Hoffman SM - Search Results

1

Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4.

Ophoff RA, Terwindt GM, Vergouwe MN, van Eijk R, Oefner PJ, Hoffman SM, Lamerdin JE, Mohrenweiser HW, Bulman DE, Ferrari M, Haan J, Lindhout D, van Ommen GJ, Hofker MH, Ferrari MD, Frants RR. Ophoff RA, et al. Among authors: hoffman sm. Cell. 1996 Nov 1;87(3):543-52. doi: 10.1016/s0092-8674(00)81373-2. Cell. 1996. PMID: 8898206 Free article.

2

Organization and evolution of the cytochrome P450 CYP2A-2B-2F subfamily gene cluster on human chromosome 19.

Hoffman SM, Fernandez-Salguero P, Gonzalez FJ, Mohrenweiser HW. Hoffman SM, et al. J Mol Evol. 1995 Dec;41(6):894-900. doi: 10.1007/BF00173169. J Mol Evol. 1995. PMID: 8587134

3

The location of MZF-1 at the telomere of human chromosome 19q makes it vulnerable to degeneration in aging cells.

Hoffman SM, Hromas R, Amemiya C, Mohrenweiser HW. Hoffman SM, et al. Leuk Res. 1996 Mar;20(3):281-3. doi: 10.1016/0145-2126(95)00158-1. Leuk Res. 1996. PMID: 8637224 Free article.

4

Complex beta-satellite repeat structures and the expansion of the zinc finger gene cluster in 19p12.

Eichler EE, Hoffman SM, Adamson AA, Gordon LA, McCready P, Lamerdin JE, Mohrenweiser HW. Eichler EE, et al. Among authors: hoffman sm. Genome Res. 1998 Aug;8(8):791-808. doi: 10.1101/gr.8.8.791. Genome Res. 1998. PMID: 9724325 Free article.

5

Organization of the multiple polymorphic sites of the D19S11 locus within a 650-kb cosmid contig.

Tynan K, Hoffman SM, Tsujimoto S, Brandriff B, Gordon L, Carrano AV, Mohrenweiser HW. Tynan K, et al. Among authors: hoffman sm. Genomics. 1993 Aug;17(2):316-23. doi: 10.1006/geno.1993.1327. Genomics. 1993. PMID: 8406482

6

JAK3 maps to human chromosome 19p12 within a cluster of proto-oncogenes and transcription factors.

Hoffman SM, Lai KS, Tomfohrde J, Bowcock A, Gordon LA, Mohrenweiser HW. Hoffman SM, et al. Genomics. 1997 Jul 1;43(1):109-11. doi: 10.1006/geno.1997.4792. Genomics. 1997. PMID: 9226382 No abstract available.

7

Pseudoachondroplasia and multiple epiphyseal dysplasia due to mutations in the cartilage oligomeric matrix protein gene.

Briggs MD, Hoffman SM, King LM, Olsen AS, Mohrenweiser H, Leroy JG, Mortier GR, Rimoin DL, Lachman RS, Gaines ES, et al. Briggs MD, et al. Among authors: hoffman sm. Nat Genet. 1995 Jul;10(3):330-6. doi: 10.1038/ng0795-330. Nat Genet. 1995. PMID: 7670472

8

A genetic polymorphism in coumarin 7-hydroxylation: sequence of the human CYP2A genes and identification of variant CYP2A6 alleles.

Fernandez-Salguero P, Hoffman SM, Cholerton S, Mohrenweiser H, Raunio H, Rautio A, Pelkonen O, Huang JD, Evans WE, Idle JR, et al. Fernandez-Salguero P, et al. Among authors: hoffman sm. Am J Hum Genet. 1995 Sep;57(3):651-60. Am J Hum Genet. 1995. PMID: 7668294 Free PMC article.

9

High-resolution genetic and physical mapping of multiple epiphyseal dysplasia and pseudoachondroplasia mutations at chromosome 19p13.1-p12.

Knowlton RG, Cekleniak JA, Cohn DH, Briggs MD, Hoffman SM, Brandriff BF, Olsen AS. Knowlton RG, et al. Among authors: hoffman sm. Genomics. 1995 Aug 10;28(3):513-9. doi: 10.1006/geno.1995.1183. Genomics. 1995. PMID: 7490089

10

Locations of human and mouse genes encoding the RFX1 and RFX2 transcription factor proteins.

Doyle J, Hoffman S, Ucla C, Reith W, Mach B, Stubbs L. Doyle J, et al. Genomics. 1996 Jul 1;35(1):227-30. doi: 10.1006/geno.1996.0343. Genomics. 1996. PMID: 8661125

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