Hagerman PJ - Search Results

1

An information-rich CGG repeat primed PCR that detects the full range of fragile X expanded alleles and minimizes the need for southern blot analysis.

Chen L, Hadd A, Sah S, Filipovic-Sadic S, Krosting J, Sekinger E, Pan R, Hagerman PJ, Stenzel TT, Tassone F, Latham GJ. Chen L, et al. Among authors: hagerman pj. J Mol Diagn. 2010 Sep;12(5):589-600. doi: 10.2353/jmoldx.2010.090227. Epub 2010 Jul 8. J Mol Diagn. 2010. PMID: 20616364 Free PMC article.

2

Elevated levels of FMR1 mRNA in carrier males: a new mechanism of involvement in the fragile-X syndrome.

Tassone F, Hagerman RJ, Taylor AK, Gane LW, Godfrey TE, Hagerman PJ. Tassone F, et al. Among authors: hagerman pj, hagerman rj. Am J Hum Genet. 2000 Jan;66(1):6-15. doi: 10.1086/302720. Am J Hum Genet. 2000. PMID: 10631132 Free PMC article.

3

Clinical involvement and protein expression in individuals with the FMR1 premutation.

Tassone F, Hagerman RJ, Taylor AK, Mills JB, Harris SW, Gane LW, Hagerman PJ. Tassone F, et al. Among authors: hagerman pj, hagerman rj. Am J Med Genet. 2000 Mar 13;91(2):144-52. doi: 10.1002/(sici)1096-8628(20000313)91:2<144::aid-ajmg14>3.0.co;2-v. Am J Med Genet. 2000. PMID: 10748416

4

Fragile X males with unmethylated, full mutation trinucleotide repeat expansions have elevated levels of FMR1 messenger RNA.

Tassone F, Hagerman RJ, Loesch DZ, Lachiewicz A, Taylor AK, Hagerman PJ. Tassone F, et al. Among authors: hagerman pj, hagerman rj. Am J Med Genet. 2000 Sep 18;94(3):232-6. doi: 10.1002/1096-8628(20000918)94:3<232::aid-ajmg9>3.0.co;2-h. Am J Med Genet. 2000. PMID: 10995510

5

A majority of fragile X males with methylated, full mutation alleles have significant levels of FMR1 messenger RNA.

Tassone F, Hagerman RJ, Taylor AK, Hagerman PJ. Tassone F, et al. Among authors: hagerman pj, hagerman rj. J Med Genet. 2001 Jul;38(7):453-6. doi: 10.1136/jmg.38.7.453. J Med Genet. 2001. PMID: 11432964 Free PMC article.

6

Transcription of the FMR1 gene in individuals with fragile X syndrome.

Tassone F, Hagerman RJ, Chamberlain WD, Hagerman PJ. Tassone F, et al. Among authors: hagerman pj, hagerman rj. Am J Med Genet. 2000 Fall;97(3):195-203. doi: 10.1002/1096-8628(200023)97:3<195::AID-AJMG1037>3.0.CO;2-R. Am J Med Genet. 2000. PMID: 11449488

7

Neuronal intranuclear inclusions in a new cerebellar tremor/ataxia syndrome among fragile X carriers.

Greco CM, Hagerman RJ, Tassone F, Chudley AE, Del Bigio MR, Jacquemont S, Leehey M, Hagerman PJ. Greco CM, et al. Among authors: hagerman pj, hagerman rj. Brain. 2002 Aug;125(Pt 8):1760-71. doi: 10.1093/brain/awf184. Brain. 2002. PMID: 12135967

8

Fragile X premutation carriers: characteristic MR imaging findings of adult male patients with progressive cerebellar and cognitive dysfunction.

Brunberg JA, Jacquemont S, Hagerman RJ, Berry-Kravis EM, Grigsby J, Leehey MA, Tassone F, Brown WT, Greco CM, Hagerman PJ. Brunberg JA, et al. Among authors: hagerman pj, hagerman rj. AJNR Am J Neuroradiol. 2002 Nov-Dec;23(10):1757-66. AJNR Am J Neuroradiol. 2002. PMID: 12427636 Free PMC article.

9

Reduced FMR1 mRNA translation efficiency in fragile X patients with premutations.

Primerano B, Tassone F, Hagerman RJ, Hagerman P, Amaldi F, Bagni C. Primerano B, et al. RNA. 2002 Dec;8(12):1482-8. RNA. 2002. PMID: 12515381 Free PMC article.

10

The FMR1 CGG repeat mouse displays ubiquitin-positive intranuclear neuronal inclusions; implications for the cerebellar tremor/ataxia syndrome.

Willemsen R, Hoogeveen-Westerveld M, Reis S, Holstege J, Severijnen LA, Nieuwenhuizen IM, Schrier M, van Unen L, Tassone F, Hoogeveen AT, Hagerman PJ, Mientjes EJ, Oostra BA. Willemsen R, et al. Among authors: hagerman pj. Hum Mol Genet. 2003 May 1;12(9):949-59. doi: 10.1093/hmg/ddg114. Hum Mol Genet. 2003. PMID: 12700164 Free article.

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