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Proceedings of the National Academy of Sciences of the United States of America
|
November 1, 1970
Detection of bacteriophage T4- and T5-coded transfer RNAs
N H Scherberg, S B Weiss
Proceedings of the National Academy of Sciences of the United States of America
|
May 1, 1972
T4 transfer RNAs: codon recognition and translational properties
N H Scherberg, S B Weiss
Endocrinologia Experimentalis
|
March 1, 1990
Anterior pituitary: triiodothyronine and/or dexamethasone induced changes in protein formation in thyroidectomized and/or adrenalectomized rats
J Brtko, J Knopp, N H Scherberg
The Journal of Clinical Endocrinology and Metabolism
|
September 1, 1983
Elevated serum thyroglobulin level in congenital thyroxine-binding globulin deficiency
D Sarne, K Barokas, N H Scherberg, et al.
Analytical Biochemistry
|
June 1, 1985
Direct application of radioiodinated aminoacyl tRNA for radiolabeling nascent proteins
N H Scherberg, K Barokas, Y Murata, et al.
The Journal of Clinical Endocrinology and Metabolism
|
January 1, 1983
The influence of percutaneous fine needle aspiration on serum thyroglobulin
E G Lever, S Refetoff, N H Scherberg, et al.
JAMA
|
November 7, 1990
Neonatal detection of generalized resistance to thyroid hormone
R E Weiss, S Balzano, N H Scherberg, et al.
The Journal of Clinical Endocrinology and Metabolism
|
December 1, 1995
Thyroid function tests and characterization of thyroxine-binding globulin in the carbohydrate-deficient glycoprotein syndrome type I
P E Macchia, H H Harrison, N H Scherberg, et al.
The Journal of Clinical Endocrinology and Metabolism
|
August 18, 2000
Familial dysalbuminemic hyperthyroxinemia in a Swiss family caused by a mutant albumin (R218P) shows an apparent discrepancy between serum concentration and affinity for thyroxine
S Pannain, M Feldman, U Eiholzer, et al.
The Journal of Clinical Endocrinology and Metabolism
|
May 20, 1998
Familial dysalbuminemic hypertriiodothyroninemia: a new, dominantly inherited albumin defect
T Sunthornthepvarakul, S Likitmaskul, S Ngowngarmratana, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 12) with videos related to
Sort By:
Page
of 2
Proceedings of the National Academy of Sciences of the United States of America
|
November 1, 1970
Detection of bacteriophage T4- and T5-coded transfer RNAs
N H Scherberg, S B Weiss
Proceedings of the National Academy of Sciences of the United States of America
|
May 1, 1972
T4 transfer RNAs: codon recognition and translational properties
N H Scherberg, S B Weiss
Endocrinologia Experimentalis
|
March 1, 1990
Anterior pituitary: triiodothyronine and/or dexamethasone induced changes in protein formation in thyroidectomized and/or adrenalectomized rats
J Brtko, J Knopp, N H Scherberg
The Journal of Clinical Endocrinology and Metabolism
|
September 1, 1983
Elevated serum thyroglobulin level in congenital thyroxine-binding globulin deficiency
D Sarne, K Barokas, N H Scherberg, et al.
Analytical Biochemistry
|
June 1, 1985
Direct application of radioiodinated aminoacyl tRNA for radiolabeling nascent proteins
N H Scherberg, K Barokas, Y Murata, et al.
The Journal of Clinical Endocrinology and Metabolism
|
January 1, 1983
The influence of percutaneous fine needle aspiration on serum thyroglobulin
E G Lever, S Refetoff, N H Scherberg, et al.
JAMA
|
November 7, 1990
Neonatal detection of generalized resistance to thyroid hormone
R E Weiss, S Balzano, N H Scherberg, et al.
The Journal of Clinical Endocrinology and Metabolism
|
December 1, 1995
Thyroid function tests and characterization of thyroxine-binding globulin in the carbohydrate-deficient glycoprotein syndrome type I
P E Macchia, H H Harrison, N H Scherberg, et al.
The Journal of Clinical Endocrinology and Metabolism
|
August 18, 2000
Familial dysalbuminemic hyperthyroxinemia in a Swiss family caused by a mutant albumin (R218P) shows an apparent discrepancy between serum concentration and affinity for thyroxine
S Pannain, M Feldman, U Eiholzer, et al.
The Journal of Clinical Endocrinology and Metabolism
|
May 20, 1998
Familial dysalbuminemic hypertriiodothyroninemia: a new, dominantly inherited albumin defect
T Sunthornthepvarakul, S Likitmaskul, S Ngowngarmratana, et al.
Page
of 2