181 related articles for article (PubMed ID: 28561018)
1. Maternal heterozygous NLRP7 variant results in recurrent reproductive failure and imprinting disturbances in the offspring.
Soellner L; Begemann M; Degenhardt F; Geipel A; Eggermann T; Mangold E
Eur J Hum Genet; 2017 Aug; 25(8):924-929. PubMed ID: 28561018
[TBL] [Abstract][Full Text] [Related]
2. NLRP7 variants in spontaneous abortions with multilocus imprinting disturbances from women with recurrent pregnancy loss.
Sazhenova EA; Nikitina TV; Vasilyev SA; Tolmacheva EN; Vasilyeva OY; Markov AV; Yuryev SY; Skryabin NA; Zarubin AA; Kolesnikov NA; Stepanov VA; Lebedev IN
J Assist Reprod Genet; 2021 Nov; 38(11):2893-2908. PubMed ID: 34554362
[TBL] [Abstract][Full Text] [Related]
3. NLRP genes and their role in preeclampsia and multi-locus imprinting disorders.
Soellner L; Kopp KM; Mütze S; Meyer R; Begemann M; Rudnik S; Rath W; Eggermann T; Zerres K
J Perinat Med; 2018 Feb; 46(2):169-173. PubMed ID: 28753543
[TBL] [Abstract][Full Text] [Related]
4. Absence of Maternal Methylation in Biparental Hydatidiform Moles from Women with NLRP7 Maternal-Effect Mutations Reveals Widespread Placenta-Specific Imprinting.
Sanchez-Delgado M; Martin-Trujillo A; Tayama C; Vidal E; Esteller M; Iglesias-Platas I; Deo N; Barney O; Maclean K; Hata K; Nakabayashi K; Fisher R; Monk D
PLoS Genet; 2015 Nov; 11(11):e1005644. PubMed ID: 26544189
[TBL] [Abstract][Full Text] [Related]
5. Maternal variants in
Begemann M; Rezwan FI; Beygo J; Docherty LE; Kolarova J; Schroeder C; Buiting K; Chokkalingam K; Degenhardt F; Wakeling EL; Kleinle S; González Fassrainer D; Oehl-Jaschkowitz B; Turner CLS; Patalan M; Gizewska M; Binder G; Bich Ngoc CT; Chi Dung V; Mehta SG; Baynam G; Hamilton-Shield JP; Aljareh S; Lokulo-Sodipe O; Horton R; Siebert R; Elbracht M; Temple IK; Eggermann T; Mackay DJG
J Med Genet; 2018 Jul; 55(7):497-504. PubMed ID: 29574422
[TBL] [Abstract][Full Text] [Related]
6. Trans-acting genetic variants causing multilocus imprinting disturbance (MLID): common mechanisms and consequences.
Eggermann T; Yapici E; Bliek J; Pereda A; Begemann M; Russo S; Tannorella P; Calzari L; de Nanclares GP; Lombardi P; Temple IK; Mackay D; Riccio A; Kagami M; Ogata T; Lapunzina P; Monk D; Maher ER; Tümer Z
Clin Epigenetics; 2022 Mar; 14(1):41. PubMed ID: 35296332
[TBL] [Abstract][Full Text] [Related]
7. A recurrent intragenic genomic duplication, other novel mutations in NLRP7 and imprinting defects in recurrent biparental hydatidiform moles.
Kou YC; Shao L; Peng HH; Rosetta R; del Gaudio D; Wagner AF; Al-Hussaini TK; Van den Veyver IB
Mol Hum Reprod; 2008 Jan; 14(1):33-40. PubMed ID: 18039680
[TBL] [Abstract][Full Text] [Related]
8. Novel NLRP7 mutations in familial recurrent hydatidiform mole: are NLRP7 mutations a risk for recurrent reproductive wastage?
Ulker V; Gurkan H; Tozkir H; Karaman V; Ozgur H; Numanoglu C; Gedikbasi A; Akbayir O; Uyguner ZO
Eur J Obstet Gynecol Reprod Biol; 2013 Sep; 170(1):188-92. PubMed ID: 23880596
[TBL] [Abstract][Full Text] [Related]
9. Mutations in NLRP7 are associated with diploid biparental hydatidiform moles, but not androgenetic complete moles.
Dixon PH; Trongwongsa P; Abu-Hayyah S; Ng SH; Akbar SA; Khawaja NP; Seckl MJ; Savage PM; Fisher RA
J Med Genet; 2012 Mar; 49(3):206-11. PubMed ID: 22315435
[TBL] [Abstract][Full Text] [Related]
10. Maternal NLRP7 and C6orf221 variants are not a common risk factor for androgenetic moles, triploidy and recurrent miscarriage.
Manokhina I; Hanna CW; Stephenson MD; McFadden DE; Robinson WP
Mol Hum Reprod; 2013 Aug; 19(8):539-44. PubMed ID: 23515668
[TBL] [Abstract][Full Text] [Related]
11. Women heterozygous for NALP7/NLRP7 mutations are at risk for reproductive wastage: report of two novel mutations.
Qian J; Deveault C; Bagga R; Xie X; Slim R
Hum Mutat; 2007 Jul; 28(7):741. PubMed ID: 17579354
[TBL] [Abstract][Full Text] [Related]
12. Disturbed genomic imprinting and its relevance for human reproduction: causes and clinical consequences.
Elbracht M; Mackay D; Begemann M; Kagan KO; Eggermann T
Hum Reprod Update; 2020 Feb; 26(2):197-213. PubMed ID: 32068234
[TBL] [Abstract][Full Text] [Related]
13. NLRP7 in the spectrum of reproductive wastage: rare non-synonymous variants confer genetic susceptibility to recurrent reproductive wastage.
Messaed C; Chebaro W; Di Roberto RB; Rittore C; Cheung A; Arseneau J; Schneider A; Chen MF; Bernishke K; Surti U; Hoffner L; Sauthier P; Buckett W; Qian J; Lau NM; Bagga R; Engert JC; Coullin P; Touitou I; Slim R;
J Med Genet; 2011 Aug; 48(8):540-8. PubMed ID: 21659348
[TBL] [Abstract][Full Text] [Related]
14. Recurrent hydatidiform mole: detection of two novel mutations in the NLRP7 gene in two Egyptian families.
Abdalla EM; Hayward BE; Shamseddin A; Nawar MM
Eur J Obstet Gynecol Reprod Biol; 2012 Oct; 164(2):211-5. PubMed ID: 22770628
[TBL] [Abstract][Full Text] [Related]
15. NLRP7 mutation analysis in sporadic hydatidiform moles in Tunisian patients: NLRP7 and sporadic mole.
Landolsi H; Rittore C; Philibert L; Hmissa S; Gribaa M; Touitou I; Yacoubi MT
Arch Pathol Lab Med; 2012 Jun; 136(6):646-51. PubMed ID: 22646272
[TBL] [Abstract][Full Text] [Related]
16. Biallelic PADI6 variants cause multilocus imprinting disturbances and miscarriages in the same family.
Eggermann T; Kadgien G; Begemann M; Elbracht M
Eur J Hum Genet; 2021 Apr; 29(4):575-580. PubMed ID: 33221824
[TBL] [Abstract][Full Text] [Related]
17. No evidence for mutations in NLRP7, NLRP2 or KHDC3L in women with unexplained recurrent pregnancy loss or infertility.
Aghajanova L; Mahadevan S; Altmäe S; Stavreus-Evers A; Regan L; Sebire N; Dixon P; Fisher RA; Van den Veyver IB
Hum Reprod; 2015 Jan; 30(1):232-8. PubMed ID: 25376457
[TBL] [Abstract][Full Text] [Related]
18. NLRP7 participates in the human subcortical maternal complex and its variants cause female infertility characterized by early embryo arrest.
Han J; Zhang N; Cao Q; Shi X; Wang C; Rui X; Ding J; Zhao C; Zhang J; Ling X; Li H; Guan Y; Meng Q; Huo R
J Mol Med (Berl); 2023 Jun; 101(6):717-729. PubMed ID: 37148315
[TBL] [Abstract][Full Text] [Related]
19. [Family pedigree analysis in family member with history of hydatidiform mole and the NLRP7 gene expression].
Li Y; Cheng Q; Qian JH; Zhou W; Xie X; Slim R
Zhonghua Fu Chan Ke Za Zhi; 2011 Aug; 46(8):600-4. PubMed ID: 22169519
[TBL] [Abstract][Full Text] [Related]
20. The p.L750V mutation in the NLRP7 gene is frequent in Mexican patients with recurrent molar pregnancies and is not associated with recurrent pregnancy loss.
Estrada H; Buentello B; Zenteno JC; Fiszman R; Aguinaga M
Prenat Diagn; 2013 Mar; 33(3):205-8. PubMed ID: 23354651
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]