127 related articles for article (PubMed ID: 38874713)
21. Identification of new variants and candidate genes in women with familial premature ovarian insufficiency using whole-exome sequencing.
Morales R; Lledo B; Ortiz JA; Lozano FM; Garcia EM; Bernabeu A; Fuentes A; Bernabeu R
J Assist Reprod Genet; 2022 Nov; 39(11):2595-2605. PubMed ID: 36208357
[TBL] [Abstract][Full Text] [Related]
22. CPEB3 deficiency in mice affect ovarian follicle development and causes premature ovarian insufficiency.
E F; Zhang H; Yin W; Wang C; Liu Y; Li Y; Wang L; Wu Y; Zhang R; Zou C; Song T; Matunda C; Zou C; Gao X
Cell Death Dis; 2021 Dec; 13(1):21. PubMed ID: 34930897
[TBL] [Abstract][Full Text] [Related]
23. FANCL gene mutations in premature ovarian insufficiency.
Yang Y; Guo T; Liu R; Ke H; Xu W; Zhao S; Qin Y
Hum Mutat; 2020 May; 41(5):1033-1041. PubMed ID: 32048394
[TBL] [Abstract][Full Text] [Related]
24. High-resolution array-CGH analysis on 46,XX patients affected by early onset primary ovarian insufficiency discloses new genes involved in ovarian function.
Bestetti I; Castronovo C; Sironi A; Caslini C; Sala C; Rossetti R; Crippa M; Ferrari I; Pistocchi A; Toniolo D; Persani L; Marozzi A; Finelli P
Hum Reprod; 2019 Mar; 34(3):574-583. PubMed ID: 30689869
[TBL] [Abstract][Full Text] [Related]
25. A novel missense variant in LAMC1 identified in a POI family by whole exome sequencing.
Xu H; Wang C; Wei H; Li T; Fang Y; Wang B
Gynecol Endocrinol; 2023 Oct; 39(1):2265507. PubMed ID: 37839437
[TBL] [Abstract][Full Text] [Related]
26. A Human Homozygous
Bakhshalizadeh S; Bird AD; Sreenivasan R; Bell KM; Robevska G; van den Bergen J; Asghari-Jafarabadi M; Kueh AJ; Touraine P; Lokchine A; Jaillard S; Ayers KL; Wilhelm D; Sinclair AH; Tucker EJ
Genes (Basel); 2024 Mar; 15(3):. PubMed ID: 38540391
[TBL] [Abstract][Full Text] [Related]
27. Landscape of pathogenic mutations in premature ovarian insufficiency.
Ke H; Tang S; Guo T; Hou D; Jiao X; Li S; Luo W; Xu B; Zhao S; Li G; Zhang X; Xu S; Wang L; Wu Y; Wang J; Zhang F; Qin Y; Jin L; Chen ZJ
Nat Med; 2023 Feb; 29(2):483-492. PubMed ID: 36732629
[TBL] [Abstract][Full Text] [Related]
28. Selective loss of kisspeptin signaling in oocytes causes progressive premature ovulatory failure.
Ruohonen ST; Gaytan F; Usseglio Gaudi A; Velasco I; Kukoricza K; Perdices-Lopez C; Franssen D; Guler I; Mehmood A; Elo LL; Ohlsson C; Poutanen M; Tena-Sempere M
Hum Reprod; 2022 Apr; 37(4):806-821. PubMed ID: 35037941
[TBL] [Abstract][Full Text] [Related]
29. Deletion of Gremlin-2 alters estrous cyclicity and disrupts female fertility in mice†.
Rydze RT; Patton BK; Briley SM; Salazar Torralba H; Gipson G; James R; Rajkovic A; Thompson T; Pangas SA
Biol Reprod; 2021 Nov; 105(5):1205-1220. PubMed ID: 34333627
[TBL] [Abstract][Full Text] [Related]
30. New mutations in non-syndromic primary ovarian insufficiency patients identified via whole-exome sequencing.
Patiño LC; Beau I; Carlosama C; Buitrago JC; González R; Suárez CF; Patarroyo MA; Delemer B; Young J; Binart N; Laissue P
Hum Reprod; 2017 Jul; 32(7):1512-1520. PubMed ID: 28505269
[TBL] [Abstract][Full Text] [Related]
31. Genetics of primary ovarian insufficiency: new developments and opportunities.
Qin Y; Jiao X; Simpson JL; Chen ZJ
Hum Reprod Update; 2015; 21(6):787-808. PubMed ID: 26243799
[TBL] [Abstract][Full Text] [Related]
32. Diminished Ovarian Reserve Chemotherapy-Induced Mouse Model: A Tool for the Preclinical Assessment of New Therapies for Ovarian Damage.
Buigues A; Marchante M; Herraiz S; Pellicer A
Reprod Sci; 2020 Aug; 27(8):1609-1619. PubMed ID: 32430713
[TBL] [Abstract][Full Text] [Related]
33. BMP15 "knockout-like" effect in familial premature ovarian insufficiency with persistent ovarian reserve.
Mayer A; Fouquet B; Pugeat M; Misrahi M
Clin Genet; 2017 Aug; 92(2):208-212. PubMed ID: 28094433
[TBL] [Abstract][Full Text] [Related]
34. Whole-exome sequencing reveals new potential genes and variants in patients with premature ovarian insufficiency.
Turkyilmaz A; Alavanda C; Ates EA; Geckinli BB; Polat H; Gokcu M; Karakaya T; Cebi AH; Soylemez MA; Guney Aİ; Ata P; Arman A
J Assist Reprod Genet; 2022 Mar; 39(3):695-710. PubMed ID: 35066699
[TBL] [Abstract][Full Text] [Related]
35. Whole-exome sequencing in patients with premature ovarian insufficiency: early detection and early intervention.
Liu H; Wei X; Sha Y; Liu W; Gao H; Lin J; Li Y; Tang Y; Wang Y; Wang Y; Su Z
J Ovarian Res; 2020 Sep; 13(1):114. PubMed ID: 32962729
[TBL] [Abstract][Full Text] [Related]
36. BMPR1A and BMPR1B Missense Mutations Cause Primary Ovarian Insufficiency.
Renault L; Patiño LC; Magnin F; Delemer B; Young J; Laissue P; Binart N; Beau I
J Clin Endocrinol Metab; 2020 Apr; 105(4):. PubMed ID: 31769494
[TBL] [Abstract][Full Text] [Related]
37. Quantitative Ubiquitylome Analysis Reveals the Specificity of RNF111/Arkadia E3 Ubiquitin Ligase for its Degradative Substrates SKI and SKIL/SnoN in TGF-β Signaling Pathway.
Laigle V; Dingli F; Amhaz S; Perron T; Chouchène M; Colasse S; Petit I; Poullet P; Loew D; Prunier C; Levy L
Mol Cell Proteomics; 2021; 20():100173. PubMed ID: 34740826
[TBL] [Abstract][Full Text] [Related]
38. Basonuclin 1 deficiency is a cause of primary ovarian insufficiency.
Zhang D; Liu Y; Zhang Z; Lv P; Liu Y; Li J; Wu Y; Zhang R; Huang Y; Xu G; Qian Y; Qian Y; Chen S; Xu C; Shen J; Zhu L; Chen K; Zhu B; Ye X; Mao Y; Bo X; Zhou C; Wang T; Chen D; Yang W; Tan Y; Song Y; Zhou D; Sheng J; Gao H; Zhu Y; Li M; Wu L; He L; Huang H
Hum Mol Genet; 2018 Nov; 27(21):3787-3800. PubMed ID: 30010909
[TBL] [Abstract][Full Text] [Related]
39. Targeted Next-Generation Sequencing Indicates a Frequent Oligogenic Involvement in Primary Ovarian Insufficiency Onset.
Rossetti R; Moleri S; Guizzardi F; Gentilini D; Libera L; Marozzi A; Moretti C; Brancati F; Bonomi M; Persani L
Front Endocrinol (Lausanne); 2021; 12():664645. PubMed ID: 34803902
[TBL] [Abstract][Full Text] [Related]
40. Next-generation sequencing of 500 POI patients identified novel responsible monogenic and oligogenic variants.
Luo W; Ke H; Tang S; Jiao X; Li Z; Zhao S; Zhang F; Guo T; Qin Y
J Ovarian Res; 2023 Feb; 16(1):39. PubMed ID: 36793102
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
