Forsman K - Search Results

1

Fine mapping of Best's macular dystrophy localizes the gene in close proximity to but distinct from the D11S480/ROM1 loci.

Graff C, Forsman K, Larsson C, Nordström S, Lind L, Johansson K, Sandgren O, Weissenbach J, Holmgren G, Gustavson KH, et al. Graff C, et al. Among authors: forsman k. Genomics. 1994 Dec;24(3):425-34. doi: 10.1006/geno.1994.1648. Genomics. 1994. PMID: 7713492

2

The gene for Best's macular dystrophy is located at 11q13 in a Swedish family.

Forsman K, Graff C, Nordström S, Johansson K, Westermark E, Lundgren E, Gustavson KH, Wadelius C, Holmgren G. Forsman K, et al. Clin Genet. 1992 Sep;42(3):156-9. doi: 10.1111/j.1399-0004.1992.tb03229.x. Clin Genet. 1992. PMID: 1395087

3

A gene for autosomal dominant progressive cone dystrophy (CORD5) maps to chromosome 17p12-p13.

Balciuniene J, Johansson K, Sandgren O, Wachtmeister L, Holmgren G, Forsman K. Balciuniene J, et al. Among authors: forsman k. Genomics. 1995 Nov 20;30(2):281-6. doi: 10.1006/geno.1995.9876. Genomics. 1995. PMID: 8586428

4

Mapping of the locus for autosomal dominant amelogenesis imperfecta (AIH2) to a 4-Mb YAC contig on chromosome 4q11-q21.

Kärrman C, Bäckman B, Dixon M, Holmgren G, Forsman K. Kärrman C, et al. Among authors: forsman k. Genomics. 1997 Jan 15;39(2):164-70. doi: 10.1006/geno.1996.4485. Genomics. 1997. PMID: 9027503

5

Refined genetic localization of the Best disease gene in 11q13 and physical mapping of linked markers on radiation hybrids.

Graff C, Eriksson A, Forsman K, Sandgren O, Holmgren G, Wadelius C. Graff C, et al. Among authors: forsman k. Hum Genet. 1997 Dec;101(3):263-70. doi: 10.1007/s004390050627. Hum Genet. 1997. PMID: 9439653

6

Localization of a gene for autosomal dominant amelogenesis imperfecta (ADAI) to chromosome 4q.

Forsman K, Lind L, Bäckman B, Westermark E, Holmgren G. Forsman K, et al. Hum Mol Genet. 1994 Sep;3(9):1621-5. doi: 10.1093/hmg/3.9.1621. Hum Mol Genet. 1994. PMID: 7833920

7

Identification of the gene responsible for Best macular dystrophy.

Petrukhin K, Koisti MJ, Bakall B, Li W, Xie G, Marknell T, Sandgren O, Forsman K, Holmgren G, Andreasson S, Vujic M, Bergen AA, McGarty-Dugan V, Figueroa D, Austin CP, Metzker ML, Caskey CT, Wadelius C. Petrukhin K, et al. Among authors: forsman k. Nat Genet. 1998 Jul;19(3):241-7. doi: 10.1038/915. Nat Genet. 1998. PMID: 9662395

8

Genetic heterogeneity of autosomal dominant amelogenesis imperfecta demonstrated by its exclusion from the AIH2 region on human chromosome 4Q.

Kärrman C, Bäckman B, Holmgren G, Forsman K. Kärrman C, et al. Among authors: forsman k. Arch Oral Biol. 1996 Aug-Sep;41(8-9):893-900. doi: 10.1016/s0003-9969(96)00010-6. Arch Oral Biol. 1996. PMID: 9022927

9

Ameloblastin gene (AMBN) maps within the critical region for autosomal dominant amelogenesis imperfecta at chromosome 4q21.

MacDougall M, DuPont BR, Simmons D, Reus B, Krebsbach P, Kärrman C, Holmgren G, Leach RJ, Forsman K. MacDougall M, et al. Among authors: forsman k. Genomics. 1997 Apr 1;41(1):115-8. doi: 10.1006/geno.1997.4643. Genomics. 1997. PMID: 9126491

10

Disease-causing mutations in the cellular retinaldehyde binding protein tighten and abolish ligand interactions.

Golovleva I, Bhattacharya S, Wu Z, Shaw N, Yang Y, Andrabi K, West KA, Burstedt MS, Forsman K, Holmgren G, Sandgren O, Noy N, Qin J, Crabb JW. Golovleva I, et al. Among authors: forsman k. J Biol Chem. 2003 Apr 4;278(14):12397-402. doi: 10.1074/jbc.M207300200. Epub 2003 Jan 20. J Biol Chem. 2003. PMID: 12536144 Free article.

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