Finnell RH - Search Results

1

Chromatin Imbalance as the Vertex Between Fetal Valproate Syndrome and Chromatinopathies.

Parodi C, Di Fede E, Peron A, Viganò I, Grazioli P, Castiglioni S, Finnell RH, Gervasini C, Vignoli A, Massa V. Parodi C, et al. Among authors: finnell rh. Front Cell Dev Biol. 2021 Apr 20;9:654467. doi: 10.3389/fcell.2021.654467. eCollection 2021. Front Cell Dev Biol. 2021. PMID: 33959609 Free PMC article. Review.

2

Valproic acid-induced skeletal malformations: associated gene expression cascades.

Massa V, Cabrera RM, Menegola E, Giavini E, Finnell RH. Massa V, et al. Among authors: finnell rh. Pharmacogenet Genomics. 2005 Nov;15(11):787-800. doi: 10.1097/01.fpc.0000170914.11898.3a. Pharmacogenet Genomics. 2005. PMID: 16220111

3

Myo-inositol enhances teratogenicity of valproic acid in the mouse.

Massa V, Wlodarczyk B, Giavini E, Finnell RH. Massa V, et al. Among authors: finnell rh. Birth Defects Res A Clin Mol Teratol. 2006 Mar;76(3):200-4. doi: 10.1002/bdra.20228. Birth Defects Res A Clin Mol Teratol. 2006. PMID: 16511884

4

Overview on neural tube defects: From development to physical characteristics.

Avagliano L, Massa V, George TM, Qureshy S, Bulfamante GP, Finnell RH. Avagliano L, et al. Among authors: finnell rh. Birth Defects Res. 2019 Nov 15;111(19):1455-1467. doi: 10.1002/bdr2.1380. Epub 2018 Nov 12. Birth Defects Res. 2019. PMID: 30421543 Free PMC article. Review.

5

Somatic and de novo Germline Variants of MEDs in Human Neural Tube Defects.

Tian T, Cao X, Chen Y, Jin L, Li Z, Han X, Lin Y, Wlodarczyk BJ, Finnell RH, Yuan Z, Wang L, Ren A, Lei Y. Tian T, et al. Among authors: finnell rh. Front Cell Dev Biol. 2021 Mar 4;9:641831. doi: 10.3389/fcell.2021.641831. eCollection 2021. Front Cell Dev Biol. 2021. PMID: 33748132 Free PMC article.

6

Embryonic Hypotaurine Levels Contribute to Strain-Dependent Susceptibility in Mouse Models of Valproate-Induced Neural Tube Defects.

Steele JW, Lin YL, Chen N, Wlodarczyk BJ, Chen Q, Attarwala N, Venkatesalu M, Cabrera RM, Gross SS, Finnell RH. Steele JW, et al. Among authors: finnell rh. Front Cell Dev Biol. 2022 Feb 21;10:832492. doi: 10.3389/fcell.2022.832492. eCollection 2022. Front Cell Dev Biol. 2022. PMID: 35265619 Free PMC article.

7

Gene Environment Interactions in the Etiology of Neural Tube Defects.

Finnell RH, Caiaffa CD, Kim SE, Lei Y, Steele J, Cao X, Tukeman G, Lin YL, Cabrera RM, Wlodarczyk BJ. Finnell RH, et al. Front Genet. 2021 May 10;12:659612. doi: 10.3389/fgene.2021.659612. eCollection 2021. Front Genet. 2021. PMID: 34040637 Free PMC article. Review.

8

Wnt1 Lineage Specific Deletion of Gpr161 Results in Embryonic Midbrain Malformation and Failure of Craniofacial Skeletal Development.

Kim SE, Robles-Lopez K, Cao X, Liu K, Chothani PJ, Bhavani N, Rahman L, Mukhopadhyay S, Wlodarczyk BJ, Finnell RH. Kim SE, et al. Among authors: finnell rh. Front Genet. 2021 Nov 23;12:761418. doi: 10.3389/fgene.2021.761418. eCollection 2021. Front Genet. 2021. PMID: 34887903 Free PMC article.

9

KDM6B Variants May Contribute to the Pathophysiology of Human Cerebral Folate Deficiency.

Han X, Cao X, Cabrera RM, Pimienta Ramirez PA, Zhang C, Ramaekers VT, Finnell RH, Lei Y. Han X, et al. Among authors: finnell rh. Biology (Basel). 2022 Dec 31;12(1):74. doi: 10.3390/biology12010074. Biology (Basel). 2022. PMID: 36671766 Free PMC article.

10

New myotonic dystrophy type 1 mouse model.

Lei Y, Finnell RH. Lei Y, et al. Among authors: finnell rh. Cell Res. 2020 Feb;30(2):99-100. doi: 10.1038/s41422-020-0276-y. Cell Res. 2020. PMID: 31953529 Free PMC article. No abstract available.

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