatoid dysplasiaSalem Alawbathani, Amit Kawalia, Mert Karakaya, et al.
Journal of Biomolecular Structure & Dynamics|June 19, 2012
Apoptotic cleavage of DNA in human lymphocyte chromatin shows high sequence specificityThomas Bettecken, Zakharia M Frenkel, Janine Altmüller, et al.
Plant Methods|January 1, 2020
A protocol for laser microdissection (LMD) followed by transcriptome analysis of plant reproductive tissue in phylogenetically distant angiospermsKimmo Kivivirta, Denise Herbert, Matthias Lange, et al.
Molecular and Cellular Probes|July 18, 2015
Exome sequencing identifies a novel heterozygous TGFB3 mutation in a disorder overlapping with Marfan and Loeys-Dietz syndromeAlma Kuechler, Janine Altmüller, Peter Nürnberg, et al.
Genome Biology|May 16, 2022
RNA modification mapping with JACUSA2Michael Piechotta, Isabel S Naarmann-de Vries, Qi Wang, et al.
Respiratory Research|April 8, 2006
Asthma families show transmission disequilibrium of gene variants in the vitamin D metabolism and signalling pathwayMatthias Wjst, Janine Altmüller, Theresia Faus-Kessler, et al.
Biological Chemistry|March 30, 2016
A systematic comparison of two new releases of exome sequencing products: the aim of use determines the choice of productJanine Altmüller, Susanne Motameny, Christian Becker, et al.
Plos One|June 13, 2015
RNA-Seq Analysis of Human Trigeminal and Dorsal Root Ganglia with a Focus on ChemoreceptorsCaroline Flegel, Nicole Schöbel, Janine Altmüller, et al.
Molecular Medicine Reports|December 20, 2017
Whole exome sequencing identifies a mutation in EYA1 and GLI3 in a patient with branchio‑otic syndrome and esophageal atresia: Coincidence or a digenic mode of inheritance?Franziska Kause, Heiko Reutter, Florian Marsch, et al.
Archives of Biochemistry and Biophysics|March 22, 2018
OR2H2 regulates the differentiation of human myoblast cells by its ligand aldehyde 13-13Benjamin Kalbe, Markus Osterloh, Viola M Schulz, et al.
Pageof 33