Y. Liang

发表

Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease

D. Pollen, J. Haines, M. Pericak-Vance, 1995, Nature.

Screening for PS1 mutations in a referral-based series of AD cases

You-Qiang Song, E. Rogaev, P. S. St George-Hyslop, 2001, Neurology.

Novel presenilin 1 mutations associated with early onset of dementia in a family with both early-onset and late-onset Alzheimer disease.

P. S. St George-Hyslop, B. Tycko, R. Mayeux, 2000, Archives of neurology.

Presenilins Interact with Armadillo Proteins Including Neural‐Specific Plakophilin‐Related Protein and β‐Catenin

J. Rommens, C. Strader, P. Fraser, 1999, Journal of neurochemistry.

Analysis of the c‐FOS gene on chromosome 14 and the promoter of the amyloid precursor protein gene in familial Alzheimer's disease

D. Pollen, J. Haines, E. Rogaev, 1993, Neurology.

Evidence for inter-generational instability in the CAG repeat in the MJD1 gene and for conserved haplotypes at flanking markers amongst Japanese and Caucasian subjects with Machado-Joseph disease.

J. Weissenbach, K. Kidd, R. Sherrington, 1995, Human molecular genetics.

Normal brain development in PS1 hypomorphic mice with markedly reduced γ-secretase cleavage of βAPP

R. Rozmahel, D. Westaway, P. George-Hyslop, 2002, Neurobiology of Aging.

A novel frameshift mutation induced by an adenosine insertion in the polycystic kidney disease 2 (PKD2) gene.

A. Paterson, P. S. St George-Hyslop, S. Somlo, 1998, Kidney international.

Mutation of the gene for the human lysosomal serine protease cathepsin G is not the cause of aberrant APP processing in familial Alzheimer disease

E. Rogaeva, P. George-Hyslop, Y. Liang, 1993, Neuroscience Letters.

Failure to detect missense mutations in the S182 gene in a series of late-onset Alzheimer's disease cases

D. Pollen, R. Sherrington, E. Rogaeva, 1995, Neuroscience Letters.

Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene

J. Rommens, R. Sherrington, E. Rogaev, 1995, Nature.

Ataxia in prion protein (PrP)-deficient mice is associated with upregulation of the novel PrP-like protein doppel.

Inyoul Y. Lee, L. Hood, F. Cohen, 1999, Journal of molecular biology.

Presenilin mutations associated with Alzheimer disease cause defective intracellular trafficking of β-catenin,a component of the presenilin protein complex

R. Rozmahel, J. Woodgett, D. Westaway, 1999, Nature Medicine.

Mutations in the open reading frame of the β-site APP cleaving enzyme (BACE) locus are not a common cause of Alzheimer's disease

E. Rogaev, P. S. St George-Hyslop, H. Medeiros, 2001, Neurogenetics.

Analysis of the 5' sequence, genomic structure, and alternative splicing of the presenilin-1 gene (PSEN1) associated with early onset Alzheimer disease.

P E Fraser, J. Rommens, P. D. de Jong, 1997, Genomics.

Alzheimer's disease associated with mutations in presenilin 2 is rare and variably penetrant.

J. Rommens, Y. Agid, R. Sherrington, 1996, Human molecular genetics.

Somatic PKD2 mutations in individual kidney and liver cysts support a "two-hit" model of cystogenesis in type 2 autosomal dominant polycystic kidney disease.

P. S. St George-Hyslop, P. Parfrey, G. Germino, 1999, Journal of the American Society of Nephrology : JASN.

Genetic evidence for a novel familial Alzheimer's disease locus on chromosome 14

D. Pollen, J. Haines, M. Pericak-Vance, 1992, Nature Genetics.

Machado-Joseph disease in pedigrees of Azorean descent is linked to chromosome 14.

J. Haines, E. Rogaev, P. S. St George-Hyslop, 1994, American journal of human genetics.

Are the associations between Alzheimer's disease and polymorphisms in the apolipoprotein E and the apolipoprotein CII genes due to linkage disequilibrium?

M. Freedman, D. Pollen, J. Haines, 1994, Annals of neurology.

Association between N-acetyltransferase 2 polymorphisms and pancreatic cancer risk: a meta-analysis.

Y. Liang, X. Zhou, J. Liang, 2015, Genetics and molecular research : GMR.