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 *

148 related articles for article (PubMed ID: 28443263)

  • 1. A 1-month-old infant with chylomicronemia due to
    Jung MK; Jin J; Kim HO; Kwon A; Chae HW; Kang SJ; Kim DH; Kim HS
    Ann Pediatr Endocrinol Metab; 2017 Mar; 22(1):68-71. PubMed ID: 28443263
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A 3-day-old neonate with severe hypertriglyceridemia from novel mutations of the GPIHBP1 gene.
    Buonuomo PS; Bartuli A; Rabacchi C; Bertolini S; Calandra S
    J Clin Lipidol; 2015; 9(2):265-70. PubMed ID: 25911085
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Autoantibodies against GPIHBP1 as a Cause of Hypertriglyceridemia.
    Beigneux AP; Miyashita K; Ploug M; Blom DJ; Ai M; Linton MF; Khovidhunkit W; Dufour R; Garg A; McMahon MA; Pullinger CR; Sandoval NP; Hu X; Allan CM; Larsson M; Machida T; Murakami M; Reue K; Tontonoz P; Goldberg IJ; Moulin P; Charrière S; Fong LG; Nakajima K; Young SG
    N Engl J Med; 2017 Apr; 376(17):1647-1658. PubMed ID: 28402248
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Chylomicronemia with a mutant GPIHBP1 (Q115P) that cannot bind lipoprotein lipase.
    Beigneux AP; Franssen R; Bensadoun A; Gin P; Melford K; Peter J; Walzem RL; Weinstein MM; Davies BS; Kuivenhoven JA; Kastelein JJ; Fong LG; Dallinga-Thie GM; Young SG
    Arterioscler Thromb Vasc Biol; 2009 Jun; 29(6):956-62. PubMed ID: 19304573
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Familial chylomicronemia syndrome: case reports of siblings with deletions of the GPIHBP1 gene.
    Kim KY; Heo YJ; Ko JM; Lee YA; Shin CH; Ki CS; Lee YJ
    BMC Endocr Disord; 2024 Apr; 24(1):47. PubMed ID: 38622573
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Homozygous missense mutation (G56R) in glycosylphosphatidylinositol-anchored high-density lipoprotein-binding protein 1 (GPI-HBP1) in two siblings with fasting chylomicronemia (MIM 144650).
    Wang J; Hegele RA
    Lipids Health Dis; 2007 Sep; 6():23. PubMed ID: 17883852
    [TBL] [Abstract][Full Text] [Related]  

  • 7. GPIHBP1 autoantibodies in a patient with unexplained chylomicronemia.
    Hu X; Dallinga-Thie GM; Hovingh GK; Chang SY; Sandoval NP; Dang TLP; Fukamachi I; Miyashita K; Nakajima K; Murakami M; Fong LG; Ploug M; Young SG; Beigneux AP
    J Clin Lipidol; 2017; 11(4):964-971. PubMed ID: 28666713
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Deletion of GPIHBP1 causing severe chylomicronemia.
    Rios JJ; Shastry S; Jasso J; Hauser N; Garg A; Bensadoun A; Cohen JC; Hobbs HH
    J Inherit Metab Dis; 2012 May; 35(3):531-40. PubMed ID: 22008945
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Familial chylomicronemia syndrome and response to medium-chain triglyceride therapy in an infant with novel mutations in GPIHBP1.
    Ahmad Z; Wilson DP
    J Clin Lipidol; 2014; 8(6):635-639. PubMed ID: 25499947
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Clinical and genetic features of 3 patients with familial chylomicronemia due to mutations in GPIHBP1 gene.
    Rabacchi C; D'Addato S; Palmisano S; Lucchi T; Bertolini S; Calandra S; Tarugi P
    J Clin Lipidol; 2016; 10(4):915-921.e4. PubMed ID: 27578123
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Chylomicronemia from GPIHBP1 autoantibodies.
    Miyashita K; Lutz J; Hudgins LC; Toib D; Ashraf AP; Song W; Murakami M; Nakajima K; Ploug M; Fong LG; Young SG; Beigneux AP
    J Lipid Res; 2020 Nov; 61(11):1365-1376. PubMed ID: 32948662
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Intermittent chylomicronemia caused by intermittent GPIHBP1 autoantibodies.
    Ashraf AP; Miyashita K; Nakajima K; Murakami M; Hegele RA; Ploug M; Fong LG; Young SG; Beigneux AP
    J Clin Lipidol; 2020; 14(2):197-200. PubMed ID: 32107180
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Management of a pregnant patient with chylomicronemia from a novel mutation in GPIHBP1: a case report.
    Lin MH; Tian XH; Hao XL; Fei H; Yin JL; Yan DD; Li T
    BMC Pregnancy Childbirth; 2020 May; 20(1):272. PubMed ID: 32375710
    [TBL] [Abstract][Full Text] [Related]  

  • 14. GPIHBP1 missense mutations often cause multimerization of GPIHBP1 and thereby prevent lipoprotein lipase binding.
    Beigneux AP; Fong LG; Bensadoun A; Davies BS; Oberer M; Gårdsvoll H; Ploug M; Young SG
    Circ Res; 2015 Feb; 116(4):624-32. PubMed ID: 25387803
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Novel mutations in the GPIHBP1 gene identified in 2 patients with recurrent acute pancreatitis.
    Ariza MJ; Martínez-Hernández PL; Ibarretxe D; Rabacchi C; Rioja J; Grande-Aragón C; Plana N; Tarugi P; Olivecrona G; Calandra S; Valdivielso P
    J Clin Lipidol; 2016; 10(1):92-100.e1. PubMed ID: 26892125
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The GPIHBP1-LPL complex and its role in plasma triglyceride metabolism: Insights into chylomicronemia.
    Jiang S; Ren Z; Yang Y; Liu Q; Zhou S; Xiao Y
    Biomed Pharmacother; 2023 Dec; 169():115874. PubMed ID: 37951027
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel mutation in GPIHBP1 causes familial chylomicronemia syndrome.
    Paquette M; Hegele RA; Paré G; Baass A
    J Clin Lipidol; 2018; 12(2):506-510. PubMed ID: 29452893
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A novel GPIHBP1 mutation related to familial chylomicronemia syndrome: A series of cases.
    Lima JG; Helena C Nobrega L; Moura Bandeira FT; Pires Sousa AG; Medeiros de Araujo Macedo TB; Cavalcante Nogueira AC; Fernandes de Oliveira Filho A; Alves RJ; Costa Gurgel Castelo MH; Silva Coelho FM; Maia RE; Lima DN; Timoteo ARS; de Melo Campos JTA
    Atherosclerosis; 2021 Apr; 322():31-38. PubMed ID: 33706081
    [TBL] [Abstract][Full Text] [Related]  

  • 19. GPIHBP1: an endothelial cell molecule important for the lipolytic processing of chylomicrons.
    Young SG; Davies BS; Fong LG; Gin P; Weinstein MM; Bensadoun A; Beigneux AP
    Curr Opin Lipidol; 2007 Aug; 18(4):389-96. PubMed ID: 17620854
    [TBL] [Abstract][Full Text] [Related]  

  • 20. GPIHBP1 autoantibody syndrome during interferon β1a treatment.
    Eguchi J; Miyashita K; Fukamachi I; Nakajima K; Murakami M; Kawahara Y; Yamashita T; Ohta Y; Abe K; Nakatsuka A; Mino M; Takase S; Okazaki H; Hegele RA; Ploug M; Hu X; Wada J; Young SG; Beigneux AP
    J Clin Lipidol; 2019; 13(1):62-69. PubMed ID: 30514621
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.