H. Tallan

发表

N-Acetyl-L-aspartic acid in brain.

H. Tallan, S. Moore, W. Stein, 1956, The Journal of biological chemistry.

Pathogenesis of Brain Dysfunction in Inborn Errors of Amino Acid Metabolism

A. Lajtha, H. Tallan, D. Rassin, 1975 .

Studies on the free amino acids and related compounds in the tissues of the cat.

H. Tallan, S. Moore, W. Stein, 1954, The Journal of biological chemistry.

Methionine adenosyltransferase: kinetic properties of human and rat liver enzymes.

H. Tallan, P. A. Cohen, 1976, Biochemical medicine.

3-Methylhistidine, a new amino acid from human urine.

H. Tallan, S. Moore, W. Stein, 1954, The Journal of biological chemistry.

Intermittent hypermethioninaemia associated with normal hepatic methionine adenosyltransferase activity: Report of a case

H. Tallan, G. Gaull, N. Buist, 1982, Journal of Inherited Metabolic Disease.

Methioninemia and myopathy: A new disorder

D. Vulovic, F. Schaffner, H. Tallan, 1981, Annals of neurology.

Hypermethioninemia associated with methionine adenosyltransferase deficiency: clinical, morphologic, and biochemical observations on four patients.

F. Schaffner, D. Lonsdale, H. Tallan, 1981, The Journal of pediatrics.

Methionine adenosyltransferase in man: evidence for multiple forms.

H. Tallan, 1979, Biochemical medicine.

Methionine Adenosyltransferase Deficiency: New Enzymatic Defect Associated with Hypermethioninemia

H. Tallan, G. Gaull, 1974, Science.

[82] Preparation and analysis of N-acetyl-d-aspartic acid

H. Tallan, 1963 .

Tyrosine-O-sulfate as a constituent of normal human urine.

H. Tallan, S. Moore, W. Stein, 1955, The Journal of biological chemistry.

Studies on the distribution of N-acetyl-L-aspartic acid in brain.

H. Tallan, 1957, The Journal of biological chemistry.

L-cystathionine in human brain.

H. Tallan, S. Moore, W. Stein, 1958, The Journal of biological chemistry.

Taurine: biological update.

H. Tallan, C. Wright, G. Gaull, 1986, Annual review of biochemistry.

A cobalamin metabolic defect with homocystinuria, methylmalonic aciduria and macrocytic anemia.

H. Tallan, D. Rassin, J. Isenberg, 1986, Neuropediatrics.

Cystathionine γ-synthesis from homocysteine and cysteine by mammalian tissue

H. Tallan, J. Sturman, G. Gaull, 1974 .

Aldosterone synthesis by adrenal mitochondria. 3. Participation of cytochrome P-450.

P. Greengard, R. Estabrook, H. Tallan, 1967, Archives of biochemistry and biophysics.

STUDIES ON LYSOZYME

H. Tallan, W. Stein, 1951 .

THE DETERMINATION AND PHYSIOLOGICAL DISTRIBUTION OF DIPYRIDAMOLE AND ITS GLUCURONIDES IN BIOLOGICAL MATERIAL.

P. Greengard, H. Tallan, I. Fratta, 1963, The Journal of pharmacology and experimental therapeutics.

Methionine Metabolism in the Brain

H. Tallan, D. Rassin, J. Sturman, 1983 .

On the proteolytic enzymes of animal tissues. X. Beef spleen cathepsin C.

H. Tallan, M. E. Jones, J. Fruton, 1952, The Journal of biological chemistry.

Chromatographic studies on lysozyme.

H. Tallan, W. Stein, 1953, The Journal of biological chemistry.

Taurine uptake by cultured human lymphoblastoid cells.

H. Tallan, E. Jacobson, C. Wright, 1983, Life sciences.

Taurine availability and function in neurogenetic retinopathies.

T. Wright, H. Tallan, J. Sturman, 1987, Advances in experimental medicine and biology.

Aldosterone synthesis by adrenal mitochondria. II. The effect of citric acid cycle intermediates; identification of the soluble stimulatory factor as fumarase.

P. Greengard, H. Tallan, P Greengard, 1967, The Journal of biological chemistry.

Aldosterone synthesis by adrenal mitochondria.

P. Greengard, H. Tallan, P Greengard, 1966, The Journal of biological chemistry.

Cystathionine synthase deficiency: Heterozygote detection using cultured skin fibroblasta

K. Hirschhorn, H. Tallan, N. Beratis, 1973 .

Hepatic cystathionase: immunochemical and electrophoretic studies of the human and rat forms.

H. Tallan, T. Pascal, B. Gillam, 1972, Biochimica et biophysica acta.

Homocystinuria: Observations on the Biosynthesis of Cystathionine and Homolanthionine

H. Tallan, D. Rassin, J. Sturman, 1971, Pediatric Research.

Homolanthionine synthesis by human liver cystathionase.

H. Tallan, G. Gaull, K. Schneidman, 1971, Biochemical and biophysical research communications.

METHIONINE-ACTIVATING ENZYME (MAE) DEFICIENCY: A NEW CAUSE FOR HYPERMETHIONINEMIA IN INFANCY

K. Hirschhorn, F. Schaffner, D. Lonsdale, 1974, Pediatric Research.

Cystathionase Deficiency: Evidence for Genetic Heterogeneity in Primary Cystathioninuria

H. Tallan, N. Beratis, G. Gaull, 1978, Pediatric Research.

Vitamin B6-responsive and -unresponsive cystathioninuria: two variant molecular forms

K. Hirschhorn, H. Tallan, N. Beratis, 1975, Science.

Cystathionine β-Synthase Deficiency: Differences in Thermostability between Normal and Abnormal Enzyme from Cultured Human Cells

H. Tallan, R. Longhi, G. Gaull, 1978, Pediatric Research.

Homocystinuria: Biosynthesis of Cystathionine and Homolanthionine

H. Tallan, D. Rassin, J. Sturman, 1970, Pediatric Research.

Homocystinuria: investigations of cystathionine synthase in cultured fetal cells and the prenatal determination of genetic status.

K. Hirschhorn, H. Tallan, N. Beratis, 1974, The Journal of pediatrics.

Cystathionine β-Synthase Deficiency: A Qualitative Abnormality of the Deficient Enzyme Modified by Vitamin B6 Therapy

H. Tallan, R. Longhi, G. Gaull, 1977, Pediatric Research.

Mitochondrial Abnormalities of Liver in Primary Ornithine Transcarbamylase Deficiency

F. Schaffner, H. Tallan, G. Gaull, 1980, Pediatric Research.

Spectrophotometric Method for Assay of Serum Antiprotease: Clinical Applications.*

H. Tallan, E. Cliffton, G. Downie, 1949, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

Ornithine carbamoyltransferase deficiency in an adult male patient: significance of hepatic ultrastructure in clinical diagnosis.

F. Schaffner, H. Tallan, G. Gaull, 1983, Pediatrics.