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 *

285 related articles for article (PubMed ID: 28686329)

  • 1. Juvenile-onset generalized lipodystrophy due to a novel heterozygous missense LMNA mutation affecting lamin C.
    Patni N; Xing C; Agarwal AK; Garg A
    Am J Med Genet A; 2017 Sep; 173(9):2517-2521. PubMed ID: 28686329
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A Novel Generalized Lipodystrophy-Associated Progeroid Syndrome Due to Recurrent Heterozygous LMNA p.T10I Mutation.
    Hussain I; Patni N; Ueda M; Sorkina E; Valerio CM; Cochran E; Brown RJ; Peeden J; Tikhonovich Y; Tiulpakov A; Stender SRS; Klouda E; Tayeh MK; Innis JW; Meyer A; Lal P; Godoy-Matos AF; Teles MG; Adams-Huet B; Rader DJ; Hegele RA; Oral EA; Garg A
    J Clin Endocrinol Metab; 2018 Mar; 103(3):1005-1014. PubMed ID: 29267953
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A LMNA splicing mutation in two sisters with severe Dunnigan-type familial partial lipodystrophy type 2.
    Morel CF; Thomas MA; Cao H; O'Neil CH; Pickering JG; Foulkes WD; Hegele RA
    J Clin Endocrinol Metab; 2006 Jul; 91(7):2689-95. PubMed ID: 16636128
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A case of familial partial lipodystrophy caused by a novel lamin A/C (LMNA) mutation in exon 1 (D47N).
    Kutbay NO; Yurekli BS; Onay H; Altay CT; Atik T; Hekimsoy Z; Saygili F; Akinci B
    Eur J Intern Med; 2016 Apr; 29():37-9. PubMed ID: 26775134
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A novel autosomal recessive lipodystrophy syndrome due to homozygous
    Patni N; Hatab S; Xing C; Zhou Z; Quittner C; Garg A
    J Med Genet; 2020 Jun; 57(6):422-426. PubMed ID: 31857427
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Atypical generalized lipoatrophy and severe insulin resistance due to a heterozygous LMNA p.T10I mutation.
    Mory PB; Crispim F; Kasamatsu T; Gabbay MA; Dib SA; Moisés RS
    Arq Bras Endocrinol Metabol; 2008 Nov; 52(8):1252-6. PubMed ID: 19169477
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Lamin A/C gene: sex-determined expression of mutations in Dunnigan-type familial partial lipodystrophy and absence of coding mutations in congenital and acquired generalized lipoatrophy.
    Vigouroux C; Magré J; Vantyghem MC; Bourut C; Lascols O; Shackleton S; Lloyd DJ; Guerci B; Padova G; Valensi P; Grimaldi A; Piquemal R; Touraine P; Trembath RC; Capeau J
    Diabetes; 2000 Nov; 49(11):1958-62. PubMed ID: 11078466
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A subtype of laminopathies: Generalized lipodystrophy-associated progeroid syndrome caused by LMNA gene c.29C>T mutation.
    Huang S; Zhang Y; Zhan Z; Gong S
    J Diabetes Investig; 2023 Oct; 14(10):1221-1225. PubMed ID: 37448194
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Multisystem dystrophy syndrome due to novel missense mutations in the amino-terminal head and alpha-helical rod domains of the lamin A/C gene.
    Garg A; Speckman RA; Bowcock AM
    Am J Med; 2002 May; 112(7):549-55. PubMed ID: 12015247
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Overlapping syndrome with familial partial lipodystrophy, Dunnigan variety and cardiomyopathy due to amino-terminal heterozygous missense lamin A/C mutations.
    Subramanyam L; Simha V; Garg A
    Clin Genet; 2010 Jul; 78(1):66-73. PubMed ID: 20041886
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mutations in the LMNA gene encoding lamin A/C.
    Genschel J; Schmidt HH
    Hum Mutat; 2000 Dec; 16(6):451-9. PubMed ID: 11102973
    [TBL] [Abstract][Full Text] [Related]  

  • 12.
    Kato K; Ohno S; Sonoda K; Fukuyama M; Makiyama T; Ozawa T; Horie M
    Circ Genom Precis Med; 2020 Oct; 13(5):435-443. PubMed ID: 32818388
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A new laminopathy caused by an Arg133/Leu mutation in
    Wang Z; Dong Y; Yang J; He Y; Lin X; Wu F; Li H; Zheng F
    Adipocyte; 2019 Dec; 8(1):280-291. PubMed ID: 31293201
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Heterogeneity of nuclear lamin A mutations in Dunnigan-type familial partial lipodystrophy.
    Hegele RA; Cao H; Anderson CM; Hramiak IM
    J Clin Endocrinol Metab; 2000 Sep; 85(9):3431-5. PubMed ID: 10999845
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A homozygous mutation in the lamin A/C gene associated with a novel syndrome of arthropathy, tendinous calcinosis, and progeroid features.
    Van Esch H; Agarwal AK; Debeer P; Fryns JP; Garg A
    J Clin Endocrinol Metab; 2006 Feb; 91(2):517-21. PubMed ID: 16278265
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A new clinical condition linked to a novel mutation in lamins A and C with generalized lipoatrophy, insulin-resistant diabetes, disseminated leukomelanodermic papules, liver steatosis, and cardiomyopathy.
    Caux F; Dubosclard E; Lascols O; Buendia B; Chazouillères O; Cohen A; Courvalin JC; Laroche L; Capeau J; Vigouroux C; Christin-Maitre S
    J Clin Endocrinol Metab; 2003 Mar; 88(3):1006-13. PubMed ID: 12629077
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The heterozygous LMNA mutation p.R471G causes a variable phenotype with features of two types of familial partial lipodystrophy.
    Muschke P; Kölsch U; Jakubiczka S; Wieland I; Brune T; Wieacker P
    Am J Med Genet A; 2007 Dec; 143A(23):2810-4. PubMed ID: 18041775
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A case of generalized lipodystrophy-associated progeroid syndrome treated by leptin replacement with short and long-term monitoring of the metabolic and endocrine profiles.
    Fukaishi T; Minami I; Masuda S; Miyachi Y; Tsujimoto K; Izumiyama H; Hashimoto K; Yoshida M; Takahashi S; Kashimada K; Morio T; Kosaki K; Maezawa Y; Yokote K; Yoshimoto T; Yamada T
    Endocr J; 2020 Feb; 67(2):211-218. PubMed ID: 31708526
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A novel lamin A/C mutation in a Dutch family with premature atherosclerosis.
    Weterings AA; van Rijsingen IA; Plomp AS; Zwinderman AH; Lekanne Deprez RH; Mannens MM; van den Bergh Weerman MA; van der Wal AC; Pinto-Sietsma SJ
    Atherosclerosis; 2013 Jul; 229(1):169-73. PubMed ID: 23659872
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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
    BMC Pediatr; 2014 Oct; 14():256. PubMed ID: 25286833
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.