Apolipoprotein E and Alzheimer disease.

Por Strittmatter, W J, Roses, A D
Publicado em 1995

Clinical overdiagnosis of vascular dementia versus necropsy confirmed series.

Por Roses, A D, Saunders, A M
Publicado em 1997

Stoichiometry of sodium and potassium transport in erythrocytes from patients with myotonic muscular dystrophy.

Por Hull, K L, Roses, A D
Publicado em 1976

A dinucleotide repeat polymorphism in the human Na(+),K(+) ATPase, alpha subunit (ATP1A3) gene

Por Kazantsev, A., Yamaoka, L.H., Roses, A.D.
Publicado em 1992

The genetic status of mothers of isolated cases of Duchenne muscular dystrophy.

Por Lane, R J, Robinow, M, Roses, A D
Publicado em 1983

A prospective study of thymectomy and serum acetylcholine receptor antibodies in myasthenia gravis.

Por Olanow, C W, Wechsler, A S, Roses, A D
Publicado em 1982

Myotonic muscular dystrophy: defective phospholipid metabolism in the erythrocyte plasma membrane.

Por Grey, J E, Gitelman, H J, Roses, A D
Publicado em 1980

Electron Spin Resonance Studies of Erythrocytes from Patients with Myotonic Muscular Dystrophy

Por Butterfield, D. A., Chesnut, D. B., Roses, A. D., Appel, S. H.
Publicado em 1974

A PvuII polymorphism detected by pEW404 (D17S64) on chromosome 17

Por Lucas, A.M., Vance, J.M., Stajich, J.M., Roses, A.D.
Publicado em 1991

RFLP analysis for APP 717 mutations associated with Alzheimer's disease.

Por Zeldenrust, S R, Murrell, J, Farlow, M, Ghetti, B, Roses, A D, Benson, M D
Publicado em 1993

RFLPs at the D19S19 locus of human chromosome 19 linked to myotonic dystrophy (DM).

Por Roses, A D, Pericak-Vance, M A, Ross, D A, Yamaoka, L, Bartlett, R J
Publicado em 1986

A PstI polymorphism detected by a genomic clone at the human slow troponin T (TNNT1) gene locus

Por Samson, F., Gilbert, J.R., Koza-Taylor, P., Speer, M.C., Lee, J., Roses, A.D.
Publicado em 1991

Beta-amyloid protein-containing inclusions in skeletal muscle of apolipoprotein-E-deficient mice.

Por Robertson, T. A., Dutton, N. S., Martins, R. N., Roses, A. D., Kakulas, B. A., Papadimitriou, J. M.
Publicado em 1997

RFLPs of the gene for the human glycine receptor on the X-chromosome.

Por Siddique, T, Phillips, K, Betz, H, Grenningloh, G, Warner, K, Hung, W Y, Laing, N, Roses, A D
Publicado em 1989

A polymorphic DNA sequence (174-3.7) on chromosome 19 [D19S58]

Por Lee, J E, Garbutt, J H, Pufky, J, Ciccone, C, Walker, A, Bartlett, R, Roses, A D
Publicado em 1989

Apolipoprotein E: high-avidity binding to beta-amyloid and increased frequency of type 4 allele in late-onset familial Alzheimer disease.

Por Strittmatter, W J, Saunders, A M, Schmechel, D, Pericak-Vance, M, Enghild, J, Salvesen, G S, Roses, A D
Publicado em 1993

Modulation of skeletal muscle sodium channels by human myotonin protein kinase.

Por Mounsey, J P, Xu, P, John, J E, Horne, L T, Gilbert, J, Roses, A D, Moorman, J R
Publicado em 1995

Relative abundance of Alzheimer A beta amyloid peptide variants in Alzheimer disease and normal aging.

Por Näslund, J, Schierhorn, A, Hellman, U, Lannfelt, L, Roses, A D, Tjernberg, L O, Silberring, J, Gandy, S E, Winblad, B, Greengard, P
Publicado em 1994

RFLP for Duchenne muscular dystrophy cDNA clone 30-2.

Por Walker, A P, Bartlett, R J, Laing, N G, Siddique, T, Yamaoka, L H, Chen, J C, Hung, W Y, Roses, A D
Publicado em 1988

RFLP for Duchenne muscular dystrophy cDNA clone 44-1.

Por Laing, N G, Siddique, T, Bartlett, R J, Yamaoka, L H, Chen, J C, Walker, A P, Hung, W Y, Roses, A D
Publicado em 1988