Advances in clinical and molecular understanding of the FMR1 premutation and fragile X-associated tremor/ataxia syndrome

Por Hagerman, Randi, Hagerman, Paul
Publicado em 2013

The Fragile-X Premutation: A Maturing Perspective

Por Hagerman, Paul J., Hagerman, Randi J.
Publicado em 2004

Testing for Fragile X Gene Mutations Throughout the Life Span

Por Hagerman, Randi J., Hagerman, Paul J.
Publicado em 2008

Fragile X and autism: Intertwined at the molecular level leading to targeted treatments

Por Hagerman, Randi, Hoem, Gry, Hagerman, Paul
Publicado em 2010

FMR1 premutation and full mutation molecular mechanisms related to autism

Por Hagerman, Randi, Au, Jacky, Hagerman, Paul
Publicado em 2011

Fragile X-associated tremor/ataxia syndrome

Por Hagerman, Paul J, Hagerman, Randi J
Publicado no Ann N Y Acad Sci (2015)

Fragile X-associated tremor/ataxia syndrome (FXTAS): Pathology and mechanisms

Por Hagerman, Paul
Publicado em 2013

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

Por Tassone, F, Hagerman, R, Taylor, A, Hagerman, P
Publicado em 2001

Fragile X Premutation

Por Tassone, Flora, Hagerman, Paul J, Hagerman, Randi J
Publicado em 2014

Do basic region-leucine zipper proteins bend their DNA targets ... does it matter?

Por Hagerman, P J
Publicado em 1996

Evidence for the existence of stable curvature of DNA in solution.

Por Hagerman, P J
Publicado em 1984

Stimulation of rat testis microsomal 17α-hydroxyprogesterone side-chain cleavage enzyme by luteinizing hormone added in vitro

Por Hagerman, Dwain D.
Publicado em 1967

Fragile X syndrome. Molecular and clinical insights and treatment issues.

Por Hagerman, R J
Publicado em 1997

DNA typing in the forensic arena.

Por Hagerman, P J
Publicado em 1990

Examination of the Recruit

Por Hagerman, A. R.
Publicado em 1940

The fragile X prevalence paradox

Por Hagerman, Paul J
Publicado em 2008

Current Gaps in Understanding the Molecular Basis of FXTAS

Por Hagerman, Paul J.
Publicado em 2012

Epilepsy drives autism in neurodevelopmental disorders

Por HAGERMAN, RANDI J
Publicado em 2013

Two FMR1 premutation cases without nuclear inclusions

Por Martínez-Cerdeño, Verónica, Lechpammer, Mirna, Hagerman, Paul J, Hagerman, Randi
Publicado no Mov Disord (2017)

UNSTABLE MUTATIONS IN THE FMR1 GENE AND THE PHENOTYPES

Por Loesch, Danuta, Hagerman, Randi
Publicado em 2012