Au SLK - Search Results

1

Diagnostic potential of the amniotic fluid cells transcriptome in deciphering mendelian disease: a proof-of-concept.

Lee M, Kwong AKY, Chui MMC, Chau JFT, Mak CCY, Au SLK, Lo HM, Chan KYK, Yépez VA, Gagneur J, Kan ASY, Chung BHY. Lee M, et al. Among authors: au slk. NPJ Genom Med. 2022 Dec 28;7(1):74. doi: 10.1038/s41525-022-00347-4. NPJ Genom Med. 2022. PMID: 36577754 Free PMC article.

2

Long-surviving Neu-Laxova syndrome confirmed by whole exome sequencing: a case report.

Kong CW, Li YY, Au SLK, Kan ASY, Chui MMC, Chung BHY, Ho YC, To WWK. Kong CW, et al. Among authors: au slk. Hong Kong Med J. 2024 Aug;30(4):328-330. doi: 10.12809/hkmj2311182. Epub 2024 May 29. Hong Kong Med J. 2024. PMID: 38807256 Free article. No abstract available.

3

Prenatal diagnosis of Myhre syndrome with a heterozygous pathogenic variant in SMAD4 gene presented with thick nuchal translucency and cardiac abnormalities.

Hui PW, Mok YK, Luk HM, Au SLK, Lau EYT, Chung B, Kan ASY. Hui PW, et al. Among authors: au slk. Prenat Diagn. 2023 Sep;43(10):1366-1369. doi: 10.1002/pd.6414. Epub 2023 Aug 2. Prenat Diagn. 2023. PMID: 37529930

4

Evaluating the Clinical Utility of Genome Sequencing for Cytogenetically Balanced Chromosomal Abnormalities in Prenatal Diagnosis.

Yu MHC, Chau JFT, Au SLK, Lo HM, Yeung KS, Fung JLF, Mak CCY, Chung CCY, Chan KYK, Chung BHY, Kan ASY. Yu MHC, et al. Among authors: au slk. Front Genet. 2021 Jan 27;11:620162. doi: 10.3389/fgene.2020.620162. eCollection 2020. Front Genet. 2021. PMID: 33584815 Free PMC article.

5

Coexistence of paternally-inherited ABCC8 mutation and mosaic paternal uniparental disomy 11p hyperinsulinism.

Tung JY, Lai SHY, Au SLK, Yeung KS, Kan ASY, Loong F, DeLeón DD, Kalish JM, Ganguly A, Chung BHY, Chan KYK. Tung JY, et al. Among authors: au slk. Int J Pediatr Endocrinol. 2020;2020:13. doi: 10.1186/s13633-020-00083-5. Epub 2020 Jul 10. Int J Pediatr Endocrinol. 2020. PMID: 32670376 Free PMC article.

6

Histone methyltransferase G9a promotes liver cancer development by epigenetic silencing of tumor suppressor gene RARRES3.

Wei L, Chiu DK, Tsang FH, Law CT, Cheng CL, Au SL, Lee JM, Wong CC, Ng IO, Wong CM. Wei L, et al. J Hepatol. 2017 Oct;67(4):758-769. doi: 10.1016/j.jhep.2017.05.015. Epub 2017 May 19. J Hepatol. 2017. PMID: 28532996

7

Up-regulation of histone methyltransferase SETDB1 by multiple mechanisms in hepatocellular carcinoma promotes cancer metastasis.

Wong CM, Wei L, Law CT, Ho DW, Tsang FH, Au SL, Sze KM, Lee JM, Wong CC, Ng IO. Wong CM, et al. Hepatology. 2016 Feb;63(2):474-87. doi: 10.1002/hep.28304. Epub 2015 Dec 14. Hepatology. 2016. PMID: 26481868

8

MicroRNA-142-3p and microRNA-142-5p are downregulated in hepatocellular carcinoma and exhibit synergistic effects on cell motility.

Tsang FH, Au SL, Wei L, Fan DN, Lee JM, Wong CC, Ng IO, Wong CM. Tsang FH, et al. Front Med. 2015 Sep;9(3):331-43. doi: 10.1007/s11684-015-0409-8. Epub 2015 Aug 19. Front Med. 2015. PMID: 26293610

9

MiR-200b/200c/429 subfamily negatively regulates Rho/ROCK signaling pathway to suppress hepatocellular carcinoma metastasis.

Wong CM, Wei L, Au SL, Fan DN, Zhou Y, Tsang FH, Law CT, Lee JM, He X, Shi J, Wong CC, Ng IO. Wong CM, et al. Oncotarget. 2015 May 30;6(15):13658-70. doi: 10.18632/oncotarget.3700. Oncotarget. 2015. PMID: 25909223 Free PMC article.

10

Switching of pyruvate kinase isoform L to M2 promotes metabolic reprogramming in hepatocarcinogenesis.

Wong CC, Au SL, Tse AP, Xu IM, Lai RK, Chiu DK, Wei LL, Fan DN, Tsang FH, Lo RC, Wong CM, Ng IO. Wong CC, et al. PLoS One. 2014 Dec 26;9(12):e115036. doi: 10.1371/journal.pone.0115036. eCollection 2014. PLoS One. 2014. PMID: 25541689 Free PMC article.

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