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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2022 | 1 |
2023 | 1 |
2024 | 0 |
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Microdeletions and microduplications linked to severe congenital disorders in infertile men.
Sci Rep. 2023 Jan 11;13(1):574. doi: 10.1038/s41598-023-27750-w.
Sci Rep. 2023.
PMID: 36631630
Free PMC article.
The Xp22.33 duplication at the PAR1/non-PAR boundary, previously linked to uterine agenesis, was detected in a patient with non-obstructive azoospermia. A novel recurrent intragenic deletion in testis-specific LRRC69 was significantly overrepresented in patients with SPGF …
The Xp22.33 duplication at the PAR1/non-PAR boundary, previously linked to uterine agenesis, was detected in a patient with non-obstructive …
Screening the hub genes and analyzing the mechanisms in discharged COVID-19 patients retesting positive through bioinformatics analysis.
Fang KY, Liang GN, Zhuang ZQ, Fang YX, Dong YQ, Liang CJ, Chen XY, Guo XG.
Fang KY, et al.
J Clin Lab Anal. 2022 Jul;36(7):e24495. doi: 10.1002/jcla.24495. Epub 2022 Jun 3.
J Clin Lab Anal. 2022.
PMID: 35657140
Free PMC article.
RESULTS: In this study, 6622 differentially expressed genes were identified in the group CR, among which RAB11B-AS1, DISP1, MICAL3, PSMG1, and DOCK4 were up-regulated genes, and ANAPC1, IGLV1-40, SORT1, PLPPR2, and ATP1A1-AS1 were down-regulated. 7335 genes were screened in the g …
RESULTS: In this study, 6622 differentially expressed genes were identified in the group CR, among which RAB11B-AS1, DISP1, MICAL3, PSMG1, a …
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