MichaelCSchneiderMD

PubMed

• 121 citations
  Newborn Screening for Lysosomal Storage Disorders in Illinois: The Initial 15-Month Experience
  Barbara K. Burton, Joel Charrow, George E. Hoganson, Darrell J. Waggoner, Brad T. Tinkle, Stephen R. Braddock, Michael Schneider, Dorothy K. Grange, Claudia Nash, Heat...> ;The Journal of Pediatrics. 2017 Nov 1
• 53 citations
  A Gene Implicated in Activation of Retinoic Acid Receptor Targets Is a Novel Renal Agenesis Gene in Humans.
  Patrick D. Brophy, Maria Rasmussen, Mrutyunjaya Parida, Greg Bonde, Benjamin W. Darbro, Xiaojing Hong, Jason C. Clarke, Kevin A. Peterson, James M. Denegre, Michael Sc...> ;Genetics. 2017 Sep 1
• Deletion of and novel missense mutation in POU3F4 in 2 families segregating X-linked nonsyndromic deafness.
  Vore, A.P., Chang, E.H., Hoppe, J.E., Butler, M.G., Forrester, S., Schneider, M.C., Smith, L.H., Burke, D.W., Campbell, C.A., Smith, R.H.> ;Arch Otolaryngol Head Neck Surg. 2005 Dec
• Activation of p21-activated kinase 6 by MAP kinase kinase 6 and p38 MAP kinase.
  Kaur, R., Liu, X., Gjoerup, O., Zhang, A., Yuan, X., Balk, S.P., Schneider, M.C., Lu, M.L.> ;J Biol Chem. 2005 Feb 4
• Large germline deletions of mitochondrial complex II subunits SDHB and SDHD in hereditary paraganglioma.
  McWhinney, S.R., Pilarski, R.T., Forrester, S.R., Schneider, M.C., Sarquis, M.M., Dias, E.P., Eng, C.> ;J Clin Endocrinol Metab. 2004 Nov
• Deoxyribonuclease I-like III is an inducible macrophage barrier to liposomal transfection.
  Wilber, A., Lu, M., Schneider, M.C.> ;Mol Ther. 2002 Jul
• Identification and localization of polycystin, the PKD1 gene product.
  Geng, L., Segal, Y., Peissel, B., Deng, N., Pei, Y., Carone, F., Rennke, H. G., Glücksmann-Kuis, A. M., Schneider, M. C., Ericsson, M., Reeders, S. T., Zhou, J.> ;J Clin Invest. 1996 Dec 15
• Advances in polycystic kidney disease.
  Schneider, M. C.> ;Mol Med Today. 1996 Feb
• Identification, localization, and expression of two novel human genes similar to deoxyribonuclease I.
  Rodriguez, A. M., Rodin, D., Nomura, H., Morton, C. C., Weremowicz, S., Schneider, M. C.> ;Genomics. 1997 Jun 15
• Caveolin-1 interacts with androgen receptor. A positive modulator of androgen receptor mediated transactivation.
  Lu, M. L., Schneider, M. C., Zheng, Y., Zhang, X., Richie, J. P.> ;J Biol Chem. 2001 Apr 20
• Mild phenotype due to tandem duplication of l7p11.2.
  Schneider, M. C., Hughes, C. R., Forrester, S., Kimonis, V.> ;Am J Med Genet. 2000 Oct 2
• Temtamy-like syndrome associated with translocation of 2p24 and 9q32.
  Talisetti, A., Forrester, S. R., Gregory, D., Johnson, L., Schneider, M. C., Kimonis, V. E.> ;Clin Dysmorphol. 2003 Jul
• Dnase1l3 deficiency in lupus-prone MRL and NZB/W F1 mice.
  Wilber, A., O'Connor, T. P., Lu, M. L., Karimi, A., Schneider, M. C.> ;Clin Exp Immunol. 2003 Oct
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