Freund CL - Search Results

1

Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor.

Freund CL, Gregory-Evans CY, Furukawa T, Papaioannou M, Looser J, Ploder L, Bellingham J, Ng D, Herbrick JA, Duncan A, Scherer SW, Tsui LC, Loutradis-Anagnostou A, Jacobson SG, Cepko CL, Bhattacharya SS, McInnes RR. Freund CL, et al. Cell. 1997 Nov 14;91(4):543-53. doi: 10.1016/s0092-8674(00)80440-7. Cell. 1997. PMID: 9390563 Free article.

2

Vsx1, a rapidly evolving paired-like homeobox gene expressed in cone bipolar cells.

Chow RL, Snow B, Novak J, Looser J, Freund C, Vidgen D, Ploder L, McInnes RR. Chow RL, et al. Mech Dev. 2001 Dec;109(2):315-22. doi: 10.1016/s0925-4773(01)00585-8. Mech Dev. 2001. PMID: 11731243 Free article.

3

Transcription factor genes and the developing eye: a genetic perspective.

Freund C, Horsford DJ, McInnes RR. Freund C, et al. Hum Mol Genet. 1996;5 Spec No:1471-88. doi: 10.1093/hmg/5.supplement_1.1471. Hum Mol Genet. 1996. PMID: 8875254 Review.

4

A ubiquitin C-terminal hydrolase gene on the proximal short arm of the X chromosome: implications for X-linked retinal disorders.

Swanson DA, Freund CL, Ploder L, McInnes RR, Valle D. Swanson DA, et al. Among authors: freund cl. Hum Mol Genet. 1996 Apr;5(4):533-8. doi: 10.1093/hmg/5.4.533. Hum Mol Genet. 1996. PMID: 8845848

5

A differential hybridization scheme to identify photoreceptor-specific genes.

Swanson DA, Freund CL, Steel JM, Xu S, Ploder L, McInnes RR, Valle D. Swanson DA, et al. Among authors: freund cl. Genome Res. 1997 May;7(5):513-21. doi: 10.1101/gr.7.5.513. Genome Res. 1997. PMID: 9149946 Free article.

6

A range of clinical phenotypes associated with mutations in CRX, a photoreceptor transcription-factor gene.

Sohocki MM, Sullivan LS, Mintz-Hittner HA, Birch D, Heckenlively JR, Freund CL, McInnes RR, Daiger SP. Sohocki MM, et al. Among authors: freund cl. Am J Hum Genet. 1998 Nov;63(5):1307-15. doi: 10.1086/302101. Am J Hum Genet. 1998. PMID: 9792858 Free PMC article.

7

Retinal degenerations with truncation mutations in the cone-rod homeobox (CRX) gene.

Jacobson SG, Cideciyan AV, Huang Y, Hanna DB, Freund CL, Affatigato LM, Carr RE, Zack DJ, Stone EM, McInnes RR. Jacobson SG, et al. Among authors: freund cl. Invest Ophthalmol Vis Sci. 1998 Nov;39(12):2417-26. Invest Ophthalmol Vis Sci. 1998. PMID: 9804150

8

De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosis.

Freund CL, Wang QL, Chen S, Muskat BL, Wiles CD, Sheffield VC, Jacobson SG, McInnes RR, Zack DJ, Stone EM. Freund CL, et al. Nat Genet. 1998 Apr;18(4):311-2. doi: 10.1038/ng0498-311. Nat Genet. 1998. PMID: 9537410 No abstract available.

9

Sequence of the clathrin heavy chain from Saccharomyces cerevisiae and requirement of the COOH terminus for clathrin function.

Lemmon SK, Pellicena-Palle A, Conley K, Freund CL. Lemmon SK, et al. Among authors: freund cl. J Cell Biol. 1991 Jan;112(1):65-80. doi: 10.1083/jcb.112.1.65. J Cell Biol. 1991. PMID: 1898742 Free PMC article.

10

Genetic instability of clathrin-deficient strains of Saccharomyces cerevisiae.

Lemmon SK, Freund C, Conley K, Jones EW. Lemmon SK, et al. Genetics. 1990 Jan;124(1):27-38. doi: 10.1093/genetics/124.1.27. Genetics. 1990. PMID: 2407603 Free PMC article.

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