Kusumi K - Search Results

1

The diastrophic dysplasia gene encodes a novel sulfate transporter: positional cloning by fine-structure linkage disequilibrium mapping.

Hästbacka J, de la Chapelle A, Mahtani MM, Clines G, Reeve-Daly MP, Daly M, Hamilton BA, Kusumi K, Trivedi B, Weaver A, et al. Hästbacka J, et al. Among authors: kusumi k. Cell. 1994 Sep 23;78(6):1073-87. doi: 10.1016/0092-8674(94)90281-x. Cell. 1994. PMID: 7923357

2

Genetic mapping of a gene causing hypertension in the stroke-prone spontaneously hypertensive rat.

Jacob HJ, Lindpaintner K, Lincoln SE, Kusumi K, Bunker RK, Mao YP, Ganten D, Dzau VJ, Lander ES. Jacob HJ, et al. Among authors: kusumi k. Cell. 1991 Oct 4;67(1):213-24. doi: 10.1016/0092-8674(91)90584-l. Cell. 1991. PMID: 1655275

3

Disruption of the nuclear hormone receptor RORalpha in staggerer mice.

Hamilton BA, Frankel WN, Kerrebrock AW, Hawkins TL, FitzHugh W, Kusumi K, Russell LB, Mueller KL, van Berkel V, Birren BW, Kruglyak L, Lander ES. Hamilton BA, et al. Among authors: kusumi k. Nature. 1996 Feb 22;379(6567):736-9. doi: 10.1038/379736a0. Nature. 1996. PMID: 8602221

4

The neuronal ceroid lipofuscinoses in human EPMR and mnd mutant mice are associated with mutations in CLN8.

Ranta S, Zhang Y, Ross B, Lonka L, Takkunen E, Messer A, Sharp J, Wheeler R, Kusumi K, Mole S, Liu W, Soares MB, Bonaldo MF, Hirvasniemi A, de la Chapelle A, Gilliam TC, Lehesjoki AE. Ranta S, et al. Among authors: kusumi k. Nat Genet. 1999 Oct;23(2):233-6. doi: 10.1038/13868. Nat Genet. 1999. PMID: 10508524

5

Construction of a large-insert yeast artificial chromosome library of the mouse genome.

Kusumi K, Smith JS, Segre JA, Koos DS, Lander ES. Kusumi K, et al. Mamm Genome. 1993;4(7):391-2. doi: 10.1007/BF00360591. Mamm Genome. 1993. PMID: 8358173 No abstract available.

6

The mouse pudgy mutation disrupts Delta homologue Dll3 and initiation of early somite boundaries.

Kusumi K, Sun ES, Kerrebrock AW, Bronson RT, Chi DC, Bulotsky MS, Spencer JB, Birren BW, Frankel WN, Lander ES. Kusumi K, et al. Nat Genet. 1998 Jul;19(3):274-8. doi: 10.1038/961. Nat Genet. 1998. PMID: 9662403

7

Human immunodeficiency virus type 1 envelope gene structure and diversity in vivo and after cocultivation in vitro.

Kusumi K, Conway B, Cunningham S, Berson A, Evans C, Iversen AK, Colvin D, Gallo MV, Coutre S, Shpaer EG, et al. Kusumi K, et al. J Virol. 1992 Feb;66(2):875-85. doi: 10.1128/JVI.66.2.875-885.1992. J Virol. 1992. PMID: 1731112 Free PMC article.

8

Direct isolation of polymorphic markers linked to a trait by genetically directed representational difference analysis.

Lisitsyn NA, Segre JA, Kusumi K, Lisitsyn NM, Nadeau JH, Frankel WN, Wigler MH, Lander ES. Lisitsyn NA, et al. Among authors: kusumi k. Nat Genet. 1994 Jan;6(1):57-63. doi: 10.1038/ng0194-57. Nat Genet. 1994. PMID: 8136836

9

Mutations in the human delta homologue, DLL3, cause axial skeletal defects in spondylocostal dysostosis.

Bulman MP, Kusumi K, Frayling TM, McKeown C, Garrett C, Lander ES, Krumlauf R, Hattersley AT, Ellard S, Turnpenny PD. Bulman MP, et al. Among authors: kusumi k. Nat Genet. 2000 Apr;24(4):438-41. doi: 10.1038/74307. Nat Genet. 2000. PMID: 10742114

10

Ducky mouse phenotype of epilepsy and ataxia is associated with mutations in the Cacna2d2 gene and decreased calcium channel current in cerebellar Purkinje cells.

Barclay J, Balaguero N, Mione M, Ackerman SL, Letts VA, Brodbeck J, Canti C, Meir A, Page KM, Kusumi K, Perez-Reyes E, Lander ES, Frankel WN, Gardiner RM, Dolphin AC, Rees M. Barclay J, et al. Among authors: kusumi k. J Neurosci. 2001 Aug 15;21(16):6095-104. doi: 10.1523/JNEUROSCI.21-16-06095.2001. J Neurosci. 2001. PMID: 11487633 Free PMC article.

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