Herbstreith M - Search Results

1

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

Mihovilovic M, Mai Y, Herbstreith M, Rubboli F, Tarroni P, Clementi F, Roses AD. Mihovilovic M, et al. Among authors: herbstreith m. Biochem Biophys Res Commun. 1993 Nov 30;197(1):137-44. doi: 10.1006/bbrc.1993.2452. Biochem Biophys Res Commun. 1993. PMID: 8250918

2

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

Constantinou-Deltas CD, Gilbert J, Bartlett RJ, Herbstreith M, Roses AD, Lee JE. Constantinou-Deltas CD, et al. Among authors: herbstreith m. Genomics. 1992 Mar;12(3):581-9. doi: 10.1016/0888-7543(92)90451-w. Genomics. 1992. PMID: 1559709

3

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

Sharp NJ, Kornegay JN, Van Camp SD, Herbstreith MH, Secore SL, Kettle S, Hung WY, Constantinou CD, Dykstra MJ, Roses AD, et al. Sharp NJ, et al. Among authors: herbstreith mh. Genomics. 1992 May;13(1):115-21. doi: 10.1016/0888-7543(92)90210-j. Genomics. 1992. PMID: 1577476

4

A molecular genetic study of intracerebral hemorrhage.

Graffagnino C, Herbstreith MH, Roses AD, Alberts MJ. Graffagnino C, et al. Among authors: herbstreith mh. Arch Neurol. 1994 Oct;51(10):981-4. doi: 10.1001/archneur.1994.00540220027011. Arch Neurol. 1994. PMID: 7945009

5

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.

Samson F, Lee JE, Hung WY, Potter TG, Herbstreith M, Roses AD, Gilbert JR. Samson F, et al. Among authors: herbstreith m. J Neurosci Res. 1990 Dec;27(4):441-51. doi: 10.1002/jnr.490270403. J Neurosci Res. 1990. PMID: 1706783

6

Myotonic dystrophy: update on progress to define the gene.

Roses AD, Pericak-Vance MA, Bartlett RJ, Yamaoka LH, Lee JE, Koh J, Chen JC, Gilbert JR, Ross DA, Herbstreith MH, et al. Roses AD, et al. Among authors: herbstreith mh. Aust Paediatr J. 1988;24 Suppl 1:66-9. Aust Paediatr J. 1988. PMID: 3060077 Review.

7

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

Graffagnino C, Herbstreith MH, Schmechel DE, Levy E, Roses AD, Alberts MJ. Graffagnino C, et al. Among authors: herbstreith mh. Stroke. 1995 Nov;26(11):2190-3. doi: 10.1161/01.str.26.11.2190. Stroke. 1995. PMID: 7482672

8

Endoglin gene polymorphism as a risk factor for sporadic intracerebral hemorrhage.

Alberts MJ, Davis JP, Graffagnino C, McClenny C, Delong D, Granger C, Herbstreith MH, Boteva K, Marchuk DA, Roses AD. Alberts MJ, et al. Among authors: herbstreith mh. Ann Neurol. 1997 May;41(5):683-6. doi: 10.1002/ana.410410519. Ann Neurol. 1997. PMID: 9153532 Clinical Trial.

9

A Bgl II polymorphism detected by LDR152 [D19S19].

Walker AP, Bartlett RJ, Yamaoka LH, Secore SL, Lee JE, Gilbert J, Herbstreith M, Pericak-Vance MA, Hung WY, Roses AD. Walker AP, et al. Among authors: herbstreith m. Nucleic Acids Res. 1988 Sep 26;16(18):9063. doi: 10.1093/nar/16.18.9063. Nucleic Acids Res. 1988. PMID: 2902564 Free PMC article.

10

Sialylated human apolipoprotein E (apoEs) is preferentially associated with neuron-enriched cultures from APOE transgenic mice.

Xu PT, Schmechel D, Qiu HL, Herbstreith M, Rothrock-Christian T, Eyster M, Roses AD, Gilbert JR. Xu PT, et al. Among authors: herbstreith m. Neurobiol Dis. 1999 Feb;6(1):63-75. doi: 10.1006/nbdi.1998.0213. Neurobiol Dis. 1999. PMID: 10078974

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