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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 dysplasia
Salem 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 specificity
Thomas 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 angiosperms
Kimmo 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 syndrome
Alma Kuechler, Janine Altmüller, Peter Nürnberg, et al.
Genome Biology
|
May 16, 2022
RNA modification mapping with JACUSA2
Michael 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 pathway
Matthias 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 product
Janine 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 Chemoreceptors
Caroline 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 13-13
Benjamin Kalbe, Markus Osterloh, Viola M Schulz, et al.
Page
of 33
Search research articles
Search
Showing results (11-20 of 326) with videos related to
Sort By:
Page
of 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 dysplasia
Salem 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 specificity
Thomas 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 angiosperms
Kimmo 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 syndrome
Alma Kuechler, Janine Altmüller, Peter Nürnberg, et al.
Genome Biology
|
May 16, 2022
RNA modification mapping with JACUSA2
Michael 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 pathway
Matthias 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 product
Janine 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 Chemoreceptors
Caroline 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 13-13
Benjamin Kalbe, Markus Osterloh, Viola M Schulz, et al.
Page
of 33