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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
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.
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
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
Exhaustive non-synonymous variants functionality prediction enables high resolution characterization of the neurofibromin architecture.
Isakov O, Wallis D, Evans DG, Ben-Shachar S. Isakov O, et al. EBioMedicine. 2018 Oct;36:508-516. doi: 10.1016/j.ebiom.2018.09.039. Epub 2018 Sep 28. EBioMedicine. 2018. PMID: 30274822 Free PMC article.
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.
Increased prevalence of ADHD in Turner syndrome with no evidence of imprinting effects.
Russell HF, Wallis D, Mazzocco MM, Moshang T, Zackai E, Zinn AR, Ross JL, Muenke M. Russell HF, et al. J Pediatr Psychol. 2006 Oct;31(9):945-55. doi: 10.1093/jpepsy/jsj106. Epub 2006 Mar 8. J Pediatr Psychol. 2006. PMID: 16524959
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