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Comparative analysis and molecular characterization of a gene BANF1 encoded a DNA-binding protein during mitosis from the Giant Panda and Black Bear.
Zeng Y, Hou YL, Ding X, Hou WR, Li J. Zeng Y, et al. Nucleosides Nucleotides Nucleic Acids. 2014;33(8):536-51. doi: 10.1080/15257770.2014.902067. Nucleosides Nucleotides Nucleic Acids. 2014. PMID: 25009988
The cDNA of the BANF1 cloned from Giant Panda and Black Bear is 297 bp in size, containing an open reading frame of 270 bp encoding 89 amino acids. ...The BANF1 gene can be readily expressed in E. coli. Results showed that the protein BANF1 fusion with the N- …
The cDNA of the BANF1 cloned from Giant Panda and Black Bear is 297 bp in size, containing an open reading frame of 270 bp encoding 8 …
Emerin in health and disease.
Koch AJ, Holaska JM. Koch AJ, et al. Semin Cell Dev Biol. 2014 May;29:95-106. doi: 10.1016/j.semcdb.2013.12.008. Epub 2013 Dec 21. Semin Cell Dev Biol. 2014. PMID: 24365856 Free PMC article. Review.
How to diagnose a lipodystrophy syndrome.
Vantyghem MC, Balavoine AS, Douillard C, Defrance F, Dieudonne L, Mouton F, Lemaire C, Bertrand-Escouflaire N, Bourdelle-Hego MF, Devemy F, Evrard A, Gheerbrand D, Girardot C, Gumuche S, Hober C, Topolinski H, Lamblin B, Mycinski B, Ryndak A, Karrouz W, Duvivier E, Merlen E, Cortet C, Weill J, Lacroix D, Wémeau JL. Vantyghem MC, et al. Ann Endocrinol (Paris). 2012 Jun;73(3):170-89. doi: 10.1016/j.ando.2012.04.010. Epub 2012 Jun 28. Ann Endocrinol (Paris). 2012. PMID: 22748602 Review.
The genetically determined partial forms usually occur as Dunnigan syndrome, which is a type of laminopathy that can also manifest as muscle, cardiac, neuropathic or progeroid involvement. Gene mutations encoding for PPAR-gamma, Akt2, CIDEC, perilipin and the ZMPSTE 24 enz …
The genetically determined partial forms usually occur as Dunnigan syndrome, which is a type of laminopathy that can also manifest as mus …
Mandibuloacral dysplasia type A-associated progeria caused by homozygous LMNA mutation in a family from Southern China.
Luo DQ, Wang XZ, Meng Y, He DY, Chen YM, Ke ZY, Yan M, Huang Y, Chen DF. Luo DQ, et al. BMC Pediatr. 2014 Oct 7;14:256. doi: 10.1186/1471-2431-14-256. BMC Pediatr. 2014. PMID: 25286833 Free PMC article.
The youngest son of 10 months showed severer lesions than those of his sisters at the same age, and presented possible muscle damage, and his symptoms progressed gradually. Three genes mutations including LMNA, ZMPSTE24 and BANF1 were tested in the family. LMNA gene …
The youngest son of 10 months showed severer lesions than those of his sisters at the same age, and presented possible muscle damage, …
Barrier-to-autointegration factor-like (BAF-L): a proposed regulator of BAF.
Tifft KE, Segura-Totten M, Lee KK, Wilson KL. Tifft KE, et al. Exp Cell Res. 2006 Feb 15;312(4):478-87. doi: 10.1016/j.yexcr.2005.11.013. Epub 2005 Dec 9. Exp Cell Res. 2006. PMID: 16337940
BAF-L mRNA was detectable at low levels in eleven other tissues and undetectable in heart and skeletal muscle which are specifically affected by Emery-Dreifuss muscular dystrophy, a disease caused by mutations in either emerin or lamin A. ...
BAF-L mRNA was detectable at low levels in eleven other tissues and undetectable in heart and skeletal muscle which are specifically …
Emerin Is Required for Proper Nucleus Reassembly after Mitosis: Implications for New Pathogenetic Mechanisms for Laminopathies Detected in EDMD1 Patients.
Dubińska-Magiera M, Kozioł K, Machowska M, Piekarowicz K, Filipczak D, Rzepecki R. Dubińska-Magiera M, et al. Cells. 2019 Mar 13;8(3):240. doi: 10.3390/cells8030240. Cells. 2019. PMID: 30871242 Free PMC article.
This disease belongs to a broader group called laminopathies-a heterogeneous group of rare genetic disorders affecting tissues of mesodermal origin. EDMD1 phenotype is characterized by progressive muscle wasting, contractures of the elbow and Achilles tendons, and cardiac …
This disease belongs to a broader group called laminopathies-a heterogeneous group of rare genetic disorders affecting tissues of mesodermal …
Transcriptional repressor germ cell-less (GCL) and barrier to autointegration factor (BAF) compete for binding to emerin in vitro.
Holaska JM, Lee KK, Kowalski AK, Wilson KL. Holaska JM, et al. J Biol Chem. 2003 Feb 28;278(9):6969-75. doi: 10.1074/jbc.M208811200. Epub 2002 Dec 18. J Biol Chem. 2003. PMID: 12493765 Free article.
Loss of emerin causes Emery-Dreifuss muscular dystrophy, a tissue-specific inherited disease that affects skeletal muscles, major tendons, and the cardiac conduction system. Although GCL alone cannot explain the disease mechanism, our results strongly support gene expressi …
Loss of emerin causes Emery-Dreifuss muscular dystrophy, a tissue-specific inherited disease that affects skeletal muscles, major ten …
'Side Population' cells in adult mouse testis express Bcrp1 gene and are enriched in spermatogonia and germinal stem cells.
Lassalle B, Bastos H, Louis JP, Riou L, Testart J, Dutrillaux B, Fouchet P, Allemand I. Lassalle B, et al. Development. 2004 Jan;131(2):479-87. doi: 10.1242/dev.00918. Epub 2003 Dec 17. Development. 2004. PMID: 14681185
Stem cells in various somatic tissues (bone marrow, skeletal muscle) can be identified by the 'Side Population' marker based on Hoechst 33342 efflux. ...
Stem cells in various somatic tissues (bone marrow, skeletal muscle) can be identified by the 'Side Population' marker based on Hoech …