Daman Kumari - Search Results

Year	Number of Results
2005	3
2007	1
2008	2
2009	2
2010	2
2011	1
2012	3
2013	1
2014	4
2015	4
2016	3
2017	1
2019	3
2020	2
2021	2
2024	2

1

The fragile X locus is prone to spontaneous DNA damage that is preferentially repaired by nonhomologous end-joining to preserve genome integrity.

Kumari D, Lokanga RA, McCann C, Ried T, Usdin K. Kumari D, et al. iScience. 2024 Jan 6;27(2):108814. doi: 10.1016/j.isci.2024.108814. eCollection 2024 Feb 16. iScience. 2024. PMID: 38303711 Free PMC article.

2

All three MutL complexes are required for repeat expansion in a human stem cell model of CAG-repeat expansion mediated glutaminase deficiency.

Hayward B, Kumari D, van Karnebeek CDM, van Kuilenburg ABP, Usdin K. Hayward B, et al. Among authors: kumari d. bioRxiv [Preprint]. 2024 Jan 8:2023.12.26.573357. doi: 10.1101/2023.12.26.573357. bioRxiv. 2024. PMID: 38260514 Free PMC article. Preprint.

3

Common Threads: Aphidicolin-Inducible and Folate-Sensitive Fragile Sites in the Human Genome.

Lokanga RA, Kumari D, Usdin K. Lokanga RA, et al. Among authors: kumari d. Front Genet. 2021 Sep 8;12:708860. doi: 10.3389/fgene.2021.708860. eCollection 2021. Front Genet. 2021. PMID: 34567068 Free PMC article. Review.

4

Modifiers of Somatic Repeat Instability in Mouse Models of Friedreich Ataxia and the Fragile X-Related Disorders: Implications for the Mechanism of Somatic Expansion in Huntington's Disease.

Zhao X, Kumari D, Miller CJ, Kim GY, Hayward B, Vitalo AG, Pinto RM, Usdin K. Zhao X, et al. Among authors: kumari d. J Huntingtons Dis. 2021;10(1):149-163. doi: 10.3233/JHD-200423. J Huntingtons Dis. 2021. PMID: 33579860 Free PMC article. Review.

5

Small Molecules Targeting H3K9 Methylation Prevent Silencing of Reactivated FMR1 Alleles in Fragile X Syndrome Patient Derived Cells.

Kumari D, Sciascia N, Usdin K. Kumari D, et al. Genes (Basel). 2020 Mar 27;11(4):356. doi: 10.3390/genes11040356. Genes (Basel). 2020. PMID: 32230785 Free PMC article.

6

Molecular analysis of FMR1 alleles for fragile X syndrome diagnosis and patient stratification.

Kumari D, Usdin K. Kumari D, et al. Expert Rev Mol Diagn. 2020 Apr;20(4):363-365. doi: 10.1080/14737159.2020.1729744. Epub 2020 Feb 18. Expert Rev Mol Diagn. 2020. PMID: 32067539 Free PMC article. Review. No abstract available.

7

Towards Mechanism-Based Treatments for Fragile X Syndrome.

Kumari D, Gazy I. Kumari D, et al. Brain Sci. 2019 Aug 16;9(8):202. doi: 10.3390/brainsci9080202. Brain Sci. 2019. PMID: 31426300 Free PMC article.

8

Glutaminase Deficiency Caused by Short Tandem Repeat Expansion in GLS.

van Kuilenburg ABP, Tarailo-Graovac M, Richmond PA, Drögemöller BI, Pouladi MA, Leen R, Brand-Arzamendi K, Dobritzsch D, Dolzhenko E, Eberle MA, Hayward B, Jones MJ, Karbassi F, Kobor MS, Koster J, Kumari D, Li M, MacIsaac J, McDonald C, Meijer J, Nguyen C, Rajan-Babu IS, Scherer SW, Sim B, Trost B, Tseng LA, Turkenburg M, van Vugt JJFA, Veldink JH, Walia JS, Wang Y, van Weeghel M, Wright GEB, Xu X, Yuen RKC, Zhang J, Ross CJ, Wasserman WW, Geraghty MT, Santra S, Wanders RJA, Wen XY, Waterham HR, Usdin K, van Karnebeek CDM. van Kuilenburg ABP, et al. Among authors: kumari d. N Engl J Med. 2019 Apr 11;380(15):1433-1441. doi: 10.1056/NEJMoa1806627. N Engl J Med. 2019. PMID: 30970188 Free PMC article.

9

Pharmacological Reactivation of the Silenced FMR1 Gene as a Targeted Therapeutic Approach for Fragile X Syndrome.

Kumari D, Gazy I, Usdin K. Kumari D, et al. Brain Sci. 2019 Feb 12;9(2):39. doi: 10.3390/brainsci9020039. Brain Sci. 2019. PMID: 30759772 Free PMC article. Review.

10

Recent advances in assays for the fragile X-related disorders.

Hayward BE, Kumari D, Usdin K. Hayward BE, et al. Among authors: kumari d. Hum Genet. 2017 Oct;136(10):1313-1327. doi: 10.1007/s00439-017-1840-5. Epub 2017 Sep 2. Hum Genet. 2017. PMID: 28866801 Free PMC article. Review.

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