PubMed (RefSeq) for id: 2462627842

Year	Number of Results
1996	3
1997	1
2002	1
2003	1
2004	1
2005	1
2006	2
2007	2
2008	2
2009	1
2010	1
2011	1
2012	4
2013	1
2015	3
2016	3
2017	2
2018	1
2019	2
2020	5
2021	4
2022	1
2023	2
2024	0

1

High-resolution photocatalytic mapping of SARS-CoV-2 spike interactions on the cell surface.

Datta S, Chen DY, Tavares AH, Reyes-Robles T, Ryu KA, Khan N, Bechtel TJ, Bertoch JM, White CH, Hazuda DJ, Vora KA, Hett EC, Fadeyi OO, Oslund RC, Emili A, Saeed M. Datta S, et al. Cell Chem Biol. 2023 Oct 19;30(10):1313-1322.e7. doi: 10.1016/j.chembiol.2023.06.028. Epub 2023 Jul 26. Cell Chem Biol. 2023. PMID: 37499664

2

Pathogenic variations in MAML2 and MAMLD1 contribute to congenital hypothyroidism due to dyshormonogenesis by regulating the Notch signalling pathway.

Wu FY, Yang RM, Zhang HY, Zhan M, Tu PH, Fang Y, Zhang CX, Song SY, Dong M, Cui RJ, Liu XY, Yang L, Yan CY, Sun F, Zhang RJ, Wang Z, Liang J, Song HD, Cheng F, Zhao SX. Wu FY, et al. J Med Genet. 2023 Sep;60(9):874-884. doi: 10.1136/jmg-2022-108866. Epub 2023 Mar 10. J Med Genet. 2023. PMID: 36898841

3

Identification of proximal SUMO-dependent interactors using SUMO-ID.

Barroso-Gomila O, Trulsson F, Muratore V, Canosa I, Merino-Cacho L, Cortazar AR, Pérez C, Azkargorta M, Iloro I, Carracedo A, Aransay AM, Elortza F, Mayor U, Vertegaal ACO, Barrio R, Sutherland JD. Barroso-Gomila O, et al. Nat Commun. 2021 Nov 18;12(1):6671. doi: 10.1038/s41467-021-26807-6. Nat Commun. 2021. PMID: 34795231 Free PMC article.

4

MAMLD1 and Differences/Disorders of Sex Development: An Update.

Miyado M, Fukami M, Ogata T. Miyado M, et al. Sex Dev. 2022;16(2-3):126-137. doi: 10.1159/000519298. Epub 2021 Oct 25. Sex Dev. 2022. PMID: 34695834 Free article. Review.

5

The genomic profiling and MAMLD1 expression in human and canines with Cushing's disease.

Wang A, Neill SG, Newman S, Tryfonidou MA, Ioachimescu A, Rossi MR, Meij BP, Oyesiku NM. Wang A, et al. BMC Endocr Disord. 2021 Sep 13;21(1):185. doi: 10.1186/s12902-021-00845-z. BMC Endocr Disord. 2021. PMID: 34517852 Free PMC article.

6

[Advance in research on the role of MAMLD1 gene in disorders of sex development].

Gao F, Gong C, Li L. Gao F, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021 Sep 10;38(9):912-916. doi: 10.3760/cma.j.cn511374-20200913-00666. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021. PMID: 34487543 Review. Chinese.

7

Disorders of Sex Development in Individuals Harbouring MAMLD1 Variants: WES and Interactome Evidence of Oligogenic Inheritance.

Li L, Gao F, Fan L, Su C, Liang X, Gong C. Li L, et al. Front Endocrinol (Lausanne). 2020 Dec 23;11:582516. doi: 10.3389/fendo.2020.582516. eCollection 2020. Front Endocrinol (Lausanne). 2020. PMID: 33424767 Free PMC article.

8

Clinical and molecular spectrum of 46,XY disorders of sex development that harbour MAMLD1 variations: case series and review of literature.

Li L, Su C, Fan L, Gao F, Liang X, Gong C. Li L, et al. Orphanet J Rare Dis. 2020 Jul 20;15(1):188. doi: 10.1186/s13023-020-01459-9. Orphanet J Rare Dis. 2020. PMID: 32690052 Free PMC article. Review.

9

Comparative Application of BioID and TurboID for Protein-Proximity Biotinylation.

May DG, Scott KL, Campos AR, Roux KJ. May DG, et al. Cells. 2020 Apr 25;9(5):1070. doi: 10.3390/cells9051070. Cells. 2020. PMID: 32344865 Free PMC article.

10

Xq28 copy number gain causing moyamoya disease and a novel moyamoya syndrome.

Aloui C, Guey S, Pipiras E, Kossorotoff M, Guéden S, Corpechot M, Bessou P, Pedespan JM, Husson M, Hervé D, Riant F, Kraemer M, Steffann J, Quenez O, Tournier-Lasserve E. Aloui C, et al. J Med Genet. 2020 May;57(5):339-346. doi: 10.1136/jmedgenet-2019-106525. Epub 2020 Jan 10. J Med Genet. 2020. PMID: 31924698

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