-
1
-
-
0036138503
-
Expression of the nonmuscle myosin heavy chain IIA in the human kidney and screening for MYH9 mutations in Epstein and Fechtner syndromes
-
Arrondel C., Vodovar N., Knebelmann B., Grunfeld J.P., Gubler M.C., Antignac C., and Heidet L. Expression of the nonmuscle myosin heavy chain IIA in the human kidney and screening for MYH9 mutations in Epstein and Fechtner syndromes. J. Am. Soc. Nephrol. 13 (2002) 65-74
-
(2002)
J. Am. Soc. Nephrol.
, vol.13
, pp. 65-74
-
-
Arrondel, C.1
Vodovar, N.2
Knebelmann, B.3
Grunfeld, J.P.4
Gubler, M.C.5
Antignac, C.6
Heidet, L.7
-
2
-
-
0035986783
-
Inherited thrombocytopenias: from genes to therapy
-
Balduini C.L., Iolascon A., and Savoia A. Inherited thrombocytopenias: from genes to therapy. Haematologica 87 (2002) 860-880
-
(2002)
Haematologica
, vol.87
, pp. 860-880
-
-
Balduini, C.L.1
Iolascon, A.2
Savoia, A.3
-
3
-
-
4744364577
-
Defects in cell adhesion and the visceral endoderm following ablation of nonmuscle myosin heavy chain II-A in mice
-
Conti M.A., Even-Ram S., Liu C., Yamada K.M., and Adelstein R.S. Defects in cell adhesion and the visceral endoderm following ablation of nonmuscle myosin heavy chain II-A in mice. J. Biol. Chem. 279 (2004) 41263-41266
-
(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
-
4
-
-
0037139605
-
Cloning of the murine non-muscle myosin heavy chain IIA gene ortholog of human MYH9 responsible for May-Hegglin, Sebastian, Fechtner, and Epstein syndromes
-
D'Apolito M., Guarnieri V., Boncristiano M., Zelante L., and Savoia A. Cloning of the murine non-muscle myosin heavy chain IIA gene ortholog of human MYH9 responsible for May-Hegglin, Sebastian, Fechtner, and Epstein syndromes. Gene 286 (2002) 215-222
-
(2002)
Gene
, vol.286
, pp. 215-222
-
-
D'Apolito, M.1
Guarnieri, V.2
Boncristiano, M.3
Zelante, L.4
Savoia, A.5
-
5
-
-
0037480960
-
Asp1424Asn MYH9 mutation results in an unstable protein responsible for the phenotypes in May-Hegglin anomaly/Fechtner syndrome
-
Deutsch S., Rideau A., Bochaton-Piallat M.L., Merla G., Geinoz A., Gabbiani G., Schwede T., Matthes T., Antonarakis S.E., and Beris P. Asp1424Asn MYH9 mutation results in an unstable protein responsible for the phenotypes in May-Hegglin anomaly/Fechtner syndrome. Blood 102 (2003) 529-534
-
(2003)
Blood
, vol.102
, pp. 529-534
-
-
Deutsch, S.1
Rideau, A.2
Bochaton-Piallat, M.L.3
Merla, G.4
Geinoz, A.5
Gabbiani, G.6
Schwede, T.7
Matthes, T.8
Antonarakis, S.E.9
Beris, P.10
-
6
-
-
0036738003
-
Defective expression of GPIb/IX/V complex in platelets from patients with May-Hegglin anomaly and Sebastian syndrome
-
Di Pumpo M., Noris P., Pecci A., Savoia A., Seri M., Ceresa I.F., and Balduini C.L. Defective expression of GPIb/IX/V complex in platelets from patients with May-Hegglin anomaly and Sebastian syndrome. Haematologica 87 (2002) 943-947
-
(2002)
Haematologica
, vol.87
, pp. 943-947
-
-
Di Pumpo, M.1
Noris, P.2
Pecci, A.3
Savoia, A.4
Seri, M.5
Ceresa, I.F.6
Balduini, C.L.7
-
7
-
-
24944506480
-
Genotype-phenotype correlation in MYH9-related thrombocytopenia
-
Dong F., Li S., Pujol-Moix N., Luban L.C., Shin S.W., Seo J.H., Ruiz-Saez A., Demeter J., Langdon S., and Kelley M.J. Genotype-phenotype correlation in MYH9-related thrombocytopenia. Br. J. Haematol. 130 (2005) 620-627
-
(2005)
Br. J. Haematol.
, vol.130
, pp. 620-627
-
-
Dong, F.1
Li, S.2
Pujol-Moix, N.3
Luban, L.C.4
Shin, S.W.5
Seo, J.H.6
Ruiz-Saez, A.7
Demeter, J.8
Langdon, S.9
Kelley, M.J.10
-
8
-
-
0037117491
-
Progressive photoreceptor degeneration, outer segment dysplasia, and rhodopsin mislocalization in mice with targeted disruption of the retinitis pigmentosa-1 (Rp1) gene
-
Gao J., Cheon K., Nusinowitz S., Liu Q., Bei D., Atkins K., Azimi A., Daiger S.P., Farber D.B., Heckenlively J.R., Pierce E.A., Sullivan L.S., and Zuo J. Progressive photoreceptor degeneration, outer segment dysplasia, and rhodopsin mislocalization in mice with targeted disruption of the retinitis pigmentosa-1 (Rp1) gene. Proc. Natl. Acad. Sci. U. S. A. 99 (2002) 5698-5703
-
(2002)
Proc. Natl. Acad. Sci. U. S. A.
, vol.99
, pp. 5698-5703
-
-
Gao, J.1
Cheon, K.2
Nusinowitz, S.3
Liu, Q.4
Bei, D.5
Atkins, K.6
Azimi, A.7
Daiger, S.P.8
Farber, D.B.9
Heckenlively, J.R.10
Pierce, E.A.11
Sullivan, L.S.12
Zuo, J.13
-
10
-
-
0037225967
-
Genetics, clinical and pathological features of glomerulonephritis associated with mutations of nonmuscle myosin IIA (Fechtner syndrome)
-
Ghiggeri G.M., Caridi G., Magrini U., Sessa A., Savoia A., Seri M., Pecci A., Romagnoli R., Gangarossa S., Noris P., Sartore S., Necchi V., Ravazzolo R., and Balduini C.L. Genetics, clinical and pathological features of glomerulonephritis associated with mutations of nonmuscle myosin IIA (Fechtner syndrome). Am. J. Kidney Dis. 41 (2003) 95-104
-
(2003)
Am. J. Kidney Dis.
, vol.41
, pp. 95-104
-
-
Ghiggeri, G.M.1
Caridi, G.2
Magrini, U.3
Sessa, A.4
Savoia, A.5
Seri, M.6
Pecci, A.7
Romagnoli, R.8
Gangarossa, S.9
Noris, P.10
Sartore, S.11
Necchi, V.12
Ravazzolo, R.13
Balduini, C.L.14
-
11
-
-
9144261091
-
Identification and characterization of nonmuscle myosin II-C, a new member of the myosin II family
-
Golomb E., Ma X., Jana S.S., Preston Y.A., Kawamoto S., Shoham N.G., Goldin E., Conti M.A., Sellers J.R., and Adelstein R.S. Identification and characterization of nonmuscle myosin II-C, a new member of the myosin II family. J. Biol. Chem. 279 (2004) 2800-2808
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 2800-2808
-
-
Golomb, E.1
Ma, X.2
Jana, S.S.3
Preston, Y.A.4
Kawamoto, S.5
Shoham, N.G.6
Goldin, E.7
Conti, M.A.8
Sellers, J.R.9
Adelstein, R.S.10
-
12
-
-
0034755959
-
Nonmuscle myosin heavy chain IIA mutations define a spectrum of autosomal dominant macrothrombocytopenias: May-Hegglin anomaly and Fechtner, Sebastian, Epstein, and Alport-like syndromes
-
Heath K.E., Campos-Barros A., Toren A., Rozenfeld-Granot G., Carlsson L.E., Savige J., Denison J.C., Gregory M.C., White J.G., Barker D.F., Greinacher A., Epstein C.J., Glucksman M.J., and Martignetti J.A. Nonmuscle myosin heavy chain IIA mutations define a spectrum of autosomal dominant macrothrombocytopenias: May-Hegglin anomaly and Fechtner, Sebastian, Epstein, and Alport-like syndromes. Am. J. Hum. Genet. 69 (2001) 1033-1045
-
(2001)
Am. J. Hum. Genet.
, vol.69
, pp. 1033-1045
-
-
Heath, K.E.1
Campos-Barros, A.2
Toren, A.3
Rozenfeld-Granot, G.4
Carlsson, L.E.5
Savige, J.6
Denison, J.C.7
Gregory, M.C.8
White, J.G.9
Barker, D.F.10
Greinacher, A.11
Epstein, C.J.12
Glucksman, M.J.13
Martignetti, J.A.14
-
13
-
-
0037195954
-
Mutations in human nonmuscle myosin IIA found in patients with May-Hegglin anomaly and Fechtner syndrome result in impaired enzymatic function
-
Hu A., Wang F., and Sellers J.R. Mutations in human nonmuscle myosin IIA found in patients with May-Hegglin anomaly and Fechtner syndrome result in impaired enzymatic function. J. Biol. Chem. 277 (2002) 46512-46517
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 46512-46517
-
-
Hu, A.1
Wang, F.2
Sellers, J.R.3
-
14
-
-
0033822065
-
Mutation of MYH9, encoding non-muscle myosin heavy chain A, in May-Hegglin anomaly
-
Kelley M.J., Jawien W., Ortel T.L., and Korczak J.F. Mutation of MYH9, encoding non-muscle myosin heavy chain A, in May-Hegglin anomaly. Nat. Genet. 26 (2000) 106-108
-
(2000)
Nat. Genet.
, vol.26
, pp. 106-108
-
-
Kelley, M.J.1
Jawien, W.2
Ortel, T.L.3
Korczak, J.F.4
-
15
-
-
29244474199
-
May-Hegglin anomaly-From genome research to clinical laboratory
-
Kunishima S. May-Hegglin anomaly-From genome research to clinical laboratory. Rinsho Byori 51 (2003) 898-904
-
(2003)
Rinsho Byori
, vol.51
, pp. 898-904
-
-
Kunishima, S.1
-
16
-
-
18244406592
-
Identification of six novel MYH9 mutations and genotype-phenotype relationships in autosomal dominant macrothrombocytopenia with leukocyte inclusions
-
Kunishima S., Matsushita T., Kojima T., Amemiya N., Choi Y.M., Hosaka N., Inoue M., Jung Y., Mamiya S., Matsumoto K., Miyajima Y., Zhang G., Ruan C., Saito K., Song K.S., Yoon H.J., Kamiya T., and Saito H. Identification of six novel MYH9 mutations and genotype-phenotype relationships in autosomal dominant macrothrombocytopenia with leukocyte inclusions. J. Hum. Genet. 46 (2001) 722-729
-
(2001)
J. Hum. Genet.
, vol.46
, pp. 722-729
-
-
Kunishima, S.1
Matsushita, T.2
Kojima, T.3
Amemiya, N.4
Choi, Y.M.5
Hosaka, 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
-
17
-
-
0037245023
-
Immunofluorescence analysis of neutrophil nonmuscle myosin heavy chain-A in MYH9 disorders: association of subcellular localization with MYH9 mutations
-
Kunishima S., Matsushita T., Kojima T., Sako M., Kimura F., Jo E.K., Inoue C., Kamiya T., and Saito H. Immunofluorescence analysis of neutrophil nonmuscle myosin heavy chain-A in MYH9 disorders: association of subcellular localization with MYH9 mutations. Lab. Invest. 83 (2003) 115-122
-
(2003)
Lab. Invest.
, vol.83
, pp. 115-122
-
-
Kunishima, S.1
Matsushita, T.2
Kojima, T.3
Sako, M.4
Kimura, F.5
Jo, E.K.6
Inoue, C.7
Kamiya, T.8
Saito, H.9
-
18
-
-
0030908919
-
A five-generation family with late-onset progressive hereditary hearing impairment due to cochleosaccular degeneration
-
Lalwani A.K., Linthicum F.H., Wilcox E.R., Moore J.K., Walters F.C., San Agustin T.B., Mislinski J., Miller M.R., Sinninger Y., Attaie A., and Luxford W.M. A five-generation family with late-onset progressive hereditary hearing impairment due to cochleosaccular degeneration. Audiol. Neuro-otol. 2 (1997) 139-154
-
(1997)
Audiol. Neuro-otol.
, vol.2
, pp. 139-154
-
-
Lalwani, A.K.1
Linthicum, F.H.2
Wilcox, E.R.3
Moore, J.K.4
Walters, F.C.5
San Agustin, T.B.6
Mislinski, J.7
Miller, M.R.8
Sinninger, Y.9
Attaie, A.10
Luxford, W.M.11
-
19
-
-
0033364309
-
A new locus for nonsyndromic hereditary hearing impairment, DFNA17, maps to chromosome 22 and represents a gene for cochleosaccular degeneration
-
Lalwani A.K., Luxford W.M., Mhatre A.N., Attaie A., Wilcox E.R., and Castelein C.M. A new locus for nonsyndromic hereditary hearing impairment, DFNA17, maps to chromosome 22 and represents a gene for cochleosaccular degeneration. Am. J. Hum. Genet. 64 (1999) 318-323
-
(1999)
Am. J. Hum. Genet.
, vol.64
, pp. 318-323
-
-
Lalwani, A.K.1
Luxford, W.M.2
Mhatre, A.N.3
Attaie, A.4
Wilcox, E.R.5
Castelein, C.M.6
-
20
-
-
0033764817
-
Human nonsyndromic hereditary deafness DFNA17 is due to a mutation in nonmuscle myosin MYH9
-
Lalwani A.K., Goldstein J.A., Kelley M.J., Luxford W., Castelein C.M., and Mhatre A.N. Human nonsyndromic hereditary deafness DFNA17 is due to a mutation in nonmuscle myosin MYH9. Am. J. Hum. Genet. 67 (2000) 1121-1128
-
(2000)
Am. J. Hum. Genet.
, vol.67
, pp. 1121-1128
-
-
Lalwani, A.K.1
Goldstein, J.A.2
Kelley, M.J.3
Luxford, W.4
Castelein, C.M.5
Mhatre, A.N.6
-
21
-
-
0141652952
-
A novel myosin heavy chain gene in human chromosome 19q13.3
-
Leal A., Endele S., Stengel C., Huehne K., Loetterle J., Barrantes R., Winterpacht A., and Rautenstrauss B. A novel myosin heavy chain gene in human chromosome 19q13.3. Gene 312 (2003) 165-171
-
(2003)
Gene
, vol.312
, pp. 165-171
-
-
Leal, A.1
Endele, S.2
Stengel, C.3
Huehne, K.4
Loetterle, J.5
Barrantes, R.6
Winterpacht, A.7
Rautenstrauss, B.8
-
22
-
-
0037136582
-
Prestin is required for electromotility of the outer hair cell and for the cochlear amplifier
-
Liberman M.C., Gao J., He D.Z., Wu X., Jia S., and Zuo J. Prestin is required for electromotility of the outer hair cell and for the cochlear amplifier. Nature 419 (2002) 300-304
-
(2002)
Nature
, vol.419
, pp. 300-304
-
-
Liberman, M.C.1
Gao, J.2
He, D.Z.3
Wu, X.4
Jia, S.5
Zuo, J.6
-
23
-
-
12444302838
-
Prestin, a cochlear motor protein, is defective in non-syndromic hearing loss
-
Liu X.Z., Ouyang X.M., Xia X.J., Zheng J., Pandya A., Li F., Du L.L., Welch K.O., Petit C., Smith R.J., Webb B.T., Yan D., Arnos K.S., Corey D., Dallos P., Nance W.E., and Chen Z.Y. Prestin, a cochlear motor protein, is defective in non-syndromic hearing loss. Hum. Mol. Genet. 12 (2003) 1155-1162
-
(2003)
Hum. Mol. Genet.
, vol.12
, pp. 1155-1162
-
-
Liu, X.Z.1
Ouyang, X.M.2
Xia, X.J.3
Zheng, J.4
Pandya, A.5
Li, F.6
Du, L.L.7
Welch, K.O.8
Petit, C.9
Smith, R.J.10
Webb, B.T.11
Yan, D.12
Arnos, K.S.13
Corey, D.14
Dallos, P.15
Nance, W.E.16
Chen, Z.Y.17
-
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 C.L., and Savoia A. Correlation between the clinical phenotype of MYH9-related disease and tissue distribution of class II nonmuscle myosin heavy chains. Genomics 83 (2004) 1125-1133
-
(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
-
-
8844261172
-
Targeted disruption of mouse ortholog of the human MYH9 responsible for macrothrombocytopenia with different organ involvement: hematological, nephrological, and otological studies of heterozygous KO mice
-
Matsushita T., Hayashi H., Kunishima S., Hayashi M., Ikejiri M., Takeshita K., Yuzawa Y., Adachi T., Hirashima K., Sone M., Yamamoto K., Takagi A., Katsumi A., Kawai K., Nezu T., Takahashi M., Nakashima T., Naoe T., Kojima T., and Saito H. Targeted disruption of mouse ortholog of the human MYH9 responsible for macrothrombocytopenia with different organ involvement: hematological, nephrological, and otological studies of heterozygous KO mice. Biochem. Biophys. Res. Commun. 325 (2004) 1163-1171
-
(2004)
Biochem. Biophys. Res. Commun.
, vol.325
, pp. 1163-1171
-
-
Matsushita, T.1
Hayashi, H.2
Kunishima, S.3
Hayashi, M.4
Ikejiri, M.5
Takeshita, K.6
Yuzawa, Y.7
Adachi, T.8
Hirashima, K.9
Sone, M.10
Yamamoto, K.11
Takagi, A.12
Katsumi, A.13
Kawai, K.14
Nezu, T.15
Takahashi, M.16
Nakashima, T.17
Naoe, T.18
Kojima, T.19
Saito, H.20
more..
-
26
-
-
0037341336
-
Macrothrombocytopenia and progressive deafness is due to a mutation in MYH9
-
Mhatre A.N., Kim Y., Brodie H.A., and Lalwani A.K. Macrothrombocytopenia and progressive deafness is due to a mutation in MYH9. Otol. Neurotol. 24 (2003) 205-209
-
(2003)
Otol. Neurotol.
, vol.24
, pp. 205-209
-
-
Mhatre, A.N.1
Kim, Y.2
Brodie, H.A.3
Lalwani, A.K.4
-
27
-
-
2342561122
-
Cloning and developmental expression of nonmuscle myosin IIA (Myh9) in the mammalian inner ear
-
Mhatre A.N., Li J., Kim Y., Coling D.E., and Lalwani A.K. Cloning and developmental expression of nonmuscle myosin IIA (Myh9) in the mammalian inner ear. J. Neurosci. Res. 76 (2004) 296-305
-
(2004)
J. Neurosci. Res.
, vol.76
, pp. 296-305
-
-
Mhatre, A.N.1
Li, J.2
Kim, Y.3
Coling, D.E.4
Lalwani, A.K.5
-
28
-
-
0036229482
-
Immunocytochemistry for the heavy chain of the non-muscle myosin IIA as a diagnostic tool for MYH9-related disorders
-
Pecci A., Noris P., Invernizzi R., Savoia A., Seri M., Ghiggeri G.M., Sartore S., Gangarossa S., Bizzaro N., and Balduini C.L. Immunocytochemistry for the heavy chain of the non-muscle myosin IIA as a diagnostic tool for MYH9-related disorders. Br. J. Haematol. 117 (2002) 164-167
-
(2002)
Br. J. Haematol.
, vol.117
, pp. 164-167
-
-
Pecci, A.1
Noris, P.2
Invernizzi, R.3
Savoia, A.4
Seri, M.5
Ghiggeri, G.M.6
Sartore, S.7
Gangarossa, S.8
Bizzaro, N.9
Balduini, C.L.10
-
29
-
-
2942709471
-
Ultrastructural analysis of granulocyte inclusions in genetically confirmed MYH9-related disorders
-
Pujol-Moix N., Kelley M.J., Hernandez A., Muniz-Diaz E., and Espanol I. Ultrastructural analysis of granulocyte inclusions in genetically confirmed MYH9-related disorders. Haematologica 89 (2004) 330-337
-
(2004)
Haematologica
, vol.89
, pp. 330-337
-
-
Pujol-Moix, N.1
Kelley, M.J.2
Hernandez, A.3
Muniz-Diaz, E.4
Espanol, I.5
-
30
-
-
0034677906
-
Myosins: a diverse superfamily
-
Sellers J.R. Myosins: a diverse superfamily. Biochim. Biophys. Acta 1496 (2000) 3-22
-
(2000)
Biochim. Biophys. Acta
, vol.1496
, pp. 3-22
-
-
Sellers, J.R.1
-
31
-
-
0033812573
-
Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes. The May-Heggllin/Fechtner Syndrome Consortium
-
Seri M., Cusano R., Gangarossa S., Caridi G., Bordo D., Lo Nigro C., Ghiggeri G.M., Ravazzolo R., Savino M., Del Vecchio M., d'Apolito M., Iolascon A., Zelante L.L., Savoia A., Balduini C.L., Noris P., Magrini U., Belletti S., Heath K.E., Babcock M., Glucksman M.J., Aliprandis E., Bizzaro N., Desnick R.J., and Martignetti J.A. Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes. The May-Heggllin/Fechtner Syndrome Consortium. Nat. Genet. 26 (2000) 103-105
-
(2000)
Nat. Genet.
, vol.26
, pp. 103-105
-
-
Seri, M.1
Cusano, R.2
Gangarossa, S.3
Caridi, G.4
Bordo, D.5
Lo Nigro, C.6
Ghiggeri, G.M.7
Ravazzolo, R.8
Savino, M.9
Del Vecchio, M.10
d'Apolito, M.11
Iolascon, A.12
Zelante, 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
Glucksman, M.J.21
Aliprandis, E.22
Bizzaro, N.23
Desnick, R.J.24
Martignetti, J.A.25
more..
-
32
-
-
0037910378
-
MYH9-related disease: May-Hegglin anomaly, Sebastian syndrome, 2003. 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., Koivisto P.A., Longo I., Musso R., Pecoraro C., Iolascon A., Magrini U., Rodriguez Soriano J., Renieri A., Ghiggeri G.M., Ravazzolo R., Balduini C.L., and Savoia A. MYH9-related disease: May-Hegglin anomaly, Sebastian syndrome, 2003. Fechtner syndrome, and Epstein syndrome are not distinct entities but represent a variable expression of a single illness. Medicine (Baltimore) 82 (2003) 203-215
-
(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
Koivisto, P.A.14
Longo, I.15
Musso, R.16
Pecoraro, C.17
Iolascon, A.18
Magrini, U.19
Rodriguez Soriano, J.20
Renieri, A.21
Ghiggeri, G.M.22
Ravazzolo, R.23
Balduini, C.L.24
Savoia, A.25
more..
-
33
-
-
0025739844
-
Human nonmuscle myosin heavy chains are encoded by two genes located on different chromosomes
-
Simons M., Wang M., McBride O.W., Kawamoto S., Yamakawa K., Gdula D., Adelstein R.S., and Weir L. Human nonmuscle myosin heavy chains are encoded by two genes located on different chromosomes. Circ. Res. 69 (1991) 530-539
-
(1991)
Circ. Res.
, vol.69
, pp. 530-539
-
-
Simons, M.1
Wang, M.2
McBride, O.W.3
Kawamoto, S.4
Yamakawa, K.5
Gdula, D.6
Adelstein, R.S.7
Weir, L.8
-
34
-
-
0037260993
-
BayGenomics: a resource of insertional mutations in mouse embryonic stem cells
-
Stryke D., Kawamoto M., Huang C.C., Johns S.J., King L.A., Harper C.A., Meng E.C., Lee R.E., Yee A., L'Italien L., Chuang P.T., Young S.G., Skarnes W.C., Babbitt P.C., and Ferrin T.E. BayGenomics: a resource of insertional mutations in mouse embryonic stem cells. Nucleic Acids Res. 31 (2003) 278-281
-
(2003)
Nucleic Acids Res.
, vol.31
, pp. 278-281
-
-
Stryke, D.1
Kawamoto, M.2
Huang, C.C.3
Johns, S.J.4
King, L.A.5
Harper, C.A.6
Meng, E.C.7
Lee, R.E.8
Yee, A.9
L'Italien, L.10
Chuang, P.T.11
Young, S.G.12
Skarnes, W.C.13
Babbitt, P.C.14
Ferrin, T.E.15
-
35
-
-
0032989251
-
Mutations in a novel retina-specific gene cause autosomal dominant retinitis pigmentosa
-
Sullivan L.S., Heckenlively J.R., Bowne S.J., Zuo J., Hide W.A., Gal A., Denton M., Inglehearn C.F., Blanton S.H., and Daiger S.P. Mutations in a novel retina-specific gene cause autosomal dominant retinitis pigmentosa. Nat. Genet. 22 (1999) 255-259
-
(1999)
Nat. Genet.
, vol.22
, pp. 255-259
-
-
Sullivan, L.S.1
Heckenlively, J.R.2
Bowne, S.J.3
Zuo, J.4
Hide, W.A.5
Gal, A.6
Denton, M.7
Inglehearn, C.F.8
Blanton, S.H.9
Daiger, S.P.10
-
36
-
-
10744226663
-
Wnk1 kinase deficiency lowers blood pressure in mice: a gene-trap screen to identify potential targets for therapeutic intervention
-
Zambrowicz B.P., Abuin A., Ramirez-Solis R., Richter L.J., Piggott J., BeltrandelRio H., Buxton E.C., Edwards J., Finch R.A., Friddle C.J., Gupta A., Hansen G., Hu Y., Huang W., Jaing C., Key Jr. B.W., Kipp P., Kohlhauff B., Ma Z.Q., Markesich D., Payne R., Potter D.G., Qian N., Shaw J., Schrick J., Shi Z.Z., Sparks M.J., Van Sligtenhorst I., Vogel P., Walke W., Xu N., Zhu Q., Person C., and Sands A.T. Wnk1 kinase deficiency lowers blood pressure in mice: a gene-trap screen to identify potential targets for therapeutic intervention. Proc. Natl. Acad. Sci. U. S. A. 100 (2003) 14109-14114
-
(2003)
Proc. Natl. Acad. Sci. U. S. A.
, vol.100
, pp. 14109-14114
-
-
Zambrowicz, B.P.1
Abuin, A.2
Ramirez-Solis, R.3
Richter, L.J.4
Piggott, J.5
BeltrandelRio, H.6
Buxton, E.C.7
Edwards, J.8
Finch, R.A.9
Friddle, C.J.10
Gupta, A.11
Hansen, G.12
Hu, Y.13
Huang, W.14
Jaing, C.15
Key Jr., B.W.16
Kipp, P.17
Kohlhauff, B.18
Ma, Z.Q.19
Markesich, D.20
Payne, R.21
Potter, D.G.22
Qian, N.23
Shaw, J.24
Schrick, J.25
Shi, Z.Z.26
Sparks, M.J.27
Van Sligtenhorst, I.28
Vogel, P.29
Walke, W.30
Xu, N.31
Zhu, Q.32
Person, C.33
Sands, A.T.34
more..
|