K. Allen

发表

doublecortin , a Brain-Specific Gene Mutated in Human X-Linked Lissencephaly and Double Cortex Syndrome, Encodes a Putative Signaling Protein

I. Scheffer, C. Walsh, M. Ross, 1998, Cell.

Association of the ADAM33 gene with asthma and bronchial hyperresponsiveness

Steuart Rorke, Stephen T. Holgate, Brooke Hayward, 2002, Nature.

Linkage and physical mapping of X-linked lissencephaly/SBH (XLIS): a gene causing neuronal migration defects in human brain.

I. Scheffer, D. Ledbetter, C. Walsh, 1997, Human molecular genetics.

Missense mutation in PAK3, R67C, causes X-linked nonspecific mental retardation.

C. Walsh, H. Bokhoven, J. Fryns, 2000, American journal of medical genetics.

Genetic analysis of nucleotide triphosphatase activity in the mouse brain.

T. Seyfried, K. Allen, Thomas N. Seyfried, 1994, Genetics.

PAK3 mutation in nonsyndromic X-linked mental retardation

C. Walsh, J. Mulley, M. Partington, 1998, Nature Genetics.

Studies of the candidate genes in X-linked congenital cerebellar hypoplasia

C. Walsh, S. Tsuji, J. Gleeson, 1999, Journal of Neurology.

A cell‐based Dkk1 binding assay reveals roles for extracellular domains of LRP5 in Dkk1 interaction and highlights differences between wild‐type and the high bone mass mutant LRP5(G171V)

R. Bhat, P. Bodine, V. Damagnez, 2009, Journal of cellular biochemistry.

Bone biomechanical properties in LRP5 mutant mice.

R. Recker, D. Cullen, M. Akhter, 2004, Bone.

Genomic Imprinting and Audiogenic Seizures in Mice

T. Seyfried, P. Neumann, K. Allen, 1997, Behavior genetics.

Genes that regulate neuronal migration in the cerebral cortex

Christopher A. Walsh, C. Walsh, K. Allen, 1999, Epilepsy Research.

Shaking down new epilepsy genes

K. Allen, C. Walsh, 1996, Nature Medicine.

A mutation in the LDL receptor-related protein 5 gene results in the autosomal dominant high-bone-mass trait.

Mark L. Johnson, P. van Eerdewegh, J. Carulli, 2002, American journal of human genetics.

LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation.

D. Ledbetter, C. Walsh, M. Ross, 1998, Human molecular genetics.

Mapping of the mouse hyh gene to a YAC/BAC contig on proximal Chromosome 7

C. Walsh, M. Davisson, K. Allen, 2002, Mammalian Genome.

Characterization of mutations in the gene doublecortin in patients with double cortex syndrome

I. Scheffer, C. Walsh, G. Holmes, 1999, Annals of neurology.

Structure-based mutation analysis shows the importance of LRP5 beta-propeller 1 in modulating Dkk1-mediated inhibition of Wnt signaling.

R. Bhat, A. Anisowicz, K. Allen, 2007, Gene.

A YAC contig in Xq22.3-q23, from DXS287 to DXS8088, spanning the brain-specific genes doublecortin (DCX) and PAK3.

C. Walsh, J. Gleeson, K. Allen, 1998, Genomics.