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 *

374 related articles for article (PubMed ID: 17666893)

  • 21. Increase of FMRP expression, raised levels of FMR1 mRNA, and clonal selection in proliferating cells with unmethylated fragile X repeat expansions: a clue to the sex bias in the transmission of full mutations?
    Salat U; Bardoni B; Wöhrle D; Steinbach P
    J Med Genet; 2000 Nov; 37(11):842-50. PubMed ID: 11073538
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Role of Taurine in Testicular Function in the Fragile x Mouse.
    Lin S; El Idrissi A
    Adv Exp Med Biol; 2019; 1155():155-162. PubMed ID: 31468394
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Transcript levels of the intermediate size or grey zone fragile X mental retardation 1 alleles are raised, and correlate with the number of CGG repeats.
    Loesch DZ; Bui QM; Huggins RM; Mitchell RJ; Hagerman RJ; Tassone F
    J Med Genet; 2007 Mar; 44(3):200-4. PubMed ID: 16905681
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Macroorchidism in FMR1 knockout mice is caused by increased Sertoli cell proliferation during testicular development.
    Slegtenhorst-Eegdeman KE; de Rooij DG; Verhoef-Post M; van de Kant HJ; Bakker CE; Oostra BA; Grootegoed JA; Themmen AP
    Endocrinology; 1998 Jan; 139(1):156-62. PubMed ID: 9421410
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Reduced FMRP and increased FMR1 transcription is proportionally associated with CGG repeat number in intermediate-length and premutation carriers.
    Kenneson A; Zhang F; Hagedorn CH; Warren ST
    Hum Mol Genet; 2001 Jul; 10(14):1449-54. PubMed ID: 11448936
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Rare intranuclear inclusions in the brains of 3 older adult males with fragile x syndrome: implications for the spectrum of fragile x-associated disorders.
    Hunsaker MR; Greco CM; Tassone F; Berman RF; Willemsen R; Hagerman RJ; Hagerman PJ
    J Neuropathol Exp Neurol; 2011 Jun; 70(6):462-9. PubMed ID: 21572337
    [TBL] [Abstract][Full Text] [Related]  

  • 27. The X chromosome and fragile X mental retardation.
    Oostra BA; Willemsen R
    Cytogenet Genome Res; 2002; 99(1-4):257-64. PubMed ID: 12900573
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Mutational analysis of the FMR1 gene in 118 mentally retarded males suspected of fragile X syndrome: absence of prevalent mutations.
    Grønskov K; Hallberg A; Brøndum-Nielsen K
    Hum Genet; 1998 Apr; 102(4):440-5. PubMed ID: 9600241
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Reduced RNA expression of the FMR1 gene in women with low (CGGn<26) repeats.
    Wang Q; Barad DH; Darmon SK; Kushnir VA; Wu YG; Lazzaroni-Tealdi E; Zhang L; Albertini DF; Gleicher N
    PLoS One; 2018; 13(12):e0209309. PubMed ID: 30576349
    [TBL] [Abstract][Full Text] [Related]  

  • 30. An origin of DNA replication in the promoter region of the human fragile X mental retardation (FMR1) gene.
    Gray SJ; Gerhardt J; Doerfler W; Small LE; Fanning E
    Mol Cell Biol; 2007 Jan; 27(2):426-37. PubMed ID: 17101793
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Two novel intragenic variants in the FMR1 gene in patients with suspect clinical diagnosis of Fragile X syndrome and no CGG repeat expansion.
    Carroll R; Shaw M; Arvio M; Gardner A; Kumar R; Hodgson B; Heron S; McKenzie F; Järvelä I; Gecz J
    Eur J Med Genet; 2020 Oct; 63(10):104010. PubMed ID: 32688058
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Fmr1 knockout mice: a model to study fragile X mental retardation. The Dutch-Belgian Fragile X Consortium.
    Cell; 1994 Jul; 78(1):23-33. PubMed ID: 8033209
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Method for the Molecular Cytogenetic Visualization of Fragile Site FRAXA].
    Bobokova TS; Lemskaya NA; Kolesnikova IS; Yudkin DV
    Mol Biol (Mosk); 2017; 51(4):704-709. PubMed ID: 28900090
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Quantitative profiling of brain lipid raft proteome in a mouse model of fragile X syndrome.
    Kalinowska M; Castillo C; Francesconi A
    PLoS One; 2015; 10(4):e0121464. PubMed ID: 25849048
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Cochlear Nucleus Transcriptome of a Fragile X Mouse Model Reveals Candidate Genes for Hyperacusis.
    Sakano H; Castle MS; Kundu P
    Laryngoscope; 2024 Mar; 134(3):1363-1371. PubMed ID: 37551886
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Induction of inclusion formation and disruption of lamin A/C structure by premutation CGG-repeat RNA in human cultured neural cells.
    Arocena DG; Iwahashi CK; Won N; Beilina A; Ludwig AL; Tassone F; Schwartz PH; Hagerman PJ
    Hum Mol Genet; 2005 Dec; 14(23):3661-71. PubMed ID: 16239243
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Somatic expansion in mouse and human carriers of fragile X premutation alleles.
    Lokanga RA; Entezam A; Kumari D; Yudkin D; Qin M; Smith CB; Usdin K
    Hum Mutat; 2013 Jan; 34(1):157-66. PubMed ID: 22887750
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Alterations of amino acids and monoamine metabolism in male Fmr1 knockout mice: a putative animal model of the human fragile X mental retardation syndrome.
    Gruss M; Braun K
    Neural Plast; 2001; 8(4):285-98. PubMed ID: 12018775
    [TBL] [Abstract][Full Text] [Related]  

  • 39. The molecular biology of FMRP: new insights into fragile X syndrome.
    Richter JD; Zhao X
    Nat Rev Neurosci; 2021 Apr; 22(4):209-222. PubMed ID: 33608673
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Expression of fragile X mental retardation-1 gene with nuclear export signal mutation changes the expression profiling of mouse cerebella immortal neuronal cell.
    Hu L; Chen Y; Evers S; Shen Y
    Proteomics; 2005 Oct; 5(15):3979-90. PubMed ID: 16130171
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 19.