DOI: 10.1016/s0960-8966(99)00003-6. Reduction of the DM-associated homeo domain protein (DMAHP) mRNA in different brain areas of myotonic dystrophy patients

Reduction of the DM-associated homeo domain protein (DMAHP) mRNA in different brain areas of myotonic dystrophy patients

10.1016/s0960-8966(99)00003-6

Crossref journal-article

Elsevier BV

Neuromuscular Disorders (78)

Bibliography

Gennarelli, M., Pavoni, M., Amicucci, P., Angelini, C., Menegazzo, E., Zelano, G., Novelli, G., & Dallapiccola, B. (1999). Reduction of the DM-associated homeo domain protein (DMAHP) mRNA in different brain areas of myotonic dystrophy patients. Neuromuscular Disorders, 9(4), 215â219.

Authors 8

M Gennarelli (first)
M Pavoni (additional)
P Amicucci (additional)
C Angelini (additional)
E Menegazzo (additional)
G Zelano (additional)
G Novelli (additional)
B Dallapiccola (additional)

References 22 Referenced 14

Harper PS. Myotonic dystrophy, 2nd ed. London: Saunders, 1989.
10.1016/0092-8674(92)90154-5 / Cell / Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member by Brook (1992)
10.1126/science.1546326 / Science / An unstable triplet repeat in a gene related to myotonic muscular dystrophy by Fu (1992)
10.1038/355545a0 / Nature / Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy by Harley (1992)
10.1016/S1097-2765(00)80058-1 / Mol Cell / GAA instability in Friedreich's Ataxia shares a common, DNA-directed and intrallelic mechanism with other trinucleotide diseases by Gacy (1998)
10.1002/(SICI)1096-8628(19961111)65:4<342::AID-AJMG18>3.0.CO;2-U / Am J Med Genet / Prediction of myotonic dystrophy clinical severity based on the number of intragenic [CTG]n trinucleotide repeats by Gennarelli (1996)
10.1007/BF02766919 / Jpn J Hum Genet / Detection of the CTG repeat expansion in congenital myotonic dystrophy by Ohya (1997)
10.1093/nar/26.6.1363 / Nucl Acid Res / Myotonic dystrophy: molecular windows on a complex etiology by Korade-Mirnics (1998)
10.1126/science.8469976 / Science / Decreased expression of myotonin-protein kinase messenger RNA and protein in adult form of myotonic dystrophy by Fu (1993)
10.1093/hmg/4.4.599 / Hum Mol Genet / Myotonic dystrophy: evidence for a possible dominant-negative RNA mutation by Wang (1995)
10.1093/hmg/5.Supplement_1.1417 / Hum Mol Genet / Myotonic dystrophy: will the real gene please step forward? by Harris (1996)
10.1038/ng0897-402 / Nat Genet / Trinucleotide repeat expansion at the myotonic dystrophy locus reduces expression of DMAHP by Klesert (1997)
10.1038/ng0897-407 / Nat Genet / Expansion of the myotonic dystrophy CTG repeat reduces expression of the flanking DMAHP gene by Thornton (1997)
10.1073/pnas.92.12.5465 / Proc Natl Acad Sci / Triplet repeat expansion in myotonic dystrophy alters the adjacent chromatin structure by Otten (1995)
Sambrook J, Fritsch EF, Maniatis T. Molecular cloning: a laboratory manual. New York: Cold Spring Harbor Laboratory Press, 1992.
10.1002/(SICI)1098-1004(1996)7:4<304::AID-HUMU3>3.0.CO;2-8 / Hum Mutat / Characterization of large CTG repeat expansions in myotonic dystrophy alleles using PCR by Cheng (1996)
10.1093/hmg/6.5.651 / Hum Molec Genet / Characterisation of expression of mDMAHP, a homeodomain-encoding gene at the murine DM locus by Healt (1997)
{'key': '10.1016/S0960-8966(99)00003-6_BIB18', 'first-page': '327', 'article-title': 'Sodium/potassium ATPase in normal and cataractous human lenses', 'volume': '5', 'author': 'Kobatashi', 'year': '1992', 'journal-title': 'Curr Eye Res'} / Curr Eye Res / Sodium/potassium ATPase in normal and cataractous human lenses by Kobatashi (1992)
10.1126/science.280.5364.737 / Science / Disruption of splicing regulated by a CUG-binding protein in myotonic dystrophy by Philips (1998)
10.1172/JCI119332 / J Clin Invest / RNA metabolism in myotonic dystrophy: patient muscle shows decreased insulin receptor RNA and protein consistent with abnormal insulin resistance by Morrone (1997)
10.1007/s004390050176 / Hum Genet / Small increase in triplet repeat length of cerebellum from patients with myotonic dystrophy by Ishii (1996)
10.1001/archneur.55.3.291 / Arch Neurol / Myotonic dystrophy as a brain disorder by Ashizawa (1998)

Dates

Type	When
Created	23 years, 1 month ago (July 25, 2002, 6:55 p.m.)
Deposited	6 years, 4 months ago (April 18, 2019, 12:56 p.m.)
Indexed	5 months, 1 week ago (March 22, 2025, 4:28 a.m.)
Issued	26 years, 3 months ago (June 1, 1999)
Published	26 years, 3 months ago (June 1, 1999)
Published Print	26 years, 3 months ago (June 1, 1999)

Funders 0

None

BibTeX

@article{Gennarelli_1999, title={Reduction of the DM-associated homeo domain protein (DMAHP) mRNA in different brain areas of myotonic dystrophy patients}, volume={9}, ISSN={0960-8966}, url={http://dx.doi.org/10.1016/s0960-8966(99)00003-6}, DOI={10.1016/s0960-8966(99)00003-6}, number={4}, journal={Neuromuscular Disorders}, publisher={Elsevier BV}, author={Gennarelli, M and Pavoni, M and Amicucci, P and Angelini, C and Menegazzo, E and Zelano, G and Novelli, G and Dallapiccola, B}, year={1999}, month=jun, pages={215–219} }

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