Hao CZ - Search Results

1

Association of novel TMEM67 variants with mild phenotypes of high gamma-glutamyl transpeptidase cholestasis and congenital hepatic fibrosis.

Qiu YL, Wang L, Huang M, Lian M, Wang F, Gong Y, Ma X, Hao CZ, Zhang J, Li ZD, Xing QH, Cao M, Wang JS. Qiu YL, et al. Among authors: hao cz. J Cell Physiol. 2022 Jun;237(6):2713-2723. doi: 10.1002/jcp.30788. Epub 2022 May 27. J Cell Physiol. 2022. PMID: 35621037

2

Severe Neonatal Cholestasis in Cerebrotendinous Xanthomatosis: Genetics, Immunostaining, Mass Spectrometry.

Gong JY, Setchell KDR, Zhao J, Zhang W, Wolfe B, Lu Y, Lackner K, Knisely AS, Wang NL, Hao CZ, Zhang MH, Wang JS. Gong JY, et al. Among authors: hao cz. J Pediatr Gastroenterol Nutr. 2017 Nov;65(5):561-568. doi: 10.1097/MPG.0000000000001730. J Pediatr Gastroenterol Nutr. 2017. PMID: 28937538

3

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: hao cz. Liver Int. 2018 Sep;38(9):1676-1685. doi: 10.1111/liv.13714. Epub 2018 Mar 12. Liver Int. 2018. PMID: 29412511

4

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.

5

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: hao cz. Hum Mutat. 2019 Dec;40(12):2247-2257. doi: 10.1002/humu.23770. Epub 2019 Sep 3. Hum Mutat. 2019. PMID: 31479177

6

TJP2 hepatobiliary disorders: Novel variants and clinical diversity.

Zhang J, Liu LL, Gong JY, Hao CZ, Qiu YL, Lu Y, Feng JY, Li JQ, Li ZD, Wang MX, Xing QH, Knisely AS, Wang JS. Zhang J, et al. Among authors: hao cz. Hum Mutat. 2020 Feb;41(2):502-511. doi: 10.1002/humu.23947. Epub 2019 Nov 28. Hum Mutat. 2020. PMID: 31696999

7

Biallelic loss-of-function ZFYVE19 mutations are associated with congenital hepatic fibrosis, sclerosing cholangiopathy and high-GGT cholestasis.

Luan W, Hao CZ, Li JQ, Wei Q, Gong JY, Qiu YL, Lu Y, Shen CH, Xia Q, Xie XB, Zhang MH, Abuduxikuer K, Li ZD, Wang L, Xing QH, Knisely AS, Wang JS. Luan W, et al. Among authors: hao cz. J Med Genet. 2021 Aug;58(8):514-525. doi: 10.1136/jmedgenet-2019-106706. Epub 2020 Jul 31. J Med Genet. 2021. PMID: 32737136

8

Defining pathogenicity of NOTCH2 variants for diagnosis of Alagille syndrome type 2 using a large cohort of patients.

Li ZD, Abuduxikuer K, Wang L, Hao CZ, Zhang J, Wang MX, Li LT, Qiu YL, Xie XB, Lu Y, Wang JS. Li ZD, et al. Among authors: hao cz. Liver Int. 2022 Aug;42(8):1836-1848. doi: 10.1111/liv.15292. Epub 2022 May 23. Liver Int. 2022. PMID: 35567760

9

ZFYVE19 deficiency: a ciliopathy involving failure of cell division, with cell death.

Yang J, Zhang YN, Wang RX, Hao CZ, Qiu Y, Chi H, Luan WS, Tang H, Zhang XJ, Sun X, Sheps JA, Ling V, Cao M, Wang JS. Yang J, et al. Among authors: hao cz. J Med Genet. 2024 Jul 19;61(8):750-758. doi: 10.1136/jmg-2023-109779. J Med Genet. 2024. PMID: 38816193 Free PMC article.

10

Inhaler personalisation based on peak inspiratory flow (PIF) among dry powder inhaler users: a pilot randomised control trial (RCT) in COPD.

Jailaini MFM, Muneswarao J, Hao CZ, Hussain R, Hamid MFA. Jailaini MFM, et al. Among authors: hao cz. J Pharm Policy Pract. 2024 Oct 18;17(1):2415425. doi: 10.1080/20523211.2024.2415425. eCollection 2024. J Pharm Policy Pract. 2024. PMID: 39434955 Free PMC article.

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