119 related articles for article (PubMed ID: 33987686)
1. Frequent DYSF rare variants/mutations in 152 Han Chinese samples with ovarian endometriosis.
Peng LS; Li ZM; Chen G; Liu FY; Luo Y; Guo JB; Gao GD; Deng YH; Xu LX; Zhou JY; Zou Y
Arch Gynecol Obstet; 2021 Sep; 304(3):671-677. PubMed ID: 33987686
[TBL] [Abstract][Full Text] [Related]
2. Novel MYH8 mutations in 152 Han Chinese samples with ovarian endometriosis.
Lou J; Zou Y; Luo Y; Zhang ZY; Liu FY; Tan J; Zeng X; Wan L; Huang OP
Gynecol Endocrinol; 2020 Jul; 36(7):632-635. PubMed ID: 32308057
[TBL] [Abstract][Full Text] [Related]
3. Molecular landscape of DYSF mutations in dysferlinopathy: From a Chinese multicenter analysis to a worldwide perspective.
Zhong H; Yu M; Lin P; Zhao Z; Zheng X; Xi J; Zhu W; Zheng Y; Zhang W; Lv H; Yan C; Hu J; Wang Z; Lu J; Zhao C; Luo S; Yuan Y
Hum Mutat; 2021 Dec; 42(12):1615-1623. PubMed ID: 34559919
[TBL] [Abstract][Full Text] [Related]
4. Mutation analysis of ZP1, ZP2, ZP3 and ZP4 genes in 152 Han Chinese samples with ovarian endometriosis.
Zou Y; Zhou JY; Guo JB; Zhang ZY; Luo Y; Liu FY; Huang H; Wang F; He M; Wang LQ; Huang OP
Mutat Res; 2019 Jan; 813():46-50. PubMed ID: 30611916
[TBL] [Abstract][Full Text] [Related]
5. Compound heterozygous DYSF variants causing limb-girdle muscular dystrophy type 2B in a Chinese family.
Li L; Jing Z; Cheng L; Liu W; Wang H; Xu Y; Zheng X; Yu X; Liu S
J Gene Med; 2020 Nov; 22(11):e3272. PubMed ID: 32889728
[TBL] [Abstract][Full Text] [Related]
6. Novel CTCF mutations in Chinese patients with ovarian endometriosis.
Guo J; Cao B; Xu X; Wu F; Zhu B
Mol Med Rep; 2018 Jul; 18(1):1031-1036. PubMed ID: 29845264
[TBL] [Abstract][Full Text] [Related]
7. Pooling-Based Genome-Wide Association Study Identifies Risk Loci in the Pathogenesis of Ovarian Endometrioma in Chinese Han Women.
Wang W; Li Y; Li S; Wu Z; Yuan M; Wang T; Wang S
Reprod Sci; 2017 Mar; 24(3):400-406. PubMed ID: 27506219
[TBL] [Abstract][Full Text] [Related]
8. UMD-DYSF, a novel locus specific database for the compilation and interactive analysis of mutations in the dysferlin gene.
Blandin G; Beroud C; Labelle V; Nguyen K; Wein N; Hamroun D; Williams B; Monnier N; Rufibach LE; Urtizberea JA; Cau P; Bartoli M; Lévy N; Krahn M
Hum Mutat; 2012 Mar; 33(3):E2317-31. PubMed ID: 22213072
[TBL] [Abstract][Full Text] [Related]
9. Novel TRERF1 mutations in Chinese patients with ovarian endometriosis.
Cao B; Zeng Y; Wu F; Liu J; Shuang Z; Xu X; Guo J
Mol Med Rep; 2018 Apr; 17(4):5435-5439. PubMed ID: 29393434
[TBL] [Abstract][Full Text] [Related]
10. The genetic profile of dysferlinopathy in a cohort of 209 cases: Genotype-phenotype relationship and a hotspot on the inner DysF domain.
Izumi R; Takahashi T; Suzuki N; Niihori T; Ono H; Nakamura N; Katada S; Kato M; Warita H; Tateyama M; Aoki Y; Aoki M
Hum Mutat; 2020 Sep; 41(9):1540-1554. PubMed ID: 32400077
[TBL] [Abstract][Full Text] [Related]
11. Novel, de novo dysferlin gene mutations in a patient with Miyoshi myopathy.
Hu YY; Lian YJ; Xu HL; Zheng YK; Li CF; Zhang JW; Yan SP
Neurosci Lett; 2018 Jan; 664():107-109. PubMed ID: 29138090
[TBL] [Abstract][Full Text] [Related]
12. Null variants in DYSF result in earlier symptom onset.
Park HJ; Hong YB; Hong JM; Yun U; Kim SW; Shin HY; Kim SM; Choi YC
Clin Genet; 2021 Mar; 99(3):396-406. PubMed ID: 33215690
[TBL] [Abstract][Full Text] [Related]
13. Identification of a novel heterozygous DYSF variant in a large family with a dominantly-inherited dysferlinopathy.
Folland C; Johnsen R; Botero Gomez A; Trajanoski D; Davis MR; Moore U; Straub V; Barresi R; Guglieri M; Hayhurst H; Schaefer AM; Laing NG; Lamont PJ; Ravenscroft G
Neuropathol Appl Neurobiol; 2022 Dec; 48(7):e12846. PubMed ID: 35962550
[TBL] [Abstract][Full Text] [Related]
14. The presence of KRAS, PPP2R1A and ARID1A mutations in 101 Chinese samples with ovarian endometriosis.
Zou Y; Zhou JY; Guo JB; Wang LQ; Luo Y; Zhang ZY; Liu FY; Tan J; Wang F; Huang OP
Mutat Res; 2018 May; 809():1-5. PubMed ID: 29547736
[TBL] [Abstract][Full Text] [Related]
15. Different mutation profiles between epithelium and stroma in endometriosis and normal endometrium.
Suda K; Nakaoka H; Yoshihara K; Ishiguro T; Adachi S; Kase H; Motoyama T; Inoue I; Enomoto T
Hum Reprod; 2019 Oct; 34(10):1899-1905. PubMed ID: 31621846
[TBL] [Abstract][Full Text] [Related]
16. Dysferlin Gene Mutation Spectrum in a Large Cohort of Chinese Patients with Dysferlinopathy.
Jin SQ; Yu M; Zhang W; Lyu H; Yuan Y; Wang ZX
Chin Med J (Engl); 2016 Oct; 129(19):2287-93. PubMed ID: 27647186
[TBL] [Abstract][Full Text] [Related]
17. Genetic variation of the E-cadherin gene is associated with primary infertility in patients with ovarian endometriosis.
Kang S; Li Y; Li B; Wang N; Zhou RM; Zhao XW
Fertil Steril; 2014 Oct; 102(4):1149-1154.e1. PubMed ID: 25150394
[TBL] [Abstract][Full Text] [Related]
18. Frequent POLE1 p.S297F mutation in Chinese patients with ovarian endometrioid carcinoma.
Zou Y; Liu FY; Liu H; Wang F; Li W; Huang MZ; Huang Y; Yuan XQ; Xu XY; Huang OP; He M
Mutat Res; 2014 Mar; 761():49-52. PubMed ID: 24472300
[TBL] [Abstract][Full Text] [Related]
19. Possible relevance of tumor-related genes mutation to malignant transformation of endometriosis.
Ma X; Hui Y; Lin L; Wu Y; Zhang X; Qin X
Eur J Gynaecol Oncol; 2016; 37(1):89-94. PubMed ID: 27048117
[TBL] [Abstract][Full Text] [Related]
20. Novel sequence variants in dysferlin-deficient muscular dystrophy leading to mRNA decay and possible C2-domain misfolding.
Wenzel K; Carl M; Perrot A; Zabojszcza J; Assadi M; Ebeling M; Geier C; Robinson PN; Kress W; Osterziel KJ; Spuler S
Hum Mutat; 2006 Jun; 27(6):599-600. PubMed ID: 16705711
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]