Figueroa KP - Search Results

1

An autosomal dominant ataxia maps to 19q13: Allelic heterogeneity of SCA13 or novel locus?

Waters MF, Fee D, Figueroa KP, Nolte D, Müller U, Advincula J, Coon H, Evidente VG, Pulst SM. Waters MF, et al. Among authors: figueroa kp. Neurology. 2005 Oct 11;65(7):1111-3. doi: 10.1212/01.wnl.0000177490.05162.41. Epub 2005 Aug 31. Neurology. 2005. PMID: 16135769

2

High frequency of nonsense mutations in the NF2 gene caused by C to T transitions in five CGA codons.

Sainz J, Figueroa K, Baser ME, Mautner VF, Pulst SM. Sainz J, et al. Hum Mol Genet. 1995 Jan;4(1):137-9. doi: 10.1093/hmg/4.1.137. Hum Mol Genet. 1995. PMID: 7711726 No abstract available.

3

Mutations of the neurofibromatosis type 2 gene and lack of the gene product in vestibular schwannomas.

Sainz J, Huynh DP, Figueroa K, Ragge NK, Baser ME, Pulst SM. Sainz J, et al. Hum Mol Genet. 1994 Jun;3(6):885-91. doi: 10.1093/hmg/3.6.885. Hum Mol Genet. 1994. PMID: 7951231

4

Identification of three neurofibromatosis type 2 (NF2) gene mutations in vestibular schwannomas.

Sainz J, Figueroa K, Baser ME, Pulst SM. Sainz J, et al. Hum Genet. 1996 Jan;97(1):121-3. doi: 10.1007/BF00218846. Hum Genet. 1996. PMID: 8557252

5

Identification of three new microsatellite markers in the spinocerebellar ataxia type 2 (SCA2) region and 1.2 Mb physical map.

Nechiporuk T, Nechiporuk A, Guan X, Frederick R, Figueroa K, Chumakov I, Korenberg JR, de Jong PJ, Pulst SM. Nechiporuk T, et al. Hum Genet. 1996 Apr;97(4):462-7. doi: 10.1007/BF02267067. Hum Genet. 1996. PMID: 8834243

6

A high-resolution PAC and BAC map of the SCA2 region.

Nechiporuk T, Nechiporuk A, Sahba S, Figueroa K, Shibata H, Chen XN, Korenberg JR, de Jong P, Pulst SM. Nechiporuk T, et al. Genomics. 1997 Sep 15;44(3):321-9. doi: 10.1006/geno.1997.4886. Genomics. 1997. PMID: 9325053

7

Spinocerebellar ataxia type 6. Frequency of the mutation and genotype-phenotype correlations.

Geschwind DH, Perlman S, Figueroa KP, Karrim J, Baloh RW, Pulst SM. Geschwind DH, et al. Among authors: figueroa kp. Neurology. 1997 Nov;49(5):1247-51. doi: 10.1212/wnl.49.5.1247. Neurology. 1997. PMID: 9371902

8

Genomic structure of the human gene for spinocerebellar ataxia type 2 (SCA2) on chromosome 12q24.1.

Sahba S, Nechiporuk A, Figueroa KP, Nechiporuk T, Pulst SM. Sahba S, et al. Among authors: figueroa kp. Genomics. 1998 Feb 1;47(3):359-64. doi: 10.1006/geno.1997.5131. Genomics. 1998. PMID: 9480749

9

The mouse SCA2 gene: cDNA sequence, alternative splicing and protein expression.

Nechiporuk T, Huynh DP, Figueroa K, Sahba S, Nechiporuk A, Pulst SM. Nechiporuk T, et al. Hum Mol Genet. 1998 Aug;7(8):1301-9. doi: 10.1093/hmg/7.8.1301. Hum Mol Genet. 1998. PMID: 9668173

10

Clinical and genetic analysis of a distinct autosomal dominant spinocerebellar ataxia.

Grewal RP, Tayag E, Figueroa KP, Zu L, Durazo A, Nunez C, Pulst SM. Grewal RP, et al. Among authors: figueroa kp. Neurology. 1998 Nov;51(5):1423-6. doi: 10.1212/wnl.51.5.1423. Neurology. 1998. PMID: 9818872

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

78 results

Search Page

Filters