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Identification and mutation analysis of a cochlear-expressed, zinc finger protein gene at the DFNB7/11 and dn hearing-loss loci on human chromosome 9q and mouse chromosome 19.
Scott DA, Greinwald JH Jr, Marietta JR, Drury S, Swiderski RE, Viñas A, DeAngelis MM, Carmi R, Ramesh A, Kraft ML, Elbedour K, Skworak AB, Friedman RA, Srikumari Srisailapathy CR, Verhoeven K, Van Gamp G, Lovett M, Deininger PL, Batzer MA, Morton CC, Keats BJ, Smith RJ, Sheffield VC. Scott DA, et al. Among authors: deangelis mm. Gene. 1998 Jul 30;215(2):461-9. doi: 10.1016/s0378-1119(98)00316-3. Gene. 1998. PMID: 9758550
The mouse deafness locus (dn) is associated with an inversion on chromosome 19.
Viñas AM, Drury SS, DeAngelis MM, Den Z, Huang JM, Berlin CI, Hunt JD, Batzer MA, Deininger PL, Keats BJ. Viñas AM, et al. Among authors: deangelis mm. Biochim Biophys Acta. 1998 Sep 30;1407(3):257-62. doi: 10.1016/s0925-4439(98)00050-7. Biochim Biophys Acta. 1998. PMID: 9748617 Free article.
A deconvolution framework that uses single-cell sequencing plus a small benchmark data set for accurate analysis of cell type ratios in complex tissue samples.
Guo S, Liu X, Cheng X, Jiang Y, Ji S, Liang Q, Koval A, Li Y, Owen LA, Kim IK, Aparicio A, Lee S, Sood AK, Kopetz S, Shen JP, Weinstein JN, DeAngelis MM, Chen R, Wang W. Guo S, et al. Among authors: deangelis mm. Genome Res. 2025 Jan 22;35(1):147-161. doi: 10.1101/gr.278822.123. Genome Res. 2025. PMID: 39586714 Free article.
Correction: Nr2e3 is a genetic modifier that rescues retinal degeneration and promotes homeostasis in multiple models of retinitis pigmentosa.
Li S, Datta S, Brabbit E, Love Z, Woytowicz V, Flattery K, Capri J, Yao K, Wu S, Imboden M, Upadhyay A, Arumugham R, Thoreson WB, DeAngelis MM, Haider NB. Li S, et al. Among authors: deangelis mm. Gene Ther. 2024 Nov;31(11-12):630-632. doi: 10.1038/s41434-024-00482-w. Gene Ther. 2024. PMID: 39294364 Free PMC article. No abstract available.
122 results