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The mechanisms of human lymphoid chromosomal translocations and their medical relevance.

Critical reviews in biochemistry and molecular biology

Liu D, Lieber MR.
PMID: 34875186
Crit Rev Biochem Mol Biol. 2021 Dec 07;1-17. doi: 10.1080/10409238.2021.2004576. Epub 2021 Dec 07.

The most common human lymphoid chromosomal translocations involve concurrent failures of the recombination activating gene (RAG) complex and Activation-Induced Deaminase (AID). These are two enzymes that are normally expressed for purposes of the two site-specific DNA recombination processes: V(D)J...

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Liu D, Lieber MR. The mechanisms of human lymphoid chromosomal translocations and their medical relevance. Crit Rev Biochem Mol Biol. 2021;1-17doi: 10.1080/10409238.2021.2004576.
Liu, D., & Lieber, M. R. (2021). The mechanisms of human lymphoid chromosomal translocations and their medical relevance. Critical reviews in biochemistry and molecular biology, 1-17. https://doi.org/10.1080/10409238.2021.2004576
Liu, Di, and Lieber, Michael R. "The mechanisms of human lymphoid chromosomal translocations and their medical relevance." Critical reviews in biochemistry and molecular biology vol. (2021): 1-17. doi: https://doi.org/10.1080/10409238.2021.2004576
Liu D, Lieber MR. The mechanisms of human lymphoid chromosomal translocations and their medical relevance. Crit Rev Biochem Mol Biol. 2021 Dec 07;1-17. doi: 10.1080/10409238.2021.2004576. Epub 2021 Dec 07. PMID: 34875186.
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4-Alkyloxyimino-cytosine nucleotides: tethering approaches to molecular probes for the P2Y.

MedChemComm

Jayasekara PS, Barrett MO, Ball CB, Brown KA, Kozma E, Costanzi S, Squarcialupi L, Balasubramanian R, Maruoka H, Jacobson KA.
PMID: 26161252
Medchemcomm. 2013 May 30;4:1156-1165. doi: 10.1039/C3MD00132F.

4-Alkyloxyimino derivatives of pyrimidine nucleotides display high potency as agonists of certain G protein-coupled P2Y receptors (P2YRs). In an effort to functionalize a P2Y

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Jayasekara PS, Barrett MO, Ball CB, et al. 4-Alkyloxyimino-cytosine nucleotides: tethering approaches to molecular probes for the P2Y. Medchemcomm. 2013;4:1156-1165doi: 10.1039/C3MD00132F.
Jayasekara, P. S., Barrett, M. O., Ball, C. B., Brown, K. A., Kozma, E., Costanzi, S., Squarcialupi, L., Balasubramanian, R., Maruoka, H., & Jacobson, K. A. (2013). 4-Alkyloxyimino-cytosine nucleotides: tethering approaches to molecular probes for the P2Y. MedChemComm, 41156-1165. https://doi.org/10.1039/C3MD00132F
Jayasekara, P Suresh, et al. "4-Alkyloxyimino-cytosine nucleotides: tethering approaches to molecular probes for the P2Y." MedChemComm vol. 4 (2013): 1156-1165. doi: https://doi.org/10.1039/C3MD00132F
Jayasekara PS, Barrett MO, Ball CB, Brown KA, Kozma E, Costanzi S, Squarcialupi L, Balasubramanian R, Maruoka H, Jacobson KA. 4-Alkyloxyimino-cytosine nucleotides: tethering approaches to molecular probes for the P2Y. Medchemcomm. 2013 May 30;4:1156-1165. doi: 10.1039/C3MD00132F. PMID: 26161252; PMCID: PMC4493932.
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ADMIRE: analysis and visualization of differential methylation in genomic regions using the Infinium HumanMethylation450 Assay.

Epigenetics & chromatin

Preussner J, Bayer J, Kuenne C, Looso M.
PMID: 26628921
Epigenetics Chromatin. 2015 Dec 01;8:51. doi: 10.1186/s13072-015-0045-1. eCollection 2015.

BACKGROUND: DNA methylation at cytosine nucleotides constitutes epigenetic gene regulation impacting cellular development and a wide range of diseases. Cytosine bases of the DNA are converted to 5-methylcytosine by the methyltransferase enzyme, acting as a reversible regulator of gene...

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Preussner J, Bayer J, Kuenne C, et al. ADMIRE: analysis and visualization of differential methylation in genomic regions using the Infinium HumanMethylation450 Assay. Epigenetics Chromatin. 2015;8:51doi: 10.1186/s13072-015-0045-1.
Preussner, J., Bayer, J., Kuenne, C., & Looso, M. (2015). ADMIRE: analysis and visualization of differential methylation in genomic regions using the Infinium HumanMethylation450 Assay. Epigenetics & chromatin, 851. https://doi.org/10.1186/s13072-015-0045-1
Preussner, Jens, et al. "ADMIRE: analysis and visualization of differential methylation in genomic regions using the Infinium HumanMethylation450 Assay." Epigenetics & chromatin vol. 8 (2015): 51. doi: https://doi.org/10.1186/s13072-015-0045-1
Preussner J, Bayer J, Kuenne C, Looso M. ADMIRE: analysis and visualization of differential methylation in genomic regions using the Infinium HumanMethylation450 Assay. Epigenetics Chromatin. 2015 Dec 01;8:51. doi: 10.1186/s13072-015-0045-1. eCollection 2015. PMID: 26628921; PMCID: PMC4666223.
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High information throughput analysis of nucleotides and their isotopically enriched isotopologues by direct-infusion FTICR-MS.

Metabolomics : Official journal of the Metabolomic Society

Lorkiewicz P, Higashi RM, Lane AN, Fan TW.
PMID: 23101002
Metabolomics. 2012;8(5):930-939. doi: 10.1007/s11306-011-0388-y. Epub 2011 Dec 09.

Fourier transform-ion cyclotron resonance-mass spectrometry (FTICR-MS) is capable of acquiring unmatched quality of isotopologue data for stable isotope resolved metabolomics (SIRM). This capability drives the need for a continuous ion introduction for obtaining optimal isotope ratios. Here we report...

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Lorkiewicz P, Higashi RM, Lane AN, et al. High information throughput analysis of nucleotides and their isotopically enriched isotopologues by direct-infusion FTICR-MS. Metabolomics. 2011;8(5):930-939doi: 10.1007/s11306-011-0388-y.
Lorkiewicz, P., Higashi, R. M., Lane, A. N., & Fan, T. W. (2012). High information throughput analysis of nucleotides and their isotopically enriched isotopologues by direct-infusion FTICR-MS. Metabolomics : Official journal of the Metabolomic Society, 8(5), 930-939. https://doi.org/10.1007/s11306-011-0388-y
Lorkiewicz, Pawel, et al. "High information throughput analysis of nucleotides and their isotopically enriched isotopologues by direct-infusion FTICR-MS." Metabolomics : Official journal of the Metabolomic Society vol. 8,5 (2012): 930-939. doi: https://doi.org/10.1007/s11306-011-0388-y
Lorkiewicz P, Higashi RM, Lane AN, Fan TW. High information throughput analysis of nucleotides and their isotopically enriched isotopologues by direct-infusion FTICR-MS. Metabolomics. 2012;8(5):930-939. doi: 10.1007/s11306-011-0388-y. Epub 2011 Dec 09. PMID: 23101002; PMCID: PMC3477816.
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Showing 1 to 4 of 4 entries