PubMed (GeneRIF) for id: 64324

Year	Number of Results
2001	1
2002	2
2003	5
2004	5
2005	4
2006	1
2007	4
2008	2
2009	5
2010	4
2011	5
2012	1
2013	6
2014	6
2015	4
2016	5
2017	6
2018	2
2019	7
2020	6
2021	8
2022	7
2023	6
2024	2

1

H3K36 methyltransferase NSD1 protects against osteoarthritis through regulating chondrocyte differentiation and cartilage homeostasis.

Shao R, Suo J, Zhang Z, Kong M, Ma Y, Wen Y, Liu M, Zhuang L, Ge K, Bi Q, Zhang C, Zou W. Shao R, et al. Cell Death Differ. 2024 Jan;31(1):106-118. doi: 10.1038/s41418-023-01244-8. Epub 2023 Nov 27. Cell Death Differ. 2024. PMID: 38012390

2

Sotos syndrome with marked overgrowth in three Japanese patients with heterozygous likely pathogenic NSD1 variants: case reports with review of literature.

Masunaga Y, Ono H, Fujisawa Y, Taniguchi K, Saitsu H, Ogata T. Masunaga Y, et al. Endocr J. 2024 Jan 29;71(1):75-81. doi: 10.1507/endocrj.EJ23-0502. Epub 2023 Nov 22. Endocr J. 2024. PMID: 37989294 Free article. Review.

3

Targeting KDM2A Enhances T-cell Infiltration in NSD1-Deficient Head and Neck Squamous Cell Carcinoma.

Chen C, Shin JH, Fang Z, Brennan K, Horowitz NB, Pfaff KL, Welsh EL, Rodig SJ, Gevaert O, Gozani O, Uppaluri R, Sunwoo JB. Chen C, et al. Cancer Res. 2023 Aug 15;83(16):2645-2655. doi: 10.1158/0008-5472.CAN-22-3114. Cancer Res. 2023. PMID: 37311054 Free PMC article.

4

NUP98::Nsd1 and FLT3-ITD collaborate to generate acute myeloid leukemia.

Matsukawa T, Yin M, Nigam N, Negi V, Li L, Small D, Zhu YJ, Walker RL, Meltzer PS, Aplan PD. Matsukawa T, et al. Leukemia. 2023 Jul;37(7):1545-1548. doi: 10.1038/s41375-023-01913-0. Epub 2023 May 5. Leukemia. 2023. PMID: 37147424 Free PMC article. No abstract available.

5

Molecular Analysis and Reclassification of NSD1 Gene Variants in a Cohort of Patients with Clinical Suspicion of Sotos Syndrome.

Testa B, Conteduca G, Grasso M, Cecconi M, Lantieri F, Baldo C, Arado A, Andraghetti L, Malacarne M, Milani D, Coviello D, Sotos Collaborative Group. Testa B, et al. Genes (Basel). 2023 Jan 22;14(2):295. doi: 10.3390/genes14020295. Genes (Basel). 2023. PMID: 36833222 Free PMC article.

6

NSD1 gene evolves under episodic selection within primates and mutations of specific exons in humans cause Sotos syndrome.

Romero VI, Arias-Almeida B, Aguiar SA. Romero VI, et al. BMC Genomics. 2022 Dec 22;23(1):849. doi: 10.1186/s12864-022-09071-w. BMC Genomics. 2022. PMID: 36550402 Free PMC article.

7

Identification of alternative transcripts of NSD1 gene in Sotos Syndrome patients and healthy subjects.

Conteduca G, Testa B, Baldo C, Arado A, Malacarne M, Candiano G, Garbarino A, Coviello DA, Cantoni C. Conteduca G, et al. Gene. 2023 Jan 30;851:146970. doi: 10.1016/j.gene.2022.146970. Epub 2022 Oct 17. Gene. 2023. PMID: 36261088 Free article.

8

Reversal of Clinical Phenotype of Sotos Syndrome Due to Microduplication of NSD1 Gene.

Takkar A, Arora V, Saxena R, Kumar P, Verma IC. Takkar A, et al. Indian J Pediatr. 2022 Nov;89(11):1137-1139. doi: 10.1007/s12098-022-04325-7. Epub 2022 Aug 4. Indian J Pediatr. 2022. PMID: 35925544

9

NSD1 mediates antagonism between SWI/SNF and polycomb complexes and is required for transcriptional activation upon EZH2 inhibition.

Drosos Y, Myers JA, Xu B, Mathias KM, Beane EC, Radko-Juettner S, Mobley RJ, Larsen ME, Piccioni F, Ma X, Low J, Hansen BS, Peters ST, Bhanu NV, Dhanda SK, Chen T, Upadhyaya SA, Pruett-Miller SM, Root DE, Garcia BA, Partridge JF, Roberts CWM. Drosos Y, et al. Mol Cell. 2022 Jul 7;82(13):2472-2489.e8. doi: 10.1016/j.molcel.2022.04.015. Epub 2022 May 9. Mol Cell. 2022. PMID: 35537449 Free PMC article.

10

The role of NSD1, NSD2, and NSD3 histone methyltransferases in solid tumors.

Topchu I, Pangeni RP, Bychkov I, Miller SA, Izumchenko E, Yu J, Golemis E, Karanicolas J, Boumber Y. Topchu I, et al. Cell Mol Life Sci. 2022 May 9;79(6):285. doi: 10.1007/s00018-022-04321-2. Cell Mol Life Sci. 2022. PMID: 35532818 Free PMC article. Review.

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