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Open AccessImproving laboratory animal genetic reporting: LAG-R guidelines
The biomedical research community addresses reproducibility challenges in animal studies through standardized nomenclature, improved experimental design, transparent reporting, data sharing, and centralized re...
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Open AccessReverse genetics reveals single gene of every candidate on Hybrid sterility, X Chromosome QTL 2 (Hstx2) are dispensable for spermatogenesis
F1 hybrid progenies between related subspecies often show hybrid sterility (HS) or inviability. HS is caused by failure of meiotic chromosome synapsis and sex body formation in house mouse. Previous studies id...
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Open AccessPathogenic POGZ mutation causes impaired cortical development and reversible autism-like phenotypes
Pogo transposable element derived with ZNF domain (POGZ) has been identified as one of the most recurrently de novo mutated genes in patients with neurodevelopmental disorders (NDDs), including autism spectrum di...
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Correction: Corrigendum: High-throughput discovery of novel developmental phenotypes
Nature 537, 508–514 (2016); doi:10.1038/nature19356 In this Article, the author Wolfgang Wurst was erroneously omitted from the author list. They are associated with the affiliations: HelmholtzZentrum Munich, ...
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High-throughput discovery of novel developmental phenotypes
Approximately one-third of all mammalian genes are essential for life. Phenotypes resulting from knockouts of these genes in mice have provided tremendous insight into gene function and congenital disorders. A...
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Addendum: An expressed pseudogene regulates the messenger-RNA stability of its homologous coding gene
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An expressed pseudogene regulates the messenger-RNA stability of its homologous coding gene
A pseudogene is a gene copy that does not produce a functional, full-length protein1. The human genome is estimated to contain up to 20,000 pseudogenes2,3. Although much effort has been devoted to understanding t...