Abramowicz M - Search Results

1

Thyroid transcription factor 1 rescues PAX8/p300 synergism impaired by a natural PAX8 paired domain mutation with dominant negative activity.

Grasberger H, Ringkananont U, Lefrancois P, Abramowicz M, Vassart G, Refetoff S. Grasberger H, et al. Among authors: abramowicz m. Mol Endocrinol. 2005 Jul;19(7):1779-91. doi: 10.1210/me.2004-0426. Epub 2005 Feb 17. Mol Endocrinol. 2005. PMID: 15718293

2

Autosomal dominant resistance to thyrotropin as a distinct entity in five multigenerational kindreds: clinical characterization and exclusion of candidate loci.

Grasberger H, Mimouni-Bloch A, Vantyghem MC, van Vliet G, Abramowicz M, Metzger DL, Abdullatif H, Rydlewski C, Macchia PE, Scherberg NH, van Sande J, Mimouni M, Weiss RE, Vassart G, Refetoff S. Grasberger H, et al. Among authors: abramowicz m. J Clin Endocrinol Metab. 2005 Jul;90(7):4025-34. doi: 10.1210/jc.2005-0572. Epub 2005 May 3. J Clin Endocrinol Metab. 2005. PMID: 15870119 Free article.

3

Characterization of a novel loss of function mutation of PAX8 in a familial case of congenital hypothyroidism with in-place, normal-sized thyroid.

Meeus L, Gilbert B, Rydlewski C, Parma J, Roussie AL, Abramowicz M, Vilain C, Christophe D, Costagliola S, Vassart G. Meeus L, et al. Among authors: abramowicz m. J Clin Endocrinol Metab. 2004 Sep;89(9):4285-91. doi: 10.1210/jc.2004-0166. J Clin Endocrinol Metab. 2004. PMID: 15356023

4

Autosomal dominant transmission of congenital thyroid hypoplasia due to loss-of-function mutation of PAX8.

Vilain C, Rydlewski C, Duprez L, Heinrichs C, Abramowicz M, Malvaux P, Renneboog B, Parma J, Costagliola S, Vassart G. Vilain C, et al. Among authors: abramowicz m. J Clin Endocrinol Metab. 2001 Jan;86(1):234-8. doi: 10.1210/jcem.86.1.7140. J Clin Endocrinol Metab. 2001. PMID: 11232006

5

Functional study of the human thyroid peroxidase gene promoter.

Abramowicz MJ, Vassart G, Christophe D. Abramowicz MJ, et al. Eur J Biochem. 1992 Feb 1;203(3):467-73. doi: 10.1111/j.1432-1033.1992.tb16571.x. Eur J Biochem. 1992. PMID: 1735431 Free article.

6

Probing the cause of thyroid dysgenesis.

Abramowicz MJ, Vassart G, Refetoff S. Abramowicz MJ, et al. Thyroid. 1997 Jun;7(3):325-6. doi: 10.1089/thy.1997.7.325. Thyroid. 1997. PMID: 9226198 No abstract available.

7

Thyroid peroxidase gene promoter confers TSH responsiveness to heterologous reporter genes in transfection experiments.

Abramowicz MJ, Vassart G, Christophe D. Abramowicz MJ, et al. Biochem Biophys Res Commun. 1990 Feb 14;166(3):1257-64. doi: 10.1016/0006-291x(90)91001-9. Biochem Biophys Res Commun. 1990. PMID: 2306241

8

Familial congenital hypothyroidism due to inactivating mutation of the thyrotropin receptor causing profound hypoplasia of the thyroid gland.

Abramowicz MJ, Duprez L, Parma J, Vassart G, Heinrichs C. Abramowicz MJ, et al. J Clin Invest. 1997 Jun 15;99(12):3018-24. doi: 10.1172/JCI119497. J Clin Invest. 1997. PMID: 9185526 Free PMC article.

9

Thyroperoxidase mRNA in quiescent and proliferating thyroid epithelial cells: expression and subcellular localization studied by in situ hybridization.

Pohl V, Abramowicz M, Vassart G, Dumont JE, Roger PP. Pohl V, et al. Among authors: abramowicz m. Eur J Cell Biol. 1993 Oct;62(1):94-104. Eur J Cell Biol. 1993. PMID: 8269983

10

Pathology of the TSH receptor.

Duprez L, Parma J, Van Sande J, Rodien P, Sabine C, Abramowicz M, Dumont JE, Vassart G. Duprez L, et al. Among authors: abramowicz m. J Pediatr Endocrinol Metab. 1999 Apr;12 Suppl 1:295-302. J Pediatr Endocrinol Metab. 1999. PMID: 10698593 Review.

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