-
1
-
-
0001864115
-
Leukocyteneinschlusse
-
May R. Leukocyteneinschlusse. Dtsch Arch Klin Med 1909; 96: 1-6.
-
(1909)
Dtsch Arch Klin Med
, vol.96
, pp. 1-6
-
-
May, R.1
-
2
-
-
84866470520
-
Simultaneous constitutional changes in neutrophils and platelets
-
Hegglin R. Simultaneous constitutional changes in neutrophils and platelets. Helv Med Acta 1945; 12: 439-40.
-
(1945)
Helv Med Acta
, vol.12
, pp. 439-440
-
-
Hegglin, R.1
-
3
-
-
0015304377
-
Hereditary macrothrombocytopathia, nephritis and deafness
-
Epstein CJ, Sahud MA, Piel CF, Goodman JR, Bernfield MR, Kushner JH, Ablin AR. Hereditary macrothrombocytopathia, nephritis and deafness. Am J Med 1972; 52: 299-310.
-
(1972)
Am J Med
, vol.52
, pp. 299-310
-
-
Epstein, C.J.1
Sahud, M.A.2
Piel, C.F.3
Goodman, J.R.4
Bernfield, M.R.5
Kushner, J.H.6
Ablin, A.R.7
-
4
-
-
0021956321
-
Fechtner syndrome-a variant of Alport's syndrome with leukocyte inclusions and macrothrombocytopenia
-
Peterson LC, Rao KV, Crosson JT, White JG. Fechtner syndrome-a variant of Alport's syndrome with leukocyte inclusions and macrothrombocytopenia. Blood 1985; 65: 397-406.
-
(1985)
Blood
, vol.65
, pp. 397-406
-
-
Peterson, L.C.1
Rao, K.V.2
Crosson, J.T.3
White, J.G.4
-
5
-
-
0025606519
-
Sebastian platelet syndrome: A new variant of hereditary macrothrombocytopenia with leukocyte inclusions
-
Greinacher A, Nieuwenhuis HK, White JG. Sebastian platelet syndrome: A new variant of hereditary macrothrombocytopenia with leukocyte inclusions. Blut 1990; 61: 282-8.
-
(1990)
Blut
, vol.61
, pp. 282-288
-
-
Greinacher, A.1
Nieuwenhuis, H.K.2
White, J.G.3
-
6
-
-
0033822065
-
Mutation of MYH9, encoding non-muscle myosin heavy chain A, in May-Hegglin anomaly
-
Kelley MJ, Jawien W, Ortel TL, Korczak JF. Mutation of MYH9, encoding non-muscle myosin heavy chain A, in May-Hegglin anomaly. Nat Genet 2000; 26: 106-8.
-
(2000)
Nat Genet
, vol.26
, pp. 106-108
-
-
Kelley, M.J.1
Jawien, W.2
Ortel, T.L.3
Korczak, J.F.4
-
7
-
-
0033812573
-
Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes
-
Seri M, Cusano R, Gangarossa S, Caridi G, Bordo D, Lo Nigros C, Gaiggeri GM, Ravazzolo R, Savino M, Del Vecchio M, d'Apolito M, Iolascon A, Zelitnte LL, Savoia A, Balduini CL, Noris P, Magrini U, Belletti S, Heath KE, Babcock M, et al. Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes. Nat Genet 2000; 26: 103-5.
-
(2000)
Nat Genet
, vol.26
, pp. 103-105
-
-
Seri, M.1
Cusano, R.2
Gangarossa, S.3
Caridi, G.4
Bordo, D.5
Lo Nigros, C.6
Gaiggeri, G.M.7
Ravazzolo, R.8
Savino, M.9
Del Vecchio, M.10
d'Apolito, M.11
Iolascon, A.12
Zelitnte, L.L.13
Savoia, A.14
Balduini, C.L.15
Noris, P.16
Magrini, U.17
Belletti, S.18
Heath, K.E.19
Babcock, M.20
more..
-
8
-
-
0035865524
-
Mutations in the NMMHC-A gene cause autosomal dominant macrothrombocytopenia with leukocyte inclusions (May-Hegglin anomaly/ Sebastian syndrome)
-
Kunishima S, Matsushita T, Kojima T, Amemiya N, Choi YM, Josika N, Inoue M, Jung Y, Mamiya S, Matsumoto K, Miyajima Y, Zhang G, Ruan C, Saito K, Song KS, Yoon HJ, Kamiya T, Saito H. Mutations in the NMMHC-A gene cause autosomal dominant macrothrombocytopenia with leukocyte inclusions (May-Hegglin anomaly/Sebastian syndrome). Blood 2001; 97: 1147-9.
-
(2001)
Blood
, vol.97
, pp. 1147-1149
-
-
Kunishima, S.1
Matsushita, T.2
Kojima, T.3
Amemiya, N.4
Choi, Y.M.5
Josika, N.6
Inoue, M.7
Jung, Y.8
Mamiya, S.9
Matsumoto, K.10
Miyajima, Y.11
Zhang, G.12
Ruan, C.13
Saito, K.14
Song, K.S.15
Yoon, H.J.16
Kamiya, T.17
Saito, H.18
-
9
-
-
29044448970
-
Nonmuscle myosin II generates forces that transmit tension and drive contraction in multiple tissues during dorsal closure
-
Franke JD, Montague RA, Kiehart DP. Nonmuscle myosin II generates forces that transmit tension and drive contraction in multiple tissues during dorsal closure. Curr Biol 2005; 15: 2208-21.
-
(2005)
Curr Biol
, vol.15
, pp. 2208-2221
-
-
Franke, J.D.1
Montague, R.A.2
Kiehart, D.P.3
-
10
-
-
0025195876
-
Microinjection of recombinant p21rho induces rapid changes in cell morphology
-
Paterson HF, Self AJ, Garrett MD, Just I, Aktories K, Hall A. Microinjection of recombinant p21rho induces rapid changes in cell morphology. J Cell Biol 1990; 111: 1001-7.
-
(1990)
J Cell Biol
, vol.111
, pp. 1001-1007
-
-
Paterson, H.F.1
Self, A.J.2
Garrett, M.D.3
Just, I.4
Aktories, K.5
Hall, A.6
-
11
-
-
0033174147
-
Rac regulates phosphorylation of the myosin-II heavy chain, actinomyosin disassembly and cell spreading
-
van Leeuwen FN, van Delft S, Kain HE, van der Kammen RA, Collard JG. Rac regulates phosphorylation of the myosin-II heavy chain, actinomyosin disassembly and cell spreading. Nat Cell Biol 1999; 1: 242-8.
-
(1999)
Nat Cell Biol
, vol.1
, pp. 242-248
-
-
van Leeuwen, F.N.1
van Delft, S.2
Kain, H.E.3
van der Kammen, R.A.4
Collard, J.G.5
-
12
-
-
0037910378
-
MYH9-related disease: May-Hegglin anomaly, Sebastian syndrome, Fechtner syndrome, and Epstein syndrome are not distinct entities but represent a variable expression of a single illness
-
Seri M, Pecci A, Di Bari F, Cusano R, Savino M, Panza E, Nigro A, Noris P, Gangarossa S, Rocca B, Gresele P, Bizzaro N, Malatesta P, Koiviso PA, Longo I, Musso R, Pecoraro C, Iolascon A, Magrini U, Rodriguez Soriano J, et al. MYH9-related disease: May-Hegglin anomaly, Sebastian syndrome, Fechtner syndrome, and Epstein syndrome are not distinct entities but represent a variable expression of a single illness. Medicine (Baltimore) 2003; 82: 203-15.
-
(2003)
Medicine (Baltimore)
, vol.82
, pp. 203-215
-
-
Seri, M.1
Pecci, A.2
Di Bari, F.3
Cusano, R.4
Savino, M.5
Panza, E.6
Nigro, A.7
Noris, P.8
Gangarossa, S.9
Rocca, B.10
Gresele, P.11
Bizzaro, N.12
Malatesta, P.13
Koiviso, P.A.14
Longo, I.15
Musso, R.16
Pecoraro, C.17
Iolascon, A.18
Magrini, U.19
Rodriguez Soriano, J.20
more..
-
13
-
-
40549091624
-
Position of nonmuscle myosin heavy chain IIA (NMMHC-IIA) mutations predicts the natural history of MYH9-related disease
-
Pecci A, Panza E, Pujol-Moix N, Klersy C, Di Bari F, Bozzi V, Giesele P, Lethagen S, Fabris F, Dufour C, Granata A, Doubek M, Pecoraro C, Koivis PA, Heller PG, Iolascon A, Alvisi P, Schwabe D, De Candia E, Rocca B, et al. Position of nonmuscle myosin heavy chain IIA (NMMHC-IIA) mutations predicts the natural history of MYH9-related disease. Hum Mutat 2008; 29: 409-17.
-
(2008)
Hum Mutat
, vol.29
, pp. 409-417
-
-
Pecci, A.1
Panza, E.2
Pujol-Moix, N.3
Klersy, C.4
Di Bari, F.5
Bozzi, V.6
Giesele, P.7
Lethagen, S.8
Fabris, F.9
Dufour, C.10
Granata, A.11
Doubek, M.12
Pecoraro, C.13
Koivis, P.A.14
Heller, P.G.15
Iolascon, A.16
Alvisi, P.17
Schwabe, D.18
De Candia, E.19
Rocca, B.20
more..
-
14
-
-
0031894136
-
Thrombocytopenia, giant platelets, and leukocyte inclusion bodies (May-Hegglin anomaly): Clinical and laboratory findings
-
Noris P, Spedini P, Belletti S, Magrini U, Balduini CL. Thrombocytopenia, giant platelets, and leukocyte inclusion bodies (May-Hegglin anomaly): Clinical and laboratory findings. Am J Med 1998; 104: 355-60.
-
(1998)
Am J Med
, vol.104
, pp. 355-360
-
-
Noris, P.1
Spedini, P.2
Belletti, S.3
Magrini, U.4
Balduini, C.L.5
-
15
-
-
23844448102
-
Altered cytoskeleton organization in platelets from patients with MYH9-related disease
-
Canobbio I, Noris P, Pecci A, Balduini A, Balduini CL, Torti M. Altered cytoskeleton organization in platelets from patients with MYH9-related disease. J Thromb Haemost 2005; 3: 1026-35.
-
(2005)
J Thromb Haemost
, vol.3
, pp. 1026-1035
-
-
Canobbio, I.1
Noris, P.2
Pecci, A.3
Balduini, A.4
Balduini, C.L.5
Torti, M.6
-
16
-
-
27744521855
-
Pathogenetic mechanisms of hematological abnormalities of patients with MYH9 mutations
-
Pecci A, Canobbio I, Balduini A, Stefanini L, Cisterna B, Marseglia C, Noris P, Savoia A, Balduini CL, Torti M. Pathogenetic mechanisms of hematological abnormalities of patients with MYH9 mutations. Hum Mol Genet 2005; 14: 3169-78.
-
(2005)
Hum Mol Genet
, vol.14
, pp. 3169-3178
-
-
Pecci, A.1
Canobbio, I.2
Balduini, A.3
Stefanini, L.4
Cisterna, B.5
Marseglia, C.6
Noris, P.7
Savoia, A.8
Balduini, C.L.9
Torti, M.10
-
17
-
-
0015978724
-
May-Hegglin anomaly: A defect in megakaryocyte fragmentation?
-
Godwin HA, Ginsburg AD. May-Hegglin anomaly: A defect in megakaryocyte fragmentation? Br J Haematol 1974; 26: 117-21.
-
(1974)
Br J Haematol
, vol.26
, pp. 117-121
-
-
Godwin, H.A.1
Ginsburg, A.D.2
-
18
-
-
0033552631
-
Blood platelets are assembled principally at the ends of proplatelet processes produced by differentiated megakaryocytes
-
Italiano JE, 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: 1299-312.
-
(1999)
J Cell Biol
, vol.147
, pp. 1299-1312
-
-
Italiano, J.E.1
Lecine, P.2
Shivdasani, R.A.3
Hartwig, J.H.4
-
19
-
-
34347390082
-
The May-Hegglin anomaly gene MYH9 is a negative regulator of platelet biogenesis modulated by the Rho-ROCK pathway
-
Chen Z, Naveiras O, Balduini A, Mammoto A, Conti MA, Adelstein RS, Ingber D, Daley GQ, Shivdasani RA. The May-Hegglin anomaly gene MYH9 is a negative regulator of platelet biogenesis modulated by the Rho-ROCK pathway. Blood 2007; 110: 171-9.
-
(2007)
Blood
, vol.110
, pp. 171-179
-
-
Chen, Z.1
Naveiras, O.2
Balduini, A.3
Mammoto, A.4
Conti, M.A.5
Adelstein, R.S.6
Ingber, D.7
Daley, G.Q.8
Shivdasani, R.A.9
-
20
-
-
4744364577
-
Defects in cell adhesion and the visceral endoderm following ablation of nonmuscle myosin heavy chain II-A in mice
-
Conti MA, Even-Ram S, Liu C, Yamada KM, Adelstein RS. Defects in cell adhesion and the visceral endoderm following ablation of nonmuscle myosin heavy chain II-A in mice. J Biol Chem 2004; 279: 41263-6.
-
(2004)
J Biol Chem
, vol.279
, pp. 41263-41266
-
-
Conti, M.A.1
Even-Ram, S.2
Liu, C.3
Yamada, K.M.4
Adelstein, R.S.5
-
21
-
-
36148955807
-
Megakaryocyte-restricted MYH9 inactivation dramatically affects hemostasis while preserving platelet aggregation and secretion
-
Leon C, Eckly A, Hechler B, Aleil B, Freund M, Ravanat C, Jourdain M, Nonne C, Weber J, Tiedt R, et al. Megakaryocyte-restricted MYH9 inactivation dramatically affects hemostasis while preserving platelet aggregation and secretion. Blood 2007; 110: 3183-91.
-
(2007)
Blood
, vol.110
, pp. 3183-3191
-
-
Leon, C.1
Eckly, A.2
Hechler, B.3
Aleil, B.4
Freund, M.5
Ravanat, C.6
Jourdain, M.7
Nonne, C.8
Weber, J.9
Tiedt, R.10
-
22
-
-
65349139574
-
Abnormal megakaryocyte morphology and proplatelet formation in mice with megakaryocyte-restricted MYH9 inactivation
-
Eckly A, Strassel C, Freund M, Cazenave JP, Lanza F, Gachet C, Leon C. Abnormal megakaryocyte morphology and proplatelet formation in mice with megakaryocyte-restricted MYH9 inactivation. Blood 2009; 113: 4-9.
-
(2009)
Blood
, vol.113
, pp. 3182-3189
-
-
Eckly, A.1
Strassel, C.2
Freund, M.3
Cazenave, J.P.4
Lanza, F.5
Gachet, C.6
Leon, C.7
-
23
-
-
0019973882
-
Characterization of the platelet membrane glycoprotein abnormalities in Bernard-Soulier syndrome and comparison with normal by surface-labeling techniques and high-resolution two-dimensional gel electrophoresis
-
Clemetson KJ, McGregor JL, James E, Dechavanne M, Luscher EF. Characterization of the platelet membrane glycoprotein abnormalities in Bernard-Soulier syndrome and comparison with normal by surface-labeling techniques and high-resolution two-dimensional gel electrophoresis. J Clin Invest 1982; 70: 304-11.
-
(1982)
J Clin Invest
, vol.70
, pp. 304-311
-
-
Clemetson, K.J.1
McGregor, J.L.2
James, E.3
Dechavanne, M.4
Luscher, E.F.5
-
24
-
-
2642537846
-
Correlation between the clinical phenotype of MYH9-related disease and tissue distribution of class II nonmuscle myosin heavy chains
-
Marigo V, Nigro A, Pecci A, Montanaro D, Di Stazio M, Balduini CL, Savoia A. Correlation between the clinical phenotype of MYH9-related disease and tissue distribution of class II nonmuscle myosin heavy chains. Genomics 2004; 83: 1125-33.
-
(2004)
Genomics
, vol.83
, pp. 1125-1133
-
-
Marigo, V.1
Nigro, A.2
Pecci, A.3
Montanaro, D.4
Di Stazio, M.5
Balduini, C.L.6
Savoia, A.7
-
25
-
-
11144225866
-
Rod mutations associated with MYH9-related disorders disrupt nonmuscle myosin-IIA assembly
-
Franke JD, Dong F, Rickoll WL, Kelley MJ, Kiehart DP. Rod mutations associated with MYH9-related disorders disrupt nonmuscle myosin-IIA assembly. Blood 2005; 105: 161-9.
-
(2005)
Blood
, vol.105
, pp. 161-169
-
-
Franke, J.D.1
Dong, F.2
Rickoll, W.L.3
Kelley, M.J.4
Kiehart, D.P.5
-
26
-
-
0018145410
-
Parasinusoidal location of megakaryocytes in marrow: A determinant of platelet release
-
Lichtman MA, Chamberlain JK, Simon W, Santillo PA. Parasinusoidal location of megakaryocytes in marrow: A determinant of platelet release. Am J Hematol 1978; 4: 303-12.
-
(1978)
Am J Hematol
, vol.4
, pp. 303-312
-
-
Lichtman, M.A.1
Chamberlain, J.K.2
Simon, W.3
Santillo, P.A.4
-
27
-
-
34648826777
-
Dynamic visualization of thrombopoiesis within bone marrow
-
Junt T, Schulze H, Chen Z, Massberg S, Goerge T, Krueger A, Wagner DD, Graf T, Italiano JE Jr, Shivdasani RA, von Andrian UH. Dynamic visualization of thrombopoiesis within bone marrow. Science 2007; 317: 1767-70.
-
(2007)
Science
, vol.317
, pp. 1767-1770
-
-
Junt, T.1
Schulze, H.2
Chen, Z.3
Massberg, S.4
Goerge, T.5
Krueger, A.6
Wagner, D.D.7
Graf, T.8
Italiano, J.E.9
Shivdasani, R.A.10
von Andrian, U.H.11
-
28
-
-
33745609531
-
Deficiency in the Wiskott-Aldrich protein induces premature proplatelet formation and platelet production in the bone marrow compartment
-
Sabri S, Foudi A, Boukour S, Franc B, Charrier S, Jandrot-Perus M, Farndale RW, Jalil A, Blundell MP, Cramer EM, Louache F, Debili N, Thrasher AJ, Vainchenker W. Deficiency in the Wiskott-Aldrich protein induces premature proplatelet formation and platelet production in the bone marrow compartment. Blood 2006; 108: 134-40.
-
(2006)
Blood
, vol.108
, pp. 134-140
-
-
Sabri, S.1
Foudi, A.2
Boukour, S.3
Franc, B.4
Charrier, S.5
Jandrot-Perus, M.6
Farndale, R.W.7
Jalil, A.8
Blundell, M.P.9
Cramer, E.M.10
Louache, F.11
Debili, N.12
Thrasher, A.J.13
Vainchenker, W.14
-
29
-
-
34248329215
-
Proplatelet formation is regulated by the Rho/ROCK pathway
-
Chang Y, Aurade F, Larbret F, Zhang Y, Le Couedic JP, Momeux L, Larghero J, Bertoglio J, Louache F, Cramer E, et al. Proplatelet formation is regulated by the Rho/ROCK pathway. Blood 2007; 109: 4229-36.
-
(2007)
Blood
, vol.109
, pp. 4229-4236
-
-
Chang, Y.1
Aurade, F.2
Larbret, F.3
Zhang, Y.4
Le Couedic, J.P.5
Momeux, L.6
Larghero, J.7
Bertoglio, J.8
Louache, F.9
Cramer, E.10
-
30
-
-
4444272147
-
Molecular mechanisms of megakaryocyte differentiation
-
Schulze H, Shivdasani RA. Molecular mechanisms of megakaryocyte differentiation. Semin Thromb Hemost 2004; 30: 389-98.
-
(2004)
Semin Thromb Hemost
, vol.30
, pp. 389-398
-
-
Schulze, H.1
Shivdasani, R.A.2
-
31
-
-
8744252579
-
Differential regulation of actin stress fiber assembly and proplatelet formation by alpha2beta1 integrin and GPVI in human megakaryocytes
-
Sabri S, Jandrot-Perrus M, Bertoglio J, Farndale RW, Mas VM, Debili N, Vainchenker W. Differential regulation of actin stress fiber assembly and proplatelet formation by alpha2beta1 integrin and GPVI in human megakaryocytes. Blood 2004; 104: 3117-25.
-
(2004)
Blood
, vol.104
, pp. 3117-3125
-
-
Sabri, S.1
Jandrot-Perrus, M.2
Bertoglio, J.3
Farndale, R.W.4
Mas, V.M.5
Debili, N.6
Vainchenker, W.7
-
32
-
-
11144356721
-
Chemokine-mediated interaction of hematopoietic progenitors with the bone marrow vascular niche is required for thrombopoiesis
-
Avecilla ST, Hattori K, Heissig B, Tejada R, Liao F, Shido K, Lin DK, Dias S, Zhang F, Hartman TE, Hackett NR, Crystal RG, Witte L, Hicklin DJ, Beilen P, Eaton D, Lyden D, de Sauvage F, Rafii S. Chemokine-mediated interaction of hematopoietic progenitors with the bone marrow vascular niche is required for thrombopoiesis. Nat Med 2004; 10: 64-71.
-
(2004)
Nat Med
, vol.10
, pp. 64-71
-
-
Avecilla, S.T.1
Hattori, K.2
Heissig, B.3
Tejada, R.4
Liao, F.5
Shido, K.6
Lin, D.K.7
Dias, S.8
Zhang, F.9
Hartman, T.E.10
Hackett, N.R.11
Crystal, R.G.12
Witte, L.13
Hicklin, D.J.14
Beilen, P.15
Eaton, D.16
Lyden, D.17
de Sauvage, F.18
Rafii, S.19
-
33
-
-
27644503703
-
RGS16 is a negative regulator of SDF-1-CXCR4 signaling in megakaryocytes
-
Berthebaud M, Riviere C, Jarrier P, Foudi A, Zhang Y, Compagno D, Galy A, Vainchenker W, Louache F. RGS16 is a negative regulator of SDF-1-CXCR4 signaling in megakaryocytes. Blood 2005; 106: 2962-8.
-
(2005)
Blood
, vol.106
, pp. 2962-2968
-
-
Berthebaud, M.1
Riviere, C.2
Jarrier, P.3
Foudi, A.4
Zhang, Y.5
Compagno, D.6
Galy, A.7
Vainchenker, W.8
Louache, F.9
-
34
-
-
0038070102
-
Control of axon elongation via an SDF-1alpha/Rho/mDia pathway in cultured cerebellar granule neurons
-
Arakawa Y, Bito H, Furuyashiki T, Tsuji T, Takemoto-Kimura S, Kimura K, Nozaki K, Hashimoto N, Narumiya S. Control of axon elongation via an SDF-1alpha/Rho/mDia pathway in cultured cerebellar granule neurons. J Cell Biol 2003; 161: 381-91.
-
(2003)
J Cell Biol
, vol.161
, pp. 381-391
-
-
Arakawa, Y.1
Bito, H.2
Furuyashiki, T.3
Tsuji, T.4
Takemoto-Kimura, S.5
Kimura, K.6
Nozaki, K.7
Hashimoto, N.8
Narumiya, S.9
|