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Molecular mechanisms of holoprosencephaly.
Wallis DE, Muenke M. Wallis DE, et al. Mol Genet Metab. 1999 Oct;68(2):126-38. doi: 10.1006/mgme.1999.2895. Mol Genet Metab. 1999. PMID: 10527664 Review.
Mutations in holoprosencephaly.
Wallis D, Muenke M. Wallis D, et al. Hum Mutat. 2000;16(2):99-108. doi: 10.1002/1098-1004(200008)16:2<99::AID-HUMU2>3.0.CO;2-0. Hum Mutat. 2000. PMID: 10923031 Review.
Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly.
Wallis DE, Roessler E, Hehr U, Nanni L, Wiltshire T, Richieri-Costa A, Gillessen-Kaesbach G, Zackai EH, Rommens J, Muenke M. Wallis DE, et al. Nat Genet. 1999 Jun;22(2):196-8. doi: 10.1038/9718. Nat Genet. 1999. PMID: 10369266
The zinc finger transcription factor Gfi1, implicated in lymphomagenesis, is required for inner ear hair cell differentiation and survival.
Wallis D, Hamblen M, Zhou Y, Venken KJ, Schumacher A, Grimes HL, Zoghbi HY, Orkin SH, Bellen HJ. Wallis D, et al. Development. 2003 Jan;130(1):221-32. doi: 10.1242/dev.00190. Development. 2003. PMID: 12441305
Vapb/Amyotrophic lateral sclerosis 8 knock-in mice display slowly progressive motor behavior defects accompanying ER stress and autophagic response.
Larroquette F, Seto L, Gaub PL, Kamal B, Wallis D, Larivière R, Vallée J, Robitaille R, Tsuda H. Larroquette F, et al. Hum Mol Genet. 2015 Nov 15;24(22):6515-29. doi: 10.1093/hmg/ddv360. Epub 2015 Sep 11. Hum Mol Genet. 2015. PMID: 26362257 Free PMC article.
Multi-Omics Profiling for NF1 Target Discovery in Neurofibromin (NF1) Deficient Cells.
Carnes RM, Mobley JA, Crossman DK, Liu H, Korf BR, Kesterson RA, Wallis D. Carnes RM, et al. Proteomics. 2019 Jun;19(11):e1800334. doi: 10.1002/pmic.201800334. Proteomics. 2019. PMID: 30908848
High-Throughput Differentiation and Screening of a Library of Mutant Stem Cell Clones Defines New Host-Based Genes Involved in Rabies Virus Infection.
Wallis D, Loesch K, Galaviz S, Sun Q, DeJesus M, Ioerger T, Sacchettini JC. Wallis D, et al. Stem Cells. 2015 Aug;33(8):2509-22. doi: 10.1002/stem.1983. Epub 2015 May 12. Stem Cells. 2015. PMID: 25752821
Initial characterization of mice null for Lphn3, a gene implicated in ADHD and addiction.
Wallis D, Hill DS, Mendez IA, Abbott LC, Finnell RH, Wellman PJ, Setlow B. Wallis D, et al. Brain Res. 2012 Jun 29;1463:85-92. doi: 10.1016/j.brainres.2012.04.053. Epub 2012 May 7. Brain Res. 2012. PMID: 22575564
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