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期刊名:Genetics

缩写:GENETICS

ISSN:0016-6731

e-ISSN:1943-2631

IF/分区:5.1/Q1

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共收录本刊相关文章索引4741
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Yunshu Song,Christopher H Seward,Chih-Ying Chen et al. Yunshu Song et al.
Rearrangements within the AUTS2 region are associated with a rare syndromic disorder with intellectual disability, developmental delay, and behavioral abnormalities as core features. In addition, smaller regional variants are linked to wide...
Erika L Ellison,Peng Zhou,Peter Hermanson et al. Erika L Ellison et al.
The highly active family of Mutator (Mu) DNA transposons has been widely used for forward and reverse genetics in maize. There are examples of Mu-suppressible alleles that result in conditional phenotypic effects based on the activity of Mu...
Matthew B Lohse,Naomi Ziv,Alexander D Johnson Matthew B Lohse
Candida albicans, a normal member of the human microbiome and an opportunistic fungal pathogen, undergoes several morphological transitions. One of these transitions is white-opaque switching, where C. albicans alternates between 2 stable c...
Bipasha Dey,Debasmita Mitra,Tirthasree Das et al. Bipasha Dey et al.
Epithelial cells contain polarity complexes on the lateral membrane and are organized in a hexagon-dominated polygonal array. The mechanisms regulating the organization of polygonal architecture in metazoan embryogenesis are not completely ...
Oscar Delaney,Andrew D Letten,Jan Engelstädter Oscar Delaney
Serial passaging is a fundamental technique in experimental evolution. The choice of bottleneck severity and frequency poses a dilemma: longer growth periods allow beneficial mutants to arise and grow over more generations, but simultaneous...
Marion Boeglin,Eduardo Leyva-Díaz,Oliver Hobert Marion Boeglin
Sec1/Munc18 (SM) proteins are important regulators of SNARE complex assembly during exocytosis throughout all major animal tissue types. However, expression of a founding member of the SM family, UNC-18, is mostly restricted to the nervous ...
Daniel Schmitz,Zhiwei Li,Valeria Lo Faro et al. Daniel Schmitz et al.
Structural variations, including copy number variations (CNVs), affect around 20 million bases in the human genome and are common causes of rare conditions. CNVs are rarely investigated in complex disease research because most CNVs are not ...
Pascale Lemieux,David Bradley,Alexandre K Dubé et al. Pascale Lemieux et al.
Protein-protein interactions (PPIs) drive many cellular processes. Some interactions are directed by Src homology 3 (SH3) domains that bind proline-rich motifs on other proteins. The evolution of the binding specificity of SH3 domains is no...