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oncogene.2018-Heterozygous IDH1R132H-WT created by "single base editing" inhibits human astroglial cell growth by downregulating YAP.pdf

oncogene.2018-Heterozygous IDH1R132H-WT created by “single base editing” inhibits human astroglial cell growth by downregulating YAPoncogene.2018-Heterozygous IDH1R132H-WT created by “single base editing” inhibits human astroglial cell growth by downregulating YAPoncogene.2018-Heterozygous IDH1R132H-WT created by “single base editing” inhibits human astroglial cell growth by downregulating YAP

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deployment of dna polymerases beta and lambda in single-nucleotide and multinucleotide pathways of mammalian base excision dna repair.dna repair (a.pdf

deployment of dna polymerases beta and lambda in single-nucleotide and multinucleotide pathways of mammalian base excision dna repair.dna repair (a

• cyjdoctor
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6

retinal dystrophy associated with a single-base deletion mutation in mitochondrial dna 3271 in patient with melas syndrome.doc ophthalmol[2019].pdf

retinal dystrophy associated with a single-base deletion mutation in mitochondrial dna 3271 in patient with melas syndrome.doc ophthalmol[2019]

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6

aligner mediated cleavage of nucleic acids for site-specific detection of single base mismatch. (2019).[10.1016_j.talanta.2019.03.106].pdf

aligner mediated cleavage of nucleic acids for site-specific detection of single base mismatch. (2019).[10.1016_j.talanta.2019.03.106]

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5

highly sensitive quantification of site-specific 5-hydroxymethylcytosine at single-base resolution by hpaii-mediated ligation pcr.[2019][10.1039_c9.pdf

highly sensitive quantification of site-specific 5-hydroxymethylcytosine at single-base resolution by hpaii-mediated ligation pcr.[2019][10.1039_c9

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7

mirror bisulfite sequencing_ a method for single-base resolution of hydroxymethylcytosine.[2018][anal chem][10.1021_acs.analchem.8b02832].pdf

mirror bisulfite sequencing_ a method for single-base resolution of hydroxymethylcytosine.[2018][anal chem][10.1021_acs.analchem.8b02832]

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from sub-microscopic variants to the resolution of a single base pair_ exome sequencing in prenatal diagnosis.[2019][eur j med genet].pdf

from sub-microscopic variants to the resolution of a single base pair_ exome sequencing in prenatal diagnosis.[2019][eur j med genet]

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6

single base resolution mapping of 2´-o-methylation sites in human mrna and in 3´ terminal ends of small rnas.[2018][methods][10.1016_j.ymeth.2018.1.pdf

single base resolution mapping of 2´-o-methylation sites in human mrna and in 3´ terminal ends of small rnas.[2018][methods][10.1016_j.ymeth.2018.1

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