Detalhe da pesquisa
1.
SOX9 and SRY binding sites on mouse mXYSRa/Enh13 enhancer redundantly regulate Sox9 expression to varying degrees.
Hum Mol Genet
; 32(1): 55-64, 2023 01 01.
Artigo
Inglês
| MEDLINE | ID: mdl-35921234
2.
Two ovarian candidate enhancers, identified by time series enhancer RNA analyses, harbor rare genetic variations identified in ovarian insufficiency.
Hum Mol Genet
; 31(13): 2223-2235, 2022 07 07.
Artigo
Inglês
| MEDLINE | ID: mdl-35134173
3.
Humanization of a tandem repeat in IG-DMR causes stochastic restoration of paternal imprinting at mouse Dlk1-Dio3 domain.
Hum Mol Genet
; 30(7): 564-574, 2021 05 12.
Artigo
Inglês
| MEDLINE | ID: mdl-33709141
4.
Nr5a1 suppression during the murine fetal period optimizes ovarian development by fine-tuning Notch signaling.
J Cell Sci
; 132(8)2019 04 15.
Artigo
Inglês
| MEDLINE | ID: mdl-30877223
5.
The progression of salt-wasting and the body weight change during the first 2 weeks of life in classical 21-hydroxylase deficiency patients.
Clin Endocrinol (Oxf)
; 94(2): 229-236, 2021 02.
Artigo
Inglês
| MEDLINE | ID: mdl-33001476
6.
Pulmonary vascular dysfunction in metabolic syndrome.
J Physiol
; 597(4): 1121-1141, 2019 02.
Artigo
Inglês
| MEDLINE | ID: mdl-30125956
7.
A hypercalcemic episode in an adolescent with autosomal dominant hypocalcemia.
Pediatr Int
; 65(1): e15707, 2023.
Artigo
Inglês
| MEDLINE | ID: mdl-38037506
8.
Molecular mechanisms of insulin resistance in 2 cases of primary insulin receptor defect-associated diseases.
Pediatr Diabetes
; 18(8): 917-924, 2017 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-28181734
9.
Lower body weight and BMI at birth were associated with early adiposity rebound in 21-hydroxylase deficiency patients.
Endocr J
; 63(11): 983-990, 2016 Nov 30.
Artigo
Inglês
| MEDLINE | ID: mdl-27545660
10.
A MinION-based Long-Read Sequencing Application With One-Step PCR for the Genetic Diagnosis of 21-Hydroxylase Deficiency.
J Clin Endocrinol Metab
; 109(3): 750-760, 2024 Feb 20.
Artigo
Inglês
| MEDLINE | ID: mdl-37804107
11.
Restoration of coronary microvascular function by OGA overexpression in a high-fat diet with low-dose streptozotocin-induced type 2 diabetic mice.
Diab Vasc Dis Res
; 20(3): 14791641231173630, 2023.
Artigo
Inglês
| MEDLINE | ID: mdl-37186669
12.
Human SRY Expression at the Sex-determining Period is Insufficient to Drive Testis Development in Mice.
Endocrinology
; 163(1)2022 01 01.
Artigo
Inglês
| MEDLINE | ID: mdl-34662386
13.
The High Relevance of 21-Deoxycortisol, (Androstenedione + 17α-Hydroxyprogesterone)/Cortisol, and 11-Deoxycortisol/17α-Hydroxyprogesterone for Newborn Screening of 21-Hydroxylase Deficiency.
J Clin Endocrinol Metab
; 107(12): 3341-3352, 2022 11 25.
Artigo
Inglês
| MEDLINE | ID: mdl-36071550
14.
Thirty-Year Lessons from the Newborn Screening for Congenital Adrenal Hyperplasia (CAH) in Japan.
Int J Neonatal Screen
; 7(3)2021 Jun 29.
Artigo
Inglês
| MEDLINE | ID: mdl-34209888
15.
HuR/Cx40 downregulation causes coronary microvascular dysfunction in type 2 diabetes.
JCI Insight
; 6(21)2021 11 08.
Artigo
Inglês
| MEDLINE | ID: mdl-34747371
16.
Chronic Hypoxia Decreases Endothelial Connexin 40, Attenuates Endothelium-Dependent Hyperpolarization-Mediated Relaxation in Small Distal Pulmonary Arteries, and Leads to Pulmonary Hypertension.
J Am Heart Assoc
; 9(24): e018327, 2020 12 15.
Artigo
Inglês
| MEDLINE | ID: mdl-33307937
17.
Overexpression of p53 due to excess protein O-GlcNAcylation is associated with coronary microvascular disease in type 2 diabetes.
Cardiovasc Res
; 116(6): 1186-1198, 2020 05 01.
Artigo
Inglês
| MEDLINE | ID: mdl-31504245
18.
Chloroquine differentially modulates coronary vasodilation in control and diabetic mice.
Br J Pharmacol
; 177(2): 314-327, 2020 01.
Artigo
Inglês
| MEDLINE | ID: mdl-31503328
19.
Gonadal failure among female patients after hematopoietic stem cell transplantation for non-malignant diseases.
Clin Pediatr Endocrinol
; 28(4): 105-112, 2019.
Artigo
Inglês
| MEDLINE | ID: mdl-31666763
20.
Clinical characteristics of adolescent cases with Type A insulin resistance syndrome caused by heterozygous mutations in the ß-subunit of the insulin receptor (INSR) gene.
J Diabetes
; 11(1): 46-54, 2019 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-29877041