IMPDH1 (Russian Wikipedia)

Analysis of information sources in references of the Wikipedia article "IMPDH1" in Russian language version.

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Kennan A., Aherne A., Palfi A., Humphries M., McKee A., Stitt A., Simpson D.A., Demtroder K., Orntoft T., Ayuso C., Kenna P.F., Farrar G.J., Humphries P. Identification of an IMPDH1 mutation in autosomal dominant retinitis pigmentosa (RP10) revealed following comparative microarray analysis of transcripts derived from retinas of wild-type and Rho(-/-) mice (англ.) // Human Molecular Genetics (англ.) (рус. : journal. — Oxford University Press, 2002. — March (vol. 11, no. 5). — P. 547—557. — doi:10.1093/hmg/11.5.547. — PMID 11875049.
Bowne S.J., Sullivan L.S., Blanton S.H., Cepko C.L., Blackshaw S., Birch D.G., Hughbanks-Wheaton D., Heckenlively J.R., Daiger S.P. Mutations in the inosine monophosphate dehydrogenase 1 gene (IMPDH1) cause the RP10 form of autosomal dominant retinitis pigmentosa (англ.) // Human Molecular Genetics (англ.) (рус. : journal. — Oxford University Press, 2002. — March (vol. 11, no. 5). — P. 559—568. — doi:10.1093/hmg/11.5.559. — PMID 11875050. — PMC 2585828.

Entrez Gene: IMP (inosine monophosphate) dehydrogenase 1 (неопр.).
Natsumeda Y., Ohno S., Kawasaki H., Konno Y., Weber G., Suzuki K. Two distinct cDNAs for human IMP dehydrogenase (англ.) // J. Biol. Chem. : journal. — 1990. — March (vol. 265, no. 9). — P. 5292—5295. — PMID 1969416.
Kennan A., Aherne A., Palfi A., Humphries M., McKee A., Stitt A., Simpson D.A., Demtroder K., Orntoft T., Ayuso C., Kenna P.F., Farrar G.J., Humphries P. Identification of an IMPDH1 mutation in autosomal dominant retinitis pigmentosa (RP10) revealed following comparative microarray analysis of transcripts derived from retinas of wild-type and Rho(-/-) mice (англ.) // Human Molecular Genetics (англ.) (рус. : journal. — Oxford University Press, 2002. — March (vol. 11, no. 5). — P. 547—557. — doi:10.1093/hmg/11.5.547. — PMID 11875049.
Bowne S.J., Sullivan L.S., Blanton S.H., Cepko C.L., Blackshaw S., Birch D.G., Hughbanks-Wheaton D., Heckenlively J.R., Daiger S.P. Mutations in the inosine monophosphate dehydrogenase 1 gene (IMPDH1) cause the RP10 form of autosomal dominant retinitis pigmentosa (англ.) // Human Molecular Genetics (англ.) (рус. : journal. — Oxford University Press, 2002. — March (vol. 11, no. 5). — P. 559—568. — doi:10.1093/hmg/11.5.559. — PMID 11875050. — PMC 2585828.

Kennan A., Aherne A., Palfi A., Humphries M., McKee A., Stitt A., Simpson D.A., Demtroder K., Orntoft T., Ayuso C., Kenna P.F., Farrar G.J., Humphries P. Identification of an IMPDH1 mutation in autosomal dominant retinitis pigmentosa (RP10) revealed following comparative microarray analysis of transcripts derived from retinas of wild-type and Rho(-/-) mice (англ.) // Human Molecular Genetics (англ.) (рус. : journal. — Oxford University Press, 2002. — March (vol. 11, no. 5). — P. 547—557. — doi:10.1093/hmg/11.5.547. — PMID 11875049.
Bowne S.J., Sullivan L.S., Blanton S.H., Cepko C.L., Blackshaw S., Birch D.G., Hughbanks-Wheaton D., Heckenlively J.R., Daiger S.P. Mutations in the inosine monophosphate dehydrogenase 1 gene (IMPDH1) cause the RP10 form of autosomal dominant retinitis pigmentosa (англ.) // Human Molecular Genetics (англ.) (рус. : journal. — Oxford University Press, 2002. — March (vol. 11, no. 5). — P. 559—568. — doi:10.1093/hmg/11.5.559. — PMID 11875050. — PMC 2585828.