Ikeda J - Search Results

1

Towards the finer mapping of facioscapulohumeral muscular dystrophy at 4q35: construction of a laser microdissection library.

Upadhyaya M, Osborn M, Maynard J, Altherr M, Ikeda J, Harper PS. Upadhyaya M, et al. Among authors: ikeda j. Am J Med Genet. 1995 Jun 19;60(3):244-51. doi: 10.1002/ajmg.1320600315. Am J Med Genet. 1995. PMID: 7573180

2

FISH detection of chromosome polymorphism and deletions in the spinal muscular atrophy (SMA) region of 5q13.

Rajcan-Separovic E, Mahadevan MS, Lefebvre C, Besner-Johnston A, Ikeda JE, Korneluk RG, MacKenzie A. Rajcan-Separovic E, et al. Among authors: ikeda je. Cytogenet Cell Genet. 1996;75(4):243-7. doi: 10.1159/000134493. Cytogenet Cell Genet. 1996. PMID: 9067434

3

Exclusion mapping of the hereditary dentatorubropallidoluysian atrophy gene from the Huntington's disease locus.

Kondo I, Ohta H, Yazaki M, Ikeda JE, Gusella JF, Kanazawa I. Kondo I, et al. Among authors: ikeda je. J Med Genet. 1990 Feb;27(2):105-8. doi: 10.1136/jmg.27.2.105. J Med Genet. 1990. PMID: 1969487 Free PMC article.

4

Identification of the origin of double minutes in normal human cells by laser-based chromosome microdissection approach.

Rajcan-Separovic E, Wang HS, Speevak MD, Janes L, Korneluk RG, Wakasa K, Ikeda JE. Rajcan-Separovic E, et al. Among authors: ikeda je. Hum Genet. 1995 Jul;96(1):39-43. doi: 10.1007/BF00214184. Hum Genet. 1995. PMID: 7607652

5

A recombination event occurring within two complex 5q13.1 microsatellite repeat polymorphisms suggests a telomeric mapping of spinal muscular atrophy.

Yaraghi Z, McLean MD, Roy N, Surh L, Ikeda JE, Korneluk RG, MacKenzie A. Yaraghi Z, et al. Among authors: ikeda je. Hum Genet. 1995 Sep;96(3):330-4. doi: 10.1007/BF00210417. Hum Genet. 1995. PMID: 7649551

6

Two 5q13 simple tandem repeat loci are in linkage disequilibrium with type 1 spinal muscular atrophy.

McLean MD, Roy N, MacKenzie AE, Salih M, Burghes AH, Simard L, Korneluk RG, Ikeda JE, Surh L. McLean MD, et al. Among authors: ikeda je. Hum Mol Genet. 1994 Nov;3(11):1951-6. doi: 10.1093/hmg/3.11.1951. Hum Mol Genet. 1994. PMID: 7874111

7

[Laser chromosome microdissection and cloning of the genetic disease loci].

Hadano S, Ikeda JE. Hadano S, et al. Among authors: ikeda je. Nihon Rinsho. 1993 Sep;51(9):2240-5. Nihon Rinsho. 1993. PMID: 8411696 Review. Japanese.

8

Laser microdissection and single unique primer PCR allow generation of regional chromosome DNA clones from a single human chromosome.

Hadano S, Watanabe M, Yokoi H, Kogi M, Kondo I, Tsuchiya H, Kanazawa I, Wakasa K, Ikeda JE. Hadano S, et al. Among authors: ikeda je. Genomics. 1991 Oct;11(2):364-73. doi: 10.1016/0888-7543(91)90144-4. Genomics. 1991. PMID: 1769652

9

Laser microdissection of the fragile X region: identification of cosmid clones and of conserved sequences in this region.

Djabali M, Nguyen C, Biunno I, Oostra BA, Mattei MG, Ikeda JE, Jordan BR. Djabali M, et al. Among authors: ikeda je. Genomics. 1991 Aug;10(4):1053-60. doi: 10.1016/0888-7543(91)90198-n. Genomics. 1991. PMID: 1916812

10

A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2.

Hadano S, Hand CK, Osuga H, Yanagisawa Y, Otomo A, Devon RS, Miyamoto N, Showguchi-Miyata J, Okada Y, Singaraja R, Figlewicz DA, Kwiatkowski T, Hosler BA, Sagie T, Skaug J, Nasir J, Brown RH Jr, Scherer SW, Rouleau GA, Hayden MR, Ikeda JE. Hadano S, et al. Among authors: ikeda je. Nat Genet. 2001 Oct;29(2):166-73. doi: 10.1038/ng1001-166. Nat Genet. 2001. PMID: 11586298

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