Henrike Indrischek
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View article: Vision-related convergent gene losses reveal SERPINE3’s unknown role in the eye
Vision-related convergent gene losses reveal SERPINE3’s unknown role in the eye Open
Despite decades of research, knowledge about the genes that are important for development and function of the mammalian eye and are involved in human eye disorders remains incomplete. During mammalian evolution, mammals that naturally exhi…
View article: Author response: Vision-related convergent gene losses reveal SERPINE3’s unknown role in the eye
Author response: Vision-related convergent gene losses reveal SERPINE3’s unknown role in the eye Open
Article Figures and data Abstract Editor's evaluation Introduction Results Discussion Materials and methods Appendix 1 Data availability References Decision letter Author response Article and author information Metrics Abstract Despite dec…
View article: Vision-related convergent gene losses reveal <i>SERPINE3</i> ’s unknown role in the eye
Vision-related convergent gene losses reveal <i>SERPINE3</i> ’s unknown role in the eye Open
Despite decades of research, knowledge about the genes that are important for development and function of the mammalian eye and are involved in human eye disorders remains incomplete. During mammalian evolution, mammals that naturally exhi…
View article: Positive Selection in Gene Regulatory Factors Suggests Adaptive Pleiotropic Changes During Human Evolution
Positive Selection in Gene Regulatory Factors Suggests Adaptive Pleiotropic Changes During Human Evolution Open
Gene regulatory factors (GRFs), such as transcription factors, co-factors and histone-modifying enzymes, play many important roles in modifying gene expression in biological processes. They have also been proposed to underlie speciation an…
View article: Divergent evolution in the genomes of closely related lacertids, <i>Lacerta viridis</i> and <i>L. bilineata</i>, and implications for speciation
Divergent evolution in the genomes of closely related lacertids, <i>Lacerta viridis</i> and <i>L. bilineata</i>, and implications for speciation Open
Background Lacerta viridis and Lacerta bilineata are sister species of European green lizards (eastern and western clades, respectively) that, until recently, were grouped together as the L. viridis complex. Genetic incompatibilities were …
View article: Introducing evolutionary biologists to the analysis of big data: guidelines to organize extended bioinformatics training courses
Introducing evolutionary biologists to the analysis of big data: guidelines to organize extended bioinformatics training courses Open
Research in evolutionary biology has been progressively influenced by big data such as massive genome and transcriptome sequencing data, scalar measurements of several phenotypes on tens to thousands of individuals, as well as from collect…
View article: Tracing the evolution of the heterotrimeric G protein α subunit in Metazoa
Tracing the evolution of the heterotrimeric G protein α subunit in Metazoa Open
View article: Additional file 5: of Tracing the evolution of the heterotrimeric G protein α subunit in Metazoa
Additional file 5: of Tracing the evolution of the heterotrimeric G protein α subunit in Metazoa Open
Supplemental file 6. ML trees of the non-Vertebrata Deuterostomia preGNAI and preGNAQ nucleotide sequences which corresponded to the mutually exclusive exons, exon6 or exon5, respectively. Bootstrapped replicates were summarized into Exten…
View article: Additional file 3: of Tracing the evolution of the heterotrimeric G protein α subunit in Metazoa
Additional file 3: of Tracing the evolution of the heterotrimeric G protein α subunit in Metazoa Open
Supplemental file 4. Maximum Likelihood Tree built on the nucleotide level further supports the emergence of GNAI1–4, GNAT1–4, and GNAZ, in addition to GNAO paralogs from the 2R WGD in Vertebrata. It shows the pattern of GNAI0-GNAT0 duplic…
View article: Additional file 4: of Tracing the evolution of the heterotrimeric G protein α subunit in Metazoa
Additional file 4: of Tracing the evolution of the heterotrimeric G protein α subunit in Metazoa Open
Supplemental file 5. Maximum Likelihood Tree of duplications of exon4 in GNAQ and GNA11 and the homologous sequence of preGNAI, encoded by exon5, duplicated in Urochordata. Bootstrapped replicates were summarized into Extended Majority Rul…
View article: Additional file 1: of Tracing the evolution of the heterotrimeric G protein α subunit in Metazoa
Additional file 1: of Tracing the evolution of the heterotrimeric G protein α subunit in Metazoa Open
Table S1. Species Evaluated. All major branches of Deuterostomia were investigated using the EMS pipeline (where sequenced genomes exist). Nine species were also included from non-Deuterostomia Opisthokonta lineages to act as outgroups. Co…
View article: Uncovering missing pieces: duplication and deletion history of arrestins in deuterostomes
Uncovering missing pieces: duplication and deletion history of arrestins in deuterostomes Open
View article: Dataset: Uncovering Missing Pieces. Duplication And Deletion History Of Arrestins In Deuterostomes.
Dataset: Uncovering Missing Pieces. Duplication And Deletion History Of Arrestins In Deuterostomes. Open
This is the dataset accompanying the following publication: Uncovering missing pieces: Duplication and deletion history of arrestins in deuterostomes. See abstract below. Background The cytosolic arrestin proteins mediate desensitization o…
View article: Dataset: Uncovering Missing Pieces. Duplication And Deletion History Of Arrestins In Deuterostomes.
Dataset: Uncovering Missing Pieces. Duplication And Deletion History Of Arrestins In Deuterostomes. Open
This is the dataset accompanying the following publication: Uncovering missing pieces: Duplication and deletion history of arrestins in deuterostomes. See abstract below. Background The cytosolic arrestin proteins mediate desensitization o…
View article: Correction: Corrigendum: Differential transcriptional responses to Ebola and Marburg virus infection in bat and human cells
Correction: Corrigendum: Differential transcriptional responses to Ebola and Marburg virus infection in bat and human cells Open
Scientific Reports 6: Article number: 34589; published online: 07 October 2016; updated: 11 January 2017 In this Article, Ivo Grosse is incorrectly affiliated to “Department of Soil Ecology, UFZ - Helmholtz Centre for Environmental Researc…
View article: Additional file 3 of Uncovering missing pieces: duplication and deletion history of arrestins in deuterostomes
Additional file 3 of Uncovering missing pieces: duplication and deletion history of arrestins in deuterostomes Open
ML tree of arrestins (depicted in Fig. 4). Starting information for tree reconstruction was an alignment of arrestins investigated in this study, for which sequence information was close to complete. Sequences derived from genomic annotati…
View article: Additional file 6 of Uncovering missing pieces: duplication and deletion history of arrestins in deuterostomes
Additional file 6 of Uncovering missing pieces: duplication and deletion history of arrestins in deuterostomes Open
Chromosomal locations: Chromosomal locations of arrestin genes. Table of chromosomal locations of arrestin genes in species with genomes assembled on chromosome-level. The columns â SAG(a)â contain the location of SAG for non-duplicated sp…
View article: Additional file 4 of Uncovering missing pieces: duplication and deletion history of arrestins in deuterostomes
Additional file 4 of Uncovering missing pieces: duplication and deletion history of arrestins in deuterostomes Open
Maximum clade credibility tree of arrestins. Starting from the same alignment as used for Additional file 3, we constructed a phylogenetic tree with BEAST2 [94] under the Birth Death model with a relaxed molecular clock (log normal) using …
View article: Additional file 5 of Uncovering missing pieces: duplication and deletion history of arrestins in deuterostomes
Additional file 5 of Uncovering missing pieces: duplication and deletion history of arrestins in deuterostomes Open
ML tree of arrestins excluding columns known to confer receptor binding. The tree was constructed from the same alignment as Additional file 3 deleting the columns known to confer receptor specificity according to [2, 17, 19, 23, 31â 33] (…
View article: Additional file 2 of Uncovering missing pieces: duplication and deletion history of arrestins in deuterostomes
Additional file 2 of Uncovering missing pieces: duplication and deletion history of arrestins in deuterostomes Open
Approximate ML tree of the arrestin fold family as extracted from UniProtKB (depicted in Additional file 1: Figure S1). Hits were assigned to the arrestin fold family if they contained at least one arrestin_N or arrestin_C domain (see Meth…
View article: Additional file 7 of Uncovering missing pieces: duplication and deletion history of arrestins in deuterostomes
Additional file 7 of Uncovering missing pieces: duplication and deletion history of arrestins in deuterostomes Open
Alignment of deuterostome arrestins with functional annotation known from experimental studies of arrestins in mammals. Note that the naming differs from the naming used throughout the manuscript with ARR1, ARR2, ARR3 and ARR4 used instead…
View article: Differential transcriptional responses to Ebola and Marburg virus infection in bat and human cells
Differential transcriptional responses to Ebola and Marburg virus infection in bat and human cells Open
View article: The paralog-to-contig assignment problem: high quality gene models from fragmented assemblies
The paralog-to-contig assignment problem: high quality gene models from fragmented assemblies Open
The ExonMatchSolver-pipeline can be employed to build highly accurate models of protein coding genes even when spanning several genomic fragments. This sets the stage for a better understanding of the evolutionary history within particular…
View article: MOESM3 of The paralog-to-contig assignment problem: high quality gene models from fragmented assemblies
MOESM3 of The paralog-to-contig assignment problem: high quality gene models from fragmented assemblies Open
Additional file 3. Memory and time requirements of the ExonMatchSolver on simulated data. The raw data is provided as Addtional_file3.xlsx. Raw data on memory and time assessment of the ExonMatchSolver on simulated data. The memory and tim…