Detalhe da pesquisa
1.
sFRP2 in the aged microenvironment drives melanoma metastasis and therapy resistance.
Nature
; 532(7598): 250-4, 2016 Apr 14.
Artigo
Inglês
| MEDLINE | ID: mdl-27042933
2.
Science surrounding the safe use of bioactive ingredients in infant formula: federal comment.
Pediatr Res
; 94(2): 420-422, 2023 08.
Artigo
Inglês
| MEDLINE | ID: mdl-36759748
3.
Revisiting the prevalence of nonclassic congenital adrenal hyperplasia in US Ashkenazi Jews and Caucasians.
Genet Med
; 19(11): 1276-1279, 2017 11.
Artigo
Inglês
| MEDLINE | ID: mdl-28541281
4.
The soluble domains of Gpi8 and Gaa1, two subunits of glycosylphosphatidylinositol transamidase (GPI-T), assemble into a complex.
Arch Biochem Biophys
; 633: 58-67, 2017 11 01.
Artigo
Inglês
| MEDLINE | ID: mdl-28893510
5.
Corrigendum: sFRP2 in the aged microenvironment drives melanoma metastasis and therapy resistance.
Nature
; 537(7619): 254, 2016 Sep 08.
Artigo
Inglês
| MEDLINE | ID: mdl-27383789
6.
Ehlers-Danlos Syndrome Caused by Biallelic TNXB Variants in Patients with Congenital Adrenal Hyperplasia.
Hum Mutat
; 37(9): 893-7, 2016 09.
Artigo
Inglês
| MEDLINE | ID: mdl-27297501
7.
Clinical and biochemical profiles suggest fibromuscular dysplasia is a systemic disease with altered TGF-ß expression and connective tissue features.
FASEB J
; 28(8): 3313-24, 2014 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-24732132
8.
A mutation in TGFB3 associated with a syndrome of low muscle mass, growth retardation, distal arthrogryposis and clinical features overlapping with Marfan and Loeys-Dietz syndrome.
Am J Med Genet A
; 161A(8): 2040-6, 2013 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-23824657
9.
Trends in ingredients added to infant formula: FDA's experiences in the GRAS notification program.
Food Chem Toxicol
; 178: 113876, 2023 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-37286029
10.
Broadening the Spectrum of Ehlers Danlos Syndrome in Patients With Congenital Adrenal Hyperplasia.
J Clin Endocrinol Metab
; 100(8): E1143-52, 2015 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-26075496
11.
Transforming growth factor-ß (TGF-ß) pathway abnormalities in tenascin-X deficiency associated with CAH-X syndrome.
Eur J Med Genet
; 57(2-3): 95-102, 2014 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-24380766
12.
Transforming growth factor-ß and inflammation in vascular (type IV) Ehlers-Danlos syndrome.
Circ Cardiovasc Genet
; 7(1): 80-8, 2014 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-24399159
13.
Tenascin-X haploinsufficiency associated with Ehlers-Danlos syndrome in patients with congenital adrenal hyperplasia.
J Clin Endocrinol Metab
; 98(2): E379-87, 2013 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-23284009
14.
Defining the boundaries of species specificity for the Saccharomyces cerevisiae glycosylphosphatidylinositol transamidase using a quantitative in vivo assay.
Biosci Rep
; 32(6): 577-86, 2012 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-22938202
15.
Tenascin-X gene defects and cardiovascular disease.
Med Hypotheses
; 83(6): 844, 2014 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-24709065