T. Kotlar

发表

Restoration of growth hormone-releasing hormone (GHRH) responsiveness in pituitary GH3 cells by adenovirus-directed expression of the human GHRH receptor.

E. J. Lee, J. Jameson, Eun-Jig Lee, 2001, Endocrinology.

Absence of constitutively activating mutations in the GHRH receptor in GH-producing pituitary tumors.

J. Jameson, I. Ciric, K. Huh, 2001, The Journal of clinical endocrinology and metabolism.

Heparin-binding apoproteins. Effects on lipoprotein lipase and hepatic uptake of remnants.

J. Borensztajn, T. Kotlar, C. A. Matza, 1986, The Biochemical journal.

Apoprotein-independent binding of chylomicron remnants to rat liver membranes.

J. Borensztajn, S. Y. Chang, T. Kotlar, 1991, The Biochemical journal.

Uptake of phospholipid-depleted chylomicrons by the perfused rat liver.

J. Borensztajn, T. Kotlar, B. McNeill, 1980, The Biochemical journal.

Liver uptake of chylomicron remnants with high and low apoprotein E:C ratios.

J. Borensztajn, T. Kotlar, 1984, Proceedings of the National Academy of Sciences of the United States of America.

Phospholipids as modulators of hepatic recognition of chylomicron remnants. Observations with emulsified lipoprotein lipids.

J. Borensztajn, T. Kotlar, 1990, The Biochemical journal.

The apoprotein B-independent hepatic uptake of chylomicron remnants.

G. Getz, J. Borensztajn, R. Padley, 1982, The Biochemical journal.

Uptake of chylomicron remnants by the liver: further evidence for the modulating role of phospholipids.

G. Getz, J. Borensztajn, T. Kotlar, 1988, Journal of lipid research.

The inhibition in vivo of lipoprotein lipase (clearing-factor lipase) activity by triton WR-1339.

J. Borensztajn, T. Kotlar, M. Rone, 1976, The Biochemical journal.

Absence of mutations in the FSH receptor in ovarian granulosa cell tumors.

R. Scully, W. Crowley, C. Albanese, 1998, The Journal of clinical endocrinology and metabolism.

A mutation in the follicle-stimulating hormone receptor occurs frequently in human ovarian sex cord tumors.

R. Scully, W. Crowley, C. Albanese, 1997, The Journal of clinical endocrinology and metabolism.

Fractionation of chylomicrons by heparin-sepharose chromatography. Characterization of two heparin-binding proteins.

S. Meredith, J. Borensztajn, T. Kotlar, 1985, The Journal of biological chemistry.

A novel loss of function mutation in exon 10 of the FSH receptor gene causing hypergonadotrophic hypogonadism: clinical and molecular characteristics.

I. Huhtaniemi, J. Jameson, P. Pakarinen, 2003, Human reproduction.

Mutational analysis of DAX1 in patients with hypogonadotropic hypogonadism or pubertal delay.

P. Hindmarsh, W. Crowley, D. Bick, 1999, The Journal of clinical endocrinology and metabolism.

Phenocopies for deafness and goiter development in a large inbred Brazilian kindred with Pendred's syndrome associated with a novel mutation in the PDS gene.

P. Kopp, J. Jameson, G. Medeiros-Neto, 1999, The Journal of clinical endocrinology and metabolism.

X-linked sex-determining region Y box 3 (SOX3) gene mutations are uncommon in men with idiopathic oligoazoospermic infertility.

J. Jameson, M. Pugeat, G. Raverot, 2004, The Journal of clinical endocrinology and metabolism.

Clinical and molecular analysis of three families with autosomal dominant neurohypophyseal diabetes insipidus associated with a novel and recurrent mutations in the vasopressin-neurophysin II gene.

P. Kopp, J. Rutishauser, G. Robertson, 2002, European journal of endocrinology.

Hydrolysis of chylomicron triacylglycerol by endothelium-bound lipoprotein lipase. Effect of decreased apoprotein C-II/C-III ratio.

J. Borensztajn, T. Kotlar, 1979, The Biochemical journal.

Adenovirus-mediated targeted expression of toxic genes to adrenocorticotropin-producing pituitary tumors using the proopiomelanocortin promoter.

J. Jameson, F. Martinson, E. J. Lee, 2001, The Journal of clinical endocrinology and metabolism.

Lack of association between the -308 polymorphism of the tumor necrosis factor-alpha gene and the insulin resistance syndrome.

S. Gapstur, W. Lowe, K. Liu, 2000, Journal of investigative medicine : the official publication of the American Federation for Clinical Research.

A novel mutation (R97C) in the neurophysin moiety of prepro-vasopressin-neurophysin II associated with autosomal-dominant neurohypophyseal diabetes insipidus.

P. Kopp, J. Rutishauser, G. Robertson, 1999, Molecular genetics and metabolism.

Hepatic uptake of phospholipid-depleted chylomicrons in vivo. Comparison with the uptake of chylomicron remnants.

J. Borensztajn, T. Kotlar, 1981, The Biochemical journal.

LETTERS TO THE EDITOR Absence of Mutations in the FSH Receptor in Ovarian Granulosa Cell Tumors a

R. Scully, C. Albanese, J. Jameson, 1998 .

Restoration of Growth Hormone-Releasing Hormone (GHRH) Responsiveness in Pituitary GH3 Cells by Adenovirus-Directed Expression of the Human GHRH Receptor* * This work was supported by a Center of Excellence grant from Knoll Pharmaceutical Co.

Eun-Jig Lee, W. Duan, T. Kotlar, 2001, Endocrinology.