BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

175 related articles for article (PubMed ID: 36927955)

  • 1. Loss-of-function variant in SPIN4 causes an X-linked overgrowth syndrome.
    Lui JC; Wagner J; Zhou E; Dong L; Barnes KM; Jee YH; Baron J
    JCI Insight; 2023 May; 8(9):. PubMed ID: 36927955
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Epigenetic Causes of Overgrowth Syndromes.
    Lui JC; Baron J
    J Clin Endocrinol Metab; 2024 Jan; 109(2):312-320. PubMed ID: 37450557
    [TBL] [Abstract][Full Text] [Related]  

  • 3. SPIN4 Is a Principal Endogenous Substrate of the E3 Ubiquitin Ligase DCAF16.
    Zhang X; Thielert M; Li H; Cravatt BF
    Biochemistry; 2021 Mar; 60(9):637-642. PubMed ID: 33636084
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mutations in Epigenetic Regulation Genes Are a Major Cause of Overgrowth with Intellectual Disability.
    Tatton-Brown K; Loveday C; Yost S; Clarke M; Ramsay E; Zachariou A; Elliott A; Wylie H; Ardissone A; Rittinger O; Stewart F; Temple IK; Cole T; ; Mahamdallie S; Seal S; Ruark E; Rahman N
    Am J Hum Genet; 2017 May; 100(5):725-736. PubMed ID: 28475857
    [TBL] [Abstract][Full Text] [Related]  

  • 5. High SPIN4 Expression Is Linked to Advanced Nodal Status and Inferior Prognosis in Nasopharyngeal Carcinoma Patients.
    Chang SL; Chan TC; Chen TJ; Yang CC; Tsai HH; Yeh CF; Lee SW; Lai HY
    Life (Basel); 2021 Sep; 11(9):. PubMed ID: 34575061
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Epigenetic signatures in overgrowth syndromes: Translational opportunities.
    Cytrynbaum C; Choufani S; Weksberg R
    Am J Med Genet C Semin Med Genet; 2019 Dec; 181(4):491-501. PubMed ID: 31828978
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A recessive syndrome of intellectual disability, moderate overgrowth, and renal dysplasia predisposing to Wilms tumor is caused by a mutation in FIBP gene.
    Akawi N; Ben-Salem S; Lahti L; Partanen J; Ali BR; Al-Gazali L
    Am J Med Genet A; 2016 Aug; 170(8):2111-8. PubMed ID: 27183861
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Whole exome sequencing identifies a novel frameshift mutation in GPC3 gene in a patient with overgrowth syndrome.
    Das Bhowmik A; Dalal A
    Gene; 2015 Nov; 572(2):303-6. PubMed ID: 26321508
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Growth plate senescence is associated with loss of DNA methylation.
    Nilsson O; Mitchum RD; Schrier L; Ferns SP; Barnes KM; Troendle JF; Baron J
    J Endocrinol; 2005 Jul; 186(1):241-9. PubMed ID: 16002553
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Ezh2 Mutations Found in the Weaver Overgrowth Syndrome Cause a Partial Loss of H3K27 Histone Methyltransferase Activity.
    Lui JC; Barnes KM; Dong L; Yue S; Graber E; Rapaport R; Dauber A; Nilsson O; Baron J
    J Clin Endocrinol Metab; 2018 Apr; 103(4):1470-1478. PubMed ID: 29244146
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Recombinant bone morphogenetic protein (BMP)-2 regulates costochondral growth plate chondrocytes and induces expression of BMP-2 and BMP-4 in a cell maturation-dependent manner.
    Erickson DM; Harris SE; Dean DD; Harris MA; Wozney JM; Boyan BD; Schwartz Z
    J Orthop Res; 1997 May; 15(3):371-80. PubMed ID: 9246083
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Molecular diagnosis of somatic overgrowth conditions: A single-center experience.
    Lalonde E; Ebrahimzadeh J; Rafferty K; Richards-Yutz J; Grant R; Toorens E; Marie Rosado J; Schindewolf E; Ganguly T; Kalish JM; Deardorff MA; Ganguly A
    Mol Genet Genomic Med; 2019 Mar; 7(3):e536. PubMed ID: 30761771
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mutations in SETD2 cause a novel overgrowth condition.
    Luscan A; Laurendeau I; Malan V; Francannet C; Odent S; Giuliano F; Lacombe D; Touraine R; Vidaud M; Pasmant E; Cormier-Daire V
    J Med Genet; 2014 Aug; 51(8):512-7. PubMed ID: 24852293
    [TBL] [Abstract][Full Text] [Related]  

  • 14. An investigation of the etiology and follow-up findings in 35 children with overgrowth syndromes, including biallelic SUZ12 variant.
    Yüksel Ülker A; Uludağ Alkaya D; Çağlayan AO; Usluer E; Aykut A; Aslanger A; Vural M; Tüysüz B
    Am J Med Genet A; 2023 Jun; 191(6):1530-1545. PubMed ID: 36919607
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Depletion of resting zone chondrocytes during growth plate senescence.
    Schrier L; Ferns SP; Barnes KM; Emons JA; Newman EI; Nilsson O; Baron J
    J Endocrinol; 2006 Apr; 189(1):27-36. PubMed ID: 16614378
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Transgenerational inheritance: how impacts to the epigenetic and genetic information of parents affect offspring health.
    Xavier MJ; Roman SD; Aitken RJ; Nixon B
    Hum Reprod Update; 2019 Sep; 25(5):518-540. PubMed ID: 31374565
    [TBL] [Abstract][Full Text] [Related]  

  • 17. mir-374-5p, mir-379-5p, and mir-503-5p Regulate Proliferation and Hypertrophic Differentiation of Growth Plate Chondrocytes in Male Rats.
    Jee YH; Wang J; Yue S; Jennings M; Clokie SJ; Nilsson O; Lui JC; Baron J
    Endocrinology; 2018 Mar; 159(3):1469-1478. PubMed ID: 29390136
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Growth disrupting mutations in epigenetic regulatory molecules are associated with abnormalities of epigenetic aging.
    Jeffries AR; Maroofian R; Salter CG; Chioza BA; Cross HE; Patton MA; Dempster E; Temple IK; Mackay DJG; Rezwan FI; Aksglaede L; Baralle D; Dabir T; Hunter MF; Kamath A; Kumar A; Newbury-Ecob R; Selicorni A; Springer A; Van Maldergem L; Varghese V; Yachelevich N; Tatton-Brown K; Mill J; Crosby AH; Baple EL
    Genome Res; 2019 Jul; 29(7):1057-1066. PubMed ID: 31160375
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Age-associated epigenetic changes in mammalian sperm: implications for offspring health and development.
    Ashapkin V; Suvorov A; Pilsner JR; Krawetz SA; Sergeyev O
    Hum Reprod Update; 2023 Jan; 29(1):24-44. PubMed ID: 36066418
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    Tlemsani C; Luscan A; Leulliot N; Bieth E; Afenjar A; Baujat G; Doco-Fenzy M; Goldenberg A; Lacombe D; Lambert L; Odent S; Pasche J; Sigaudy S; Buffet A; Violle-Poirsier C; Briand-Suleau A; Laurendeau I; Chin M; Saugier-Veber P; Vidaud D; Cormier-Daire V; Vidaud M; Pasmant E; Burglen L
    J Med Genet; 2016 Nov; 53(11):743-751. PubMed ID: 27317772
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.