Arbogast L - Search Results

1

Identification of the first intragenic deletion of the PITX2 gene causing an Axenfeld-Rieger Syndrome: case report.

de la Houssaye G, Bieche I, Roche O, Vieira V, Laurendeau I, Arbogast L, Zeghidi H, Rapp P, Halimi P, Vidaud M, Dufier JL, Menasche M, Abitbol M. de la Houssaye G, et al. Among authors: arbogast l. BMC Med Genet. 2006 Nov 29;7:82. doi: 10.1186/1471-2350-7-82. BMC Med Genet. 2006. PMID: 17134502 Free PMC article.

2

Identification of four new PITX2 gene mutations in patients with Axenfeld-Rieger syndrome.

Vieira V, David G, Roche O, de la Houssaye G, Boutboul S, Arbogast L, Kobetz A, Orssaud C, Camand O, Schorderet DF, Munier F, Rossi A, Delezoide AL, Marsac C, Ricquier D, Dufier JL, Menasche M, Abitbol M. Vieira V, et al. Among authors: arbogast l. Mol Vis. 2006 Dec 1;12:1448-60. Mol Vis. 2006. PMID: 17167399 Free article.

3

Mutational analysis of the OA1 gene in ocular albinism.

Camand O, Boutboul S, Arbogast L, Roche O, Sternberg C, Sutherland J, Levin A, Héon E, Menasche M, Dufier J, Abitbol M. Camand O, et al. Among authors: arbogast l. Ophthalmic Genet. 2003 Sep;24(3):167-73. doi: 10.1076/opge.24.3.167.15605. Ophthalmic Genet. 2003. PMID: 12868035

4

The RNA-binding protein Musashi-1 is produced in the developing and adult mouse eye.

Raji B, Dansault A, Leemput J, de la Houssaye G, Vieira V, Kobetz A, Arbogast L, Masson C, Menasche M, Abitbol M. Raji B, et al. Among authors: arbogast l. Mol Vis. 2007 Aug 10;13:1412-27. Mol Vis. 2007. PMID: 17768378

5

Analysis of partner of inscuteable (mPins) expression in the developing mouse eye.

Raji B, Dansault A, Vieira V, de la Houssaye G, Lacassagne E, Kobetz A, Arbogast L, Dufier JL, Blumer JB, Menasche M, Abitbol M. Raji B, et al. Among authors: arbogast l. Mol Vis. 2008;14:2575-96. Epub 2008 Dec 31. Mol Vis. 2008. PMID: 19122831 Free PMC article.

6

Gamma-D crystallin gene (CRYGD) mutation causes autosomal dominant congenital cerulean cataracts.

Nandrot E, Slingsby C, Basak A, Cherif-Chefchaouni M, Benazzouz B, Hajaji Y, Boutayeb S, Gribouval O, Arbogast L, Berraho A, Abitbol M, Hilal L. Nandrot E, et al. Among authors: arbogast l. J Med Genet. 2003 Apr;40(4):262-7. doi: 10.1136/jmg.40.4.262. J Med Genet. 2003. PMID: 12676897 Free PMC article.

7

Solid-State NMR Characterization of Lyophilized Formulations of Monoclonal Antibody Therapeutics.

Perodeau J, Arbogast LW, Nieuwkoop AJ. Perodeau J, et al. Among authors: arbogast lw. Mol Pharm. 2023 Mar 6;20(3):1480-1489. doi: 10.1021/acs.molpharmaceut.2c00676. Epub 2023 Jan 26. Mol Pharm. 2023. PMID: 36702622

8

Expansion and mechanistic insights into de novo DEAF1 variants in DEAF1-associated neurodevelopmental disorders.

McGee SR, Rajamanickam S, Adhikari S, Falayi OC, Wilson TA, Shayota BJ, Cooley Coleman JA, Skinner C, Caylor RC, Stevenson RE, Quaio CRAC, Wilke BC, Bain JM, Anyane-Yeboa K, Brown K, Greally JM, Bijlsma EK, Ruivenkamp CAL, Politi K, Arbogast LA, Collard MW, Huggenvik JI, Elsea SH, Jensik PJ. McGee SR, et al. Among authors: arbogast la. Hum Mol Genet. 2023 Jan 13;32(3):386-401. doi: 10.1093/hmg/ddac200. Hum Mol Genet. 2023. PMID: 35981081 Free PMC article.

9

Interlaboratory Studies Using the NISTmAb to Advance Biopharmaceutical Structural Analytics.

Yandrofski K, Mouchahoir T, De Leoz ML, Duewer D, Hudgens JW, Anderson KW, Arbogast L, Delaglio F, Brinson RG, Marino JP, Phinney K, Tarlov M, Schiel JE. Yandrofski K, et al. Among authors: arbogast l. Front Mol Biosci. 2022 May 5;9:876780. doi: 10.3389/fmolb.2022.876780. eCollection 2022. Front Mol Biosci. 2022. PMID: 35601836 Free PMC article. Review.

10

Principal Component Analysis of 1D 1H Diffusion Edited NMR Spectra of Protein Therapeutics.

Elliott KW, Delaglio F, Wikström M, Marino JP, Arbogast LW. Elliott KW, et al. Among authors: arbogast lw. J Pharm Sci. 2021 Oct;110(10):3385-3394. doi: 10.1016/j.xphs.2021.06.027. Epub 2021 Jun 21. J Pharm Sci. 2021. PMID: 34166704 Free PMC article.

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