PubMed for id: 77812697

Year	Number of Results
1989	1
1990	2
1992	1
2014	1
2023	5
2024	2

1

The TTN p. Tyr4418Ter mutation causes cardiomyopathy in human and mice.

Sun W, Liu X, Song L, Tao L, Lai K, Jiang H, Xiao H. Sun W, et al. PLoS One. 2024 Feb 21;19(2):e0296802. doi: 10.1371/journal.pone.0296802. eCollection 2024. PLoS One. 2024. PMID: 38381767 Free PMC article.

2

Titin takes centerstage among cytoskeletal contributions to myocardial passive stiffness.

Loescher CM, Linke WA. Loescher CM, et al. Cytoskeleton (Hoboken). 2024 Feb-Mar;81(2-3):184-187. doi: 10.1002/cm.21827. Epub 2023 Dec 29. Cytoskeleton (Hoboken). 2024. PMID: 38158587

3

Spatiotemporal transcriptomic maps of whole mouse embryos at the onset of organogenesis.

Sampath Kumar A, Tian L, Bolondi A, Hernández AA, Stickels R, Kretzmer H, Murray E, Wittler L, Walther M, Barakat G, Haut L, Elkabetz Y, Macosko EZ, Guignard L, Chen F, Meissner A. Sampath Kumar A, et al. Nat Genet. 2023 Jul;55(7):1176-1185. doi: 10.1038/s41588-023-01435-6. Epub 2023 Jul 6. Nat Genet. 2023. PMID: 37414952 Free PMC article.

4

Gse1, a component of the CoREST complex, is required for placenta development in the mouse.

Hiver S, Shimizu-Mizuno N, Ikawa Y, Kajikawa E, Sai X, Nishimura H, Takaoka K, Nishimura O, Kuraku S, Tanaka S, Hamada H. Hiver S, et al. Dev Biol. 2023 Jun;498:97-105. doi: 10.1016/j.ydbio.2023.03.009. Epub 2023 Apr 4. Dev Biol. 2023. PMID: 37019373

5

Insights into the Role of a Cardiomyopathy-Causing Genetic Variant in ACTN2.

Broadway-Stringer S, Jiang H, Wadmore K, Hooper C, Douglas G, Steeples V, Azad AJ, Singer E, Reyat JS, Galatik F, Ehler E, Bennett P, Kalisch-Smith JI, Sparrow DB, Davies B, Djinovic-Carugo K, Gautel M, Watkins H, Gehmlich K. Broadway-Stringer S, et al. Cells. 2023 Feb 24;12(5):721. doi: 10.3390/cells12050721. Cells. 2023. PMID: 36899856 Free PMC article.

6

Urine titin as a novel biomarker for Duchenne muscular dystrophy.

Ishii MN, Nakashima M, Kamiguchi H, Zach N, Kuboki R, Baba R, Hirakawa T, Suzuki K, Quinton M. Ishii MN, et al. Neuromuscul Disord. 2023 Apr;33(4):302-308. doi: 10.1016/j.nmd.2023.02.003. Epub 2023 Feb 13. Neuromuscul Disord. 2023. PMID: 36871413

7

Upstream open reading frame in 5'-untranslated region reduces titin mRNA translational efficiency.

Cadar AG, Zhong L, Lin A, Valenzuela MO, Lim CC. Cadar AG, et al. Biochem Biophys Res Commun. 2014 Oct 10;453(1):185-91. doi: 10.1016/j.bbrc.2014.09.085. Epub 2014 Sep 27. Biochem Biophys Res Commun. 2014. PMID: 25264194 Free PMC article.

8

Differential timing of nuclear lamin A/C expression in the various organs of the mouse embryo and the young animal: a developmental study.

Röber RA, Weber K, Osborn M. Röber RA, et al. Development. 1989 Feb;105(2):365-78. doi: 10.1242/dev.105.2.365. Development. 1989. PMID: 2680424

9

Localisation of a dystrophin-related autosomal gene to 6q24 in man, and to mouse chromosome 10 in the region of the dystrophia muscularis (dy) locus.

Buckle VJ, Guenet JL, Simon-Chazottes D, Love DR, Davies KE. Buckle VJ, et al. Hum Genet. 1990 Aug;85(3):324-6. doi: 10.1007/BF00206755. Hum Genet. 1990. PMID: 2203673

10

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, et al. Labeit S, et al. Nature. 1990 May 17;345(6272):273-6. doi: 10.1038/345273a0. Nature. 1990. PMID: 2129545

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