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6 results for author:"Stenger J.E." in Literature citations

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Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease.

Zuechner S., Noureddine M., Kennerson M., Verhoeven K., Claeys K., De Jonghe P., Merory J., Oliveira S.A., Speer M.C., Stenger J.E. et al.

Nat. Genet. 37:289-294(2005) · UniProtKB (1) · Mapped (10)

Analysis of the RELN gene as a genetic risk factor for autism.

Skaar D.A., Shao Y., Haines J.L., Stenger J.E., Jaworski J., Martin E.R., DeLong G.R., Moore J.H., McCauley J.L., Sutcliffe J.S. et al.

Mol. Psychiatry 10:563-571(2005) · Mapped (5)

Comprehensive association analysis of APOE regulatory region polymorphisms in Alzheimer disease.

Nicodemus K.K., Stenger J.E., Schmechel D.E., Welsh-Bohmer K.A., Saunders A.M., Roses A.D., Gilbert J.R., Vance J.M., Haines J.L., Pericak-Vance M.A. et al.

Neurogenetics 5:201-208(2004) · Mapped (5)

Glutathione S-transferase omega-1 modifies age-at-onset of Alzheimer disease and Parkinson disease.

Li Y.J., Oliveira S.A., Xu P., Martin E.R., Stenger J.E., Scherzer C.R., Hauser M.A., Scott W.K., Small G.W., Nance M.A. et al.

Hum. Mol. Genet. 12:3259-3267(2003) · Mapped (10)

Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21.

Baxter R.V., Ben-Othmane K., Rochelle J.M., Stajich J.E., Hulette C., Dew-Knight S., Hentati F., Ben-Hamida M., Bel S., Stenger J.E. et al.

Nat. Genet. 30:21-22(2002) · UniProtKB (1)

The zinc finger region of simian virus 40 large T antigen is needed for hexamer assembly and origin melting.

Loeber G., Stenger J.E., Ray S., Parsons R.E., Anderson M.E., Tegtmeyer P.

J. Virol. 65:3167-3174(1991) · UniProtKB (1)

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