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Links from Nucleotide

Items: 9

1.
Abundant expression of myosin heavy-chain IIB RNA in a subset of human masseter muscle fibres
Michael J. Horton, Carla A. Brandon, Terence J. Morris, Thomas W. Braun, Kenneth M. Yaw, James J. Sciote
Arch Oral Biol. Author manuscript; available in PMC 2013 Dec 3.
Published in final edited form as: Arch Oral Biol. 2001 Nov; 46(11): 1039–1050. doi: 10.1016/s0003-9969(01)00066-8
PMCID:
PMC3848045
AbstractArticlePDF–6.4M
2.
Temporal spatial expression and function of non-muscle myosin II isoforms IIA and IIB in scar remodeling
Jennifer E Bond, Trung Q Ho, Maria Angelica Selim, Cedric L Hunter, Edith V Bowers, Howard Levinson
Lab Invest. Author manuscript; available in PMC 2012 Jul 28.
Published in final edited form as: Lab Invest. 2011 Apr; 91(4): 499–508. Published online 2010 Nov 22. doi: 10.1038/labinvest.2010.181
PMCID:
PMC3407540
AbstractArticlePDF–1.7M
3.
Maximum velocity of shortening in relation to myosin isoform composition in single fibres from human skeletal muscles.
L Larsson, R L Moss
J Physiol. 1993 Dec; 472: 595–614. doi: 10.1113/jphysiol.1993.sp019964
PMCID:
PMC1160504
SummaryPage BrowsePDF–2.9M
4.
The myosin alkali light chain proteins and their genes.
P J Barton, M E Buckingham
Biochem J. 1985 Oct 15; 231(2): 249–261. doi: 10.1042/bj2310249
PMCID:
PMC1152739
SummaryPage BrowsePDF–2.8M
5.
Duplication of ALK F1245 missense mutation due to acquired uniparental disomy associated with aggressive progression in a patient with relapsed neuroblastoma
Shunsuke Kimura, Daisuke Hasegawa, Yuri Yoshimoto, Masafumi Seki, Atsuro Daida, Masahiro Sekiguchi, Shinsuke Hirabayashi, Yosuke Hosoya, Masao Kobayashi, Satoru Miyano, Seishi Ogawa, Junko Takita, Atsushi Manabe
Oncol Lett. 2019 Mar; 17(3): 3323–3329. Published online 2019 Jan 29. doi: 10.3892/ol.2019.9985
PMCID:
PMC6396392
AbstractArticlePDF–1.5M
6.
Parental Whole-Exome Sequencing Enables Sialidosis Type II Diagnosis due to an NEU1 Missense Mutation as an Underlying Cause of Nephrotic Syndrome in the Child
Reza Maroofian, Isabel Schuele, Maryam Najafi, Zeineb Bakey, Abolfazl Rad, Dinu Antony, Haleh Habibi, Miriam Schmidts
Kidney Int Rep. 2018 Nov; 3(6): 1454–1463. Published online 2018 Jul 29. doi: 10.1016/j.ekir.2018.07.015
PMCID:
PMC6224678
AbstractArticlePDF–784K
7.
Genomic variants link to hepatitis C racial disparities
Matthew M. Yeh, Sarag Boukhar, Benjamin Roberts, Nairanjana Dasgupta, Sayed S. Daoud
Oncotarget. 2017 Aug 29; 8(35): 59455–59475. Published online 2017 Aug 1. doi: 10.18632/oncotarget.19755
PMCID:
PMC5601746
AbstractArticlePDF–6.3M
8.
Myosin content of individual human muscle fibers isolated by laser capture microdissection
Charles A. Stuart, William L. Stone, Mary E. A. Howell, Marianne F. Brannon, H. Kenton Hall, Andrew L. Gibson, Michael H. Stone
Am J Physiol Cell Physiol. 2016 Mar 1; 310(5): C381–C389. Published online 2015 Dec 16. doi: 10.1152/ajpcell.00317.2015
PMCID:
PMC4971827
AbstractArticle
9.
MYH9-related disease: Five novel mutations expanding the spectrum of causative mutations and confirming genotype/phenotype correlations
Daniela De Rocco, Barbara Zieger, Helen Platokouki, Paula G. Heller, Annalisa Pastore, Roberta Bottega, Patrizia Noris, Serena Barozzi, Ana C. Glembotsky, Helen Pergantou, Carlo L. Balduini, Anna Savoia, Alessandro Pecci
Eur J Med Genet. 2013 Jan; 56(1): 7–12. doi: 10.1016/j.ejmg.2012.10.009
PMCID:
PMC3546164
AbstractArticle

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