10 results for author:"Cuajungco M.P." in Literature citations
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| Abnormal accumulation of human transmembrane (TMEM)-176A and 176B proteins is associated with cancer pathology. Cuajungco M.P., Podevin W., Valluri V.K., Bui Q., Nguyen V.H., Taylor K. Acta Histochem. 114:705-712(2012) · Mapped (4) |
| Zinc dyshomeostasis is linked with the loss of mucolipidosis IV-associated TRPML1 ion channel. Eichelsdoerfer J.L., Evans J.A., Slaugenhaupt S.A., Cuajungco M.P. J. Biol. Chem. 285:34304-34308(2010) · Mapped (4) |
| The tissue-specific expression of TRPML2 (MCOLN-2) gene is influenced by the presence of TRPML1. Samie M.A., Grimm C., Evans J.A., Curcio-Morelli C., Heller S., Slaugenhaupt S.A., Cuajungco M.P. Pflugers Arch. 459:79-91(2009) · Mapped (8) |
| Stimulus-specific modulation of the cation channel TRPV4 by PACSIN 3. D'hoedt D., Owsianik G., Prenen J., Cuajungco M.P., Grimm C., Heller S., Voets T., Nilius B. J. Biol. Chem. 283:6272-6280(2008) · Mapped (9) |
| A helix-breaking mutation in TRPML3 leads to constitutive activity underlying deafness in the varitint-waddler mouse. Grimm C., Cuajungco M.P., van Aken A.F., Schnee M., Jors S., Kros C.J., Ricci A.J., Heller S. Proc. Natl. Acad. Sci. U.S.A. 104:19583-19588(2007) · Mapped (4) |
| PACSINs bind to the TRPV4 cation channel. PACSIN 3 modulates the subcellular localization of TRPV4. Cuajungco M.P., Grimm C., Oshima K., D'hoedt D., Nilius B., Mensenkamp A.R., Bindels R.J., Plomann M., Heller S. J. Biol. Chem. 281:18753-18762(2006) · Mapped (11) |
| Tissue-specific reduction in splicing efficiency of IKBKAP due to the major mutation associated with familial dysautonomia. Cuajungco M.P., Leyne M., Mull J., Gill S.P., Lu W., Zagzag D., Axelrod F.B., Maayan C., Gusella J.F., Slaugenhaupt S.A. Am. J. Hum. Genet. 72:749-758(2003) · Mapped (9) |
| Cloning, characterization, and genomic structure of the mouse Ikbkap gene. Cuajungco M.P., Leyne M., Mull J., Gill S.P., Gusella J.F., Slaugenhaupt S.A. DNA Cell Biol. 20:579-586(2001) · UniProtKB (1) · Mapped (24) |
| Tissue-specific expression of a splicing mutation in the IKBKAP gene causes familial dysautonomia. Slaugenhaupt S.A., Blumenfeld A., Gill S.P., Leyne M., Mull J., Cuajungco M.P., Liebert C.B., Chadwick B.P., Idelson M., Reznik L. et al. Am. J. Hum. Genet. 68:598-605(2001) · UniProtKB (1) · Mapped (3) |
| The A beta peptide of Alzheimer's disease directly produces hydrogen peroxide through metal ion reduction. Huang X., Atwood C.S., Hartshorn M.A., Multhaup G., Goldstein L.E., Scarpa R.C., Cuajungco M.P., Gray D.N., Lim J., Moir R.D. et al. Biochemistry 38:7609-7616(1999) · UniProtKB (1) |