From: Charles Plessy Date: Tue, 12 Sep 2017 03:31:31 +0000 (+0900) Subject: Old. X-Git-Url: https://source.charles.plessy.org/?a=commitdiff_plain;h=083c8502e2e8e0f443255ae30f43c1110335fba0;p=source.git Old. --- diff --git a/biblio/15520289.mdwn b/biblio/15520289.mdwn index 4544374d..42fcc474 100644 --- a/biblio/15520289.mdwn +++ b/biblio/15520289.mdwn @@ -1,3 +1,10 @@ [[!meta title="The human L1 promoter: variable transcription initiation sites and a major impact of upstream flanking sequence on promoter activity."]] [[!tag cap enzyme]] + +Lavie L, Maldener E, Brouha B, Meese EU, Mayer J. + +Genome Res. 2004 Nov;14(11):2253-60 doi:10.1101/gr.2745804 + +The human L1 promoter: variable transcription initiation sites and a major impact of upstream flanking sequence on promoter activity. + [[!pmid 15520289 desc="The presence of an extra G in pseudogenes suggests that many reverse-transcriptases can reverse transcribe the cap."]] diff --git a/biblio/15897197.mdwn b/biblio/15897197.mdwn new file mode 100644 index 00000000..dd5b00c6 --- /dev/null +++ b/biblio/15897197.mdwn @@ -0,0 +1,10 @@ +[[!meta title="Novel 3'-ribonuclease and 3'-phosphatase activities of the bacterial non-homologous end-joining protein, DNA ligase D."]] +[[!tag ligase enzyme]] + +Zhu H, Shuman S. + +J Biol Chem. 2005 Jul 15;280(28):25973-81 doi:10.1074/jbc.M504002200 + +Novel 3′-ribonuclease and 3′-phosphatase activities of the bacterial non-homologous end-joining protein, DNA ligase D. + +[[!pmid 15897197 desc="These activities depend on Mn2+, and could be used to generate a 3'rNOH or 3'rNp oligo."]] diff --git a/biblio/To_Do b/biblio/To_Do index fa184b44..de90bf13 100644 --- a/biblio/To_Do +++ b/biblio/To_Do @@ -563,9 +563,6 @@ Conserved in human, mouse and oppossum. What about fish ? 15919954 [miRNA] Very sharp expression patterns. -15897197 [enzymes] -These activities depend on Mn2+, and could be used to generate a 3'rNOH or 3'rNp oligo. - 15979195 [enhancers] A 5' GC-rich / AT-rich, and a conversely 3' AT-rich / GC-rich motifs were discovered. The change in nucleotide composition seems to delinate the boundaries of the enhancers.