Cargando…

P1475: MUTATIONS IN THE GAP DOMAIN OF RACGAP1 CAUSE DEVELOPMENTAL AND ERYTHROID DEFECTS IN ZEBRAFISH

Detalles Bibliográficos
Autores principales:	Romero-Cortadellas, Lídia, Bañón, Aitor, Hernández, Gonzalo, Pérez-Montero, Santiago, Tornador, Cristian, Alsina, Berta, Sanchez, Mayka
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Lippincott Williams & Wilkins 2023
Materias:	Posters
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10430497/ http://dx.doi.org/10.1097/01.HS9.0000972784.01629.bb

Ejemplares similares

Mutations in the RACGAP1 gene cause autosomal recessive congenital dyserythropoietic anemia type III
por: Hernández, Gonzalo, et al.
Publicado: (2022)

Turning RacGAP into a RhoGAP
por: Tuma, Rabiya S.
Publicado: (2003)

New Cases of Hypochromic Microcytic Anemia Due to Mutations in the SLC11A2 Gene and Functional Characterization of the G75R Mutation
por: Romero-Cortadellas, Lídia, et al.
Publicado: (2022)

Michelangelo, 1475-1564 /
por: Néret, Gilles
Publicado: (2000)

Pioneer statoacoustic neurons guide neuroblast behaviour during otic ganglion assembly
por: Bañón, Aitor, et al.
Publicado: (2023)

Miguel Ángel, 1475-1564 /
por: Néret, Gilles
Publicado: (2000)

Miguel Ángel, 1475-1564 /
por: Néret, Gilles
Publicado: (1998)

The RacGAP β-Chimaerin is essential for cerebellar granule cell migration
por: Estep, Jason A., et al.
Publicado: (2018)

Tum/RacGAP functions as a switch activating the Pav/kinesin-6 motor
por: Tao, Li, et al.
Publicado: (2016)

Around the World in 1,475 Salmonella Geo-serotypes
por: Gossner, Céline M., et al.
Publicado: (2016)

1475. A Retrospective Study Analyzing Recurrent LVAD Driveline Infections
por: Tin, Kathy, et al.
Publicado: (2023)

New Cases and Mutations in SEC23B Gene Causing Congenital Dyserythropoietic Anemia Type II
por: Musri, Melina Mara, et al.
Publicado: (2023)

Pseudogene RACGAP1P activates RACGAP1/Rho/ERK signalling axis as a competing endogenous RNA to promote hepatocellular carcinoma early recurrence
por: Wang, Meng-Yao, et al.
Publicado: (2019)

Hereditary Hyperferritinemia Cataract Syndrome: Ferritin L Gene and Physiopathology behind the Disease—Report of New Cases
por: Celma Nos, Ferran, et al.
Publicado: (2021)

Dutch medical biography. A biographical dictionary of Dutch physicians and surgeons 1475–1975
por: Schupbach, W.
Publicado: (1985)

RacGAP1 promotes the malignant progression of cervical cancer by regulating AP-1 via miR-192 and p-JNK
por: Zhang, Tianli, et al.
Publicado: (2022)

Long non‐coding RNA RACGAP1P promotes breast cancer invasion and metastasis via miR‐345‐5p/RACGAP1‐mediated mitochondrial fission
por: Zhou, Danmei, et al.
Publicado: (2020)

Comparative evaluation of three proliferation markers, Ki-67, TOP2A, and RacGAP1, in bronchopulmonary neuroendocrine neoplasms: Issues and prospects
por: Neubauer, Elisa, et al.
Publicado: (2016)

A late self-portrait of Michelangelo Buonarroti (1475-1564) in the cartoon of the Epifania in the British Museum
por: de Campos, Deivis, et al.
Publicado: (2020)

Deaf sign language hidden in the fresco The Crucifixion of Saint Peter by Michelangelo Buonarroti (1475-1564)
por: de Campos, Deivis, et al.
Publicado: (2020)

P1496: TRANSFERRIN NON-CODING VARIANTS CAUSE MRNA DESTABILISATION IN CONGENITAL HYPOTRANSFERRINEMIA
por: Ferrer, Xenia, et al.
Publicado: (2023)

Expression of aurora kinase A correlates with the Wnt‐modulator RACGAP1 in gastric cancer
por: Bornschein, Jan, et al.
Publicado: (2016)

Inclusive single-particle distributions in p.bar.p interactions at 14.75 GeV/c
por: Dao, F T, et al.
Publicado: (1974)

1475 Hamsi scoring in the prediction of unfavorable outcomes in tuberculous meningitis: Results of multinational Haydarpasa-2 Study
por: Erdem, Hakan, et al.
Publicado: (2014)

RCP-driven α5β1 recycling suppresses Rac and promotes RhoA activity via the RacGAP1–IQGAP1 complex
por: Jacquemet, Guillaume, et al.
Publicado: (2013)

Effects of Shenkang Pills on Early-Stage Diabetic Nephropathy in db/db Mice via Inhibiting AURKB/RacGAP1/RhoA Signaling Pathway
por: Wang, Fujing, et al.
Publicado: (2022)

Hematopoietic Cytokine Gene Duplication in Zebrafish Erythroid and Myeloid Lineages
por: Oltova, Jana, et al.
Publicado: (2018)

L-Ferritin: One Gene, Five Diseases; from Hereditary Hyperferritinemia to Hypoferritinemia—Report of New Cases
por: Cadenas, Beatriz, et al.
Publicado: (2019)

RACGAP1 variants in a sporadic case of CDA III implicate the dysfunction of centralspindlin as the basis of the disease
por: Wontakal, Sandeep N., et al.
Publicado: (2022)

Assessment of RACGAP1 as a Prognostic and Immunological Biomarker in Multiple Human Tumors: A Multiomics Analysis
por: Eid, Refaat A., et al.
Publicado: (2022)

HIF‑1α and RACGAP1 promote the progression of hepatocellular carcinoma in a mutually regulatory way
por: Wu, Xianjian, et al.
Publicado: (2023)

1475. Understanding Prescribing Practices for Uncomplicated Urinary Tract Infections (UTIs) in the Primary Care Setting: A Pilot Study
por: Pinkerton, Mark, et al.
Publicado: (2019)

CoDysAn: A Telemedicine Tool to Improve Awareness and Diagnosis for Patients With Congenital Dyserythropoietic Anemia
por: Tornador, Cristian, et al.
Publicado: (2019)

The fibronectin receptor on mammalian erythroid precursor cells: characterization and developmental regulation
Publicado: (1986)

Control of developmentally primed erythroid genes by combinatorial co-repressor actions
por: Stadhouders, Ralph, et al.
Publicado: (2015)

Jak2a regulates erythroid and myeloid hematopoiesis during zebrafish embryogenesis
por: Zhu, Xianmin, et al.
Publicado: (2017)

Tpr Deficiency Disrupts Erythroid Maturation With Impaired Chromatin Condensation in Zebrafish Embryogenesis
por: Wu, Shuang, et al.
Publicado: (2021)

1475. Etiology and Outcome of Fever and Respiratory Distress in Adult Patients Presenting to Medical Emergency in a Tertiary Care Hospital in North India
por: Suri, Vikas, et al.
Publicado: (2018)

PLAGL2 promotes bladder cancer progression via RACGAP1/RhoA GTPase/YAP1 signaling
por: Chen, Hualin, et al.
Publicado: (2023)

Disruption of the folate pathway in zebrafish causes developmental defects
por: Lee, Marina S, et al.
Publicado: (2012)

Cannot write session to /tmp/vufind_sessions/sess_605nohsgdtvpm5oukldt387m0r