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1.
Synthesis and Comparative Structure-Activity Study of Carbohydrate-Based Phenolic Compounds as α-Glucosidase Inhibitors and Antioxidants.
Molecules
; 24(23)2019 Nov 27.
Artículo
en Inglés
| MEDLINE | ID: mdl-31783621
2.
Hypodysfibrinogenemia with a Heterozygous Mutation of γCys326Ser by the Novel Transversion of TGT to TCT in a Patient with Pulmonary Thromboembolism and Right Ventricular Thrombus.
Cardiology
; 137(3): 167-172, 2017.
Artículo
en Inglés
| MEDLINE | ID: mdl-28419986
3.
Clinical utility of urinary mulberry bodies/cells testing in the diagnosis of Fabry disease.
Mol Genet Metab Rep
; 36: 100983, 2023 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-37323223
4.
γD318Y fibrinogen shows no fibrin polymerization due to defective "A-a" and "B-b" interactions, whereas that of γK321E fibrinogen is nearly normal.
Thromb Res
; 182: 150-158, 2019 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-31484085
5.
The fibrous form of intracellular inclusion bodies in recombinant variant fibrinogen-producing cells is specific to the hepatic fibrinogen storage disease-inducible variant fibrinogen.
Int J Hematol
; 105(6): 758-768, 2017 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-28161763
6.
Genetic analyses of novel compound heterozygous hypodysfibrinogenemia, Tsukuba I: FGG c.1129+62_65 del AATA and FGG c.1299+4 del A.
Thromb Res
; 148: 111-117, 2016 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-27837696
7.
Differences in the function and secretion of congenital aberrant fibrinogenemia between heterozygous γD320G (Okayama II) and γΔN319-ΔD320 (Otsu I).
Thromb Res
; 136(6): 1318-24, 2015 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-26573395
8.
Novel heterozygous dysfibrinogenemia, Sumida (AαC472S), showed markedly impaired lateral aggregation of protofibrils and mildly lower functional fibrinogen levels.
Thromb Res
; 135(4): 710-7, 2015 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-25613923
9.
Complete measurable residual disease response after combination chemotherapy with AML-type and ALL-type regimens in pediatric B/myeloid acute bilineal leukemia.
Leuk Lymphoma
; 61(4): 967-970, 2020 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-31809628
10.
Recombinant γT305A fibrinogen indicates severely impaired fibrin polymerization due to the aberrant function of hole 'A' and calcium binding sites.
Thromb Res
; 134(2): 518-25, 2014 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-24968960
11.
Factor H gene variants in Japanese: its relation to atypical hemolytic uremic syndrome.
Mol Immunol
; 49(1-2): 48-55, 2011 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-21868097
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