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 *

142 related articles for article (PubMed ID: 35494534)

  • 21. A study of FRAXE in mentally retarded individuals referred for fragile X syndrome (FRAXA) testing in the United Kingdom.
    Knight SJ; Ritchie RJ; Chakrabarti L; Cross G; Taylor GR; Mueller RF; Hurst J; Paterson J; Yates JR; Dow DJ; Davies KE
    Am J Hum Genet; 1996 May; 58(5):906-13. PubMed ID: 8651274
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Simultaneous Screening of the FRAXA and FRAXE Loci for Rapid Detection of FMR1 CGG and/or AFF2 CCG Repeat Expansions by Triplet-Primed PCR.
    Liu T; Wang FS; Cheah FSH; Gu Y; Shaw M; Law HY; Tay SKH; Lee CG; Nelson DL; Gecz J; Chong SS
    J Mol Diagn; 2021 Aug; 23(8):941-951. PubMed ID: 34111553
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Expansion and methylation status at FRAXE can be detected on EcoRI blots used for FRAXA diagnosis: analysis of four FRAXE families with mild mental retardation in males.
    Biancalana V; Taine L; Bouix JC; Finck S; Chauvin A; De Verneuil H; Knight SJ; Stoll C; Lacombe D; Mandel JL
    Am J Hum Genet; 1996 Oct; 59(4):847-54. PubMed ID: 8808600
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Microdeletions in FMR2 may be a significant cause of premature ovarian failure.
    Murray A; Webb J; Dennis N; Conway G; Morton N
    J Med Genet; 1999 Oct; 36(10):767-70. PubMed ID: 10528856
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Identification of FMR2, a novel gene associated with the FRAXE CCG repeat and CpG island.
    Gu Y; Shen Y; Gibbs RA; Nelson DL
    Nat Genet; 1996 May; 13(1):109-13. PubMed ID: 8673086
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Possible founder effects for FRAXE alleles.
    Limprasert P; Zhong N; Currie JR; Brown WT
    Am J Med Genet; 1999 May; 84(3):286-90. PubMed ID: 10331609
    [TBL] [Abstract][Full Text] [Related]  

  • 27. FMR2 expression in families with FRAXE mental retardation.
    Gécz J; Oostra BA; Hockey A; Carbonell P; Turner G; Haan EA; Sutherland GR; Mulley JC
    Hum Mol Genet; 1997 Mar; 6(3):435-41. PubMed ID: 9147647
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Identification of the gene FMR2, associated with FRAXE mental retardation.
    Gecz J; Gedeon AK; Sutherland GR; Mulley JC
    Nat Genet; 1996 May; 13(1):105-8. PubMed ID: 8673085
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Lack of expansion of triplet repeats in the FMR1, FRAXE, and FRAXF loci in male multiplex families with autism and pervasive developmental disorders.
    Holden JJ; Wing M; Chalifoux M; Julien-Inalsingh C; Schutz C; Robinson P; Szatmari P; White BN
    Am J Med Genet; 1996 Aug; 64(2):399-403. PubMed ID: 8844091
    [TBL] [Abstract][Full Text] [Related]  

  • 30. FRAXE intermediate alleles are associated with Parkinson's disease.
    Annesi G; Nicoletti G; Tarantino P; Cutuli N; Annesi F; Marco EV; Zappia M; Morgante L; Arabia G; Pugliese P; Condino F; Carrideo S; Civitelli D; Caracciolo M; Romeo N; Spadafora P; Candiano IC; Quattrone A
    Neurosci Lett; 2004 Sep; 368(1):21-4. PubMed ID: 15342126
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Studies of FRAXA and FRAXE in women with premature ovarian failure.
    Murray A; Webb J; Grimley S; Conway G; Jacobs P
    J Med Genet; 1998 Aug; 35(8):637-40. PubMed ID: 9719368
    [TBL] [Abstract][Full Text] [Related]  

  • 32. FRAXE mutation in a mentally retarded subject and in his phenotypically normal twin brother.
    Lo Nigro C; Faravelli F; Cavani S; Perroni L; Novello P; Vitali M; Bricarelli FD; Grasso M
    Eur J Hum Genet; 2000 Mar; 8(3):157-62. PubMed ID: 10780779
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Molecular screening of fragile X (FRAXA) and FRAXE mental retardation syndromes in the Hellenic population of Greece and Cyprus: incidence, genetic variation, and stability.
    Patsalis PC; Sismani C; Hettinger JA; Boumba I; Georgiou I; Stylianidou G; Anastasiadou V; Koukoulli R; Pagoulatos G; Syrrou M
    Am J Med Genet; 1999 May; 84(3):184-90. PubMed ID: 10331587
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Folic acid supplementation and malaria susceptibility and severity among people taking antifolate antimalarial drugs in endemic areas.
    Crider K; Williams J; Qi YP; Gutman J; Yeung L; Mai C; Finkelstain J; Mehta S; Pons-Duran C; Menéndez C; Moraleda C; Rogers L; Daniels K; Green P
    Cochrane Database Syst Rev; 2022 Feb; 2(2022):. PubMed ID: 36321557
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Lack of FMR3 expression in a male with non-syndromic mental retardation and a microdeletion immediately distal to FRAXE CCG repeat.
    Santos-Rebouças CB; Abdalla CB; Fullston T; Campos M; Pimentel MM; Gécz J
    Neurosci Lett; 2006 Apr; 397(3):245-8. PubMed ID: 16469443
    [TBL] [Abstract][Full Text] [Related]  

  • 36. FRAXA and FRAXE prevalence in patients with nonspecific mental retardation in the Hellenic population.
    Syrrou M; Georgiou I; Grigoriadou M; Petersen MB; Kitsiou S; Pagoulatos G; Patsalis PC
    Genet Epidemiol; 1998; 15(1):103-9. PubMed ID: 9523214
    [TBL] [Abstract][Full Text] [Related]  

  • 37. FRAXE expansion is not a common etiological factor among developmentally delayed males.
    Allingham-Hawkins DJ; Ray PN
    Am J Hum Genet; 1995 Jul; 57(1):72-6. PubMed ID: 7541938
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Polymorphism of trinucleotide repeats at loci FRAXA and FRAXE in the population of Tomsk].
    Tolmacheva EN; Nazarenko SA
    Genetika; 2002 Feb; 38(2):268-73. PubMed ID: 11898618
    [TBL] [Abstract][Full Text] [Related]  

  • 39. FMR3 is a novel gene associated with FRAXE CpG island and transcriptionally silent in FRAXE full mutations.
    Gécz J
    J Med Genet; 2000 Oct; 37(10):782-4. PubMed ID: 11015457
    [TBL] [Abstract][Full Text] [Related]  

  • 40. FRAXA and FRAXE: evidence against segregation distortion and for an effect of intermediate alleles on learning disability.
    Teague JW; Morton NE; Dennis NR; Curtis G; McKechnie N; Macpherson JN; Murray A; Pound MC; Sharrock AJ; Youings SA; Jacobs PA
    Proc Natl Acad Sci U S A; 1998 Jan; 95(2):719-24. PubMed ID: 9435259
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.