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Role of maternal spiralian-specific homeobox gene SPILE-E in the specification of blastomeres along the animal-vegetal axis during the early cleavage stages of mollusks. onlinelibrary.wiley.com/doi/10 in Nipponacmea fuscoviridis (limpet)

Nsp14 of SARS-CoV-2 inhibits mRNA processing and nuclear export by targeting the nuclear cap-binding complex. academic.oup.com/nar/advance-a

Calcium dynamics at the neural cell primary cilium regulate Hedgehog signaling-dependent neurogenesis in the embryonic neural tube. pnas.org/doi/10.1073/pnas.2220

Development of a Gene and Nucleic Acid Delivery System for Skeletal Muscle Administration via Limb Perfusion Using Nanobubbles and Ultrasound. mdpi.com/1999-4923/15/6/1665 mdpi.com/1999-4923/15/6/1665

Jak2 and Jaw Muscles Are Required for Buccopharyngeal Membrane Perforation during Mouth Development. mdpi.com/2221-3759/11/2/24

Mitochondrial calcium signaling mediated transcriptional regulation of keratin filaments is a critical determinant of melanogenesis. biorxiv.org/content/10.1101/20

Genetic and protein interaction studies between the ciliary dyslexia candidate genes DYX1C1 and DCDC2. bmcmolcellbiol.biomedcentral.c

Etv5a suppresses neural progenitor cell proliferation by inhibiting sox2 transcription. liebertpub.com/doi/10.1089/scd

Development and validation of a high throughput screening platform to enable target identification in skeletal muscle cells from Duchenne Muscular Dystrophy (DMD) patients. biorxiv.org/content/10.1101/20 Vivo-

A median fin derived from the lateral plate mesoderm and the origin of paired fins. nature.com/articles/s41586-023

Cerebellar granular neuron progenitors exit their germinative niche via Barhl1 mediated silencing of T-Cell Factor transcriptional activity. biorxiv.org/content/10.1101/20

Neural crest E-cadherin loss drives cleft lip/palate by epigenetic modulation via pro-inflammatory gene-environment interaction. nature.com/articles/s41467-023

Mutation of vsx genes in zebrafish highlights the robustness of the retinal specification network. elifesciences.org/articles/855

Identification of an α-l-iduronidase (IDUA) M1T mutation in a Chinese family with autosomal recessive mucopolysaccharidosis I. nyaspubs.onlinelibrary.wiley.c

Cryo-EM structure of the Mon1–Ccz1–RMC1 complex reveals molecular basis of metazoan RAB7A activation. pnas.org/doi/10.1073/pnas.2301

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