Fei YL - Search Results

1

Alterations of H19 imprinting and IGF2 replication timing are infrequent in Beckwith-Wiedemann syndrome.

Squire JA, Li M, Perlikowski S, Fei YL, Bayani J, Zhang ZM, Weksberg R. Squire JA, et al. Among authors: fei yl. Genomics. 2000 May 1;65(3):234-42. doi: 10.1006/geno.2000.6155. Genomics. 2000. PMID: 10857747

2

Discordant KCNQ1OT1 imprinting in sets of monozygotic twins discordant for Beckwith-Wiedemann syndrome.

Weksberg R, Shuman C, Caluseriu O, Smith AC, Fei YL, Nishikawa J, Stockley TL, Best L, Chitayat D, Olney A, Ives E, Schneider A, Bestor TH, Li M, Sadowski P, Squire J. Weksberg R, et al. Among authors: fei yl. Hum Mol Genet. 2002 May 15;11(11):1317-25. doi: 10.1093/hmg/11.11.1317. Hum Mol Genet. 2002. PMID: 12019213

3

Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome.

Weksberg R, Shen DR, Fei YL, Song QL, Squire J. Weksberg R, et al. Among authors: fei yl. Nat Genet. 1993 Oct;5(2):143-50. doi: 10.1038/ng1093-143. Nat Genet. 1993. PMID: 8252039

4

Imprinting status of 11p15 genes in Beckwith-Wiedemann syndrome patients with CDKN1C mutations.

Li M, Squire J, Shuman C, Fei YL, Atkin J, Pauli R, Smith A, Nishikawa J, Chitayat D, Weksberg R. Li M, et al. Among authors: fei yl. Genomics. 2001 Jun 15;74(3):370-6. doi: 10.1006/geno.2001.6549. Genomics. 2001. PMID: 11414765

5

Tumor development in the Beckwith-Wiedemann syndrome is associated with a variety of constitutional molecular 11p15 alterations including imprinting defects of KCNQ1OT1.

Weksberg R, Nishikawa J, Caluseriu O, Fei YL, Shuman C, Wei C, Steele L, Cameron J, Smith A, Ambus I, Li M, Ray PN, Sadowski P, Squire J. Weksberg R, et al. Among authors: fei yl. Hum Mol Genet. 2001 Dec 15;10(26):2989-3000. doi: 10.1093/hmg/10.26.2989. Hum Mol Genet. 2001. PMID: 11751681

6

CDKN1C mutation in Wiedemann-Beckwith syndrome patients reduces RNA splicing efficiency and identifies a splicing enhancer.

Lew JM, Fei YL, Aleck K, Blencowe BJ, Weksberg R, Sadowski PD. Lew JM, et al. Among authors: fei yl. Am J Med Genet A. 2004 Jun 15;127A(3):268-76. doi: 10.1002/ajmg.a.30020. Am J Med Genet A. 2004. PMID: 15150778

7

GPC3 mutation analysis in a spectrum of patients with overgrowth expands the phenotype of Simpson-Golabi-Behmel syndrome.

Li M, Shuman C, Fei YL, Cutiongco E, Bender HA, Stevens C, Wilkins-Haug L, Day-Salvatore D, Yong SL, Geraghty MT, Squire J, Weksberg R. Li M, et al. Among authors: fei yl. Am J Med Genet. 2001 Aug 1;102(2):161-8. doi: 10.1002/1096-8628(20010801)102:2<161::aid-ajmg1453>3.0.co;2-o. Am J Med Genet. 2001. PMID: 11477610

8

Expression of p57(KIP2) potently blocks the growth of human astrocytomas and induces cell senescence.

Tsugu A, Sakai K, Dirks PB, Jung S, Weksberg R, Fei YL, Mondal S, Ivanchuk S, Ackerley C, Hamel PA, Rutka JT. Tsugu A, et al. Among authors: fei yl. Am J Pathol. 2000 Sep;157(3):919-32. doi: 10.1016/S0002-9440(10)64605-6. Am J Pathol. 2000. PMID: 10980131 Free PMC article.

9

Efficacy and Safety of Thermal Ablation for Solitary Low-Risk T2N0M0 Papillary Thyroid Carcinoma.

Fei YL, Wei Y, Zhao ZL, Peng LL, Li Y, Cao SL, Wu J, Zhou HD, Yu MA. Fei YL, et al. Korean J Radiol. 2024 Aug;25(8):756-766. doi: 10.3348/kjr.2023.1279. Korean J Radiol. 2024. PMID: 39109502 Free PMC article.

10

Non‑persistence to Oral Anticoagulation Therapy in Elderly Patients with Non‑valvular Atrial Fibrillation.

Cao Y, Feng YY, Du W, Li J, Fei YL, Yang H, Wang M, Li SJ, Li XJ, Han B. Cao Y, et al. Among authors: fei yl. Patient Prefer Adherence. 2023 Dec 6;17:3185-3194. doi: 10.2147/PPA.S435592. eCollection 2023. Patient Prefer Adherence. 2023. PMID: 38084322 Free PMC article.

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