Lu C - Search Results

1

Novel RSPH4A Variants Associated With Primary Ciliary Dyskinesia-Related Infertility in Three Chinese Families.

Wang L, Wang R, Yang D, Lu C, Xu Y, Liu Y, Guo T, Lei C, Luo H. Wang L, et al. Among authors: lu c. Front Genet. 2022 Jun 22;13:922287. doi: 10.3389/fgene.2022.922287. eCollection 2022. Front Genet. 2022. PMID: 35812741 Free PMC article.

2

Identification of Two Novel DNAAF2 Variants in Two Consanguineous Families with Primary Ciliary Dyskinesia.

Lu C, Yang D, Lei C, Wang R, Guo T, Luo H. Lu C, et al. Pharmgenomics Pers Med. 2021 Nov 10;14:1415-1423. doi: 10.2147/PGPM.S338981. eCollection 2021. Pharmgenomics Pers Med. 2021. PMID: 34785929 Free PMC article.

3

Novel Compound Heterozygous Variants in CCDC40 Associated with Primary Ciliary Dyskinesia and Multiple Morphological Abnormalities of the Sperm Flagella.

Xu Y, Yang B, Lei C, Yang D, Ding S, Lu C, Wang L, Guo T, Wang R, Luo H. Xu Y, et al. Among authors: lu c. Pharmgenomics Pers Med. 2022 Apr 15;15:341-350. doi: 10.2147/PGPM.S359821. eCollection 2022. Pharmgenomics Pers Med. 2022. PMID: 35449766 Free PMC article.

4

Identification of a Novel OFD1 Variant in a Patient with Primary Ciliary Dyskinesia.

Yang B, Lei C, Yang D, Lu C, Xu Y, Wang L, Guo T, Wang R, Luo H. Yang B, et al. Among authors: lu c. Pharmgenomics Pers Med. 2022 Jul 11;15:697-704. doi: 10.2147/PGPM.S365740. eCollection 2022. Pharmgenomics Pers Med. 2022. PMID: 35847568 Free PMC article.

5

Case Report: Whole-Exome Sequencing-Based Copy Number Variation Analysis Identified a Novel DRC1 Homozygous Exon Deletion in a Patient With Primary Ciliary Dyskinesia.

Liu Y, Lei C, Wang R, Yang D, Yang B, Xu Y, Lu C, Wang L, Ding S, Guo T, Liu S, Luo H. Liu Y, et al. Among authors: lu c. Front Genet. 2022 Jul 6;13:940292. doi: 10.3389/fgene.2022.940292. eCollection 2022. Front Genet. 2022. PMID: 35873463 Free PMC article.

6

Case Report: DNAAF4 Variants Cause Primary Ciliary Dyskinesia and Infertility in Two Han Chinese Families.

Guo T, Lu C, Yang D, Lei C, Liu Y, Xu Y, Yang B, Wang R, Luo H. Guo T, et al. Among authors: lu c. Front Genet. 2022 Jul 12;13:934920. doi: 10.3389/fgene.2022.934920. eCollection 2022. Front Genet. 2022. PMID: 35903363 Free PMC article.

7

A novel COL3A1 variant associated with vascular Ehlers-Danlos syndrome in a patient presents as recurrent pneumothorax with cavities.

Guo T, Liu Y, Lvqiu S, Lei C, He WL, Jiang Y, Yang D, Wang R, Yang B, Lu C, Xu Y, Ding S, Wang L, Luo H, Peng H. Guo T, et al. Among authors: lu c. QJM. 2023 Sep 12;116(8):691-693. doi: 10.1093/qjmed/hcad059. QJM. 2023. PMID: 37074961 No abstract available.

8

Whole-exome sequencing identified novel DNAH5 homozygous variants in two consanguineous families with primary ciliary dyskinesia.

Yang B, Lei C, Xu Y, Yang D, Lu C, Liu Y, Guo T, Luo H. Yang B, et al. Among authors: lu c. Chin Med J (Engl). 2024 Jan 5;137(1):115-116. doi: 10.1097/CM9.0000000000002736. Epub 2023 Jun 16. Chin Med J (Engl). 2024. PMID: 37319416 Free PMC article. No abstract available.

9

Differences in examination results of small anastomotic fistula after radical gastrectomy with afterward treatments: A case report.

Lu CY, Liu YL, Liu KJ, Xu S, Yao HL, Li L, Guo ZS. Lu CY, et al. World J Clin Cases. 2022 Jul 26;10(21):7609-7616. doi: 10.12998/wjcc.v10.i21.7609. World J Clin Cases. 2022. PMID: 36157983 Free PMC article.

10

Research on Intelligent Monitoring and Protection Equipment of Vital Signs of Underground Personnel in Coal Mines: Review.

Liang Y, Liu Y, Lu C, Cui D, Yang J, Zhou R. Liang Y, et al. Among authors: lu c. Sensors (Basel). 2024 Dec 25;25(1):63. doi: 10.3390/s25010063. Sensors (Basel). 2024. PMID: 39796854

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