These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

118 related articles for article (PubMed ID: 17513488)

  • 21. Lamin A/C assembly defects in Emery-Dreifuss muscular dystrophy can be regulated by culture medium composition.
    Holt I; Nguyen TM; Wehnert M; Morris GE
    Neuromuscul Disord; 2006 Jun; 16(6):368-73. PubMed ID: 16697197
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Nuclear accumulation of androgen receptor in gender difference of dilated cardiomyopathy due to lamin A/C mutations.
    Arimura T; Onoue K; Takahashi-Tanaka Y; Ishikawa T; Kuwahara M; Setou M; Shigenobu S; Yamaguchi K; Bertrand AT; Machida N; Takayama K; Fukusato M; Tanaka R; Somekawa S; Nakano T; Yamane Y; Kuba K; Imai Y; Saito Y; Bonne G; Kimura A
    Cardiovasc Res; 2013 Aug; 99(3):382-94. PubMed ID: 23631840
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A Novel Lamin A Mutant Responsible for Congenital Muscular Dystrophy Causes Distinct Abnormalities of the Cell Nucleus.
    Barateau A; Vadrot N; Vicart P; Ferreiro A; Mayer M; Héron D; Vigouroux C; Buendia B
    PLoS One; 2017; 12(1):e0169189. PubMed ID: 28125586
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Both lamin A and lamin C mutations cause lamina instability as well as loss of internal nuclear lamin organization.
    Broers JL; Kuijpers HJ; Ostlund C; Worman HJ; Endert J; Ramaekers FC
    Exp Cell Res; 2005 Apr; 304(2):582-92. PubMed ID: 15748902
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Heart-specific expression of laminopathic mutations in transgenic zebrafish.
    Verma AD; Parnaik VK
    Cell Biol Int; 2017 Jul; 41(7):809-819. PubMed ID: 28464412
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Effect of lamin A/C knockdown on osteoblast differentiation and function.
    Akter R; Rivas D; Geneau G; Drissi H; Duque G
    J Bone Miner Res; 2009 Feb; 24(2):283-93. PubMed ID: 18847334
    [TBL] [Abstract][Full Text] [Related]  

  • 27. LMNA Mutation c.917T>G (p.L306R) Leads to Deleterious Hyper-Assembly of Lamin A/C and Associates with Severe Right Ventricular Cardiomyopathy and Premature Aging.
    Alastalo TP; West G; Li SP; Keinänen A; Helenius M; Tyni T; Lapatto R; Turanlahti M; Heikkilä P; Kääriäinen H; Laakso M; Mauermann M; Herrmann H; Pihkala J; Taimen P
    Hum Mutat; 2015 Jul; 36(7):694-703. PubMed ID: 25820511
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Pathology and nuclear abnormalities in hearts of transgenic mice expressing M371K lamin A encoded by an LMNA mutation causing Emery-Dreifuss muscular dystrophy.
    Wang Y; Herron AJ; Worman HJ
    Hum Mol Genet; 2006 Aug; 15(16):2479-89. PubMed ID: 16825283
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Effect of pathogenic mis-sense mutations in lamin A on its interaction with emerin in vivo.
    Holt I; Ostlund C; Stewart CL; Man Nt; Worman HJ; Morris GE
    J Cell Sci; 2003 Jul; 116(Pt 14):3027-35. PubMed ID: 12783988
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Deleterious assembly of the lamin A/C mutant p.S143P causes ER stress in familial dilated cardiomyopathy.
    West G; Gullmets J; Virtanen L; Li SP; Keinänen A; Shimi T; Mauermann M; Heliö T; Kaartinen M; Ollila L; Kuusisto J; Eriksson JE; Goldman RD; Herrmann H; Taimen P
    J Cell Sci; 2016 Jul; 129(14):2732-43. PubMed ID: 27235420
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Lamin A and lamin-associated polypeptide 2 (LAP-2) in human skin in the process of aging.
    Golubtsova NN; Filippov FN; Gunin AG
    Adv Gerontol; 2016; 29(4):577-585. PubMed ID: 28539015
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Nuclear matrix metalloproteinase-2 in the cardiomyocyte and the ischemic-reperfused heart.
    Baghirova S; Hughes BG; Poirier M; Kondo MY; Schulz R
    J Mol Cell Cardiol; 2016 May; 94():153-161. PubMed ID: 27079252
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Lamin B2 Levels Regulate Polyploidization of Cardiomyocyte Nuclei and Myocardial Regeneration.
    Han L; Choudhury S; Mich-Basso JD; Ammanamanchi N; Ganapathy B; Suresh S; Khaladkar M; Singh J; Maehr R; Zuppo DA; Kim J; Eberwine JH; Wyman SK; Wu YL; Kühn B
    Dev Cell; 2020 Apr; 53(1):42-59.e11. PubMed ID: 32109383
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Functional Characterization of a Novel Truncating Mutation in Lamin A/C Gene in a Family with a Severe Cardiomyopathy with Conduction Defects.
    Gerbino A; Bottillo I; Milano S; Lipari M; Zio R; Morlino S; Mola MG; Procino G; Re F; Zachara E; Grammatico P; Svelto M; Carmosino M
    Cell Physiol Biochem; 2017; 44(4):1559-1577. PubMed ID: 29197877
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Expression and localization of nuclear proteins in autosomal-dominant Emery-Dreifuss muscular dystrophy with LMNA R377H mutation.
    Reichart B; Klafke R; Dreger C; Krüger E; Motsch I; Ewald A; Schäfer J; Reichmann H; Müller CR; Dabauvalle MC
    BMC Cell Biol; 2004 Mar; 5():12. PubMed ID: 15053843
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Lamin C Counteracts Glucose Intolerance in Aging, Obesity, and Diabetes Through β-Cell Adaptation.
    de Toledo M; Lopez-Mejia IC; Cavelier P; Pratlong M; Barrachina C; Gromada X; Annicotte JS; Tazi J; Chavey C
    Diabetes; 2020 Apr; 69(4):647-660. PubMed ID: 32005707
    [TBL] [Abstract][Full Text] [Related]  

  • 37. DNA Damage Response/TP53 Pathway Is Activated and Contributes to the Pathogenesis of Dilated Cardiomyopathy Associated With LMNA (Lamin A/C) Mutations.
    Chen SN; Lombardi R; Karmouch J; Tsai JY; Czernuszewicz G; Taylor MRG; Mestroni L; Coarfa C; Gurha P; Marian AJ
    Circ Res; 2019 Mar; 124(6):856-873. PubMed ID: 30696354
    [TBL] [Abstract][Full Text] [Related]  

  • 38. In vivo and in vitro examination of the functional significances of novel lamin gene mutations in heart failure patients.
    Sylvius N; Bilinska ZT; Veinot JP; Fidzianska A; Bolongo PM; Poon S; McKeown P; Davies RA; Chan KL; Tang AS; Dyack S; Grzybowski J; Ruzyllo W; McBride H; Tesson F
    J Med Genet; 2005 Aug; 42(8):639-47. PubMed ID: 16061563
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Laminopathies; Mutations on single gene and various human genetic diseases.
    Kang SM; Yoon MH; Park BJ
    BMB Rep; 2018 Jul; 51(7):327-337. PubMed ID: 29764566
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Partial cleavage of A-type lamins concurs with their total disintegration from the nuclear lamina during apoptosis.
    Broers JL; Bronnenberg NM; Kuijpers HJ; Schutte B; Hutchison CJ; Ramaekers FC
    Eur J Cell Biol; 2002 Dec; 81(12):677-91. PubMed ID: 12553668
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.