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 *

213 related articles for article (PubMed ID: 35646065)

  • 1.
    Jiraanont P; Manor E; Tabatadze N; Zafarullah M; Mendoza G; Melikishvili G; Tassone F
    Front Genet; 2022; 13():884424. PubMed ID: 35646065
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Epigenetic characterization of the FMR1 gene and aberrant neurodevelopment in human induced pluripotent stem cell models of fragile X syndrome.
    Sheridan SD; Theriault KM; Reis SA; Zhou F; Madison JM; Daheron L; Loring JF; Haggarty SJ
    PLoS One; 2011; 6(10):e26203. PubMed ID: 22022567
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Fragile X Syndrome Caused by Maternal Somatic Mosaicism of
    Gómez-Rodríguez MJ; Morales-Conejo M; Arteche-López A; Sánchez-Calvín MT; Quesada-Espinosa JF; Gómez-Manjón I; Palma-Milla C; Lezana-Rosales JM; Pérez de la Fuente R; Martin-Ramos ML; Fernández-Guijarro M; Moreno-García M; Alvarez-Mora MI
    Genes (Basel); 2022 Sep; 13(9):. PubMed ID: 36140775
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Double Genetic Hit: Fragile X Syndrome and Partial Deletion of Protein Patched Homolog 1 Antisense as Cause of Severe Autism Spectrum Disorder.
    Saldarriaga W; Payán-Gómez C; González-Teshima LY; Rosa L; Tassone F; Hagerman RJ
    J Dev Behav Pediatr; 2020 Dec; 41(9):724-728. PubMed ID: 32947579
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Unstable mutations in the FMR1 gene and the phenotypes.
    Loesch D; Hagerman R
    Adv Exp Med Biol; 2012; 769():78-114. PubMed ID: 23560306
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Changes in expression of the long non-coding RNA FMR4 associate with altered gene expression during differentiation of human neural precursor cells.
    Peschansky VJ; Pastori C; Zeier Z; Motti D; Wentzel K; Velmeshev D; Magistri M; Bixby JL; Lemmon VP; Silva JP; Wahlestedt C
    Front Genet; 2015; 6():263. PubMed ID: 26322075
    [TBL] [Abstract][Full Text] [Related]  

  • 7. CNS expression of murine fragile X protein (FMRP) as a function of CGG-repeat size.
    Ludwig AL; Espinal GM; Pretto DI; Jamal AL; Arque G; Tassone F; Berman RF; Hagerman PJ
    Hum Mol Genet; 2014 Jun; 23(12):3228-38. PubMed ID: 24463622
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Methylated premutation of the FMR1 gene in three sisters: correlating CGG expansion and epigenetic inactivation.
    Tabolacci E; Pomponi MG; Remondini L; Pietrobono R; Nobile V; Pennacchio G; Gurrieri F; Neri G; Genuardi M; Chiurazzi P
    Eur J Hum Genet; 2020 May; 28(5):567-575. PubMed ID: 31804632
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Fragile X spectrum disorders.
    Lozano R; Rosero CA; Hagerman RJ
    Intractable Rare Dis Res; 2014 Nov; 3(4):134-46. PubMed ID: 25606363
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mosaic FMR1 deletion causes fragile X syndrome and can lead to molecular misdiagnosis: a case report and review of the literature.
    Coffee B; Ikeda M; Budimirovic DB; Hjelm LN; Kaufmann WE; Warren ST
    Am J Med Genet A; 2008 May; 146A(10):1358-67. PubMed ID: 18412117
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Germinal mosaicism for a deletion of the FMR1 gene leading to fragile X syndrome.
    Jiraanont P; Hagerman RJ; Neri G; Zollino M; Murdolo M; Tassone F
    Eur J Med Genet; 2016 Sep; 59(9):459-62. PubMed ID: 27546052
    [TBL] [Abstract][Full Text] [Related]  

  • 12. De novo microduplication of the FMR1 gene in a patient with developmental delay, epilepsy and hyperactivity.
    Vengoechea J; Parikh AS; Zhang S; Tassone F
    Eur J Hum Genet; 2012 Nov; 20(11):1197-200. PubMed ID: 22549406
    [TBL] [Abstract][Full Text] [Related]  

  • 13. microRNAs and Fragile X Syndrome.
    Lin SL
    Adv Exp Med Biol; 2015; 888():107-21. PubMed ID: 26663181
    [TBL] [Abstract][Full Text] [Related]  

  • 14. FMRP Levels in Human Peripheral Blood Leukocytes Correlates with Intellectual Disability.
    Roth M; Ronco L; Cadavid D; Durbin-Johnson B; Hagerman RJ; Tassone F
    Diagnostics (Basel); 2021 Sep; 11(10):. PubMed ID: 34679478
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A mouse model of the human Fragile X syndrome I304N mutation.
    Zang JB; Nosyreva ED; Spencer CM; Volk LJ; Musunuru K; Zhong R; Stone EF; Yuva-Paylor LA; Huber KM; Paylor R; Darnell JC; Darnell RB
    PLoS Genet; 2009 Dec; 5(12):e1000758. PubMed ID: 20011099
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Selective Deletion of Astroglial FMRP Dysregulates Glutamate Transporter GLT1 and Contributes to Fragile X Syndrome Phenotypes In Vivo.
    Higashimori H; Schin CS; Chiang MS; Morel L; Shoneye TA; Nelson DL; Yang Y
    J Neurosci; 2016 Jul; 36(27):7079-94. PubMed ID: 27383586
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Modeling fragile X syndrome in the Fmr1 knockout mouse.
    Kazdoba TM; Leach PT; Silverman JL; Crawley JN
    Intractable Rare Dis Res; 2014 Nov; 3(4):118-33. PubMed ID: 25606362
    [TBL] [Abstract][Full Text] [Related]  

  • 18. FMR1 gene mutations in patients with fragile X syndrome and obligate carriers: 30 years of experience in Chile.
    Santa María L; Aliaga S; Faundes V; Morales P; Pugin Á; Curotto B; Soto P; Peña MI; Salas I; Alliende MA
    Genet Res (Camb); 2016 Jun; 98():e11. PubMed ID: 27350105
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Long Noncoding RNA Can Be a Probable Mechanism and a Novel Target for Diagnosis and Therapy in Fragile X Syndrome.
    Huang G; Zhu H; Wu S; Cui M; Xu T
    Front Genet; 2019; 10():446. PubMed ID: 31191598
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Intragenic FMR1 disease-causing variants: a significant mutational mechanism leading to Fragile-X syndrome.
    Quartier A; Poquet H; Gilbert-Dussardier B; Rossi M; Casteleyn AS; Portes VD; Feger C; Nourisson E; Kuentz P; Redin C; Thevenon J; Mosca-Boidron AL; Callier P; Muller J; Lesca G; Huet F; Geoffroy V; El Chehadeh S; Jung M; Trojak B; Le Gras S; Lehalle D; Jost B; Maury S; Masurel A; Edery P; Thauvin-Robinet C; Gérard B; Mandel JL; Faivre L; Piton A
    Eur J Hum Genet; 2017 Apr; 25(4):423-431. PubMed ID: 28176767
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.