R. M. Clark

发表

Acidic Proline-rich Protein Db and Caries in Young Children

W. L. Owen, S. Bidichandani, R. Slayton, 2007, Journal of dental research.

The GAA triplet-repeat sequence in Friedreich ataxia shows a high level of somatic instability in vivo, with a significant predilection for large contractions.

T. Ashizawa, S. Bidichandani, M. Gómez, 2002, Human molecular genetics.

Replication in mammalian cells recapitulates the locus-specific differences in somatic instability of genomic GAA triplet-repeats

S. Bidichandani, I. De Biase, R. M. Clark, 2006, Nucleic acids research.

The GAA triplet-repeat is unstable in the context of the human FXN locus and displays age-dependent expansions in cerebellum and DRG in a transgenic mouse model

S. Bidichandani, M. Pook, A. Malykhina, 2006, Human Genetics.

Expansion of GAA triplet repeats in the human genome: unique origin of the FRDA mutation at the center of an Alu.

G. Dalgliesh, S. Bidichandani, D. Endres, 2004, Genomics.

A novel candidate gene for mouse and human preaxial polydactyly with altered expression in limbs of Hemimelic extra-toes mutant mice.

D. Kingsley, P. Marker, R. M. Clark, 2000, Genomics.

Expansion of GAA trinucleotide repeats in mammals.

G. Dalgliesh, S. Bidichandani, Rhonda M Clark, 2006, Genomics.

Genetic admixture of European FRDA genes is the cause of Friedreich ataxia in the Mexican population.

S. Bidichandani, S. Nath, A. Rasmussen, 2004, Genomics.

Reciprocal mouse and human limb phenotypes caused by gain- and loss-of-function mutations affecting Lmbr1.

D. Kingsley, M. Muenke, P. Marker, 2001, Genetics.