These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

179 related articles for article (PubMed ID: 8380383)

  • 1. Molecular basis of the thyroglobulin synthesis defect in Dutch goats.
    Veenboer GJ; de Vijlder JJ
    Endocrinology; 1993 Jan; 132(1):377-81. PubMed ID: 8380383
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Defective thyroglobulin synthesis and secretion causing goiter and hypothyroidism.
    Medeiros-Neto G; Targovnik HM; Vassart G
    Endocr Rev; 1993 Apr; 14(2):165-83. PubMed ID: 8325250
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A nonsense mutation causes human hereditary congenital goiter with preferential production of a 171-nucleotide-deleted thyroglobulin ribonucleic acid messenger.
    Targovnik HM; Medeiros-Neto G; Varela V; Cochaux P; Wajchenberg BL; Vassart G
    J Clin Endocrinol Metab; 1993 Jul; 77(1):210-5. PubMed ID: 8325944
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Normal-sized thyroglobulin messenger ribonucleic acid in Dutch goats with a thyroglobulin synthesis defect is translated into a 35,000 molecular weight N-terminal fragment.
    Sterk A; van Dijk JE; Veenboer GJ; Moorman AF; de Vijlder JJ
    Endocrinology; 1989 Jan; 124(1):477-83. PubMed ID: 2642421
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A premature stopcodon in thyroglobulin messenger RNA results in familial goiter and moderate hypothyroidism.
    van de Graaf SA; Ris-Stalpers C; Veenboer GJ; Cammenga M; Santos C; Targovnik HM; de Vijlder JJ; Medeiros-Neto G
    J Clin Endocrinol Metab; 1999 Jul; 84(7):2537-42. PubMed ID: 10404833
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Congenital goiter with hypothyroidism caused by a 5' splice site mutation in the thyroglobulin gene.
    Targovnik HM; Rivolta CM; Mendive FM; Moya CM; Vono J; Medeiros-Neto G
    Thyroid; 2001 Jul; 11(7):685-90. PubMed ID: 11484898
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Evidence for the segregation of three different mutated alleles of the thyroglobulin gene in a Brazilian family with congenital goiter and hypothyroidism.
    Targovnik HM; Frechtel GD; Mendive FM; Vono J; Cochaux P; Vassart G; Medeiros-Neto G
    Thyroid; 1998 Apr; 8(4):291-7. PubMed ID: 9588493
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A 138-nucleotide deletion in the thyroglobulin ribonucleic acid messenger in a congenital goiter with defective thyroglobulin synthesis.
    Targovnik HM; Vono J; Billerbeck AE; Cerrone GE; Varela V; Mendive F; Wajchenberg BL; Medeiros-Neto G
    J Clin Endocrinol Metab; 1995 Nov; 80(11):3356-60. PubMed ID: 7593451
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Thyroglobulin (Tg) gene and familial Tg synthesis defect].
    Ieiri T
    Nihon Rinsho; 1994 Apr; 52(4):869-74. PubMed ID: 8196172
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A new case of congenital goiter with hypothyroidism caused by a homozygous p.R277X mutation in the exon 7 of the thyroglobulin gene: a mutational hot spot could explain the recurrence of this mutation.
    Rivolta CM; Moya CM; Gutnisky VJ; Varela V; Miralles-García JM; González-Sarmiento R; Targovnik HM
    J Clin Endocrinol Metab; 2005 Jun; 90(6):3766-70. PubMed ID: 15769978
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A 3' splice site mutation in the thyroglobulin gene responsible for congenital goiter with hypothyroidism.
    Ieiri T; Cochaux P; Targovnik HM; Suzuki M; Shimoda S; Perret J; Vassart G
    J Clin Invest; 1991 Dec; 88(6):1901-5. PubMed ID: 1752952
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Low levels of thyroglobulin messenger ribonucleic acid in congenital goitrous hypothyroidism with defective thyroglobulin synthesis.
    Targovnik H; Propato F; Varela V; Wajchenberg B; Knobel M; D'Abronzo HF; Medeiros-Neto G
    J Clin Endocrinol Metab; 1989 Dec; 69(6):1137-47. PubMed ID: 2584351
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Compound heterozygous mutations in the thyroglobulin gene (1143delC and 6725G-->A [R2223H]) resulting in fetal goitrous hypothyroidism.
    Caron P; Moya CM; Malet D; Gutnisky VJ; Chabardes B; Rivolta CM; Targovnik HM
    J Clin Endocrinol Metab; 2003 Aug; 88(8):3546-53. PubMed ID: 12915634
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Nonfunctional thyroglobulin messenger RNA in goats with hereditary congenital goiter.
    de Vijlder JJ; van Ommen GJ; van Voorthuizen WF; Koch CA; Arnberg AC; Vassart G; Dinsart C; Flavell RA
    J Mol Appl Genet; 1981; 1(1):51-9. PubMed ID: 6125553
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Studies on the structures of the normal and abnormal goat thyroglobulin genes.
    Van Ommen GJ; Sterk A; Mercken LO; Arnberg AC; Baas F; De Vijlder JJ
    Biochimie; 1989 Feb; 71(2):211-21. PubMed ID: 2495821
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A single amino acid change in the acetylcholinesterase-like domain of thyroglobulin causes congenital goiter with hypothyroidism in the cog/cog mouse: a model of human endoplasmic reticulum storage diseases.
    Kim PS; Hossain SA; Park YN; Lee I; Yoo SE; Arvan P
    Proc Natl Acad Sci U S A; 1998 Aug; 95(17):9909-13. PubMed ID: 9707574
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Two distinct compound heterozygous constellations (R277X/IVS34-1G>C and R277X/R1511X) in the thyroglobulin (TG) gene in affected individuals of a Brazilian kindred with congenital goiter and defective TG synthesis.
    Gutnisky VJ; Moya CM; Rivolta CM; Domené S; Varela V; Toniolo JV; Medeiros-Neto G; Targovnik HM
    J Clin Endocrinol Metab; 2004 Feb; 89(2):646-57. PubMed ID: 14764776
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular analysis of congenital goitres with hypothyroidism caused by defective thyroglobulin synthesis. Identification of a novel c.7006C>T [p.R2317X] mutation and expression of minigenes containing nonsense mutations in exon 7.
    Machiavelli GA; Caputo M; Rivolta CM; Olcese MC; Gruñeiro-Papendieck L; Chiesa A; González-Sarmiento R; Targovnik HM
    Clin Endocrinol (Oxf); 2010 Jan; 72(1):112-21. PubMed ID: 19438905
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Clinical and genetic analysis of a compound heterozygous mutation in the thyroglobulin gene in a Chinese twin family with congenital goiter and hypothyroidism.
    Liu S; Zhang S; Li W; Zhang A; Qi F; Zheng G; Yan S; Ma X
    Twin Res Hum Genet; 2012 Feb; 15(1):126-32. PubMed ID: 22784463
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Molecular genetics of hereditary thyroid diseases due to a defect in the thyroglobulin or thyroperoxidase synthesis.
    Targovnik HM; Varela V; Frechtel GD; Cerrone GE; Copelli SB; Propato FV; Mendive F
    Braz J Med Biol Res; 1994 Dec; 27(12):2745-57. PubMed ID: 7549998
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.