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...esulting in the depletion of thymidine triphosphate (TTP), one of the four nucleotide triphosphates used in the ''in vivo'' synthesis of DNA. Other fluorouracil

Fatty liver and [[steatohepatitis]] may be caused by the [[single-nucleotide polymorphism]]s [http://www.ncbi.nlm.nih.gov/projects/SNP/snp_ref.cgi?rs=28

* [http://www.ncbi.nlm.nih.gov/sites/entrez?db=nuccore Entrez Nucleotide]: [http://www.ncbi.nlm.nih.gov/nuccore/NG_008376 NG_008376]; [[PubMed]] [ht

...d one [[amino acid]] of protein [[S12]], interfering with decoding around nucleotide 1400 of 16S thereby inhibiting the formation of an initiation complex, caus

...so that the drug gets incorporated into new viral RNA or DNA, but the next nucleotide base cannot be added because a linkage group is missing. Anti-metabolites a

{{r|Single-nucleotide polymorphism}}

...rtant and widely known products of biosynthesis include [[amino acid]]s, [[nucleotide]]s, and , [[vitamin]]s but all components of living beings depend on this p

...rRNA and one amino acid in protein S12. This interferes with decoding near nucleotide 1400 in 16S rRNA of the 30S subunit, interfering with the formation of an i

...2178}}</ref> Patient response to IVIG, however, is influenced by a single nucleotide polymorphism in the transient axonal glycoprotein 1 gene (TAG-1)<ref>{{cita

[[Single-nucleotide polymorphism]] of the beta-1 (ADRB1) [[adrenergic receptor]], specifically [[Single-nucleotide polymorphism]] of the beta-2 (ADRB2) [[adrenergic receptor]], specifically

...s of [[rifampin]]-resistant organisms. I. A punctual mutation was found in nucleotide 1367 of the rpoBgene. That mutation show strains of rifampin-resistant M.l

...mith, J.B. & Smith, D.B. (1974) Genome size and the proportion of repeated nucleotide sequence DNA in plants. Biochemical Genetics 12, 257−269 (1974).</ref> of

...2178}}</ref> Patient response to IVIG, however, is influenced by a single nucleotide polymorphism in the transient axonal glycoprotein 1 gene (TAG-1)<ref>{{cita

...between the uracil H3 proton and the adenine N1 nitrogen atom. Like other nucleotide bases, it is subject to oxidative damage.

.... A point mutation can be reversed by another point mutation, in which the nucleotide is changed back to its original state (true reversion) or by second-site re ...to a higher energy level. DNA absorbs one form, [[ultraviolet light]]. Two nucleotide bases in DNA - cytosine and thymine - are most vulnerable to excitation tha

...bon source for the synthesis of other molecules . Also, if the body needs nucleotide precursors of DNA for growth and synthesis, G6P will also be dehydrogenate

...v/articlerender.fcgi?tool=pmcentrez&artid=135101 183:3194–202]</ref> The [[nucleotide]] sequencing of Rts1 was completed at Shinshu University School of Medicine

...gene defect responsible for an inheritable disease. The search for Single Nucleotide Polymorphisms (SNiPs), which are single (point) mutations in a gene, is one

...classified in a new genus along with the similar Hendra virus (70% to 88% nucleotide homology, 67% to 92% amino acid homology): Henipavirus <ref name=Bossart>{{

...du&retmode=ref&cmd=prlinks&id=11007705 }}</ref> Various have been [[single-nucleotide polymorphism]]s suggested.<ref name="pmid16610949">{{cite journal| author=S ...Coelho L, Gurbaxani B, Maloney EM, Jones JF| title=Combinations of single nucleotide polymorphisms in neuroendocrine effector and receptor genes predict chronic