All Stories

  1. CED-3 caspase acts with miRNAs to regulate non-apoptotic gene expression dynamics for robust development in C. elegans
  2. Peroxisome Protein Transportation Affects Metabolism of Branched-Chain Fatty Acids That Critically Impact Growth and Development of C. elegans
  3. Functional Analysis of Neuronal MicroRNAs in Caenorhabditis elegans Dauer Formation by Combinational Genetics and Neuronal miRISC Immunoprecipitation
  4. A novel sphingolipid-TORC1 pathway critically promotes postembryonic development in Caenorhabditis elegans
  5. Fat chance for longevity
  6. Systematic Analysis of Tissue-Restricted miRISCs Reveals a Broad Role for MicroRNAs in Suppressing Basal Activity of the C. elegans Pathogen Response
  7. Regulation of maternal phospholipid composition and IP3-dependent embryonic membrane dynamics by a specific fatty acid metabolic event in C. elegans
  8. The fatty acid synthasefasn-1acts upstream of WNK and Ste20/GCK-VI kinases to modulate antimicrobial peptide expression inC. elegansepidermis
  9. Systematic analysis of dynamic miRNA-target interactions during C. elegans development
  10. P-Type ATPase TAT-2 Negatively Regulates Monomethyl Branched-Chain Fatty Acid Mediated Function in Post-Embryonic Growth and Development in C. elegans
  11. A branched-chain fatty acid is involved in post-embryonic growth control in parallel to the insulin receptor pathway and its biosynthesis is feedback-regulated in C. elegans
  12. Systematic Identification of C. elegans miRISC Proteins, miRNAs, and mRNA Targets by Their Interactions with GW182 Proteins AIN-1 and AIN-2
  13. GW182 family proteins are crucial for microRNA-mediated gene silencing
  14. The Developmental Timing Regulator AIN-1 Interacts with miRISCs and May Target the Argonaute Protein ALG-1 to Cytoplasmic P Bodies in C. elegans
  15. Monomethyl Branched-Chain Fatty Acids Play an Essential Role in Caenorhabditis elegans Development
  16. lin-35/Rb Cooperates With the SWI/SNF Complex to Control Caenorhabditis elegans Larval Development
  17. A 5-bp deletion in ELOVL4 is associated with two related forms of autosomal dominant macular dystrophy. Zhang K,∗ Kniazeva M, Han M, Li W, Yu Z, Yang Z, Li Y, Metzker ML, Allikmets R, Zack DJ, Kakuk L, Lagali PS, Wong PW, MacDonald IM, Sieving PA, Figu...
  18. A new locus for dominant drusen and macular degeneration maps to chromosome 6q14
  19. A novel mutation in the ABCR gene in four patients with autosomal recessive Stargardt disease
  20. The ABCR Gene in Recessive and Dominant Stargardt Diseases: A Genetic Pathway in Macular Degeneration
  21. A New Locus for Autosomal Dominant Stargardt-Like Disease Maps to Chromosome 4
  22. Clinical and genetic studies of an autosomal dominant cone-rod dystrophy with features of Stargardt disease
  23. Addition of second primer after initial denaturation step in PCR cycling: a simple way to avoid low-molecular-weight non-specific products