Factors influencing premature induction of enzyme in cultured chick-embryo liver cells

Por Skea, B. R., Nemeth, A. M.
Publicado em 1969

Changes in the mechanism regulating liver uridine diphosphate glucuronyltransferase activity during embryonic life.

Por Burchell, B, Dutton, G J, Nemeth, A M
Publicado em 1971

Induction of uridine diphosphate glucuronyltransferase: relation to protein and ribonucleic acid synthesis.

Por Burchell, B, Nemeth, A M, Dutton, G J
Publicado em 1972

Development of uridine diphosphate-glucuronyltransferase activity in cultures of chick-embryo liver

Por Ko, Vivian, Dutton, G. J., Nemeth, A. M.
Publicado em 1967

The ramification and connections of retinal fibres in layer 7 of the domestic chick optic tectum: a Golgi impregnation, anterograde tracer and GABA-immunogold study

Por Sebestény, T, Davies, DC, Zayats, N, Németh, A, Tömböl, T
Publicado em 2002

Autoantibodies against cytochrome P450s in sera of children treated with immunosuppressive drugs

Por LYTTON, S D, BERG, U, NEMETH, A, INGELMAN-SUNDBERG, M
Publicado em 2002

Klinefelter-like phenotype and primary infertility in a male with a paracentric Xq inversion

Por Nemeth, A, Gallen, I, Crocker, M, Levy, E, Maher, E
Publicado em 2002

Cytomegalovirus DNA detection on Guthrie cards in patients with neonatal cholestasis

Por Fischler, B., Rodensjo, P., Nemeth, A., Forsgren, M., Lewensohn-Fuchs, I.
Publicado em 1999

Isolation of genomic and cDNA clones encoding bovine poly(A) binding protein II.

Por Nemeth, A, Krause, S, Blank, D, Jenny, A, Jenö, P, Lustig, A, Wahle, E
Publicado em 1995

Some Biochemical Changes in the Transplanted Kidney

Por Williams, M. A., Tyler, H. M., Morton, Mary, Nemeth, A., Dempster, W. J.
Publicado em 1962

The Drosophila poly(A)-binding protein II is ubiquitous throughout Drosophila development and has the same function in mRNA polyadenylation as its bovine homolog in vitro.

Por Benoit, B, Nemeth, A, Aulner, N, Kühn, U, Simonelig, M, Wahle, E, Bourbon, H M
Publicado em 1999

Density of γ/δ(+) T cells in the jejunal epithelium of patients with coeliac disease and dermatitis herpetiformis is increased with age

Por SAVILAHTI, E, ÖRMÄLÄ, T, ARATO, A, HACSEK, G, HOLM, K, KLEMOLA, T, NEMETH, A, MÄKI, M, REUNALA, T
Publicado em 1997

Growth in Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency

Por Haglind, C. Bieneck, Stenlid, M. Halldin, Ask, S., Alm, J., Nemeth, A., Döbeln, Uv., Nordenström, A.
Publicado em 2012

Neuropsychological Development in Patients with Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase (LCHAD) Deficiency

Por Strandqvist, A., Haglind, C. Bieneck, Zetterström, R. H., Nemeth, A., von Döbeln, U., Stenlid, M. Halldin, Nordenström, A.
Publicado no JIMD Rep (2015)

Relation between GB virus C/hepatitis G virus and fulminant hepatic failure may be secondary to treatment with contaminated blood and/or blood products

Por Halasz, R, Barkholt, L, Lara, C, Hultgren, C, Ando, Y, Broome, U, Fischler, B, Nemeth, A, Ericzon, B, Sonnerborg, A, Sallberg, M
Publicado em 1999

Genetic mapping of a cone and rod dysfunction (Aland Island eye disease) to the proximal short arm of the human X chromosome.

Por Glass, I A, Good, P, Coleman, M P, Fullwood, P, Giles, M G, Lindsay, S, Nemeth, A H, Davies, K E, Willshaw, H A, Fielder, A
Publicado em 1993

De Novo Donor‐Specific HLA Antibody Formation in Two Patients With Crigler‐Najjar Syndrome Type I Following Human Hepatocyte Transplantation With Partial Hepatectomy Preconditionin...

Por Jorns, C., Nowak, G., Nemeth, A., Zemack, H., Mörk, L.‐M., Johansson, H., Gramignoli, R., Watanabe, M., Karadagi, A., Alheim, M., Hauzenberger, D., van Dijk, R., Bosma, P. J., Ebbesen, F., Szakos, A., Fischler, B., Strom, S., Ellis, E., Ericzon, B.‐G.
Publicado no Am J Transplant (2015)

Chorea-acanthocytosis: genetic linkage to chromosome 9q21.

Por Rubio, J P, Danek, A, Stone, C, Chalmers, R, Wood, N, Verellen, C, Ferrer, X, Malandrini, A, Fabrizi, G M, Manfredi, M, Vance, J, Pericak-Vance, M, Brown, R, Rudolf, G, Picard, F, Alonso, E, Brin, M, Németh, A H, Farrall, M, Monaco, A P
Publicado em 1997

Phenotypic heterogeneity and genetic modification of P102L inherited prion disease in an international series

Por Webb, T. E. F., Poulter, M., Beck, J., Uphill, J., Adamson, G., Campbell, T., Linehan, J., Powell, C., Brandner, S., Pal, S., Siddique, D., Wadsworth, J. D., Joiner, S., Alner, K., Petersen, C., Hampson, S., Rhymes, C., Treacy, C., Storey, E., Geschwind, M. D., Nemeth, A. H., Wroe, S., Collinge, J., Mead, S.
Publicado em 2008