Benzow K - Search Results

1

Delineating regional vulnerability in the neurodegenerative disease SCA1 using a conditional mutant ATXN1 mouse.

Duvick L, Southern WM, Benzow K, Burch ZN, Handler HP, Mitchell JS, Kuivinen H, Gadiparthi UK, Yang P, Soles A, Scheeler C, Rainwater O, Serres S, Lind E, Nichols-Meade T, O'Callaghan B, Zoghbi HY, Cvetanovic M, Wheeler VC, Ervasti JM, Koob MD, Orr HT. Duvick L, et al. Among authors: benzow k. bioRxiv [Preprint]. 2023 Jun 30:2023.02.08.527710. doi: 10.1101/2023.02.08.527710. bioRxiv. 2023. PMID: 36798410 Free PMC article. Preprint.

2

Comparison of expanded CAG repeat tracts in sperm and lymphocyte DNA from Machado Joseph disease and spinocerebellar ataxia type I patients.

Maurer DJ, Benzow KA, Schut LJ, Ranum LP, Livingston DM. Maurer DJ, et al. Among authors: benzow ka. Hum Mutat. 1998;Suppl 1:S74-7. doi: 10.1002/humu.1380110126. Hum Mutat. 1998. PMID: 9452047 No abstract available.

3

Clinical and genetic characteristics of a five-generation family with a novel form of myotonic dystrophy (DM2).

Day JW, Roelofs R, Leroy B, Pech I, Benzow K, Ranum LP. Day JW, et al. Among authors: benzow k. Neuromuscul Disord. 1999 Jan;9(1):19-27. doi: 10.1016/s0960-8966(98)00094-7. Neuromuscul Disord. 1999. PMID: 10063831

4

The KLHL1-antisense transcript ( KLHL1AS) is evolutionarily conserved.

Benzow KA, Koob MD. Benzow KA, et al. Mamm Genome. 2002 Mar;13(3):134-41. doi: 10.1007/s00335-001-2105-2. Mamm Genome. 2002. PMID: 11919683

5

The spinocerebellar ataxia 8 noncoding RNA causes neurodegeneration and associates with staufen in Drosophila.

Mutsuddi M, Marshall CM, Benzow KA, Koob MD, Rebay I. Mutsuddi M, et al. Curr Biol. 2004 Feb 17;14(4):302-8. doi: 10.1016/j.cub.2004.01.034. Curr Biol. 2004. PMID: 14972680 Free article.

6

Targeted deletion of a single Sca8 ataxia locus allele in mice causes abnormal gait, progressive loss of motor coordination, and Purkinje cell dendritic deficits.

He Y, Zu T, Benzow KA, Orr HT, Clark HB, Koob MD. He Y, et al. J Neurosci. 2006 Sep 27;26(39):9975-82. doi: 10.1523/JNEUROSCI.2595-06.2006. J Neurosci. 2006. PMID: 17005861 Free PMC article.

7

Markerless modification of trinucleotide repeat loci in BACs.

Benzow KA, Koob MD. Benzow KA, et al. Methods Mol Biol. 2013;1010:265-76. doi: 10.1007/978-1-62703-411-1_17. Methods Mol Biol. 2013. PMID: 23754231

8

The Transcription Factor, α1ACT, Acts Through a MicroRNA Network to Regulate Neurogenesis and Cell Death During Neonatal Cerebellar Development.

Wei C, Benzow K, Koob MD, Gomez CM, Du X. Wei C, et al. Among authors: benzow k. Cerebellum. 2023 Aug;22(4):651-662. doi: 10.1007/s12311-022-01431-2. Epub 2022 Jun 22. Cerebellum. 2023. PMID: 35729466 Free PMC article.

9

Correction: The Transcription Factor, α1ACT, Acts Through a MicroRNA Network to Regulate Neurogenesis and Cell Death During Neonatal Cerebellar Development.

Wei C, Benzow K, Koob MD, Gomez CM, Du X. Wei C, et al. Among authors: benzow k. Cerebellum. 2024 Apr;23(2):876. doi: 10.1007/s12311-023-01567-9. Cerebellum. 2024. PMID: 37198370 Free PMC article. No abstract available.

10

Mapping SCA1 regional vulnerabilities reveals neural and skeletal muscle contributions to disease.

Duvick L, Southern WM, Benzow KA, Burch ZN, Handler HP, Mitchell JS, Kuivinen H, Gadiparthi U, Yang P, Soles A, Sheeler CA, Rainwater O, Serres S, Lind EB, Nichols-Meade T, You Y, O'Callaghan B, Zoghbi HY, Cvetanovic M, Wheeler VC, Ervasti JM, Koob MD, Orr HT. Duvick L, et al. Among authors: benzow ka. JCI Insight. 2024 Mar 21;9(9):e176057. doi: 10.1172/jci.insight.176057. JCI Insight. 2024. PMID: 38512434 Free PMC article.

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