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.
26. VPS33B and VIPAR are essential for epidermal lamellar body biogenesis and function. Rogerson C; Gissen P Biochim Biophys Acta Mol Basis Dis; 2018 May; 1864(5 Pt A):1609-1621. PubMed ID: 29409756 [TBL] [Abstract][Full Text] [Related]
27. Platelets of the Wistar Furth rat have reduced levels of alpha-granule proteins. An animal model resembling gray platelet syndrome. Jackson CW; Hutson NK; Steward SA; Saito N; Cramer EM J Clin Invest; 1991 Jun; 87(6):1985-91. PubMed ID: 2040691 [TBL] [Abstract][Full Text] [Related]
28. Comparative evolutionary analysis of VPS33 homologues: genetic and functional insights. Gissen P; Johnson CA; Gentle D; Hurst LD; Doherty AJ; O'Kane CJ; Kelly DA; Maher ER Hum Mol Genet; 2005 May; 14(10):1261-70. PubMed ID: 15790593 [TBL] [Abstract][Full Text] [Related]
29. Clinical characteristics and VPS33B mutations in patients with ARC syndrome. Jang JY; Kim KM; Kim GH; Yu E; Lee JJ; Park YS; Yoo HW J Pediatr Gastroenterol Nutr; 2009 Mar; 48(3):348-54. PubMed ID: 19274792 [TBL] [Abstract][Full Text] [Related]
30. Incorporation of a circulating protein into alpha granules of megakaryocytes. Handagama PJ; Bainton DF Blood Cells; 1989; 15(1):59-72. PubMed ID: 2930854 [TBL] [Abstract][Full Text] [Related]
31. Acidification of α-granules in megakaryocytes by vacuolar-type adenosine triphosphatase is essential for organelle biogenesis. Lu CY; Wu JZ; Yao HHY; Liu RJY; Li L; Pluthero FG; Freeman SA; Kahr WHA J Thromb Haemost; 2024 Aug; 22(8):2294-2305. PubMed ID: 38718926 [TBL] [Abstract][Full Text] [Related]
32. Immature dense granules in platelets from mice with platelet storage pool disease. Reddington M; Novak EK; Hurley E; Medda C; McGarry MP; Swank RT Blood; 1987 May; 69(5):1300-6. PubMed ID: 3567357 [TBL] [Abstract][Full Text] [Related]
33. Incorporation of a circulating protein into megakaryocyte and platelet granules. Handagama PJ; George JN; Shuman MA; McEver RP; Bainton DF Proc Natl Acad Sci U S A; 1987 Feb; 84(3):861-5. PubMed ID: 3468513 [TBL] [Abstract][Full Text] [Related]
34. Identification of novel mutations in the VPS33B gene involved in arthrogryposis, renal dysfunction, and cholestasis syndrome. Seo SH; Hwang SM; Ko JM; Ko JS; Hyun YJ; Cho SI; Park H; Kim SY; Seong MW; Park SS Clin Genet; 2015 Jul; 88(1):80-4. PubMed ID: 24917129 [TBL] [Abstract][Full Text] [Related]
35. Kistrin, an integrin antagonist, blocks endocytosis of fibrinogen into guinea pig megakaryocyte and platelet alpha-granules. Handagama P; Bainton DF; Jacques Y; Conn MT; Lazarus RA; Shuman MA J Clin Invest; 1993 Jan; 91(1):193-200. PubMed ID: 8423218 [TBL] [Abstract][Full Text] [Related]
36. Zebrafish vps33b, an ortholog of the gene responsible for human arthrogryposis-renal dysfunction-cholestasis syndrome, regulates biliary development downstream of the onecut transcription factor hnf6. Matthews RP; Plumb-Rudewiez N; Lorent K; Gissen P; Johnson CA; Lemaigre F; Pack M Development; 2005 Dec; 132(23):5295-306. PubMed ID: 16284120 [TBL] [Abstract][Full Text] [Related]
37. Munc18-2, but not Munc18-1 or Munc18-3, regulates platelet exocytosis, hemostasis, and thrombosis. Cardenas EI; Gonzalez R; Breaux K; Da Q; Gutierrez BA; Ramos MA; Cardenas RA; Burns AR; Rumbaut RE; Adachi R J Biol Chem; 2019 Mar; 294(13):4784-4792. PubMed ID: 30696774 [TBL] [Abstract][Full Text] [Related]
39. ARC syndrome with high GGT cholestasis caused by VPS33B mutations. Wang JS; Zhao J; Li LT World J Gastroenterol; 2014 Apr; 20(16):4830-4. PubMed ID: 24782640 [TBL] [Abstract][Full Text] [Related]