Search Results - "Astrin, K.H." :: K.UTB vyhledávací portál | TBU Library Retrieval Portal

Congenital erythropoietic porphyria successfully treated by allogeneic bone marrow transplantation

Congenital erythropoietic porphyria successfully treated by allogeneic bone marrow transplantation

by TEZCAN, I, XU, W, DESNICK, R. J, GURGEY, A, TUNCER, M, CETIN, M, ÖNER, C, YETGIN, S, ERSOY, F, AIZENCANG, G, ASTRIN, K. H
Published in Blood (01.12.1998)

Get full text

Journal Article

Congenital Erythropoietic Porphyria Successfully Treated by Allogeneic Bone Marrow Transplantation

Congenital Erythropoietic Porphyria Successfully Treated by Allogeneic Bone Marrow Transplantation

by Tezcan, I., Xu, W., Gurgey, A., Tuncer, M., Cetin, M., Öner, C., Yetgin, S., Ersoy, F., Aizencang, G., Astrin, K.H., Desnick, R.J.
Published in Blood (01.12.1998)

Get full text

Journal Article

Congenital Erythropoietic Porphyria: Prolonged High-Level Expression and Correction of the Heme Biosynthetic Defect by Retroviral-Mediated Gene Transfer into Porphyric and Erythroid Cells

Congenital Erythropoietic Porphyria: Prolonged High-Level Expression and Correction of the Heme Biosynthetic Defect by Retroviral-Mediated Gene Transfer into Porphyric and Erythroid Cells

by Kauppinen, R., Glass, I.A., Aizencang, G., Astrin, K.H., Atweh, G.F., Desnick, R.J.
Published in Molecular genetics and metabolism (01.09.1998)

Get full text

Journal Article

Nature and frequency of mutations in the [alpha]-galactosidase A gene that cause Fabry disease

Nature and frequency of mutations in the [alpha]-galactosidase A gene that cause Fabry disease

by Eng, C.M., Resnick-Silverman, L.A., Niehaus, D.J., Astrin, K.H., Desnick, R.J.
Published in American journal of human genetics (01.12.1993)

Get full text

Journal Article

Rsal polymorphism in the human §-aminolevulinate dehydratase gene at 9q34

Rsal polymorphism in the human §-aminolevulinate dehydratase gene at 9q34

by Astrin, K.H., Kaya, A.H., Wetmur, J.G., Desnick, R.J.
Published in Nucleic acids research (11.08.1991)

Get full text

Journal Article

RsaI polymorphism in the human delta-aminolevulinate dehydratase gene at 9q34

RsaI polymorphism in the human delta-aminolevulinate dehydratase gene at 9q34

by Astrin, K H, Kaya, A H, Wetmur, J G, Desnick, R J
Published in Nucleic acids research (11.08.1991)

Get full text

Journal Article

Acute intermittent porphyria: a single-base deletion and a nonsense mutation in the human hydroxymethylbilane synthase gene, predicting truncations of the enzyme polypeptide

Acute intermittent porphyria: a single-base deletion and a nonsense mutation in the human hydroxymethylbilane synthase gene, predicting truncations of the enzyme polypeptide

by Lee, G Y, Astrin, K H, Desnick, R J
Published in American journal of medical genetics (28.08.1995)

Get more information

Journal Article

Measurement of free nucleotides in cultured human lymphoid cells using high pressure liquid chromatography

Measurement of free nucleotides in cultured human lymphoid cells using high pressure liquid chromatography

by Brenton, D.P., Astrin, K.H., Cruikshank, M.K., Seegmiller, J.E.
Published in Biochemical medicine (01.06.1977)

Get full text

Journal Article