Detalhe da pesquisa
1.
Steroid-induced diabetes: a clinical and molecular approach to understanding and treatment.
Diabetes Metab Res Rev
; 30(2): 96-102, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24123849
2.
Role of type 2 deiodinase in response to acute lung injury (ALI) in mice.
Proc Natl Acad Sci U S A
; 108(49): E1321-9, 2011 Dec 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-22065740
3.
Mutations in SECISBP2 result in abnormal thyroid hormone metabolism.
Nat Genet
; 37(11): 1247-52, 2005 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-16228000
4.
STR mutations on chromosome 15q cause thyrotropin resistance by activating a primate-specific enhancer of MIR7-2/MIR1179.
Nat Genet
; 56(5): 877-888, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38714869
5.
Delayed development of specific thyroid hormone-regulated events in transthyretin null mice.
Am J Physiol Endocrinol Metab
; 304(1): E23-31, 2013 Jan 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23092911
6.
Thyroid hormone receptor-ß agonists prevent hepatic steatosis in fat-fed rats but impair insulin sensitivity via discrete pathways.
Am J Physiol Endocrinol Metab
; 305(1): E89-100, 2013 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23651850
7.
Congenital Hypothyroidism in Two Sudanese Families Harboring a Novel Iodotyrosine Deiodinase Mutation (IYD R279C).
Thyroid
; 33(2): 261-266, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36633921
8.
Eyes on the Prize: Decoding the Ophthalmic Product Regulations and Intricacies of the U.S. Food and Drug Administration Approval.
J Ocul Pharmacol Ther
; 39(8): 572-582, 2023 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37797226
9.
Combined Use of RT-qPCR and NGS for Identification and Surveillance of SARS-CoV-2 Variants of Concern in Residual Clinical Laboratory Samples in Miami-Dade County, Florida.
Viruses
; 15(3)2023 02 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-36992302
10.
Rivalry between human ideation and virus mutation: two competing means of sustainability.
Women Health Care Issues
; 4(3)2021 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-34527953
11.
Early Diagnosis and Treatment of an Infant with a Novel Thyroid Hormone Receptor α Gene (pC380SfsX9) Mutation.
Thyroid
; 31(6): 1003-1005, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33198587
12.
Novel DIO1 Gene Mutation Acting as Phenotype Modifier for Novel Compound Heterozygous TPO Gene Mutations Causing Congenital Hypothyroidism.
Thyroid
; 31(10): 1589-1591, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34128397
13.
Automation of mass vaccination against COVID-19 at an academic health center.
JAMIA Open
; 4(4): ooab102, 2021 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-34927000
14.
Measurement of Reverse Triiodothyronine Level and the Triiodothyronine to Reverse Triiodothyronine Ratio in Dried Blood Spot Samples at Birth May Facilitate Early Detection of Monocarboxylate Transporter 8 Deficiency.
Thyroid
; 31(9): 1316-1321, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34049438
15.
Prenatal Treatment of Thyroid Hormone Cell Membrane Transport Defect Caused by MCT8 Gene Mutation.
Thyroid
; 31(5): 713-720, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32746752
16.
Insertion of an Alu Element in Thyroglobulin Gene as a Novel Cause of Congenital Hypothyroidism.
Thyroid
; 30(5): 780-782, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-31868128
17.
Sorting Variants of Unknown Significance Identified by Whole Exome Sequencing: Genetic and Laboratory Investigations of Two Novel MCT8 Variants.
Thyroid
; 30(3): 463-465, 2020 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31856685
18.
Clinical and Molecular Analysis in 2 Families With Novel Compound Heterozygous SBP2 (SECISBP2) Mutations.
J Clin Endocrinol Metab
; 105(3)2020 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32084277
19.
Increased Prevalence of TG and TPO Mutations in Sudanese Children With Congenital Hypothyroidism.
J Clin Endocrinol Metab
; 105(5)2020 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31867598
20.
A lack of thyroid hormones rather than excess thyrotropin causes abnormal skeletal development in hypothyroidism.
Mol Endocrinol
; 22(2): 501-12, 2008 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-17932107