Rust K - Search Results

1

Weill-Marchesani syndrome--possible linkage of the autosomal dominant form to 15q21.1.

Wirtz MK, Samples JR, Kramer PL, Rust K, Yount J, Acott TS, Koler RD, Cisler J, Jahed A, Gorlin RJ, Godfrey M. Wirtz MK, et al. Among authors: rust k. Am J Med Genet. 1996 Oct 2;65(1):68-75. doi: 10.1002/(SICI)1096-8628(19961002)65:1<68::AID-AJMG11>3.0.CO;2-P. Am J Med Genet. 1996. PMID: 8914744

2

Mapping a gene for adult-onset primary open-angle glaucoma to chromosome 3q.

Wirtz MK, Samples JR, Kramer PL, Rust K, Topinka JR, Yount J, Koler RD, Acott TS. Wirtz MK, et al. Among authors: rust k. Am J Hum Genet. 1997 Feb;60(2):296-304. Am J Hum Genet. 1997. PMID: 9012402 Free PMC article.

3

Age-related macular degeneration. Clinical features in a large family and linkage to chromosome 1q.

Klein ML, Schultz DW, Edwards A, Matise TC, Rust K, Berselli CB, Trzupek K, Weleber RG, Ott J, Wirtz MK, Acott TS. Klein ML, et al. Among authors: rust k. Arch Ophthalmol. 1998 Aug;116(8):1082-8. doi: 10.1001/archopht.116.8.1082. Arch Ophthalmol. 1998. PMID: 9715689

4

Malattia leventinese: refinement of the genetic locus and phenotypic variability in autosomal dominant macular drusen.

Edwards AO, Klein ML, Berselli CB, Hejtmancik JF, Rust K, Wirtz MK, Weleber RG, Acott TS. Edwards AO, et al. Among authors: rust k. Am J Ophthalmol. 1998 Sep;126(3):417-24. doi: 10.1016/s0002-9394(98)00097-x. Am J Ophthalmol. 1998. PMID: 9744375

5

GLC1F, a new primary open-angle glaucoma locus, maps to 7q35-q36.

Wirtz MK, Samples JR, Rust K, Lie J, Nordling L, Schilling K, Acott TS, Kramer PL. Wirtz MK, et al. Among authors: rust k. Arch Ophthalmol. 1999 Feb;117(2):237-41. doi: 10.1001/archopht.117.2.237. Arch Ophthalmol. 1999. PMID: 10037570

6

Refining the primary open-angle glaucoma GLC1C region on chromosome 3 by haplotype analysis.

Samples JR, Kitsos G, Economou-Petersen E, Steinkamp P, Sykes R, Rust K, Patzer C, Grigoriadou M, Aperis G, Psilas K, Petersen MB, Wirtz MK. Samples JR, et al. Among authors: rust k. Clin Genet. 2004 Jan;65(1):40-4. doi: 10.1111/j..2004.00182.x. Clin Genet. 2004. PMID: 15032973

7

Insulin-like growth factor binding protein-5 expression by human trabecular meshwork.

Wirtz MK, Xu H, Rust K, Alexander JP, Acott TS. Wirtz MK, et al. Among authors: rust k. Invest Ophthalmol Vis Sci. 1998 Jan;39(1):45-53. Invest Ophthalmol Vis Sci. 1998. PMID: 9430544

8

A large GLC1C Greek family with a myocilin T377M mutation: inheritance and phenotypic variability.

Petersen MB, Kitsos G, Samples JR, Gaudette ND, Economou-Petersen E, Sykes R, Rust K, Grigoriadou M, Aperis G, Choi D, Psilas K, Craig JE, Kramer PL, Mackey DA, Wirtz MK. Petersen MB, et al. Among authors: rust k. Invest Ophthalmol Vis Sci. 2006 Feb;47(2):620-5. doi: 10.1167/iovs.05-0631. Invest Ophthalmol Vis Sci. 2006. PMID: 16431959

9

Uveitis in patients with sarcoidosis is not associated with mutations in NOD2 (CARD15).

Martin TM, Doyle TM, Smith JR, Dinulescu D, Rust K, Rosenbaum JT. Martin TM, et al. Among authors: rust k. Am J Ophthalmol. 2003 Nov;136(5):933-5. doi: 10.1016/s0002-9394(03)00892-4. Am J Ophthalmol. 2003. PMID: 14597055

10

Deletion of the auxiliary α2δ1 voltage sensitive calcium channel subunit in osteocytes and late-stage osteoblasts impairs femur strength and load-induced bone formation in male mice.

Wright CS, Lewis KJ, Semon K, Yi X, Reyes Fernandez PC, Rust K, Prideaux M, Schneider A, Pederson M, Deosthale P, Plotkin LI, Hum JM, Sankar U, Farach-Carson MC, Robling AG, Thompson WR. Wright CS, et al. Among authors: rust k. J Bone Miner Res. 2024 Apr 19;39(3):298-314. doi: 10.1093/jbmr/zjae010. J Bone Miner Res. 2024. PMID: 38477790

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