John SW - Search Results

1

Mouse mutants from chemically mutagenized embryonic stem cells.

Munroe RJ, Bergstrom RA, Zheng QY, Libby B, Smith R, John SW, Schimenti KJ, Browning VL, Schimenti JC. Munroe RJ, et al. Among authors: john sw. Nat Genet. 2000 Mar;24(3):318-21. doi: 10.1038/73563. Nat Genet. 2000. PMID: 10700192 Free PMC article.

2

Mutations in genes encoding melanosomal proteins cause pigmentary glaucoma in DBA/2J mice.

Anderson MG, Smith RS, Hawes NL, Zabaleta A, Chang B, Wiggs JL, John SW. Anderson MG, et al. Among authors: john sw. Nat Genet. 2002 Jan;30(1):81-5. doi: 10.1038/ng794. Epub 2001 Dec 17. Nat Genet. 2002. PMID: 11743578

3

Interacting loci cause severe iris atrophy and glaucoma in DBA/2J mice.

Chang B, Smith RS, Hawes NL, Anderson MG, Zabaleta A, Savinova O, Roderick TH, Heckenlively JR, Davisson MT, John SW. Chang B, et al. Among authors: john sw. Nat Genet. 1999 Apr;21(4):405-9. doi: 10.1038/7741. Nat Genet. 1999. PMID: 10192392

4

Mouse genetics: a tool to help unlock the mechanisms of glaucoma.

John SW, Anderson MG, Smith RS. John SW, et al. J Glaucoma. 1999 Dec;8(6):400-12. J Glaucoma. 1999. PMID: 10604301 Review.

5

A goniolens for clinical monitoring of the mouse iridocorneal angle and optic nerve.

Smith RS, Korb D, John SW. Smith RS, et al. Among authors: john sw. Mol Vis. 2002 Feb 25;8:26-31. Mol Vis. 2002. PMID: 11889463 Free article.

6

Anterior segment development relevant to glaucoma.

Gould DB, Smith RS, John SW. Gould DB, et al. Among authors: john sw. Int J Dev Biol. 2004;48(8-9):1015-29. doi: 10.1387/ijdb.041865dg. Int J Dev Biol. 2004. PMID: 15558492 Free article. Review.

7

Mutations in Col4a1 cause perinatal cerebral hemorrhage and porencephaly.

Gould DB, Phalan FC, Breedveld GJ, van Mil SE, Smith RS, Schimenti JC, Aguglia U, van der Knaap MS, Heutink P, John SW. Gould DB, et al. Among authors: john sw. Science. 2005 May 20;308(5725):1167-71. doi: 10.1126/science.1109418. Science. 2005. PMID: 15905400

8

Col4a1 mutation causes endoplasmic reticulum stress and genetically modifiable ocular dysgenesis.

Gould DB, Marchant JK, Savinova OV, Smith RS, John SW. Gould DB, et al. Among authors: john sw. Hum Mol Genet. 2007 Apr 1;16(7):798-807. doi: 10.1093/hmg/ddm024. Epub 2007 Feb 22. Hum Mol Genet. 2007. PMID: 17317786

9

Alteration of the serine protease PRSS56 causes angle-closure glaucoma in mice and posterior microphthalmia in humans and mice.

Nair KS, Hmani-Aifa M, Ali Z, Kearney AL, Ben Salem S, Macalinao DG, Cosma IM, Bouassida W, Hakim B, Benzina Z, Soto I, Söderkvist P, Howell GR, Smith RS, Ayadi H, John SW. Nair KS, et al. Among authors: john sw. Nat Genet. 2011 Jun;43(6):579-84. doi: 10.1038/ng.813. Epub 2011 May 1. Nat Genet. 2011. PMID: 21532570 Free PMC article.

10

Haploinsufficiency of the transcription factors FOXC1 and FOXC2 results in aberrant ocular development.

Smith RS, Zabaleta A, Kume T, Savinova OV, Kidson SH, Martin JE, Nishimura DY, Alward WL, Hogan BL, John SW. Smith RS, et al. Among authors: john sw. Hum Mol Genet. 2000 Apr 12;9(7):1021-32. doi: 10.1093/hmg/9.7.1021. Hum Mol Genet. 2000. PMID: 10767326

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