Results 201 to 210 of about 30,427,296 (288)

A single base pair substitution in zebrafish distinguishes between innate and acute startle behavior regulation. [PDF]

PLoS One
Ortiz EA, Campbell PD, Nelson JC, Granato M.   +3 more
europepmc   +1 more source

Staggered intercalation of DNA duplexes with base-pair modulation by two distinct drug molecules induces asymmetric backbone twisting and structure polymorphism. [PDF]

Nucleic Acids Res, 2022
Satange R, Kao SH, Chien CM, Chou SH, Lin CC, Neidle S, Hou MH.   +6 more
europepmc   +1 more source

Unusual Base Pair between Two 2-Thiouridines and Its Implication for Nonenzymatic RNA Copying. [PDF]

J Am Chem Soc
Ding D, Fang Z, Kim SC, O'Flaherty DK, Jia X, Stone TB, Zhou L, Szostak JW.   +7 more
europepmc   +1 more source

Importance of base-pair opening for mismatch recognition. [PDF]

Nucleic Acids Res, 2020
Bouchal T, Durník I, Illík V, Réblová K, Kulhánek P.   +4 more
europepmc   +1 more source

Genetic Code Engineering by Natural and Unnatural Base Pair Systems for the Site-Specific Incorporation of Non-Standard Amino Acids Into Proteins. [PDF]

Front Mol Biosci, 2022
Kimoto M, Hirao I.
europepmc   +1 more source

The simian virus 40 minimal origin and the 72-base-pair repeat are required simultaneously for efficient induction of late gene expression with large tumor antigen.

, 1984
S W Hartzell, Barry J. Byrne, K. N. Subramanian   +2 more
openalex   +1 more source

The 21-base pair deletion mutant Calpain3 does not inhibit wild-type Calpain3 activity. [PDF]

Genes Dis
Maitra S, Oh S, Choe YJ, Kim J, Kim NC.
europepmc   +1 more source

A paired comparison of cream and ointment-based dithranol in short contact treatment of psoriasis [PDF]

, 1987
Clive Grattan, A Christopher, Michael K. Robinson   +2 more
openalex   +1 more source

ISWI Remodelers Slide Nucleosomes with Coordinated Multi-Base-Pair Entry Steps and Single-Base-Pair Exit Steps

Cell, 2013
S. Deindl, William L. Hwang, Swetansu K. Hota, Timothy R Blosser, P. Prasad, B. Bartholomew, X. Zhuang   +6 more
semanticscholar   +1 more source

A novel 11 base pair deletion in KMT2C resulting in Kleefstra syndrome 2. [PDF]

Mol Genet Genomic Med
Whitford W, Taylor J, Hayes I, Smith W, Snell RG, Lehnert K, Jacobsen JC.   +6 more
europepmc   +1 more source