PubMed for id: 2263

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Results by year

Year	Number of Results
1990	3
1991	5
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2024	4

702 results

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Page 1

Genetic insights into the 'sandwich fusion' subtype of Klippel-Feil syndrome: novel FGFR2 mutations identified by 21 cases of whole-exome sequencing.

Xu N, Hung KL, Gong X, Fan D, Tian Y, Yan M, Wei Y, Wang S. Xu N, et al. Orphanet J Rare Dis. 2024 Apr 1;19(1):141. doi: 10.1186/s13023-024-03134-9. Orphanet J Rare Dis. 2024. PMID: 38561822 Free PMC article.

Investigating FGFR2 gene as a blood-based epigenetic biomarker in gastric cancer.

Aleyasin SA, Moradi A, Abolhasani N, Abdollahi M. Aleyasin SA, et al. Mol Biol Rep. 2024 Feb 1;51(1):253. doi: 10.1007/s11033-023-09082-0. Mol Biol Rep. 2024. PMID: 38302798

Expansion of the complex genotypic and phenotypic spectrum of FGFR2-associated neurocutaneous syndromes.

Schmidt J, Kaulfuß S, Ott H, Gaubert M, Reintjes N, Bremmer F, Dreha-Kulaczewski S, Stroebel P, Yigit G, Wollnik B. Schmidt J, et al. Hum Genet. 2024 Feb;143(2):159-168. doi: 10.1007/s00439-023-02634-1. Epub 2024 Jan 24. Hum Genet. 2024. PMID: 38265560 Free PMC article.

FGFR2 genetic variants in women with breast cancer.

Dix-Peek T, Dickens C, Augustine TN, Phakathi BP, Van Den Berg EJ, Joffe M, Ayeni OA, Cubasch H, Nietz S, Mathew CG, Hayat M, Neugut AI, Jacobson JS, Ruff P, Duarte RAB. Dix-Peek T, et al. Mol Med Rep. 2023 Dec;28(6):226. doi: 10.3892/mmr.2023.13113. Epub 2023 Oct 13. Mol Med Rep. 2023. PMID: 37830168 Free PMC article.

Functional Distinctions of Endometrial Cancer-Associated Mutations in the Fibroblast Growth Factor Receptor 2 Gene.

Dixit G, Pappas BA, Bhardwaj G, Schanz W, Maretzky T. Dixit G, et al. Cells. 2023 Sep 7;12(18):2227. doi: 10.3390/cells12182227. Cells. 2023. PMID: 37759450 Free PMC article.

Postzygotic gain-of-function variants in FGFR2 in two patients with hair follicle naevus.

Cheng Q, Yang F, Xue R, Wang H, Lin Z. Cheng Q, et al. Br J Dermatol. 2023 Oct 25;189(5):641-643. doi: 10.1093/bjd/ljad267. Br J Dermatol. 2023. PMID: 37540986 No abstract available.

Integrating transcriptomics and genomics to identify fibroblast growth factor/receptor candidate genes for non-syndromic orofacial cleft in Chinese.

Ge B, Lin Y, Shi B, Jia Z. Ge B, et al. Arch Oral Biol. 2023 Sep;153:105750. doi: 10.1016/j.archoralbio.2023.105750. Epub 2023 Jun 15. Arch Oral Biol. 2023. PMID: 37348362

Facial skeleton dysmorphology in syndromic craniosynostosis: differences between FGFR2 and no-FGFR2-related syndromes and relationship with skull base and facial sutural patterns.

Calandrelli R, Pilato F, Massimi L, D'Apolito G, Colosimo C. Calandrelli R, et al. Childs Nerv Syst. 2023 Nov;39(11):3235-3247. doi: 10.1007/s00381-023-05962-9. Epub 2023 May 17. Childs Nerv Syst. 2023. PMID: 37195419

FGFR2 mutations promote endometrial cancer progression through dual engagement of EGFR and Notch signalling pathways.

Dixit G, Gonzalez-Bosquet J, Skurski J, Devor EJ, Dickerson EB, Nothnick WB, Issuree PD, Leslie KK, Maretzky T. Dixit G, et al. Clin Transl Med. 2023 May;13(5):e1223. doi: 10.1002/ctm2.1223. Clin Transl Med. 2023. PMID: 37165578 Free PMC article.

FGFR2 modulates the Akt/Nrf2/ARE signaling pathway to improve angiotensin II-induced hypertension-related endothelial dysfunction.

Jiao K, Su P, Li Y. Jiao K, et al. Clin Exp Hypertens. 2023 Dec 31;45(1):2208777. doi: 10.1080/10641963.2023.2208777. Clin Exp Hypertens. 2023. PMID: 37154169 Free article.

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