Detalhe da pesquisa
1.
An engineered multicellular stem cell niche for the 3D derivation of human myogenic progenitors from iPSCs.
EMBO J;
41(14): e110655, 2022 07 18.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35703167
2.
Longitudinal Human Milk miRNA Composition over the First 3 mo of Lactation in a Cohort of Healthy Mothers Delivering Term Infants.
J Nutr;
152(1): 94-106, 2022 01 11.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34510208
3.
Bifidobacterium longum subsp. iuvenis subsp. nov., a novel subspecies isolated from the faeces of weaning infants.
Int J Syst Evol Microbiol;
73(10)2023 Oct.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37851001
4.
Mutations in endothelin 1 cause recessive auriculocondylar syndrome and dominant isolated question-mark ears.
Am J Hum Genet;
93(6): 1118-25, 2013 Dec 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24268655
5.
Improving mutation screening in familial hematuric nephropathies through next generation sequencing.
J Am Soc Nephrol;
25(12): 2740-51, 2014 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24854265
6.
The Pleiotropic Effects of Carbohydrate-Mediated Growth Rate Modifications in Bifidobacterium longum NCC 2705.
Microorganisms;
11(3)2023 Feb 26.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36985162
7.
Maternal uniparental disomy of chromosome 2 in a patient with a DGUOK mutation associated with hepatocerebral mitochondrial DNA depletion syndrome.
Mol Genet Metab;
107(4): 700-4, 2012 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23141463
8.
Contribution of genetic ancestry and polygenic risk score in meeting vitamin B12 needs in healthy Brazilian children and adolescents.
Sci Rep;
11(1): 11992, 2021 06 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34099811
9.
A new TRPV3 missense mutation in a patient with Olmsted syndrome and erythromelalgia.
JAMA Dermatol;
150(3): 303-6, 2014 Mar.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24452206
10.
Intellectual disability associated with retinal dystrophy in the Xp11.3 deletion syndrome: ZNF674 on trial. Guilty or innocent?
Eur J Hum Genet;
20(3): 352-6, 2012 Mar.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22126752
11.
KIF7 mutations cause fetal hydrolethalus and acrocallosal syndromes.
Nat Genet;
43(6): 601-6, 2011 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-21552264