-
1
-
-
0029563253
-
The Rab protein family: Genetic mapping of six Rab genes in the mouse
-
1. Barbosa, M. D. F. S., Johnson, S. A., Achey, K., Gutierrez, M. J., Wakeland, E. K., Zerial, M., and Kingsmore, S. F. (1995). The Rab protein family: Genetic mapping of six Rab genes in the mouse. Genomics 30: 439-444.
-
(1995)
Genomics
, vol.30
, pp. 439-444
-
-
Barbosa, M.D.F.S.1
Johnson, S.A.2
Achey, K.3
Gutierrez, M.J.4
Wakeland, E.K.5
Zerial, M.6
Kingsmore, S.F.7
-
2
-
-
0030074255
-
Genetic mapping of the Rab5a and Rab5b genes on mouse chromosomes 17 and 2, respectively
-
2. Barbosa, M. D. F. S., Wakeland, E. K., Zerial, M., and Kingsmore, S. F. (1995). Genetic mapping of the Rab5a and Rab5b genes on mouse chromosomes 17 and 2, respectively. Mamm. Genome 7: 166-167.
-
(1995)
Mamm. Genome
, vol.7
, pp. 166-167
-
-
Barbosa, M.D.F.S.1
Wakeland, E.K.2
Zerial, M.3
Kingsmore, S.F.4
-
3
-
-
15844397403
-
Identification of the homologous beige and Chediak-Higashi syndrome genes
-
3. Barbosa, M. D., Nguyen, Q. A., Tchernev, V. T., Ashley, J. A., Detter, J. C., Blaydes, S. M., Brandt, S. J., Chotai, D., Hodgman, C., Solari, R. C., Lovett, M., and Kingsmore, S. F. (1996). Identification of the homologous beige and Chediak-Higashi syndrome genes. Nature 382: 262-265.
-
(1996)
Nature
, vol.382
, pp. 262-265
-
-
Barbosa, M.D.1
Nguyen, Q.A.2
Tchernev, V.T.3
Ashley, J.A.4
Detter, J.C.5
Blaydes, S.M.6
Brandt, S.J.7
Chotai, D.8
Hodgman, C.9
Solari, R.C.10
Lovett, M.11
Kingsmore, S.F.12
-
4
-
-
0027288548
-
Human erythrocyte membrane protein band 4.2 (pallidin)
-
4. Cohen, C. M., Dotimas, E., and Korsgren, C. (1993). Human erythrocyte membrane protein band 4.2 (pallidin). Semin. Hematol. 30: 119-137.
-
(1993)
Semin. Hematol.
, vol.30
, pp. 119-137
-
-
Cohen, C.M.1
Dotimas, E.2
Korsgren, C.3
-
5
-
-
0027355255
-
Molecular markers that define the distal ends of mouse autosomes 4,13, 19, and the sex chromosomes
-
5. Eicher, E. M., and Shown, E. P. (1993). Molecular markers that define the distal ends of mouse autosomes 4,13, 19, and the sex chromosomes. Mamm. Genome 4: 226-229.
-
(1993)
Mamm. Genome
, vol.4
, pp. 226-229
-
-
Eicher, E.M.1
Shown, E.P.2
-
6
-
-
85030296604
-
Human erythrocyte membrane protein 4.2 (pallidin) in non-erythroid cells: Localization in human platelets
-
6. Hamilton, C. M., and Cohen, C. M. (1995). Human erythrocyte membrane protein 4.2 (pallidin) in non-erythroid cells: Localization in human platelets. Mol. Cell. Biol. 6: 338a.
-
(1995)
Mol. Cell. Biol.
, vol.6
-
-
Hamilton, C.M.1
Cohen, C.M.2
-
7
-
-
0028794760
-
A deletional frameshift mutation in protein 4.2 gene (Allele 4.2 Lisboa) associated with hereditary hemolytic anemia
-
7. Hayette, S., Dhermy, D., dos Santos, M.-E., Bozon, M., Drenckhahn, D., Alloisio, N., Texier, P., Delaunay, J., and Morle, L. (1995). A deletional frameshift mutation in protein 4.2 gene (Allele 4.2 Lisboa) associated with hereditary hemolytic anemia. Blood 85: 250-256.
-
(1995)
Blood
, vol.85
, pp. 250-256
-
-
Hayette, S.1
Dhermy, D.2
Dos Santos, M.-E.3
Bozon, M.4
Drenckhahn, D.5
Alloisio, N.6
Texier, P.7
Delaunay, J.8
Morle, L.9
-
8
-
-
0028286547
-
cDNA sequence, gene sequence, and properties of murine pallidin (band 4.2), the protein implicated in the murine pallid mutation
-
8. Korsgren, C., and Cohen, C. M. (1994). cDNA sequence, gene sequence, and properties of murine pallidin (band 4.2), the protein implicated in the murine pallid mutation. Genomics 21: 478-485.
-
(1994)
Genomics
, vol.21
, pp. 478-485
-
-
Korsgren, C.1
Cohen, C.M.2
-
9
-
-
0014949207
-
Cleavage of structural proteins during the assembly of the head of bacteriophage T4
-
9. Laemmli, U. K. (1970). Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227: 680-685.
-
(1970)
Nature
, vol.227
, pp. 680-685
-
-
Laemmli, U.K.1
-
10
-
-
0029047129
-
Ank3 (epithelial ankyrin), a widely distributed new member of the ankyrin gene family and the major ankyrin in kidney, is expressed in alternatively spliced forms, including forms that lack the repeat domain
-
10. Peters, L. L., John, K. M., Lu, F. M., Eicher, E. M., Higgins, A., Yialamas, M., Turtzo, L. C., Otsuka, A. J., and Lux, S. E. (1995). Ank3 (epithelial ankyrin), a widely distributed new member of the ankyrin gene family and the major ankyrin in kidney, is expressed in alternatively spliced forms, including forms that lack the repeat domain. J. Cell Biol. 130: 313-330.
-
(1995)
J. Cell Biol.
, vol.130
, pp. 313-330
-
-
Peters, L.L.1
John, K.M.2
Lu, F.M.3
Eicher, E.M.4
Higgins, A.5
Yialamas, M.6
Turtzo, L.C.7
Otsuka, A.J.8
Lux, S.E.9
-
11
-
-
0011130389
-
Melanocytes cultured from pallid mice are less melanized than c57 melanocytes and demonstrate differences in pallidin (band 4.2) localization
-
11. Risinger, M. A., Derick, L. H., and Cohen, C. M. (1994). Melanocytes cultured from pallid mice are less melanized than c57 melanocytes and demonstrate differences in pallidin (band 4.2) localization. Mol. Biol. Cell. 5: 366a.
-
(1994)
Mol. Biol. Cell.
, vol.5
-
-
Risinger, M.A.1
Derick, L.H.2
Cohen, C.M.3
-
12
-
-
0000484985
-
A new mutation in the house mouse (M. Musculus)
-
12. Roberts, E. (1931) A new mutation in the house mouse (M. musculus). Science 74: 569.
-
(1931)
Science
, vol.74
, pp. 569
-
-
Roberts, E.1
-
13
-
-
0017681196
-
DNA sequencing with chain terminating inhibitors
-
13. Sanger, F., Nicklen, S., and Coulson, A. R. (1977). DNA sequencing with chain terminating inhibitors. Proc. Natl. Acad. Sci. USA 74: 5463-5467.
-
(1977)
Proc. Natl. Acad. Sci. USA
, vol.74
, pp. 5463-5467
-
-
Sanger, F.1
Nicklen, S.2
Coulson, A.R.3
-
14
-
-
0025993470
-
Platelet storage pool deficiency associated with inherited abnormalities of the inner ear in the mouse pigment mutants muted and mocha
-
14. Swank, R., Reddington, M., Howlett, O., and Novak, E. (1991). Platelet storage pool deficiency associated with inherited abnormalities of the inner ear in the mouse pigment mutants muted and mocha. Blood 78: 2036-2044.
-
(1991)
Blood
, vol.78
, pp. 2036-2044
-
-
Swank, R.1
Reddington, M.2
Howlett, O.3
Novak, E.4
-
15
-
-
0021200816
-
Genes for serum amyloid a proteins map to chromosome 7 in the mouse
-
15. Taylor, B. A., and Rowe, L. B. (1984). Genes for serum amyloid A proteins map to chromosome 7 in the mouse. Mol. Gen. Genet. 195: 491-499.
-
(1984)
Mol. Gen. Genet.
, vol.195
, pp. 491-499
-
-
Taylor, B.A.1
Rowe, L.B.2
-
16
-
-
0026922667
-
The murine pallid mutation is a platelet storage pool disease associated with the protein 4.2 (pallidin) gene
-
16. White, R., Peters, L., Adkinson, L., Korsgren, C., Cohen, C., and Lux, S. (1992). The murine pallid mutation is a platelet storage pool disease associated with the protein 4.2 (pallidin) gene. Nature Genet. 2: 80-83.
-
(1992)
Nature Genet.
, vol.2
, pp. 80-83
-
-
White, R.1
Peters, L.2
Adkinson, L.3
Korsgren, C.4
Cohen, C.5
Lux, S.6
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