128 related articles for article (PubMed ID: 34225611)
1. Screening of Candidate Pathogenic Genes for Spontaneous Abortion Using Whole Exome Sequencing.
Zhu Q; Liu J; Chen L; Zhou Y; Zhou T; Bian W; Ding G; Li G; Ding J
Comb Chem High Throughput Screen; 2022; 25(9):1462-1473. PubMed ID: 34225611
[TBL] [Abstract][Full Text] [Related]
2. Whole exome sequencing in recurrent early pregnancy loss.
Qiao Y; Wen J; Tang F; Martell S; Shomer N; Leung PC; Stephenson MD; Rajcan-Separovic E
Mol Hum Reprod; 2016 May; 22(5):364-72. PubMed ID: 26826164
[TBL] [Abstract][Full Text] [Related]
3. Genome variation in colorectal cancer patient with liver metastasis measured by whole-exome sequencing.
Yi H; Liao ZW; Chen JJ; Shi XY; Chen GL; Wu GT; Zhou DY; Zhou GQ; Huang JY; Lian L; Yu ZY; He SB
J Gastrointest Oncol; 2021 Apr; 12(2):507-515. PubMed ID: 34012644
[TBL] [Abstract][Full Text] [Related]
4. Identification of ACOT13 and PTGER2 as novel candidate genes of autosomal dominant polycystic kidney disease through whole exome sequencing.
Du N; Dong D; Sun L; Che L; Li X; Liu Y; Wang B
Eur J Med Res; 2021 Dec; 26(1):142. PubMed ID: 34886911
[TBL] [Abstract][Full Text] [Related]
5. Specific genetic aberrations of parathyroid in Chinese patients with tertiary hyperparathyroidism using whole-exome sequencing.
Li L; Sheng Q; Zeng H; Li W; Wang Q; Ma G; Xu X; Qiu M; Zhang W; Shan C
Front Endocrinol (Lausanne); 2023; 14():1221060. PubMed ID: 37854190
[TBL] [Abstract][Full Text] [Related]
6. Key Gene and Functional Pathways Identified in Unexplained Recurrent Spontaneous Abortion Using Targeted RNA Sequencing and Clinical Analysis.
Gu H; Li L; Du M; Xu H; Gao M; Liu X; Wei X; Zhong X
Front Immunol; 2021; 12():717832. PubMed ID: 34421922
[TBL] [Abstract][Full Text] [Related]
7. Identification of somatic mutations using whole-exome sequencing in Korean patients with acute myeloid leukemia.
Heo SG; Koh Y; Kim JK; Jung J; Kim HL; Yoon SS; Park JW
BMC Med Genet; 2017 Mar; 18(1):23. PubMed ID: 28249600
[TBL] [Abstract][Full Text] [Related]
8. Identification of genetic polymorphisms in unexplained recurrent spontaneous abortion based on whole exome sequencing.
Mou JT; Huang SX; Yu LL; Xu J; Deng QL; Xie YS; Deng K
Ann Transl Med; 2022 May; 10(10):603. PubMed ID: 35722368
[TBL] [Abstract][Full Text] [Related]
9. The present and future of whole-exome sequencing in studying and treating human reproductive disorders.
Guo W; Zhu X; Yan L; Qiao J
J Genet Genomics; 2018 Oct; 45(10):517-525. PubMed ID: 30391409
[TBL] [Abstract][Full Text] [Related]
10. Whole exome sequencing and transcriptome-wide profiling identify potentially subtype-relevant genes of nasopharyngeal carcinoma.
Liu J; Li X; Yang S; Mou J; Lu H
Pathol Res Pract; 2020 Dec; 216(12):153244. PubMed ID: 33113455
[TBL] [Abstract][Full Text] [Related]
11. Analysis of the inheritance pattern of a Chinese family with phaeochromocytomas through whole exome sequencing.
Cao M; Sun F; Huang X; Dai J; Cui B; Ning G
Gene; 2013 Sep; 526(2):164-9. PubMed ID: 23707928
[TBL] [Abstract][Full Text] [Related]
12. Experimental Study of Somatic Variants of Osteosarcoma by Whole-Exome Sequencing.
Hou J; Liu G; Zhang P; Wang B; Yan Q; Wu P; Wang C; Yao W
Med Sci Monit; 2020 Mar; 26():e920826. PubMed ID: 32193367
[TBL] [Abstract][Full Text] [Related]
13. Whole-Exome Sequencing Indicated New Candidate Genes Associated with Unilateral Cryptorchidism in Pigs.
da Silva AN; Ibelli AMG; Savoldi IR; Cantão ME; Zanella EL; Marques MG; da Silva MVGB; de Peixoto JO; Ledur MC; Lopes JS; Vargas JE; Zanella R
Sex Dev; 2023; 17(1):56-66. PubMed ID: 36758533
[TBL] [Abstract][Full Text] [Related]
14. Whole-Genome Re-sequencing and Transcriptome Reveal Oogenesis-Related Genes in Autotetraploid Carassius auratus.
Wang C; Qin H; Zhao C; Yang L; Yu T; Zhang Y; Luo X; Qin Q; Liu S
Mar Biotechnol (NY); 2021 Apr; 23(2):233-241. PubMed ID: 33675430
[TBL] [Abstract][Full Text] [Related]
15. Targeted next-generation sequencing for cancer-associated gene mutation and copy number detection in 206 patients with non-small-cell lung cancer.
Zheng S; Wang X; Fu Y; Li B; Xu J; Wang H; Huang Z; Xu H; Qiu Y; Shi Y; Li K
Bioengineered; 2021 Dec; 12(1):791-802. PubMed ID: 33629637
[TBL] [Abstract][Full Text] [Related]
16. Next generation sequencing exome data analysis aids in the discovery of SNP and INDEL patterns in Parkinson's disease.
Odumpatta R; Mohanapriya A
Genomics; 2020 Sep; 112(5):3722-3728. PubMed ID: 32348865
[TBL] [Abstract][Full Text] [Related]
17. Whole exome sequencing identifies novel candidate mutations in a Chinese family with left ventricular noncompaction.
Zhou Y; Qian Z; Yang J; Zhu M; Hou X; Wang Y; Wu H; Zou J
Mol Med Rep; 2018 May; 17(5):7325-7330. PubMed ID: 29568952
[TBL] [Abstract][Full Text] [Related]
18. Genomic and transcriptional alterations in first-line chemotherapy exert a potentially unfavorable influence on subsequent immunotherapy in NSCLC.
He Y; Chen L; Zhao L; Dang S; Liu G; Sasada S; Ma PC; van Zandwijk N; Rosell R; Popper HH; Wang H; Jiang M; Guo H; Liu X; Chen S; Zhang X; Xu M; Zhu B; Liu M; Zhou C
Theranostics; 2021; 11(14):7092-7109. PubMed ID: 34093873
[No Abstract] [Full Text] [Related]
19. Concurrent exome-targeted next-generation sequencing and single nucleotide polymorphism array to identify the causative genetic aberrations of isolated Mayer-Rokitansky-Küster-Hauser syndrome.
Chen MJ; Wei SY; Yang WS; Wu TT; Li HY; Ho HN; Yang YS; Chen PL
Hum Reprod; 2015 Jul; 30(7):1732-42. PubMed ID: 25924657
[TBL] [Abstract][Full Text] [Related]
20. Next generation sequencing in recurrent pregnancy loss-approaches and outcomes.
Rajcan-Separovic E
Eur J Med Genet; 2020 Feb; 63(2):103644. PubMed ID: 30991114
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]