Results 41 to 50 of about 185 (76)

Modelling fragile X-associated neuropsychiatric disorders in young inducible 90CGG premutation mice. [PDF]

Brain
Çalışkan G, Lacalle SE, Kul E, Del Ángel M, Zambrano AL, Hukema R, Santos M, Stork O.   +7 more
europepmc   +1 more source

Disruption of Ephx2 in cardiomyocytes but not endothelial cells improves functional recovery after ischemia-reperfusion in isolated mouse hearts. [PDF]

J Biol Chem, 2023
Edin ML, Gruzdev A, Bradbury JA, Graves JP, Lih FB, DeGraff LM, Fleming I, Zeldin DC.   +7 more
europepmc   +1 more source

Overlapping Pathways: Autism Spectrum Disorder in Fragile X Carrier States and the Need for Greater Awareness. [PDF]

Cureus
Fernandez MV, Sirven A, Pickles B, Hamid S, Nunez Selva A.   +4 more
europepmc   +1 more source

Neurodevelopmental origins of age-related neurodegenerative diseases. [PDF]

EBioMedicine
Chow KH, Abel T.
europepmc   +1 more source

The International Fragile X Premutation Registry: building a resource for research and clinical trial readiness. [PDF]

J Med Genet, 2022
Hessl D, Rosselot H, Miller R, Espinal G, Famula J, Sherman SL, Todd PK, Cabal Herrera AM, Lipworth K, Cohen J, Hall DA, Leehey M, Grigsby J, Weber JD, Alusi S, Wheeler A, Raspa M, Hudson T, Sobrian SK.   +18 more
europepmc   +1 more source

A Comprehensive Review of Fragile X Syndrome and Fragile X Premutation Associated Conditions in Africa. [PDF]

Genes (Basel)
Mbachu CNP, Mbachu II, Hagerman R.
europepmc   +1 more source

Social and physical predictors of mental health impact in adult women who have an FMR1 premutation. [PDF]

Genet Med Open, 2023
Kraan CM, Bui M, Archibald A, Davison S, Cvejic RC, Metcalfe S, Amor DJ, Trollor JN, Cohen J, Cornish K.   +9 more
europepmc   +1 more source

Reduced Respiratory Sinus Arrhythmia in Infants with the FMR1 Premutation. [PDF]

Int J Mol Sci
Chase A, Hamrick L, Arnold H, Smith J, Hantman R, Cortez K, Adayev T, Tortora ND, Dahlman A, Roberts J.   +9 more
europepmc   +1 more source

Cardiovascular Problems in the Fragile X Premutation. [PDF]

Front Genet, 2020
Tassanakijpanich N, Cohen J, Cohen R, Srivatsa UN, Hagerman RJ.   +4 more
europepmc   +1 more source

Unmethylated Mosaic Full Mutation Males without Fragile X Syndrome. [PDF]

Genes (Basel)
Tak Y, Schneider A, Santos E, Randol JL, Tassone F, Hagerman P, Hagerman RJ.   +6 more
europepmc   +1 more source