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Francisco Mora‐López

Observed names: F Mora-López, F. Mora‐López, Francisco Mora López, Francisco Mora-Lopez, Francisco Mora-López, Francisco Mora-López
ORCID: 0000-0002-6423-0222
Observed ORCID: 0000-0002-6423-0222
OpenAlex ID: A5026085689
Human BSAP and BLIMP1 conform an autoregulatory feedback loop
2007 · Francisco Mora-López, Elena Reales, et al. · Blood · 43
Transcriptional correlates of the pathological phenotype in a Huntington’s disease mouse model
2019 · Andrea Gallardo-Orihuela, Irati Hervás-Corpión, et al. · Scientific Reports · 40
Identification of Soluble N-Ethylmaleimide-Sensitive Factor Attachment Protein Receptor Exocytotic Machinery in Human Plasma Cells: SNAP-23 Is Essential for Antibody Secretion
2005 · Elena Reales, Francisco Mora-López, et al. · The Journal of Immunology · 36
Transcription of PRDM1 , the master regulator for plasma cell differentiation, depends on an SP1/SP3/EGR‐1 GC‐box
2008 · Francisco Mora‐López, Nuria Pedreño‐Horrillo, et al. · European Journal of Immunology · 31
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Increased survival is a selective feature of human circulating antigen-induced plasma cells synthesizing high-affinity antibodies
2007 · Inés González-García, Beatriz Rodríguez-Bayona, et al. · Blood · 29
Three cases with L1 syndrome and two novel mutations in the L1CAM gene
2015 · Rosario Marín, Miriam Ley-Martos, et al. · European Journal of Pediatrics · 21
Syntaxin-4 is implicated in the secretion of antibodies by human plasma cells
2013 · Laura Gómez-Jaramillo, Luis Delgado-Pérez, et al. · Journal of Leukocyte Biology · 21
The expression of PRDI-BF1 beta isoform in multiple myeloma plasma cells.
2006 · Esther Ocaña, Inés González-García, et al. · PubMed · 19
Novel mutation in the epithelial sodium channel causing type I pseudohypoaldosteronism in a patient misdiagnosed with cystic fibrosis
2012 · Francisco Mora-Lopez, Manuel Bernal-Quiros, et al. · European Journal of Pediatrics · 16
Vexas syndrome successfully treated with canakinumab
2023 · Cristina Collantes‐Rodríguez, David Jiménez‐Gallo, et al. · JDDG Journal der Deutschen Dermatologischen Gesellschaft · 12
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Potential Diagnostic Value of the Differential Expression of Histone H3 Variants between Low- and High-Grade Gliomas
2021 · Irati Hervás-Corpión, Andrea Gallardo-Orihuela, et al. · Cancers · 10
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Response to flecainide test in Andersen‐Tawil syndrome with incessant ventricular tachycardia
2017 · Marcos Fernández, María Del Rosario Marín, et al. · Pacing and Clinical Electrophysiology · 8
Different Phenotypes of Schimke Immuno-Osseous Dysplasia (SIOD) in Two Sisters with the Same Mutation in the SMARCAL1 Gene
2022 · Ana Castellano-Martinez, Silvia Acuñas-Soto, et al. · Endocrine Metabolic & Immune Disorders - Drug Targets · 7
Differential epigenetic regulation between the alternative promoters, PRDM1α and PRDM1β, of the tumour suppressor gene PRDM1 in human multiple myeloma cells
2020 · Raquel Romero-García, Laura Gómez-Jaramillo, et al. · Scientific Reports · 7
Novel splice mutation in CDSN gene causing type b peeling skin syndrome
2022 · I. Navarro‐Navarro, D. Jiménez‐Gallo, et al. · Journal of the European Academy of Dermatology and Venereology · 5
VEXAS‐Syndrom erfolgreich mit Canakinumab therapiert
2023 · Cristina Collantes‐Rodríguez, David Jiménez‐Gallo, et al. · JDDG Journal der Deutschen Dermatologischen Gesellschaft · 2
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X-linked Lymphoproliferative Disease Type 1 in a Patient With the p.Gly93Asp SH2D1A Gene Mutation and Hemophagocytic Lymphohistiocytosis
2017 · Raquel de la Varga-Martínez, Francisco Mora-López, et al. · Journal of Pediatric Hematology/Oncology · 1
A New Variant of the PTEN Gene in Relation to Cowden Syndrome Type 1
2024 · Marina Fernández-Villares, Isabel Villegas-Romero, et al. · Indian Journal of Dermatology
Hyper IgM Syndrome Type 2 Presenting as Intestinal Lymphoid Polyposis Without Recurrent Infection
2020 · R de la Varga-Martínez, M Vilches-Moreno, et al. · Journal of Investigational Allergology and Clinical Immunology
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Two new mutations in the PPOX gene in a patient with variegate porphyria
2020 · Cristina Collantes‐Rodríguez, Raquel de la Varga‐Martínez, et al. · JDDG Journal der Deutschen Dermatologischen Gesellschaft
Zwei neue Mutationen im PPOX‐Gen bei einem Patienten mit Porphyria variegata
2020 · Cristina Collantes‐Rodríguez, Raquel de la Varga‐Martínez, et al. · JDDG Journal der Deutschen Dermatologischen Gesellschaft
Glomulin mutation and glomuvenous malformations: two case reports with the same mutation but different phenotypes
2018 · Cristina Collantes-Rodríguez, Raquel De La Varga-Martínez, et al. · European Journal of Dermatology
Nueva mutación en el gen ALDH3A2 en un niño con síndrome de Sjögren-Larsson
2018 · Francisco Mora López, Miriam Vilches Moreno, et al. · Revista de Neurología
Works count: 23
Citation count: 308
H-index: 10
I10-index: 11
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