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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2005 5
2006 5
2007 3
2008 2
2009 2
2010 1
2011 3
2012 2
2014 2
2015 2
2019 2
2020 4
2021 1
2022 1
2023 1
2024 2

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37 results

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Page 1
Bone dysplasia in Hutchinson-Gilford progeria syndrome is associated with dysregulated differentiation and function of bone cell populations.
Cabral WA, Stephan C, Terajima M, Thaivalappil AA, Blanchard O, Tavarez UL, Narisu N, Yan T, Wincovitch SM, Taga Y, Yamauchi M, Kozloff KM, Erdos MR, Collins FS. Cabral WA, et al. Among authors: wincovitch sm. Aging Cell. 2023 Sep;22(9):e13903. doi: 10.1111/acel.13903. Epub 2023 Jun 26. Aging Cell. 2023. PMID: 37365004 Free PMC article.
Progressive pulmonary fibrosis in a murine model of Hermansky-Pudlak syndrome.
Abudi-Sinreich S, Bodine SP, Yokoyama T, Tolman NJ, Tyrlik M, Testa LC, Han CG, Dorward HM, Wincovitch SM, Anikster Y, Gahl WA, Cinar R, Gochuico BR, Malicdan MCV. Abudi-Sinreich S, et al. Among authors: wincovitch sm. Respir Res. 2022 May 4;23(1):112. doi: 10.1186/s12931-022-02002-z. Respir Res. 2022. PMID: 35509004 Free PMC article.
Redundant mechanisms driven independently by RUNX1 and GATA2 for hematopoietic development.
Bresciani E, Carrington B, Yu K, Kim EM, Zhen T, Guzman VS, Broadbridge E, Bishop K, Kirby M, Harper U, Wincovitch S, Dell'Orso S, Sartorelli V, Sood R, Liu P. Bresciani E, et al. Among authors: wincovitch s. Blood Adv. 2021 Dec 14;5(23):4949-4962. doi: 10.1182/bloodadvances.2020003969. Blood Adv. 2021. PMID: 34492681 Free PMC article.
Genetic background modifies phenotypic severity and longevity in a mouse model of Niemann-Pick disease type C1.
Rodriguez-Gil JL, Watkins-Chow DE, Baxter LL, Elliot G, Harper UL, Wincovitch SM, Wedel JC, Incao AA, Huebecker M, Boehm FJ, Garver WS, Porter FD, Broman KW, Platt FM, Pavan WJ. Rodriguez-Gil JL, et al. Among authors: wincovitch sm. Dis Model Mech. 2020 Mar 13;13(3):dmm042614. doi: 10.1242/dmm.042614. Dis Model Mech. 2020. PMID: 31996359 Free PMC article.
Comparative study of enriched dopaminergic neurons from siblings with Gaucher disease discordant for parkinsonism.
Hertz E, Perez G, Hao Y, Rytel K, Ma C, Kirby M, Anderson S, Wincovitch S, Andersh K, Ahfeldt T, Blanchard J, Andy Qi Y, Lopez G, Tayebi N, Sidransky E, Chen Y. Hertz E, et al. Among authors: wincovitch s. bioRxiv [Preprint]. 2024 Feb 28:2024.02.25.581985. doi: 10.1101/2024.02.25.581985. bioRxiv. 2024. PMID: 38529501 Free PMC article. Preprint.
Structural and molecular hair abnormalities in trichothiodystrophy.
Liang C, Morris A, Schlücker S, Imoto K, Price VH, Menefee E, Wincovitch SM, Levin IW, Tamura D, Strehle KR, Kraemer KH, DiGiovanna JJ. Liang C, et al. Among authors: wincovitch sm. J Invest Dermatol. 2006 Oct;126(10):2210-6. doi: 10.1038/sj.jid.5700384. Epub 2006 May 25. J Invest Dermatol. 2006. PMID: 16728971 Free article.
37 results