Han X - Search Results

1

Folate regulation of planar cell polarity pathway and F-actin through folate receptor alpha.

Han X, Cao X, Cabrera RM, Ramirez PAP, Lin YL, Wlodarczyk BJ, Zhang C, Finnell RH, Lei Y. Han X, et al. FASEB J. 2024 Jan;38(1):e23346. doi: 10.1096/fj.202300202R. FASEB J. 2024. PMID: 38095297

2

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. Biology (Basel). 2022 Dec 31;12(1):74. doi: 10.3390/biology12010074. Biology (Basel). 2022. PMID: 36671766 Free PMC article.

3

CIC de novo loss of function variants contribute to cerebral folate deficiency by downregulating FOLR1 expression.

Cao X, Wolf A, Kim SE, Cabrera RM, Wlodarczyk BJ, Zhu H, Parker M, Lin Y, Steele JW, Han X, Ramaekers VT, Steinfeld R, Finnell RH, Lei Y. Cao X, et al. Among authors: han x. J Med Genet. 2021 Jul;58(7):484-494. doi: 10.1136/jmedgenet-2020-106987. Epub 2020 Aug 20. J Med Genet. 2021. PMID: 32820034 Free PMC article.

4

FKBP8 variants are risk factors for spina bifida.

Tian T, Cao X, Kim SE, Lin YL, Steele JW, Cabrera RM, Karki M, Yang W, Marini NJ, Hoffman EN, Han X, Hu C, Wang L, Wlodarczyk BJ, Shaw GM, Ren A, Finnell RH, Lei Y. Tian T, et al. Among authors: han x. Hum Mol Genet. 2020 Nov 4;29(18):3132-3144. doi: 10.1093/hmg/ddaa211. Hum Mol Genet. 2020. PMID: 32969478 Free PMC article.

5

Hypermethylation of PI3K-AKT signalling pathway genes is associated with human neural tube defects.

Tian T, Lai X, Xiang K, Han X, Yin S, Cabrera RM, Steele JW, Lei Y, Cao X, Finnell RH, Wang L, Ren A. Tian T, et al. Among authors: han x. Epigenetics. 2022 Jan-Feb;17(2):133-146. doi: 10.1080/15592294.2021.1878725. Epub 2021 Feb 17. Epigenetics. 2022. PMID: 33491544 Free PMC article.

6

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: han x. 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.

7

CIC missense variants contribute to susceptibility for spina bifida.

Han X, Cao X, Aguiar-Pulido V, Yang W, Karki M, Ramirez PAP, Cabrera RM, Lin YL, Wlodarczyk BJ, Shaw GM, Ross ME, Zhang C, Finnell RH, Lei Y. Han X, et al. Hum Mutat. 2022 Dec;43(12):2021-2032. doi: 10.1002/humu.24460. Epub 2022 Sep 12. Hum Mutat. 2022. PMID: 36054333 Free PMC article.

8

The role of miRNAs in polycystic ovary syndrome with insulin resistance.

Luo Y, Cui C, Han X, Wang Q, Zhang C. Luo Y, et al. Among authors: han x. J Assist Reprod Genet. 2021 Feb;38(2):289-304. doi: 10.1007/s10815-020-02019-7. Epub 2021 Jan 6. J Assist Reprod Genet. 2021. PMID: 33405004 Free PMC article. Review.

9

Cumulative live birth and surplus embryo incidence after frozen-thaw cycles in PCOS: how many oocytes do we need?

Chen YH, Wang Q, Zhang YN, Han X, Li DH, Zhang CL. Chen YH, et al. Among authors: han x. J Assist Reprod Genet. 2017 Sep;34(9):1153-1159. doi: 10.1007/s10815-017-0959-6. Epub 2017 Jun 3. J Assist Reprod Genet. 2017. PMID: 28580513 Free PMC article.

10

Increased maternal hCG concentrations in early in vitro pregnancy with elevated basal FSH.

Han X, Yin B, Lin S, Wang Q, Su N, Zhang C. Han X, et al. PLoS One. 2018 Sep 10;13(9):e0203610. doi: 10.1371/journal.pone.0203610. eCollection 2018. PLoS One. 2018. PMID: 30199550 Free PMC article.

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