Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Laura E. Yu"'
Publikováno v:
PLoS ONE, Vol 5, Iss 8, p e12235 (2010)
Mitochondrial mRNA editing in Trypanosoma brucei requires the specific interaction of a guide RNA with its cognate mRNA. Hundreds of gRNAs are involved in the editing process, each needing to target their specific editing domain within the target mes
Externí odkaz:
https://doaj.org/article/7424945d2c3e47e2abf1425dec09d8d0
Publikováno v:
RNA Biology. 1:27-33
The most dramatic example of RNA editing is found in the mitochondria of trypanosomes. In these organisms, U-insertions/deletions can create mRNAs that are twice as large as the gene that encodes them. Guide RNAs (gRNAs) that are complementary to sho
Autor:
Donna J. Koslowsky, Laura E. Yu
Publikováno v:
RNA (New York, N.Y.). 12(6)
Expression of mitochondrial genes in Trypanosoma brucei requires RNA editing of its mRNA transcripts. During editing, uridylates are precisely inserted and deleted as directed by the gRNA template to create the protein open reading frame. This proces
Autor:
Larissa Reifur, Donna J. Koslowsky, Laura E. Yu, Sandra L. Clement, Andrea M. Hingst, Melissa K. Mingler
Publikováno v:
Molecular and biochemical parasitology. 150(1)
A new class of organellar proteins, characterized by pentatricopeptide repeat (PPR) motifs, has been identified in plants. These proteins contain multiple 35-amino acid repeats that are proposed to form a super helix capable of binding a strand of RN
Autor:
Diana E. Northup, Laura E. Yu, Kathleen E. Dano, Cynthia A. Connolly, Susan M. Barns, Michael N. Spilde, Clifford N. Dahm, Rachel T. Schelble, Donald O. Natvig, Penelope J. Boston, Laura J. Crossey
Publikováno v:
Environmental microbiology. 5(11)
Summary Lechuguilla Cave is an ancient, deep, oligotrophic subterranean environment that contains an abundance of low-density ferromanganese deposits, the origin of which is uncertain. To assess the possibility that biotic factors may be involved in
Autor:
Jill L. Elfenbein, Edi Lúcia Sartorato, Rachel Fisher, Karen H. Friderici, Caryn R. Rothrock, Alessandra Murgia, Emanuela Leonardi, Laura E. Yu, Sarah L. Lebeis, Sainan Wei
Publikováno v:
Human genetics. 113(1)
Non-syndromic hearing impairment (NSHI) is the most common form of deafness and presents with no other symptoms or sensory defects. Mutations in the gap junction gene GJB2 account for a high proportion of recessive NSHI. The GJB2 gene encodes connexi