M. Herbstreith

发表

Increased phosphorylated components of erythrocyte membrane spectrin band II with reference to Duchenne muscular dystrophy

A. Roses, S. Appel, M. Herbstreith, 1976, Journal of the Neurological Sciences.

2-D Fluorescence Difference Gel Electrophoresis (DIGE) in Neuroproteomics

C. Osorio, O. Alzate, M. Herbstreith, 2010 .

Membrane protein kinase alteration in Duchenne muscular dystrophy

A. Roses, S. Appel, M. Herbstreith, 1975, Nature.

Endoglin gene polymorphism as a risk factor for sporadic intracerebral hemorrhage

C. Graffagnino, D. Marchuk, J. Davis, 1997, Annals of neurology.

Isolation and localization of a slow troponin (TnT) gene on chromosome 19 by subtraction hybridization of a cDNA muscle library using myotonic dystrophy muscle cDNA

J. Gilbert, W. Hung, A. Roses, 1990, Journal of Neuroscience Research.

Identification of abnormally [32P]‐phosphorylated cyanogen bromide cleavage product of erythrocyte membrane spectrin in Duchenne muscular dystrophy

P. E. Shile, A. Roses, A. Roses, 1981, Neurology.

An error in dystrophin mRNA processing in golden retriever muscular dystrophy, an animal homologue of Duchenne muscular dystrophy.

R. Bartlett, W. Hung, J. Kornegay, 1992, Genomics.

SB-431542, a small molecule transforming growth factor-beta-receptor antagonist, inhibits human glioma cell line proliferation and motility.

D. Bigner, Xiao-Fan Wang, H. Friedman, 2004, Molecular cancer therapeutics.

Splicing of an anti-sense Alu sequence generates a coding sequence variant for the alpha-3 subunit of a neuronal acetylcholine receptor.

A. Roses, F. Clementi, F. Rubboli, 1993, Biochemical and biophysical research communications.

A new probe for the diagnosis of myotonic muscular dystrophy.

J. Gilbert, M. Pericak-Vance, T. Mohandas, 1987, Science.

Dystrophin mRNA Processing in the Canine Homologue of Duchenne Muscular Dystrophy: An Authentic Model for Gene Therapy

R. Bartlett, J. Kornegay, S. Secore, 1992 .

The identification and characterization of KRAB-domain-containing zinc finger proteins.

J. Gilbert, R. Bartlett, A. Roses, 1992, Genomics.

Sialylated Human Apolipoprotein E (apoEs) Is Preferentially Associated with Neuron-Enriched Cultures from APOE Transgenic Mice

J. Gilbert, A. Roses, P. Xu, 1999, Neurobiology of Disease.

Localization of cloned unique DNA to three different regions of chromosome 19: screen for linkage probes for myotonic dystrophy.

D. Ledbetter, M. Pericak-Vance, R. Bartlett, 1985, Journal of neurogenetics.

A molecular genetic study of intracerebral hemorrhage.

C. Graffagnino, A. Roses, M. Alberts, 1994, Archives of neurology.

Cystatin C mutation in an elderly man with sporadic amyloid angiopathy and intracerebral hemorrhage.

C. Graffagnino, D. Schmechel, E. Levy, 1995, Stroke.

Endogenous apolipoprotein E suppresses LPS‐stimulated microglial nitric oxide production

D. Laskowitz, E. Bennett, M. McMillian, 1998, Neuroreport.

Vesicles with transport capability isolated from cultured fibroblasts.

A. Roses, L. Mokrasch, M. Herbstreith, 1984, Preparative biochemistry.