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| Title : Maintaining the thyroid gland in mutant thyroglobulin-induced hypothyroidism requires thyroid cell proliferation that must continue in adulthood - Zhang_2022_J.Biol.Chem_298_102066 |
| Author(s) : Zhang X , Malik B , Young C , Zhang H , Larkin D , Liao XH , Refetoff S , Liu M , Arvan P |
| Ref : Journal of Biological Chemistry , 298 :102066 , 2022 |
| Abstract : Zhang_2022_J.Biol.Chem_298_102066 |
| ESTHER : Zhang_2022_J.Biol.Chem_298_102066 |
| PubMedSearch : Zhang_2022_J.Biol.Chem_298_102066 |
| PubMedID: 35618019 |
| Title : Insertion of an Alu Element in Thyroglobulin Gene as a Novel Cause of Congenital Hypothyroidism - Bruellman_2020_Thyroid__ |
| Author(s) : Bruellman R , Watanabe Y , Shareef R , Abdullah MA , Dumitrescu A , Strauss BS , Refetoff S , Weiss RE |
| Ref : Thyroid , : , 2020 |
| Abstract : Bruellman_2020_Thyroid__ |
| ESTHER : Bruellman_2020_Thyroid__ |
| PubMedSearch : Bruellman_2020_Thyroid__ |
| PubMedID: 31868128 |
| Title : Increased Prevalence of TG and TPO Mutations in Sudanese Children With Congenital Hypothyroidism - Bruellman_2020_J.Clin.Endocrinol.Metab_105_1564 |
| Author(s) : Bruellman RJ , Watanabe Y , Ebrhim RS , Creech MK , Abdullah MA , Dumitrescu AM , Refetoff S , Weiss RE |
| Ref : J Clinical Endocrinology Metab , 105 :1564 , 2020 |
| Abstract : Bruellman_2020_J.Clin.Endocrinol.Metab_105_1564 |
| ESTHER : Bruellman_2020_J.Clin.Endocrinol.Metab_105_1564 |
| PubMedSearch : Bruellman_2020_J.Clin.Endocrinol.Metab_105_1564 |
| PubMedID: 31867598 |
| Title : A novel mutation in the TG gene (G2322S) causing congenital hypothyroidism in a Sudanese family: a case report - Watanabe_2018_BMC.Med.Genet_19_69 |
| Author(s) : Watanabe Y , Sharwood E , Goodwin B , Creech MK , Hassan HY , Netea MG , Jaeger M , Dumitrescu A , Refetoff S , Huynh T , Weiss RE |
| Ref : BMC Med Genet , 19 :69 , 2018 |
| Abstract : Watanabe_2018_BMC.Med.Genet_19_69 |
| ESTHER : Watanabe_2018_BMC.Med.Genet_19_69 |
| PubMedSearch : Watanabe_2018_BMC.Med.Genet_19_69 |
| PubMedID: 29720101 |
| Gene_locus related to this paper: human-TG |
| Title : A clinically euthyroid child with a large goiter due to a thyroglobulin gene defect: clinical features and genetic studies - Hermanns_2013_J.Pediatr.Endocrinol.Metab_26_119 |
| Author(s) : Hermanns P , Refetoff S , Sriphrapradang C , Pohlenz J , Okamato J , Slyper L , Slyper AH |
| Ref : J Pediatr Endocrinol Metab , 26 :119 , 2013 |
| Abstract : Hermanns_2013_J.Pediatr.Endocrinol.Metab_26_119 |
| ESTHER : Hermanns_2013_J.Pediatr.Endocrinol.Metab_26_119 |
| PubMedSearch : Hermanns_2013_J.Pediatr.Endocrinol.Metab_26_119 |
| PubMedID: 23457313 |
| Gene_locus related to this paper: human-TG |
| Title : Defective thyroglobulin storage in LDL receptor-associated protein-deficient mice - Lisi_2006_Am.J.Physiol.Cell.Physiol_290_C1160 |
| Author(s) : Lisi S , Botta R , Pinchera A , Collins AB , Refetoff S , Arvan P , Bu G , Grasso L , Marshansky V , Bechoua S , Hurtado-Lorenzo A , Marcocci C , Brown D , McCluskey RT , Marino M |
| Ref : American Journal of Physiology Cell Physiol , 290 :C1160 , 2006 |
| Abstract : Lisi_2006_Am.J.Physiol.Cell.Physiol_290_C1160 |
| ESTHER : Lisi_2006_Am.J.Physiol.Cell.Physiol_290_C1160 |
| PubMedSearch : Lisi_2006_Am.J.Physiol.Cell.Physiol_290_C1160 |
| PubMedID: 16306127 |