Maria Luisa
Lozano Almela
Catedraticos de Universidad Vinculados
Publikationen (167) Publikationen von Maria Luisa Lozano Almela
2024
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Analysis of AlphaFold and molecular dynamics structure predictions of mutations in serpins
PLoS ONE, Vol. 19, Núm. 7 JULY
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Fostamatinib effectiveness and safety for immune thrombocytopenia in clinical practice
Blood, Vol. 144, Núm. 6, pp. 646-656
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Germline assessment for alloHSCT candidates over 50 years: A ‘Fast-Track’ screening in myeloid neoplasms
British Journal of Haematology, Vol. 205, Núm. 2, pp. 503-509
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Recommendations for the future management of thrombocytopenia in patients with liver cirrhosis: A modified RAND/UCLA appropriateness method
Gastroenterologia y Hepatologia, Vol. 47, Núm. 1, pp. 32-50
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Targeted long-read sequencing identifies and characterizes structural variants in cases of inherited platelet disorders
Journal of Thrombosis and Haemostasis, Vol. 22, Núm. 3, pp. 851-859
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The importance of genetic variant cleaners: From patient to wet lab and back to clinical practice
British Journal of Haematology
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The whole is greater than the sum of its parts: Long-read sequencing for solving clinical problems in haematology
Journal of Cellular and Molecular Medicine, Vol. 28, Núm. 3
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Thrombotic risk and features of patients with inferior vena cava agenesis: a multicentre, retrospective, observational study
The Lancet Haematology, Vol. 11, Núm. 8, pp. e606-e616
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miR-146a−/− mice model reveals that NF-κB inhibition reverts inflammation-driven myelofibrosis-like phenotype
American Journal of Hematology, Vol. 99, Núm. 7, pp. 1326-1337
2023
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Congenital factor XI deficiency and risk of heart failure in humans
Journal of Thrombosis and Haemostasis
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Expanding therapeutic options for patients with primary immune thrombocytopenia
The Lancet Haematology
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Factor XI in Carriers of Antiphospholipid Antibodies: Elevated Levels Associated with Symptomatic Thrombotic Cases, While Low Levels Linked to Asymptomatic Cases
International Journal of Molecular Sciences, Vol. 24, Núm. 22
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Impact of genetic structural variants in factor XI deficiency: identification, accurate characterization, and inferred mechanism by long-read sequencing
Journal of Thrombosis and Haemostasis, Vol. 21, Núm. 7, pp. 1779-1788
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Lentiviral gene therapy reverts GPIX expression and phenotype in Bernard-Soulier syndrome type C
Molecular Therapy - Nucleic Acids, Vol. 33, pp. 75-92
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NLRP3 inflammasome activation and symptom burden in KRAS-mutated CMML patients is reverted by IL-1 blocking therapy
Cell Reports Medicine, Vol. 4, Núm. 12
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Suramin, a drug for the treatment of trypanosomiasis, reduces the prothrombotic and metastatic phenotypes of colorectal cancer cells by inhibiting hepsin
Biomedicine and Pharmacotherapy, Vol. 168
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Venetoclax is a potent hepsin inhibitor that reduces the metastatic and prothrombotic phenotypes of hepsin-expressing colorectal cancer cells
Frontiers in Molecular Biosciences, Vol. 10
2022
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A Novel GATA1 Variant in the C-Terminal Zinc Finger Compared with the Platelet Phenotype of Patients with A Likely Pathogenic Variant in the N-Terminal Zinc Finger
Cells, Vol. 11, Núm. 20
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Full-length antithrombin frameshift variant with aberrant C-terminus causes endoplasmic reticulum retention with a dominant-negative effect
JCI Insight, Vol. 7, Núm. 19
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Implication of Hepsin from Primary Tumor in the Prognosis of Colorectal Cancer Patients
Cancers, Vol. 14, Núm. 13