Detalhe da pesquisa
1.
One fits all: a highly sensitive combined ddPCR/pyrosequencing system for the quantification of microchimerism after hematopoietic and solid organ transplantation.
Clin Chem Lab Med
; 61(11): 1994-2001, 2023 10 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-37167203
2.
Hereditary Spherocytosis: Can Next-Generation Sequencing of the Five Most Frequently Affected Genes Replace Time-Consuming Functional Investigations?
Int J Mol Sci
; 24(23)2023 Nov 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-38069343
3.
Evaluation of a laboratory-based high-throughput SARS-CoV-2 antigen assay for non-COVID-19 patient screening at hospital admission.
Med Microbiol Immunol
; 210(2-3): 165-171, 2021 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-33856557
4.
A non-invasive diagnostic assay for rapid detection and characterization of aberrant mRNA-splicing by nonsense mediated decay inhibition.
Mol Genet Metab
; 130(1): 27-35, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32222271
5.
Hepatitis E virus genotype 3 is a common finding in liver-transplanted patients undergoing liver biopsy for elevated liver enzymes with a low De Ritis ratio and suspected acute rejection: A real-world cohort.
Clin Transplant
; 32(11): e13411, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30230607
6.
Heme oxygenase-1 suppresses a pro-inflammatory phenotype in monocytes and determines endothelial function and arterial hypertension in mice and humans.
Eur Heart J
; 36(48): 3437-46, 2015 Dec 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-26516175
7.
A novel von Willebrand factor multimer ratio as marker of disease activity in thrombotic thrombocytopenic purpura.
Blood Adv
; 7(17): 5091-5102, 2023 09 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-37399489
8.
Severe high-molecular-weight kininogen deficiency: clinical characteristics, deficiency-causing KNG1 variants, and estimated prevalence.
J Thromb Haemost
; 21(2): 237-254, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36700498
9.
CEP162 deficiency causes human retinal degeneration and reveals a dual role in ciliogenesis and neurogenesis.
J Clin Invest
; 133(8)2023 04 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-36862503
10.
Biallelic MAD2L1BP (p31comet) mutation is associated with mosaic aneuploidy and juvenile granulosa cell tumors.
JCI Insight
; 8(22)2023 Nov 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-37796616
11.
Novel GATA1 Variant Causing a Bleeding Phenotype Associated with Combined Platelet α-/δ-Storage Pool Deficiency and Mild Dyserythropoiesis Modified by a SLC4A1 Variant.
Cells
; 11(19)2022 09 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-36231035
12.
Lipid presentation by the protein C receptor links coagulation with autoimmunity.
Science
; 371(6534)2021 03 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-33707237
13.
Severe plasma prekallikrein deficiency: Clinical characteristics, novel KLKB1 mutations, and estimated prevalence.
J Thromb Haemost
; 18(7): 1598-1617, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32202057
14.
A novel approach to CFTR mutation testing by pyrosequencing-based assay panels adapted to ethnicities.
Clin Chem
; 55(6): 1083-91, 2009 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-19372188
15.
Platelet Activation by Antiphospholipid Antibodies Depends on Epitope Specificity and is Prevented by mTOR Inhibitors.
Thromb Haemost
; 119(7): 1147-1153, 2019 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-31018220
16.
Structural and functional characterization of a human IgG monoclonal antiphospholipid antibody.
Immunobiology
; 216(1-2): 145-51, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-20591533