Nouri N - Search Results

1

Single-nucleotide polymorphism genotyping using microarrays.

Patil N, Nouri N, McAllister L, Matsukaki H, Ryder T. Patil N, et al. Among authors: nouri n. Curr Protoc Hum Genet. 2001 May;Chapter 2:Unit 2.9. doi: 10.1002/0471142905.hg0209s27. Curr Protoc Hum Genet. 2001. PMID: 18428273

2

Dinucleotide repeat polymorphism at the hormone sensitive lipase (LIPE) locus.

Levitt RC, Jedlicka AE, Nouri N. Levitt RC, et al. Among authors: nouri n. Hum Mol Genet. 1992 May;1(2):139. doi: 10.1093/hmg/1.2.139. Hum Mol Genet. 1992. PMID: 1301154 No abstract available.

3

Mapping of the gene for hormone sensitive lipase (LIPE) to chromosome 19q13.1-->q13.2.

Levitt RC, Liu Z, Nouri N, Meyers DA, Brandriff B, Mohrenweiser HM. Levitt RC, et al. Among authors: nouri n. Cytogenet Cell Genet. 1995;69(3-4):211-4. doi: 10.1159/000133966. Cytogenet Cell Genet. 1995. PMID: 7698015

4

Evidence for genetic heterogeneity in malignant hyperthermia susceptibility.

Levitt RC, Nouri N, Jedlicka AE, McKusick VA, Marks AR, Shutack JG, Fletcher JE, Rosenberg H, Meyers DA. Levitt RC, et al. Among authors: nouri n. Genomics. 1991 Nov;11(3):543-7. doi: 10.1016/0888-7543(91)90061-i. Genomics. 1991. PMID: 1774061 Free article.

5

Linkage mapping of the human thromboxane A2 receptor (TBXA2R) to chromosome 19p13.3 using transcribed 3' untranslated DNA sequence polymorphisms.

Schwengel DA, Nouri N, Meyers DA, Levitt RC. Schwengel DA, et al. Among authors: nouri n. Genomics. 1993 Nov;18(2):212-5. doi: 10.1006/geno.1993.1457. Genomics. 1993. PMID: 8288221

6

Genome-wide association study and mouse model identify interaction between RET and EDNRB pathways in Hirschsprung disease.

Carrasquillo MM, McCallion AS, Puffenberger EG, Kashuk CS, Nouri N, Chakravarti A. Carrasquillo MM, et al. Among authors: nouri n. Nat Genet. 2002 Oct;32(2):237-44. doi: 10.1038/ng998. Epub 2002 Sep 23. Nat Genet. 2002. PMID: 12355085

7

Analysis of CAG repeat of the Machado-Joseph gene in human, chimpanzee and monkey populations: a variant nucleotide is associated with the number of CAG repeats.

Limprasert P, Nouri N, Heyman RA, Nopparatana C, Kamonsilp M, Deininger PL, Keats BJ. Limprasert P, et al. Among authors: nouri n. Hum Mol Genet. 1996 Feb;5(2):207-13. doi: 10.1093/hmg/5.2.207. Hum Mol Genet. 1996. PMID: 8824876

8

Tightly linked flanking microsatellite markers for the Usher syndrome type I locus on the short arm of chromosome 11.

Keats BJ, Nouri N, Pelias MZ, Deininger PL, Litt M. Keats BJ, et al. Among authors: nouri n. Am J Hum Genet. 1994 Apr;54(4):681-6. Am J Hum Genet. 1994. PMID: 8128966 Free PMC article.

9

A locus for axonal motor-sensory neuropathy with deafness and mental retardation maps to Xq24-q26.

Priest JM, Fischbeck KH, Nouri N, Keats BJ. Priest JM, et al. Among authors: nouri n. Genomics. 1995 Sep 20;29(2):409-12. doi: 10.1006/geno.1995.9987. Genomics. 1995. PMID: 8666389 Free article.

10

A gene for Crouzon craniofacial dysostosis maps to the long arm of chromosome 10.

Preston RA, Post JC, Keats BJ, Aston CE, Ferrell RE, Priest J, Nouri N, Losken HW, Morris CA, Hurtt MR, et al. Preston RA, et al. Among authors: nouri n. Nat Genet. 1994 Jun;7(2):149-53. doi: 10.1038/ng0694-149. Nat Genet. 1994. PMID: 7920632

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