CHROMOSOMAL LOCALIZATION OF THE MOUSE TITIN GENE AND ITS RELATION TO MUSCULAR-DYSTROPHY WITH MYOSITIS AND NEBULIN GENES ON CHROMOSOME-2

MULLER-SEITZ M, KAUPMANN K, LABEIT S, Jockusch H (1993)
GENOMICS 18(3): 559-561.

Journal Article | Published | English

No fulltext has been uploaded

Author
; ; ;
Publishing Year
ISSN
PUB-ID

Cite this

MULLER-SEITZ M, KAUPMANN K, LABEIT S, Jockusch H. CHROMOSOMAL LOCALIZATION OF THE MOUSE TITIN GENE AND ITS RELATION TO MUSCULAR-DYSTROPHY WITH MYOSITIS AND NEBULIN GENES ON CHROMOSOME-2. GENOMICS. 1993;18(3):559-561.
MULLER-SEITZ, M., KAUPMANN, K., LABEIT, S., & Jockusch, H. (1993). CHROMOSOMAL LOCALIZATION OF THE MOUSE TITIN GENE AND ITS RELATION TO MUSCULAR-DYSTROPHY WITH MYOSITIS AND NEBULIN GENES ON CHROMOSOME-2. GENOMICS, 18(3), 559-561.
MULLER-SEITZ, M., KAUPMANN, K., LABEIT, S., and Jockusch, H. (1993). CHROMOSOMAL LOCALIZATION OF THE MOUSE TITIN GENE AND ITS RELATION TO MUSCULAR-DYSTROPHY WITH MYOSITIS AND NEBULIN GENES ON CHROMOSOME-2. GENOMICS 18, 559-561.
MULLER-SEITZ, M., et al., 1993. CHROMOSOMAL LOCALIZATION OF THE MOUSE TITIN GENE AND ITS RELATION TO MUSCULAR-DYSTROPHY WITH MYOSITIS AND NEBULIN GENES ON CHROMOSOME-2. GENOMICS, 18(3), p 559-561.
M. MULLER-SEITZ, et al., “CHROMOSOMAL LOCALIZATION OF THE MOUSE TITIN GENE AND ITS RELATION TO MUSCULAR-DYSTROPHY WITH MYOSITIS AND NEBULIN GENES ON CHROMOSOME-2”, GENOMICS, vol. 18, 1993, pp. 559-561.
MULLER-SEITZ, M., KAUPMANN, K., LABEIT, S., Jockusch, H.: CHROMOSOMAL LOCALIZATION OF THE MOUSE TITIN GENE AND ITS RELATION TO MUSCULAR-DYSTROPHY WITH MYOSITIS AND NEBULIN GENES ON CHROMOSOME-2. GENOMICS. 18, 559-561 (1993).
MULLER-SEITZ, M, KAUPMANN, K, LABEIT, S, and Jockusch, Harald. “CHROMOSOMAL LOCALIZATION OF THE MOUSE TITIN GENE AND ITS RELATION TO MUSCULAR-DYSTROPHY WITH MYOSITIS AND NEBULIN GENES ON CHROMOSOME-2”. GENOMICS 18.3 (1993): 559-561.
This data publication is cited in the following publications:
This publication cites the following data publications:

12 Citations in Europe PMC

Data provided by Europe PubMed Central.

Titin: physiological function and role in cardiomyopathy and failure.
Granzier H, Wu Y, Siegfried L, LeWinter M., Heart Fail Rev 10(3), 2005
PMID: 16416044
Tibial muscular dystrophy is a titinopathy caused by mutations in TTN, the gene encoding the giant skeletal-muscle protein titin.
Hackman P, Vihola A, Haravuori H, Marchand S, Sarparanta J, De Seze J, Labeit S, Witt C, Peltonen L, Richard I, Udd B., Am. J. Hum. Genet. 71(3), 2002
PMID: 12145747
Distal myopathies.
Udd B, Griggs R., Curr. Opin. Neurol. 14(5), 2001
PMID: 11562566
A 7.5-kb 3'-Terminal cDNA Sequence of Chicken Skeletal Muscle Nebulin Reveals Its Actin Binding Regions.
Suzuki T, Yajima H, Maruyama K, Kimura S., Zool. Sci. 17(8), 2000
PMID: 18522464
Terminal regions of mouse nebulin: sequence analysis and complementary localization with N-RAP.
Herrera AH, Elzey B, Law DJ, Horowits R., Cell Motil. Cytoskeleton 45(3), 2000
PMID: 10706776
The titin cDNA sequence and partial genomic sequences: insights into the molecular genetics, cell biology and physiology of the titin filament system.
Kolmerer B, Witt CC, Freiburg A, Millevoi S, Stier G, Sorimachi H, Pelin K, Carrier L, Schwartz K, Labeit D, Gregorio CC, Linke WA, Labeit S., Rev. Physiol. Biochem. Pharmacol. 138(), 1999
PMID: 10396137
A gene for autosomal recessive limb-girdle muscular dystrophy in Manitoba Hutterites maps to chromosome region 9q31-q33: evidence for another limb-girdle muscular dystrophy locus.
Weiler T, Greenberg CR, Zelinski T, Nylen E, Coghlan G, Crumley MJ, Fujiwara TM, Morgan K, Wrogemann K., Am. J. Hum. Genet. 63(1), 1998
PMID: 9634523
Skeletal muscle connectin primary structures as related to animal species and muscle type.
Tanabe R, Muroya S, Nakajima I, Chikuni K, Nakai H., J. Food Sci. 62(3), 1997
PMID: IND21634934
Deletion in the Z-line region of the titin gene in a baby hamster kidney cell line, BHK-21-Bi.
Jackel M, Witt C, Antonova O, Curdt I, Labeit S, Jockusch H., FEBS Lett. 408(1), 1997
PMID: 9180260
Nebulette: a 107 kD nebulin-like protein in cardiac muscle.
Moncman CL, Wang K., Cell Motil. Cytoskeleton 32(3), 1995
PMID: 8581976
Chromosomal mapping in the mouse of eight K(+)-channel genes representing the four Shaker-like subfamilies Shaker, Shab, Shaw, and Shal.
Klocke R, Roberds SL, Tamkun MM, Gronemeier M, Augustin A, Albrecht B, Pongs O, Jockusch H., Genomics 18(3), 1993
PMID: 7905852

20 References

Data provided by Europe PubMed Central.

Sequence of an unusually large protein implicated in regulation of myosin activity in C. elegans.
Benian GM, Kiff JE, Neckelmann N, Moerman DG, Waterston RH., Nature 342(6245), 1989
PMID: 2812002
Drosophila projectin: Relatedness to titin and twitchin and correlation with lethal (4) 102 CDa and bent-Dominant mutants
Fyrberg, 1992
Muscle pathology and density of satellite cells in the mouse mutant “muscular dystrophy with myositis” (mdm/mdm)
Heimann, J. Musc. Res. Cell Motil. 14(), 1993
Nucleotide sequence of the mouse muscle nicotinic acetylcholine receptor alpha subunit.
Isenberg KE, Mudd J, Shah V, Merlie JP., Nucleic Acids Res. 14(12), 1986
PMID: 3755237
Wobbler, a mutation affecting motoneuron survival and gonadal functions in the mouse, maps to proximal chromosome 11
Kaupmann, Genomics 12(), 1992
A regular pattern of two types of 100-residue motif in the sequence of titin.
Labeit S, Barlow DP, Gautel M, Gibson T, Holt J, Hsieh CL, Francke U, Leonard K, Wardale J, Whiting A., Nature 345(6272), 1990
PMID: 2129545
Towards a molecular understanding of titin.
Labeit S, Gautel M, Lakey A, Trinick J., EMBO J. 11(5), 1992
PMID: 1582406
Evidence that nebulin is a protein-ruler in muscle thin filaments.
Labeit S, Gibson T, Lakey A, Leonard K, Zeviani M, Knight P, Wardale J, Trinick J., FEBS Lett. 282(2), 1991
PMID: 2037050
Muscular dystrophy with myositis (mdm)
Lane, Mouse News Lett. 73(), 1985
Mouse chromosome atlas
Lyon, Mouse Genome 91(), 1993
Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia.
Saiki RK, Scharf S, Faloona F, Mullis KB, Horn GT, Erlich HA, Arnheim N., Science 230(4732), 1985
PMID: 2999980
A molecular genetic linkage map of mouse chromosome 2.
Siracusa LD, Silan CM, Justice MJ, Mercer JA, Bauskin AR, Ben-Neriah Y, Duboule D, Hastie ND, Copeland NG, Jenkins NA., Genomics 6(3), 1990
PMID: 1970329
Nebulin cDNAs detect a 25-kilobase transcript in skeletal muscle and localize to human chromosome 2.
Stedman H, Browning K, Oliver N, Oronzi-Scott M, Fischbeck K, Sarkar S, Sylvester J, Schmickel R, Wang K., Genomics 2(1), 1988
PMID: 2838409
Pax: a murine multigene family of paired box-containing genes.
Walther C, Guenet JL, Simon D, Deutsch U, Jostes B, Goulding MD, Plachov D, Balling R, Gruss P., Genomics 11(2), 1991
PMID: 1685142
Does titin regulate the length of muscle thick filaments?
Whiting A, Wardale J, Trinick J., J. Mol. Biol. 205(1), 1989
PMID: 2926807
Cloning and expression of human nebulin cDNAs and assignment of the gene to chromosome 2q31-q32.
Zeviani M, Darras BT, Rizzuto R, Salviati G, Betto R, Bonilla E, Miranda AF, Du J, Samitt C, Dickson G., Genomics 2(3), 1988
PMID: 3397062

Export

0 Marked Publications

Open Data PUB

Web of Science

View record in Web of Science®

Sources

PMID: 8307566
PubMed | Europe PMC

Search this title in

Google Scholar