BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

284 related articles for article (PubMed ID: 31847873)

  • 1. A KHDC3L mutation resulting in recurrent hydatidiform mole causes genome-wide DNA methylation loss in oocytes and persistent imprinting defects post-fertilisation.
    Demond H; Anvar Z; Jahromi BN; Sparago A; Verma A; Davari M; Calzari L; Russo S; Jahromi MA; Monk D; Andrews S; Riccio A; Kelsey G
    Genome Med; 2019 Dec; 11(1):84. PubMed ID: 31847873
    [TBL] [Abstract][Full Text] [Related]  

  • 2. DNA Methylation Dynamics in the Female Germline and Maternal-Effect Mutations That Disrupt Genomic Imprinting.
    Anvar Z; Chakchouk I; Demond H; Sharif M; Kelsey G; Van den Veyver IB
    Genes (Basel); 2021 Aug; 12(8):. PubMed ID: 34440388
    [TBL] [Abstract][Full Text] [Related]  

  • 3. NLRPs, the subcortical maternal complex and genomic imprinting.
    Monk D; Sanchez-Delgado M; Fisher R
    Reproduction; 2017 Dec; 154(6):R161-R170. PubMed ID: 28916717
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The loss of imprinted DNA methylation in mouse blastocysts is inflicted to a similar extent by in vitro follicle culture and ovulation induction.
    Saenz-de-Juano MD; Billooye K; Smitz J; Anckaert E
    Mol Hum Reprod; 2016 Jun; 22(6):427-41. PubMed ID: 26908643
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. NLRP7 and KHDC3L, the two maternal-effect proteins responsible for recurrent hydatidiform moles, co-localize to the oocyte cytoskeleton.
    Akoury E; Zhang L; Ao A; Slim R
    Hum Reprod; 2015 Jan; 30(1):159-69. PubMed ID: 25358348
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Novel pathogenic variants in NLRP7, NLRP5, and PADI6 in patients with recurrent hydatidiform moles and reproductive failure.
    Rezaei M; Suresh B; Bereke E; Hadipour Z; Aguinaga M; Qian J; Bagga R; Fardaei M; Hemida R; Jagadeesh S; Majewski J; Slim R
    Clin Genet; 2021 Jun; 99(6):823-828. PubMed ID: 33583041
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Aberrant hypomethylation at imprinted differentially methylated regions is involved in biparental placental mesenchymal dysplasia.
    Aoki S; Higashimoto K; Hidaka H; Ohtsuka Y; Aoki S; Mishima H; Yoshiura KI; Nakabayashi K; Hata K; Yatsuki H; Hara S; Ohba T; Katabuchi H; Soejima H
    Clin Epigenetics; 2022 May; 14(1):64. PubMed ID: 35581658
    [TBL] [Abstract][Full Text] [Related]  

  • 9. NLRP7 and KHDC3L variants in Chinese patients with recurrent hydatidiform moles.
    Ji M; Shi X; Xiang Y; Cui Q; Zhao J
    Jpn J Clin Oncol; 2019 Jul; 49(7):620-627. PubMed ID: 31220306
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Lack of involvement of known DNA methyltransferases in familial hydatidiform mole implies the involvement of other factors in establishment of imprinting in the human female germline.
    Hayward BE; De Vos M; Judson H; Hodge D; Huntriss J; Picton HM; Sheridan E; Bonthron DT
    BMC Genet; 2003 Jan; 4():2. PubMed ID: 12546714
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Allele-Specific Methylome and Transcriptome Analysis Reveals Widespread Imprinting in the Human Placenta.
    Hamada H; Okae H; Toh H; Chiba H; Hiura H; Shirane K; Sato T; Suyama M; Yaegashi N; Sasaki H; Arima T
    Am J Hum Genet; 2016 Nov; 99(5):1045-1058. PubMed ID: 27843122
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Loss-of-function maternal-effect mutations of PADI6 are associated with familial and sporadic Beckwith-Wiedemann syndrome with multi-locus imprinting disturbance.
    Cubellis MV; Pignata L; Verma A; Sparago A; Del Prete R; Monticelli M; Calzari L; Antona V; Melis D; Tenconi R; Russo S; Cerrato F; Riccio A
    Clin Epigenetics; 2020 Sep; 12(1):139. PubMed ID: 32928291
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Recurrent complete hydatidiform mole: where we are, is there a safe gestational horizon? Opinion and mini-review.
    Kalogiannidis I; Kalinderi K; Kalinderis M; Miliaras D; Tarlatzis B; Athanasiadis A
    J Assist Reprod Genet; 2018 Jun; 35(6):967-973. PubMed ID: 29737470
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Novel genetic variants of KHDC3L and other members of the subcortical maternal complex associated with Beckwith-Wiedemann syndrome or Pseudohypoparathyroidism 1B and multi-locus imprinting disturbances.
    Pignata L; Cecere F; Verma A; Hay Mele B; Monticelli M; Acurzio B; Giaccari C; Sparago A; Hernandez Mora JR; Monteagudo-Sánchez A; Esteller M; Pereda A; Tenorio-Castano J; Palumbo O; Carella M; Prontera P; Piscopo C; Accadia M; Lapunzina P; Cubellis MV; de Nanclares GP; Monk D; Riccio A; Cerrato F
    Clin Epigenetics; 2022 May; 14(1):71. PubMed ID: 35643636
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Contribution of intragenic DNA methylation in mouse gametic DNA methylomes to establish oocyte-specific heritable marks.
    Kobayashi H; Sakurai T; Imai M; Takahashi N; Fukuda A; Yayoi O; Sato S; Nakabayashi K; Hata K; Sotomaru Y; Suzuki Y; Kono T
    PLoS Genet; 2012 Jan; 8(1):e1002440. PubMed ID: 22242016
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Human Oocyte-Derived Methylation Differences Persist in the Placenta Revealing Widespread Transient Imprinting.
    Sanchez-Delgado M; Court F; Vidal E; Medrano J; Monteagudo-Sánchez A; Martin-Trujillo A; Tayama C; Iglesias-Platas I; Kondova I; Bontrop R; Poo-Llanillo ME; Marques-Bonet T; Nakabayashi K; Simón C; Monk D
    PLoS Genet; 2016 Nov; 12(11):e1006427. PubMed ID: 27835649
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mutations causing familial biparental hydatidiform mole implicate c6orf221 as a possible regulator of genomic imprinting in the human oocyte.
    Parry DA; Logan CV; Hayward BE; Shires M; Landolsi H; Diggle C; Carr I; Rittore C; Touitou I; Philibert L; Fisher RA; Fallahian M; Huntriss JD; Picton HM; Malik S; Taylor GR; Johnson CA; Bonthron DT; Sheridan EG
    Am J Hum Genet; 2011 Sep; 89(3):451-8. PubMed ID: 21885028
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Biparental hydatidiform moles: a maternal effect mutation affecting imprinting in the offspring.
    Van den Veyver IB; Al-Hussaini TK
    Hum Reprod Update; 2006; 12(3):233-42. PubMed ID: 16540529
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A familial case of recurrent hydatidiform mole with p.Asp108Ilefs∗30 causing mutation in KHDC3L: A genetic and clinical report.
    Fatemi N; Varkiani M; Ramazanali F; Almadani N; Totonchi M
    Taiwan J Obstet Gynecol; 2022 Mar; 61(2):395-398. PubMed ID: 35361411
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.