Carlsson P - Search Results

1

Mutations of the forkhead/winged-helix gene, FKHL7, in patients with Axenfeld-Rieger anomaly.

Mears AJ, Jordan T, Mirzayans F, Dubois S, Kume T, Parlee M, Ritch R, Koop B, Kuo WL, Collins C, Marshall J, Gould DB, Pearce W, Carlsson P, Enerbäck S, Morissette J, Bhattacharya S, Hogan B, Raymond V, Walter MA. Mears AJ, et al. Among authors: carlsson p. Am J Hum Genet. 1998 Nov;63(5):1316-28. doi: 10.1086/302109. Am J Hum Genet. 1998. PMID: 9792859 Free PMC article.

2

Fox's in development and disease.

Lehmann OJ, Sowden JC, Carlsson P, Jordan T, Bhattacharya SS. Lehmann OJ, et al. Among authors: carlsson p. Trends Genet. 2003 Jun;19(6):339-44. doi: 10.1016/S0168-9525(03)00111-2. Trends Genet. 2003. PMID: 12801727 Review.

3

Novel anterior segment phenotypes resulting from forkhead gene alterations: evidence for cross-species conservation of function.

Lehmann OJ, Tuft S, Brice G, Smith R, Blixt A, Bell R, Johansson B, Jordan T, Hitchings RA, Khaw PT, John SW, Carlsson P, Bhattacharya SS. Lehmann OJ, et al. Among authors: carlsson p. Invest Ophthalmol Vis Sci. 2003 Jun;44(6):2627-33. doi: 10.1167/iovs.02-0609. Invest Ophthalmol Vis Sci. 2003. PMID: 12766066

4

The winged helix transcription factor Fkh10 is required for normal development of the inner ear.

Hulander M, Wurst W, Carlsson P, Enerbäck S. Hulander M, et al. Among authors: carlsson p. Nat Genet. 1998 Dec;20(4):374-6. doi: 10.1038/3850. Nat Genet. 1998. PMID: 9843211

5

The kidney-expressed winged helix transcription factor FREAC-4 is regulated by Ets-1. A possible role in kidney development.

Cederberg A, Hulander M, Carlsson P, Enerbäck S. Cederberg A, et al. Among authors: carlsson p. J Biol Chem. 1999 Jan 1;274(1):165-9. doi: 10.1074/jbc.274.1.165. J Biol Chem. 1999. PMID: 9867825 Free article.

6

Chromosomal localization of six human forkhead genes, freac-1 (FKHL5), -3 (FKHL7), -4 (FKHL8), -5 (FKHL9), -6 (FKHL10), and -8 (FKHL12).

Larsson C, Hellqvist M, Pierrou S, White I, Enerbäck S, Carlsson P. Larsson C, et al. Among authors: carlsson p. Genomics. 1995 Dec 10;30(3):464-9. doi: 10.1006/geno.1995.1266. Genomics. 1995. PMID: 8825632

7

Haploinsufficiency of the forkhead gene Foxf1, a target for sonic hedgehog signaling, causes lung and foregut malformations.

Mahlapuu M, Enerbäck S, Carlsson P. Mahlapuu M, et al. Among authors: carlsson p. Development. 2001 Jun;128(12):2397-406. doi: 10.1242/dev.128.12.2397. Development. 2001. PMID: 11493558

8

FOXF2 is required for cochlear development in humans and mice.

Bademci G, Abad C, Incesulu A, Elian F, Reyahi A, Diaz-Horta O, Cengiz FB, Sineni CJ, Seyhan S, Atli EI, Basmak H, Demir S, Nik AM, Footz T, Guo S, Duman D, Fitoz S, Gurkan H, Blanton SH, Walter MA, Carlsson P, Walz K, Tekin M. Bademci G, et al. Among authors: carlsson p. Hum Mol Genet. 2019 Apr 15;28(8):1286-1297. doi: 10.1093/hmg/ddy431. Hum Mol Genet. 2019. PMID: 30561639 Free PMC article.

9

Chromosome localization, sequence analysis, and expression pattern identify FKHL 18 as a novel human forkhead gene.

Cederberg A, Betz R, Lagercrantz S, Larsson C, Hulander M, Carlsson P, Enerbäck S. Cederberg A, et al. Among authors: carlsson p. Genomics. 1997 Sep 15;44(3):344-6. doi: 10.1006/geno.1997.4864. Genomics. 1997. PMID: 9325056

10

FOXC2 is a winged helix gene that counteracts obesity, hypertriglyceridemia, and diet-induced insulin resistance.

Cederberg A, Grønning LM, Ahrén B, Taskén K, Carlsson P, Enerbäck S. Cederberg A, et al. Among authors: carlsson p. Cell. 2001 Sep 7;106(5):563-73. doi: 10.1016/s0092-8674(01)00474-3. Cell. 2001. PMID: 11551504 Free article.

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