Alisch R - Search Results

1

Positional cloning of the Werner's syndrome gene.

Yu CE, Oshima J, Fu YH, Wijsman EM, Hisama F, Alisch R, Matthews S, Nakura J, Miki T, Ouais S, Martin GM, Mulligan J, Schellenberg GD. Yu CE, et al. Among authors: alisch r. Science. 1996 Apr 12;272(5259):258-62. doi: 10.1126/science.272.5259.258. Science. 1996. PMID: 8602509

2

Purified regenerating retinal neurons reveal regulatory role of DNA methylation-mediated Na+/K+-ATPase in murine axon regeneration.

Rizk E, Madrid A, Koueik J, Sun D, Stewart K, Chen D, Luo S, Hong F, Papale LA, Hariharan N, Alisch RS, Iskandar BJ. Rizk E, et al. Commun Biol. 2023 Jan 30;6(1):120. doi: 10.1038/s42003-023-04463-4. Commun Biol. 2023. PMID: 36717618 Free PMC article.

3

FMRP Regulates the Nuclear Export of Adam9 and Psen1 mRNAs: Secondary Analysis of an N⁶-Methyladenosine Dataset.

Westmark CJ, Maloney B, Alisch RS, Sokol DK, Lahiri DK. Westmark CJ, et al. Sci Rep. 2020 Jul 1;10(1):10781. doi: 10.1038/s41598-020-66394-y. Sci Rep. 2020. PMID: 32612155 Free PMC article.

4

Hippocampal and peripheral blood DNA methylation signatures correlate at the gene and pathway level in a mouse model of autism.

Alberca CD, Papale LA, Madrid A, Alisch RS. Alberca CD, et al. Among authors: alisch rs. Hum Mol Genet. 2023 Dec 1;32(24):3312-3322. doi: 10.1093/hmg/ddad137. Hum Mol Genet. 2023. PMID: 37658766

5

Influence of chronic administration of antidepressant drugs on mRNA for galanin, galanin receptors, and tyrosine hydroxylase in catecholaminergic and serotonergic cell-body regions in rat brain.

Rovin ML, Boss-Williams KA, Alisch RS, Ritchie JC, Weinshenker D, West CH, Weiss JM. Rovin ML, et al. Neuropeptides. 2012 Apr;46(2):81-91. doi: 10.1016/j.npep.2012.01.001. Epub 2012 Feb 10. Neuropeptides. 2012. PMID: 22317959 Free PMC article.

6

Early-life disruption of epigenetic marks may contribute to the origins of mental illness.

Lee ER, Alisch RS. Lee ER, et al. Among authors: alisch rs. Epigenomics. 2012 Aug;4(4):355-7. doi: 10.2217/epi.12.35. Epigenomics. 2012. PMID: 22920174 No abstract available.

7

Bone dysplasia sclerosteosis results from loss of the SOST gene product, a novel cystine knot-containing protein.

Brunkow ME, Gardner JC, Van Ness J, Paeper BW, Kovacevich BR, Proll S, Skonier JE, Zhao L, Sabo PJ, Fu Y, Alisch RS, Gillett L, Colbert T, Tacconi P, Galas D, Hamersma H, Beighton P, Mulligan J. Brunkow ME, et al. Among authors: alisch rs. Am J Hum Genet. 2001 Mar;68(3):577-89. doi: 10.1086/318811. Epub 2001 Feb 9. Am J Hum Genet. 2001. PMID: 11179006 Free PMC article.

8

ATLAS: a system to selectively identify human-specific L1 insertions.

Badge RM, Alisch RS, Moran JV. Badge RM, et al. Am J Hum Genet. 2003 Apr;72(4):823-38. doi: 10.1086/373939. Epub 2003 Mar 11. Am J Hum Genet. 2003. PMID: 12632328 Free PMC article.

9

A transient assay reveals that cultured human cells can accommodate multiple LINE-1 retrotransposition events.

Wei W, Morrish TA, Alisch RS, Moran JV. Wei W, et al. Among authors: alisch rs. Anal Biochem. 2000 Sep 10;284(2):435-8. doi: 10.1006/abio.2000.4675. Anal Biochem. 2000. PMID: 10964437 No abstract available.

10

Unconventional translation of mammalian LINE-1 retrotransposons.

Alisch RS, Garcia-Perez JL, Muotri AR, Gage FH, Moran JV. Alisch RS, et al. Genes Dev. 2006 Jan 15;20(2):210-24. doi: 10.1101/gad.1380406. Genes Dev. 2006. PMID: 16418485 Free PMC article.

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