-
1
-
-
79961094789
-
Inherited platelet disorders: A clinical approach to diagnosis and management
-
Cox K, Price V, Kahr WH. Inherited platelet disorders: a clinical approach to diagnosis and management. Expert Rev Hematol. 2011;4(4):455-472.
-
(2011)
Expert Rev Hematol
, vol.4
, Issue.4
, pp. 455-472
-
-
Cox, K.1
Price, V.2
Kahr, W.H.3
-
2
-
-
79960636704
-
Advances in our understanding of the molecular basis of disorders of platelet function
-
Nurden A, Nurden P. Advances in our understanding of the molecular basis of disorders of platelet function. J Thromb Haemost. 2011;9 (Suppl 1):76-91.
-
(2011)
J Thromb Haemost
, vol.9
, Issue.SUPPL. 1
, pp. 76-91
-
-
Nurden, A.1
Nurden, P.2
-
3
-
-
0033552631
-
Blood platelets are assembled principally at the ends of proplatelet processes produced by differentiated megakaryocytes
-
DOI 10.1083/jcb.147.6.1299
-
Italiano JE Jr, Lecine P, Shivdasani RA, Hartwig JH. Blood platelets are assembled principally at the ends of proplatelet processes produced by differentiated megakaryocytes. J Cell Biol. 1999; 147(6):1299-1312. (Pubitemid 30012814)
-
(1999)
Journal of Cell Biology
, vol.147
, Issue.6
, pp. 1299-1312
-
-
Italiano Jr., J.E.1
Lecine, P.2
Shivdasani, R.A.3
Hartwig, J.H.4
-
5
-
-
65849360502
-
Platelet alpha-granules: Basic biology and clinical correlates
-
Blair P, Flaumenhaft R. Platelet alpha-granules: basic biology and clinical correlates. Blood Rev. 2009;23(4):177-189.
-
(2009)
Blood Rev
, vol.23
, Issue.4
, pp. 177-189
-
-
Blair, P.1
Flaumenhaft, R.2
-
6
-
-
0032055178
-
Multivesicular bodies are an intermediate stage in the formation of platelet alpha-granules
-
Heijnen HF, Debili N, VainchenckerW, Breton-Gorius J, Geuze HJ, Sixma JJ. Multivesicular bodies are an intermediate stage in the formation of platelet alpha-granules. Blood. 1998;91(7):2313-2325. (Pubitemid 28155504)
-
(1998)
Blood
, vol.91
, Issue.7
, pp. 2313-2325
-
-
Heijnen, H.F.G.1
Debili, N.2
Vainchencker, W.3
Breton-Gorius, J.4
Geuze, H.J.5
Sixma, J.J.6
-
8
-
-
28844492181
-
Mechanisms of organelle transport and capture along proplatelets during platelet production
-
DOI 10.1182/blood-2005-06-2206
-
Richardson J, Shivdasani R, Boers C, Hartwig J, Italiano JE Jr. Mechanisms of organelle transport and capture along proplatelets during platelet production. Blood. 2005;106:4066-4075. (Pubitemid 41775911)
-
(2005)
Blood
, vol.106
, Issue.13
, pp. 4066-4075
-
-
Richardson, J.L.1
Shivdasani, R.A.2
Boers, C.3
Hartwig, J.H.4
Italiano Jr., J.E.5
-
9
-
-
52949149668
-
Disorders of lysosome-related organelle biogenesis: Clinical and molecular genetics
-
Huizing M, Helip-Wooley A, Westbroek W, Gunay-Aygun M, Gahl WA. Disorders of lysosome-related organelle biogenesis: clinical and molecular genetics. Annu Rev Genomics Hum Genet. 2008;9:359-386.
-
(2008)
Annu Rev Genomics Hum Genet
, vol.9
, pp. 359-386
-
-
Huizing, M.1
Helip-Wooley, A.2
Westbroek, W.3
Gunay-Aygun, M.4
Gahl, W.A.5
-
10
-
-
2942562170
-
Murine Hermansky-Pudlak syndrome genes: Regulators of lysosome-related organelles
-
DOI 10.1002/bies.20042
-
Li W, Rusiniak ME, Chintala S, Gautam R, Novak EK, Swank RT. Murine Hermansky-Pudlak syndrome genes: regulators of lysosome-related organelles. Bioessays. 2004;26(6):616-628. (Pubitemid 38758339)
-
(2004)
BioEssays
, vol.26
, Issue.6
, pp. 616-628
-
-
Li, W.1
Rusiniak, M.E.2
Chintala, S.3
Gautam, R.4
Novak, E.K.5
Swank, R.T.6
-
11
-
-
33645057693
-
Hermansky-Pudlak syndrome: A disease of protein trafficking and organelle function
-
Wei ML. Hermansky-Pudlak syndrome: a disease of protein trafficking and organelle function. Pigment Cell Res. 2006;19(1):19-42.
-
(2006)
Pigment Cell Res
, vol.19
, Issue.1
, pp. 19-42
-
-
Wei, M.L.1
-
13
-
-
34648828526
-
Melanosomes - Dark organelles enlighten endosomal membrane transport
-
DOI 10.1038/nrm2258, PII NRM2258
-
Raposo G, Marks MS. Melanosomes: dark organelles enlighten endosomal membrane transport. Nat Rev Mol Cell Biol. 2007;8(10):786-797. (Pubitemid 47462136)
-
(2007)
Nature Reviews Molecular Cell Biology
, vol.8
, Issue.10
, pp. 786-797
-
-
Raposo, G.1
Marks, M.S.2
-
14
-
-
0035880246
-
Platelets from patients with the Quebec platelet disorder contain and secrete abnormal amounts of urokinase-type plasminogen activator
-
Kahr WH, Zheng S, Sheth PM, et al. Platelets from patients with the Quebec platelet disorder contain and secrete abnormal amounts of urokinase-type plasminogen activator. Blood. 2001;98(2):257-265.
-
(2001)
Blood
, vol.98
, Issue.2
, pp. 257-265
-
-
Kahr, W.H.1
Zheng, S.2
Sheth, P.M.3
-
15
-
-
0043064058
-
Intracellular activation of the fibrinolytic cascade in the Quebec Platelet Disorder
-
Sheth PM, Kahr WH, Haq MA, Veljkovic DK, Rivard GE, Hayward CP. Intracellular activation of the fibrinolytic cascade in the Quebec platelet disorder. Thromb Haemost. 2003;90(2):293-298. (Pubitemid 36992505)
-
(2003)
Thrombosis and Haemostasis
, vol.90
, Issue.2
, pp. 293-298
-
-
Sheth, P.M.1
Kahr, W.H.A.2
Haq, M.A.3
Veljkovic, D.K.4
Rivard, G.E.5
Hayward, C.P.M.6
-
16
-
-
77949516918
-
Persons with Quebec platelet disorder have a tandem duplication of PLAU, the urokinase plasminogen activator gene
-
Paterson AD, Rommens JM, Bharaj B, et al. Persons with Quebec platelet disorder have a tandem duplication of PLAU, the urokinase plasminogen activator gene. Blood. 2010;115(6):1264-1266.
-
(2010)
Blood
, vol.115
, Issue.6
, pp. 1264-1266
-
-
Paterson, A.D.1
Rommens, J.M.2
Bharaj, B.3
-
17
-
-
33846201270
-
The gray platelet syndrome: Clinical spectrum of the disease
-
DOI 10.1016/j.blre.2005.12.003, PII S0268960X05000718
-
Nurden AT, Nurden P. The gray platelet syndrome: clinical spectrum of the disease. Blood Rev. 2007;21(1):21-36. (Pubitemid 46097190)
-
(2007)
Blood Reviews
, vol.21
, Issue.1
, pp. 21-36
-
-
Nurden, A.T.1
Nurden, P.2
-
18
-
-
0018333833
-
Ultrastuctural studies of the gray platelet syndrome
-
White JG. Ultrastructural studies of the gray platelet syndrome. Am J Pathol. 1979;95(2):445-462. (Pubitemid 9187084)
-
(1979)
American Journal of Pathology
, vol.95
, Issue.2
, pp. 445-462
-
-
White, J.G.1
-
19
-
-
79960903114
-
Mutations in NBEAL2, encoding a BEACH protein, cause gray platelet syndrome
-
Kahr WH, Hinckley J, Li L, et al. Mutations in NBEAL2, encoding a BEACH protein, cause gray platelet syndrome. Nat Genet. 2011;43(8):738-740.
-
(2011)
Nat Genet
, vol.43
, Issue.8
, pp. 738-740
-
-
Kahr, W.H.1
Hinckley, J.2
Li, L.3
-
20
-
-
79960921968
-
NBEAL2 is mutated in gray platelet syndrome and is required for biogenesis of platelet alphagranules
-
Gunay-Aygun M, Falik-Zaccai TC, Vilboux T, et al. NBEAL2 is mutated in gray platelet syndrome and is required for biogenesis of platelet alphagranules. Nat Genet. 2011;43(8):732-734.
-
(2011)
Nat Genet
, vol.43
, Issue.8
, pp. 732-734
-
-
Gunay-Aygun, M.1
Falik-Zaccai, T.C.2
Vilboux, T.3
-
21
-
-
79960895154
-
Exome sequencing identifies NBEAL2 as the causative gene for gray platelet syndrome
-
Albers CA, Cvejic A, Favier R, et al. Exome sequencing identifies NBEAL2 as the causative gene for gray platelet syndrome. Nat Genet. 2011;43(8):735-737.
-
(2011)
Nat Genet
, vol.43
, Issue.8
, pp. 735-737
-
-
Albers, C.A.1
Cvejic, A.2
Favier, R.3
-
22
-
-
12144290067
-
Mutations in VPS33B, encoding a regulator of SNARE-dependent membrane fusion, cause arthrogryposis-renal dysfunction-cholestasis (ARC) syndrome
-
DOI 10.1038/ng1325
-
Gissen P, Johnson CA, Morgan NV, et al. Mutations in VPS33B, encoding a regulator of SNARE-dependent membrane fusion, cause arthrogryposis-renal dysfunction-cholestasis (ARC) syndrome. Nat Genet. 2004;36(4):400-404. (Pubitemid 38437264)
-
(2004)
Nature Genetics
, vol.36
, Issue.4
, pp. 400-404
-
-
Gissen, P.1
Johnson, C.A.2
Morgan, N.V.3
Stapelbroek, J.M.4
Forshew, T.5
Cooper, W.N.6
McKiernan, P.J.7
Klomp, L.W.J.8
Morris, A.A.M.9
Wraith, J.E.10
McClean, P.11
Lynch, S.A.12
Thompson, R.J.13
Lo, B.14
Quarrell, O.W.15
Di, R.M.16
Trembath, R.C.17
Mandel, H.18
Wali, S.19
Karet, F.E.20
Knisely, A.S.21
Houwen, R.H.J.22
Kelly, D.A.23
Maher, E.R.24
more..
-
23
-
-
28844469933
-
Requirement of VPS33B, a member of the Sec1/Munc18 protein family, in megakaryocyte and platelet α-granule biogenesis
-
DOI 10.1182/blood-2005-04-1356
-
Lo B, Li L, Gissen P, et al. Requirement of VPS33B, a member of the Sec1/Munc18 protein family, in megakaryocyte and platelet α-granule biogenesis. Blood. 2005;106(13):4159-4166. (Pubitemid 41775922)
-
(2005)
Blood
, vol.106
, Issue.13
, pp. 4159-4166
-
-
Lo, B.1
Li, L.2
Gissen, P.3
Christensen, H.4
McKiernan, P.J.5
Ye, C.6
Abdelhaleem, M.7
Hayes, J.A.8
Williams, M.D.9
Chitayat, D.10
Kahr, W.H.A.11
-
24
-
-
77952764560
-
Agranular platelets as a cardinal feature of ARC syndrome
-
Kim SM, Chang HK, Song JW, Koh H, Han SJ. Agranular platelets as a cardinal feature of ARC syndrome. J Pediatr Hematol Oncol. 2010;32(4):253-258.
-
(2010)
J Pediatr Hematol Oncol
, vol.32
, Issue.4
, pp. 253-258
-
-
Kim, S.M.1
Chang, H.K.2
Song, J.W.3
Koh, H.4
Han, S.J.5
-
25
-
-
77955914628
-
Usefulness of gray platelets observation in ARC syndrome
-
Benet B, Lainey E, Fenneteau O, Baudouin V, Hurtaud-Roux MF. Usefulness of gray platelets observation in ARC syndrome. Ann Biol Clin (Paris). 2010;68(4):485-489.
-
(2010)
Ann Biol Clin (Paris)
, vol.68
, Issue.4
, pp. 485-489
-
-
Benet, B.1
Lainey, E.2
Fenneteau, O.3
Baudouin, V.4
Hurtaud-Roux, M.F.5
-
26
-
-
0037377234
-
Vesicle trafficking: Pleasure and pain from SM genes
-
DOI 10.1016/S0962-8924(03)00031-X
-
Toonen RF, Verhage M. Vesicle trafficking: pleasure and pain from SM genes. Trends Cell Biol. 2003;13(4):177-186. (Pubitemid 36351533)
-
(2003)
Trends in Cell Biology
, vol.13
, Issue.4
, pp. 177-186
-
-
Toonen, R.F.G.1
Verhage, M.2
-
27
-
-
0035800740
-
Molecular characterization of mammalian homologues of class C Vps proteins that interact with syntaxin-7
-
Kim BY, Kramer H, Yamamoto A, Kominami E, Kohsaka S, Akazawa C. Molecular characterization of mammalian homologues of class C Vps proteins that interact with syntaxin-7. J Biol Chem. 2001;276(31):29393-29402.
-
(2001)
J Biol Chem
, vol.276
, Issue.31
, pp. 29393-29402
-
-
Kim, B.Y.1
Kramer, H.2
Yamamoto, A.3
Kominami, E.4
Kohsaka, S.5
Akazawa, C.6
-
28
-
-
0037417972
-
The mouse organellar biogenesis mutant buff results from a mutation in Vps33a, a homologue of yeast vps33 and Drosophila carnation
-
DOI 10.1073/pnas.0237292100
-
Suzuki T, Oiso N, Gautam R, et al. The mouse organellar biogenesis mutant buff results from a mutation in Vps33a, a homologue of yeast vps33 and Drosophila carnation. Proc Natl Acad Sci U S A. 2003;100(3):1146-1150. (Pubitemid 36183970)
-
(2003)
Proceedings of the National Academy of Sciences of the United States of America
, vol.100
, Issue.3
, pp. 1146-1150
-
-
Suzuki, T.1
Oiso, N.2
Gautam, R.3
Novak, E.K.4
Panthier, J.-J.5
Suprabha, P.G.6
Vida, T.7
Swank, R.T.8
Spritz, R.A.9
-
29
-
-
67949091245
-
Vps-C complexes: Gatekeepers of endolysosomal traffic
-
Nickerson DP, Brett CL, Merz AJ. Vps-C complexes: gatekeepers of endolysosomal traffic. Curr Opin Cell Biol. 2009;21(4):543-551.
-
(2009)
Curr Opin Cell Biol
, vol.21
, Issue.4
, pp. 543-551
-
-
Nickerson, D.P.1
Brett, C.L.2
Merz, A.J.3
-
30
-
-
0033213257
-
A role for the deep orange and carnation eye color genes in lysosomal delivery in Drosophila
-
DOI 10.1016/S1097-2765(00)80199-9
-
Sevrioukov EA, He JP, Moghrabi N, Sunio A, Kramer H. A role for the deep orange and carnation eye color genes in lysosomal delivery in Drosophila. Mol Cell. 1999;4(4):479-486. (Pubitemid 29531128)
-
(1999)
Molecular Cell
, vol.4
, Issue.4
, pp. 479-486
-
-
Sevrioukov, E.A.1
He, J.-P.2
Moghrabi, N.3
Sunio, A.4
Kramer, H.5
-
31
-
-
33744914606
-
A dual function for Deep orange in programmed autophagy in the Drosophila melanogaster fat body
-
DOI 10.1016/j.yexcr.2006.03.002, PII S0014482706000887
-
Lindmo K, Simonsen A, Brech A, Finley K, Rusten TE, Stenmark H. A dual function for Deep orange in programmed autophagy in the Drosophila melanogaster fat body. Exp Cell Res. 2006;312(11):2018-2027. (Pubitemid 43850927)
-
(2006)
Experimental Cell Research
, vol.312
, Issue.11
, pp. 2018-2027
-
-
Lindmo, K.1
Simonsen, A.2
Brech, A.3
Finley, K.4
Rusten, T.E.5
Stenmark, H.6
-
32
-
-
24944583279
-
Drosophila Vps16A is required for trafficking to lysosomes and biogenesis of pigment granules
-
DOI 10.1242/jcs.02502
-
Pulipparacharuvil S, Akbar MA, Ray S, et al. Drosophila Vps16A is required for trafficking to lysosomes and biogenesis of pigment granules. J Cell Sci. 2005;118(Pt 16):3663-3673. (Pubitemid 41309413)
-
(2005)
Journal of Cell Science
, vol.118
, Issue.16
, pp. 3663-3673
-
-
Pulipparacharuvil, S.1
Akbar, M.A.2
Ray, S.3
Sevrioukov, E.A.4
Haberman, A.S.5
Rohrer, J.6
Kramer, H.7
-
33
-
-
0037598597
-
Deep-orange and carnation define distinct stages in late endosomal biogenesis in Drosophila melanogaster
-
DOI 10.1083/jcb.200210166
-
Sriram V, Krishnan KS, Mayor S. deep-orange and carnation define distinct stages in late endosomal biogenesis in Drosophila melanogaster. J Cell Biol. 2003;161(3):593-607. (Pubitemid 36578583)
-
(2003)
Journal of Cell Biology
, vol.161
, Issue.3
, pp. 593-607
-
-
Sriram, V.1
Krishnan, K.S.2
Mayor, S.3
-
34
-
-
65249172588
-
The SM protein Car/ Vps33A regulates SNARE-mediated trafficking to lysosomes and lysosome-related organelles
-
Akbar MA, Ray S, Kramer H. The SM protein Car/ Vps33A regulates SNARE-mediated trafficking to lysosomes and lysosome-related organelles. Mol Biol Cell. 2009;20(6):1705-1714.
-
(2009)
Mol Biol Cell
, vol.20
, Issue.6
, pp. 1705-1714
-
-
Akbar, M.A.1
Ray, S.2
Kramer, H.3
-
35
-
-
79551692756
-
The full-of-bacteria gene is required for phagosome maturation during immune defense in Drosophila
-
Akbar MA, Tracy C, Kahr WH, Kramer H. The full-of-bacteria gene is required for phagosome maturation during immune defense in Drosophila. J Cell Biol. 2011;192(3):383-390.
-
(2011)
J Cell Biol
, vol.192
, Issue.3
, pp. 383-390
-
-
Akbar, M.A.1
Tracy, C.2
Kahr, W.H.3
Kramer, H.4
-
36
-
-
77950300024
-
Mutations in VIPAR cause an arthrogryposis, renal dysfunction and cholestasis syndrome phenotype with defects in epithelial polarization
-
Cullinane AR, Straatman-Iwanowska A, Zaucker A, et al. Mutations in VIPAR cause an arthrogryposis, renal dysfunction and cholestasis syndrome phenotype with defects in epithelial polarization. Nat Genet. 2010;42(4):303-312.
-
(2010)
Nat Genet
, vol.42
, Issue.4
, pp. 303-312
-
-
Cullinane, A.R.1
Straatman-Iwanowska, A.2
Zaucker, A.3
-
37
-
-
64149113031
-
SPE-39 family proteins interact with the HOPS complex and function in lysosomal delivery
-
Zhu GD, Salazar G, Zlatic SA, et al. SPE-39 family proteins interact with the HOPS complex and function in lysosomal delivery. Mol Biol Cell. 2009;20(4):1223-1240.
-
(2009)
Mol Biol Cell
, vol.20
, Issue.4
, pp. 1223-1240
-
-
Zhu, G.D.1
Salazar, G.2
Zlatic, S.A.3
-
38
-
-
73349110958
-
Platelet-associated complement factor H in healthy persons and patients with atypical HUS
-
Licht C, Pluthero FG, Li L, et al. Platelet-associated complement factor H in healthy persons and patients with atypical HUS. Blood. 2009;114(20):4538- 4545.
-
(2009)
Blood
, vol.114
, Issue.20
, pp. 4538-4545
-
-
Licht, C.1
Pluthero, F.G.2
Li, L.3
-
39
-
-
0027278869
-
The protein CD63 is in platelet dense granules, is deficient in a patient with Hermansky-Pudlak syndrome, and appears identical to granulophysin
-
Nishibori M, Cham B, McNicol A, Shalev A, Jain N, Gerrard JM. The protein CD63 is in platelet dense granules, is deficient in a patient with Hermansky-Pudlak syndrome, and appears identical to granulophysin. J Clin Invest. 1993;91(4):1775-1782. (Pubitemid 23127384)
-
(1993)
Journal of Clinical Investigation
, vol.91
, Issue.4
, pp. 1775-1782
-
-
Nishibori, M.1
Cham, B.2
McNicol, A.3
Shalev, A.4
Jain, N.5
Gerrard, J.M.6
-
40
-
-
77952564450
-
Anucleate platelets generate progeny
-
Schwertz H, Koster S, Kahr WH, et al. Anucleate platelets generate progeny. Blood. 2010;115(18):3801-3809.
-
(2010)
Blood
, vol.115
, Issue.18
, pp. 3801-3809
-
-
Schwertz, H.1
Koster, S.2
Kahr, W.H.3
-
41
-
-
0033165875
-
Platelet dense granules: Structure, function and implications for haemostasis
-
DOI 10.1016/S0049-3848(99)00015-8, PII S0049384899000158
-
McNicol A, Israels SJ. Platelet dense granules: structure, function and implications for haemostasis. Thromb Res. 1999;95(1):1-18. (Pubitemid 29325256)
-
(1999)
Thrombosis Research
, vol.95
, Issue.1
, pp. 1-18
-
-
McNicol, A.1
Israels, S.J.2
-
42
-
-
59049104632
-
Protein synthesis by platelets: Historical and new perspectives
-
Weyrich AS, Schwertz H, Kraiss LW, Zimmerman GA. Protein synthesis by platelets: historical and new perspectives. J Thromb Haemost. 2009;7(2):241-246.
-
(2009)
J Thromb Haemost
, vol.7
, Issue.2
, pp. 241-246
-
-
Weyrich, A.S.1
Schwertz, H.2
Kraiss, L.W.3
Zimmerman, G.A.4
-
43
-
-
38949178835
-
Angiogenesis is regulated by a novel mechanism: Pro- and antiangiogenic proteins are organized into separate platelet alpha granules and differentially released
-
DOI 10.1182/blood-2007-09-113837
-
Italiano JE Jr, Richardson JL, Patel-Hett S, et al. Angiogenesis is regulated by a novel mechanism: pro- and antiangiogenic proteins are organized into separate platelet alpha granules and differentially released. Blood. 2008;111(3):1227-1233. (Pubitemid 351213404)
-
(2008)
Blood
, vol.111
, Issue.3
, pp. 1227-1233
-
-
Italiano Jr., J.E.1
Richardson, J.L.2
Patel-Hett, S.3
Battinelli, E.4
Zaslavsky, A.5
Short, S.6
Ryeom, S.7
Folkman, J.8
Klement, G.L.9
-
44
-
-
34548823786
-
Evidence that differential packaging of the major platelet granule proteins von Willebrand factor and fibrinogen can support their differential release
-
DOI 10.1111/j.1538-7836.2007.02698.x
-
Sehgal S, Storrie B. Evidence that differential packaging of the major platelet granule proteins von Willebrand factor and fibrinogen can support their differential release. J Thromb Haemost. 2007;5(10):2009-2016. (Pubitemid 47450016)
-
(2007)
Journal of Thrombosis and Haemostasis
, vol.5
, Issue.10
, pp. 2009-2016
-
-
Sehgal, S.1
Storrie, B.2
-
45
-
-
80051562142
-
Quantitative immunofluorescence mapping reveals little functional coclustering of proteins within platelet alpha-granules
-
Kamykowski J, Carlton P, Sehgal S, Storrie B. Quantitative immunofluorescence mapping reveals little functional coclustering of proteins within platelet alpha-granules. Blood. 2011; 118(5):1370-1373.
-
(2011)
Blood
, vol.118
, Issue.5
, pp. 1370-1373
-
-
Kamykowski, J.1
Carlton, P.2
Sehgal, S.3
Storrie, B.4
-
46
-
-
77956502480
-
The platelet interior revisited: Electron tomography reveals tubular alpha-granule subtypes
-
van Nispen tot Pannerden H, de Haas F, GeertsW, Posthuma G, van Dijk S, Heijnen HF. The platelet interior revisited: electron tomography reveals tubular alpha-granule subtypes. Blood. 2010; 116(7):1147-1156.
-
(2010)
Blood
, vol.116
, Issue.7
, pp. 1147-1156
-
-
Van Nispen Tot Pannerden, H.1
De Haas, F.2
Geerts, W.3
Posthuma, G.4
Van Dijk, S.5
Heijnen, H.F.6
-
47
-
-
80052614265
-
Actomyosin II contractility expels von Willebrand factor from Weibel-Palade bodies during exocytosis
-
Nightingale TD, White IJ, Doyle EL, et al. Actomyosin II contractility expels von Willebrand factor from Weibel-Palade bodies during exocytosis. J Cell Biol. 2011;194(4):613-629.
-
(2011)
J Cell Biol
, vol.194
, Issue.4
, pp. 613-629
-
-
Nightingale, T.D.1
White, I.J.2
Doyle, E.L.3
-
48
-
-
0034918524
-
A journey with platelet P-selectin: The molecular basis of granule secretion, signalling and cell adhesion
-
Furie B, Furie BC, Flaumenhaft R. A journey with platelet P-selectin: the molecular basis of granule secretion, signalling and cell adhesion. Thromb Haemost. 2001;86(1):214-221. (Pubitemid 32666187)
-
(2001)
Thrombosis and Haemostasis
, vol.86
, Issue.1
, pp. 214-221
-
-
Furie, B.1
Furie, B.C.2
Flaumenhaft, R.3
-
49
-
-
0023574858
-
Gray platelet syndrome. Demonstration of alpha granule membranes that can fuse with the cell surface
-
Rosa JP, George JN, Bainton DF, Nurden AT, Caen JP, McEver RP. Gray platelet syndrome. Demonstration of alpha granule membranes that can fuse with the cell surface. J Clin Invest. 1987; 80(4):1138-1146. (Pubitemid 18075653)
-
(1987)
Journal of Clinical Investigation
, vol.80
, Issue.4
, pp. 1138-1146
-
-
Rosa, J.-P.1
George, J.N.2
Bainton, D.F.3
Nurden, A.T.4
Caen, J.P.5
McEver, R.P.6
|