Yan YY - Search Results

1

A Specially Designed Multi-Gene Panel Facilitates Genetic Diagnosis in Children with Intrahepatic Cholestasis: Simultaneous Test of Known Large Insertions/Deletions.

Wang NL, Lu YL, Zhang P, Zhang MH, Gong JY, Lu Y, Xie XB, Qiu YL, Yan YY, Wu BB, Wang JS. Wang NL, et al. Among authors: yan yy. PLoS One. 2016 Oct 5;11(10):e0164058. doi: 10.1371/journal.pone.0164058. eCollection 2016. PLoS One. 2016. PMID: 27706244 Free PMC article.

2

Comprehensive bile acid profiling in hereditary intrahepatic cholestasis: Genetic and clinical correlations.

Liu T, Wang RX, Han J, Hao CZ, Qiu YL, Yan YY, Li LT, Wang NL, Gong JY, Lu Y, Zhang MH, Xie XB, Yang JC, You YJ, Li JQ, Knisely AS, Borchers CH, Ling V, Wang JS. Liu T, et al. Among authors: yan yy. Liver Int. 2018 Sep;38(9):1676-1685. doi: 10.1111/liv.13714. Epub 2018 Mar 12. Liver Int. 2018. PMID: 29412511

3

Defects in myosin VB are associated with a spectrum of previously undiagnosed low γ-glutamyltransferase cholestasis.

Qiu YL, Gong JY, Feng JY, Wang RX, Han J, Liu T, Lu Y, Li LT, Zhang MH, Sheps JA, Wang NL, Yan YY, Li JQ, Chen L, Borchers CH, Sipos B, Knisely AS, Ling V, Xing QH, Wang JS. Qiu YL, et al. Among authors: yan yy. Hepatology. 2017 May;65(5):1655-1669. doi: 10.1002/hep.29020. Epub 2017 Mar 23. Hepatology. 2017. PMID: 28027573 Free PMC article.

4

Novel missense mutation in VPS33B is associated with isolated low gamma-glutamyltransferase cholestasis: Attenuated, incomplete phenotype of arthrogryposis, renal dysfunction, and cholestasis syndrome.

Qiu YL, Liu T, Abuduxikuer K, Hao CZ, Gong JY, Zhang MH, Li LT, Yan YY, Li JQ, Wang JS. Qiu YL, et al. Among authors: yan yy. Hum Mutat. 2019 Dec;40(12):2247-2257. doi: 10.1002/humu.23770. Epub 2019 Sep 3. Hum Mutat. 2019. PMID: 31479177

5

Serum Golgi protein 73 is a marker comparable to APRI for diagnosing significant fibrosis in children with liver disease.

Liu L, Wang J, Feng J, Yao M, Hao C, You Y, Yan Y, Gong J, Lu Y, Xie X, Zhang M, Chen L, Li T, Lu F, Wang JS. Liu L, et al. Sci Rep. 2018 Nov 13;8(1):16730. doi: 10.1038/s41598-018-34714-y. Sci Rep. 2018. PMID: 30425268 Free PMC article.

6

NTCP Deficiency Causes Gallbladder Abnormalities in Mice and Human Beings.

Mao F, Wang MX, Hou X, Zhou Z, Yan YY, Fang LJ, Tan Z, Fang WY, Liu T, He W, Li C, Xie XB, Lu SQ, Sui J, Wang F, Han J, Wang JS, Li W. Mao F, et al. Among authors: yan yy. Cell Mol Gastroenterol Hepatol. 2021;11(3):831-839. doi: 10.1016/j.jcmgh.2020.09.001. Epub 2020 Sep 9. Cell Mol Gastroenterol Hepatol. 2021. PMID: 32919083 Free PMC article. No abstract available.

7

Abnormal Bilirubin Metabolism in Patients With Sodium Taurocholate Cotransporting Polypeptide Deficiency.

Yan YY, Wang MX, Gong JY, Liu LL, Setchell KDR, Xie XB, Wang NL, Li W, Wang JS. Yan YY, et al. J Pediatr Gastroenterol Nutr. 2020 Nov;71(5):e138-e141. doi: 10.1097/MPG.0000000000002862. J Pediatr Gastroenterol Nutr. 2020. PMID: 33093374

8

[No title available]

[No authors listed] [No authors listed] PMID: 32796433

9

m⁶A modification of lncRNA PHKA1-AS1 enhances Actinin Alpha 4 stability and promotes non-small cell lung cancer metastasis.

Guo QR, Zhang GB, Zhou WM, Lu Y, Chen XZ, Deng ZF, Li JS, Bi H, Wu MS, Xie MR, Yan YY, Zhang JY. Guo QR, et al. Among authors: yan yy. MedComm (2020). 2024 May 17;5(6):e547. doi: 10.1002/mco2.547. eCollection 2024 Jun. MedComm (2020). 2024. PMID: 38764726 Free PMC article.

10

The discovery of a novel pyrrolo[2,3-b]pyridine as a selective CDK8 inhibitor offers a new approach against psoriasis.

Yan YY, Wang YM, Shen JH, Jian YJ, Lei CC, Wang Q, Liu C, Zhang XX, Liu XH. Yan YY, et al. Biomed Pharmacother. 2024 May 6;175:116705. doi: 10.1016/j.biopha.2024.116705. Online ahead of print. Biomed Pharmacother. 2024. PMID: 38713949 Free article.

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