Qi M - Search Results

1

Retinol dehydrogenase 12 (RDH12) knock out may cause hyperuricemia phenotype in mice.

Bian J, Chen H, Sun J, Han S, Qi M, Pan Q. Bian J, et al. Among authors: qi m. Biochem Biophys Res Commun. 2024 May 21;709:149809. doi: 10.1016/j.bbrc.2024.149809. Epub 2024 Mar 20. Biochem Biophys Res Commun. 2024. PMID: 38552555

2

Identification and characterization of novel compound heterozygous variants in FSHR causing primary ovarian insufficiency with resistant ovary syndrome.

Chen X, Chen L, Wang Y, Shu C, Zhou Y, Wu R, Jin B, Yang L, Sun J, Qi M, Shu J. Chen X, et al. Among authors: qi m. Front Endocrinol (Lausanne). 2023 Jan 10;13:1013894. doi: 10.3389/fendo.2022.1013894. eCollection 2022. Front Endocrinol (Lausanne). 2023. PMID: 36704038 Free PMC article.

3

Genetic analysis of RET, EDNRB, and EDN3 genes and three SNPs in MCS + 9.7 in Chinese Patients with isolated Hirschsprung disease.

Zhang XN, Zhou MN, Qiu YQ, Ding SP, Qi M, Li JC. Zhang XN, et al. Among authors: qi m. Biochem Genet. 2007 Aug;45(7-8):523-7. doi: 10.1007/s10528-007-9093-y. Epub 2007 Jun 7. Biochem Genet. 2007. PMID: 17554617 No abstract available.

4

Confrontment and solution to gonadotropin resistance and low oocyte retrieval in in vitro fertilization for type I BPES: a case series with review of literature.

Yu Y, Ji M, Xu W, Zhang L, Qi M, Shu J. Yu Y, et al. Among authors: qi m. J Ovarian Res. 2021 Oct 28;14(1):143. doi: 10.1186/s13048-021-00900-2. J Ovarian Res. 2021. PMID: 34711234 Free PMC article. Review.

5

A retrospective study on epidemiological analysis of pre-hospital emergency care in Hangzhou, China.

Wang J, He Y, Chen X, Chen M, Tang C, Lu F, Qi M, Zhang J. Wang J, et al. Among authors: qi m. PLoS One. 2023 Apr 18;18(4):e0282870. doi: 10.1371/journal.pone.0282870. eCollection 2023. PLoS One. 2023. PMID: 37071636 Free PMC article.

6

Classical investigation of incomplete collagen C-propeptide processing reveals a distinctive high bone mass OI phenotype.

Qi M. Qi M. Hum Mutat. 2011 Jun;32(6):v. doi: 10.1002/humu.21531. Hum Mutat. 2011. PMID: 21618347 No abstract available.

7

A Chinese family with cat eye syndrome and abnormality of eye movement: First case report.

Lu Y, Shen L, Zheng Y, Zhang H, Liu Y, Qi M, Huang S, Shen B. Lu Y, et al. Among authors: qi m. Front Pediatr. 2023 Apr 11;11:1145183. doi: 10.3389/fped.2023.1145183. eCollection 2023. Front Pediatr. 2023. PMID: 37114001 Free PMC article.

8

Whole Exome Sequencing Identified Novel ARMC9 Variations in Two Cases With Joubert Syndrome.

Wang H, Luo G, Hu W, Mei J, Shen Y, Wang M, Tan Y, Yang Y, Lu C, Zhao Y, Qi M. Wang H, et al. Among authors: qi m. Front Genet. 2022 Feb 4;13:817153. doi: 10.3389/fgene.2022.817153. eCollection 2022. Front Genet. 2022. PMID: 35186037 Free PMC article.

9

Mitochondrion and its related disorders: making a comeback.

Zhang XN, Qi M. Zhang XN, et al. Among authors: qi m. J Zhejiang Univ Sci B. 2008 Feb;9(2):90-2. doi: 10.1631/jzus.B0710621. J Zhejiang Univ Sci B. 2008. PMID: 18257129 Free PMC article. Review.

10

PDCD6 is an independent predictor of progression free survival in epithelial ovarian cancer.

Su D, Xu H, Feng J, Gao Y, Gu L, Ying L, Katsaros D, Yu H, Xu S, Qi M. Su D, et al. Among authors: qi m. J Transl Med. 2012 Feb 27;10:31. doi: 10.1186/1479-5876-10-31. J Transl Med. 2012. PMID: 22369209 Free PMC article.

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