These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

164 related articles for article (PubMed ID: 34554362)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. Embryoscopy and karyotype findings of repeated miscarriages in recurrent pregnancy loss and spontaneous pregnancy loss.
    Feichtinger M; Reiner A; Hartmann B; Philipp T
    J Assist Reprod Genet; 2018 Aug; 35(8):1401-1406. PubMed ID: 29916100
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. DNA methylation defects in spermatozoa of male partners from couples experiencing recurrent pregnancy loss.
    Khambata K; Raut S; Deshpande S; Mohan S; Sonawane S; Gaonkar R; Ansari Z; Datar M; Bansal V; Patil A; Warke H; Balasinor NH
    Hum Reprod; 2021 Jan; 36(1):48-60. PubMed ID: 33319906
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. NLRP7 or KHDC3L genes and the etiology of molar pregnancies and recurrent miscarriage.
    Andreasen L; Christiansen OB; Niemann I; Bolund L; Sunde L
    Mol Hum Reprod; 2013 Nov; 19(11):773-81. PubMed ID: 23963444
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A genetic association study of NLRP2 and NLRP7 genes in idiopathic recurrent miscarriage.
    Huang JY; Su M; Lin SH; Kuo PL
    Hum Reprod; 2013 Apr; 28(4):1127-34. PubMed ID: 23360675
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Karyotype evaluation of repeated abortions in primary and secondary recurrent pregnancy loss.
    Nikitina TV; Sazhenova EA; Zhigalina DI; Tolmacheva EN; Sukhanova NN; Lebedev IN
    J Assist Reprod Genet; 2020 Mar; 37(3):517-525. PubMed ID: 32009222
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disorders.
    Fontana L; Bedeschi MF; Maitz S; Cereda A; Faré C; Motta S; Seresini A; D'Ursi P; Orro A; Pecile V; Calvello M; Selicorni A; Lalatta F; Milani D; Sirchia SM; Miozzo M; Tabano S
    Epigenetics; 2018; 13(9):897-909. PubMed ID: 30221575
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Germline variants in genes of the subcortical maternal complex and Multilocus Imprinting Disturbance are associated with miscarriage/infertility or Beckwith-Wiedemann progeny.
    Tannorella P; Calzari L; Daolio C; Mainini E; Vimercati A; Gentilini D; Soli F; Pedrolli A; Bonati MT; Larizza L; Russo S
    Clin Epigenetics; 2022 Mar; 14(1):43. PubMed ID: 35317853
    [TBL] [Abstract][Full Text] [Related]  

  • 20. IL-10 gene promoter and intron polymorphisms and changes in IL-10 secretion in women with idiopathic recurrent miscarriage.
    Qaddourah RH; Magdoud K; Saldanha FL; Mahmood N; Mustafa FE; Mahjoub T; Almawi WY
    Hum Reprod; 2014 May; 29(5):1025-34. PubMed ID: 24626804
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.