1 - 25 of
225
results
for author:"Scherer S."
in Literature Citations
| Matrix metalloproteinase gene polymorphisms in patients with rheumatoid arthritis. Scherer S., de Souza T.B., de Paoli J., Brenol C.V., Xavier R.M., Brenol J.C., Chies J.A., Simon D. Rheumatol. Int. 0:0-0(2009) · Mapped (17) |
| Mutations in smooth muscle alpha-actin (ACTA2) cause coronary artery disease, stroke, and Moyamoya disease, along with thoracic aortic disease. Guo D.C., Papke C.L., Tran-Fadulu V., Regalado E.S., Avidan N., Johnson R.J., Kim D.H., Pannu H., Willing M.C., Sparks E. et al. Am. J. Hum. Genet. 84:617-627(2009) · Mapped (4) |
| Reassessing the impact of donor HLA-C genotype on long-term liver transplant survival. Tran T.H., Middleton D., Dohler B., Scherer S., Meenagh A., Sleator C., Opelz G. Am. J. Transplant. 9:1674-1678(2009) · Mapped (370) |
| Connexin32 mutations cause loss of function in Schwann cells and oligodendrocytes leading to PNS and CNS myelination defects. Sargiannidou I., Vavlitou N., Aristodemou S., Hadjisavvas A., Kyriacou K., Scherer S.S., Kleopa K.A. J. Neurosci. 29:4736-4749(2009) · Mapped (2) |
| Copy number variation analysis and sequencing of the X-linked mental retardation gene TSPAN7/TM4SF2 in patients with autism spectrum disorder. Noor A., Gianakopoulos P.J., Fernandez B., Marshall C.R., Szatmari P., Roberts W., Scherer S.W., Vincent J.B. Psychiatr. Genet. 19:154-155(2009) · Mapped (10) |
| Improved cutaneous healing in diabetic mice exposed to healthy peripheral circulation. Pietramaggiori G., Scherer S.S., Alperovich M., Chen B., Orgill D.P., Wagers A.J. J. Invest. Dermatol. 129:2265-2274(2009) · Mapped (4) |
| Association and mutation analyses of 16p11.2 autism candidate genes. Kumar R.A., Marshall C.R., Badner J.A., Babatz T.D., Mukamel Z., Aldinger K.A., Sudi J., Brune C.W., Goh G., Karamohamed S. et al. PLoS ONE 4:e4582-e4582(2009) · Mapped (39) |
| Hereditary spastic paraplegia is a novel phenotype for GJA12/GJC2 mutations. Orthmann-Murphy J.L., Salsano E., Abrams C.K., Bizzi A., Uziel G., Freidin M.M., Lamantea E., Zeviani M., Scherer S.S., Pareyson D. Brain 132:426-438(2009) · Mapped (1) |
| Characterization of the differentially methylated region of the Impact gene that exhibits Glires-specific imprinting. Okamura K., Wintle R.F., Scherer S.W. Genome Biol. 9:R160-R160(2008) · UniProtKB (16) |
| Interaction of Muc2 and Apc on Wnt signaling and in intestinal tumorigenesis: potential role of chronic inflammation. Yang K., Popova N.V., Yang W.C., Lozonschi I., Tadesse S., Kent S., Bancroft L., Matise I., Cormier R.T., Scherer S.J. et al. Cancer Res. 68:7313-7322(2008) · Mapped (16) |
| Epigenetic regulation of HYAL-1 hyaluronidase expression. identification of HYAL-1 promoter. Lokeshwar V.B., Gomez P., Kramer M., Knapp J., McCornack M.A., Lopez L.E., Fregien N., Dhir N., Scherer S., Klumpp D.J. et al. J. Biol. Chem. 283:29215-29227(2008) · Mapped (3) |
| Excessive genomic DNA copy number variation in the Li-Fraumeni cancer predisposition syndrome. Shlien A., Tabori U., Marshall C.R., Pienkowska M., Feuk L., Novokmet A., Nanda S., Druker H., Scherer S.W., Malkin D. Proc. Natl. Acad. Sci. U.S.A. 105:11264-11269(2008) · Mapped (31) |
| Dynamic variation in allele-specific gene expression of Paraoxonase-1 in murine and human tissues. Parker-Katiraee L., Bousiaki E., Monk D., Moore G.E., Nakabayashi K., Scherer S.W. Hum. Mol. Genet. 17:3263-3270(2008) · Mapped (5) |
| Infantile spasms is associated with deletion of the MAGI2 gene on chromosome 7q11.23-q21.11. Marshall C.R., Young E.J., Pani A.M., Freckmann M.L., Lacassie Y., Howald C., Fitzgerald K.K., Peippo M., Morris C.A., Shane K. et al. Am. J. Hum. Genet. 83:106-111(2008) · Mapped (6) |
| Comparative analysis of human chromosome 7q21 and mouse proximal chromosome 6 reveals a placental-specific imprinted gene, TFPI2/Tfpi2, which requires EHMT2 and EED for allelic-silencing. Monk D., Wagschal A., Arnaud P., Muller P.S., Parker-Katiraee L., Bourc'his D., Scherer S.W., Feil R., Stanier P., Moore G.E. Genome Res. 18:1270-1281(2008) · Mapped (26) |
| Human oligodendrocytes express Cx31.3: function and interactions with Cx32 mutants. Sargiannidou I., Ahn M., Enriquez A.D., Peinado A., Reynolds R., Abrams C., Scherer S.S., Kleopa K.A. Neurobiol. Dis. 30:221-233(2008) · Mapped (1) |
| Distinct effects of the recurrent Mlh1G67R mutation on MMR functions, cancer, and meiosis. Avdievich E., Reiss C., Scherer S.J., Zhang Y., Maier S.M., Jin B., Hou H. Jr., Rosenwald A., Riedmiller H., Kucherlapati R. et al. Proc. Natl. Acad. Sci. U.S.A. 105:4247-4252(2008) · Mapped (5) |
| Role of minor histocompatibility antigens in renal transplantation. Heinold A., Opelz G., Scherer S., Ruhenstroth A., Laux G., Doehler B., Tran T.H. Am. J. Transplant. 8:95-102(2008) · Mapped (2,493) |
| Cell expression of GDAP1 in the nervous system and pathogenesis of Charcot-Marie-Tooth type 4A disease. Pedrola L., Espert A., Valdes-Sanchez T., Sanchez-Piris M., Sirkowski E.E., Scherer S.S., Farinas I., Palau F. J. Cell. Mol. Med. 12:679-689(2008) · Mapped (3) |
| Contribution of SHANK3 mutations to autism spectrum disorder. Moessner R., Marshall C.R., Sutcliffe J.S., Skaug J., Pinto D., Vincent J., Zwaigenbaum L., Fernandez B., Roberts W., Szatmari P. et al. Am. J. Hum. Genet. 81:1289-1297(2007) · Mapped (4) |
| Mutations in smooth muscle alpha-actin (ACTA2) lead to thoracic aortic aneurysms and dissections. Guo D.-C., Pannu H., Tran-Fadulu V., Papke C.L., Yu R.K., Avidan N., Bourgeois S., Estrera A.L., Safi H.J., Sparks E. et al. |
| Identification and characterization of three novel HLA alleles, HLA-A*240214, HLA-A*3215 and HLA-DQB1*060302. Heinold A., Bauer M., Opelz G., Scherer S., Schmidt A.H., Tran T.H. Tissue Antigens 70:511-514(2007) · UniProtKB (3) |
| Characterization of a new HLA-B allele, HLA-B*5312, and re-evaluation of the published sequences of the untranslated regions of HLA-B*35 and HLA-B*53. Heinold A., Bauer M., Scherer S., Opelz G., Tran T.H. Tissue Antigens 70:319-323(2007) · UniProtKB (1) |
| Nectin-like proteins mediate axon Schwann cell interactions along the internode and are essential for myelination. Maurel P., Einheber S., Galinska J., Thaker P., Lam I., Rubin M.B., Scherer S.S., Murakami Y., Gutmann D.H., Salzer J.L. J. Cell Biol. 178:861-874(2007) · UniProtKB (1) · Mapped (3) |
| MYH11 mutations result in a distinct vascular pathology driven by insulin-like growth factor 1 and angiotensin II. Pannu H., Tran-Fadulu V., Papke C.L., Scherer S., Liu Y., Presley C., Guo D., Estrera A.L., Safi H.J., Brasier A.R. et al. Hum. Mol. Genet. 16:2453-2462(2007) · Mapped (21) |
