Zobrazeno 1 - 10 of 14 pro vyhledávání: '"Carolina, Muchnik"'
1
Akademický článek
Memory reconsolidation as a tool to endure encoding deficits in elderly.
Autor: Leonela M Tassone, Facundo A Urreta Benítez, Delfina Rochon, Paula B Martínez, Matias Bonilla, Candela S Leon, Carolina Muchnik, Patricia Solis, Nancy Medel, Silvia Kochen, Luis I Brusco, Malen D Moyano, Cecilia Forcato
Publikováno v: PLoS ONE, Vol 15, Iss 8, p e0237361 (2020)
Normal aging involves changes in the ability to acquire, consolidate and recall new information. It has been recently proposed that the reconsolidation process is also affected in older adults. Reconsolidation is triggered after reminder presentation
Externí odkaz: https://doaj.org/article/3841c9e9d2654dfab3bfcd09667fd001
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2
Akademický článek
Nevoid Basal Cell Carcinoma Syndrome: PTCH1 Mutation Profile and Expression of Genes Involved in the Hedgehog Pathway in Argentinian Patients
Autor: Maria Florencia Martinez, Maria Vanesa Romano, Alfredo Pedro Martinez, Abel González, Carolina Muchnik, Fernando Miguel Stengel, Luis Daniel Mazzuoccolo, Pablo Javier Azurmendi
Publikováno v: Cells, Vol 8, Iss 2, p 144 (2019)
Nevoid basal cell carcinoma syndrome (NBCCS) is an autosomal dominant disorder characterized by multiple basal cell carcinomas (BCC), mainly caused by PTCH1 gene mutations. Our current study aimed to establish (1) PTCH1 germinal and somatic mutationa
Externí odkaz: https://doaj.org/article/1b76c0514d1a48fda247bdbd62fe6517
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3
Memory reconsolidation as a tool to endure encoding deficits in elderly
Autor: Carolina Muchnik, Delfina Rochon, Patricia Solís, Malen D. Moyano, Facundo A. Urreta Benítez, Paula B. Martínez, Leonela M. Tassone, Nancy Medel, Luis Ignacio Brusco, Silvia Kochen, Cecilia Forcato, Candela S. Leon, Matías Bonilla
Publikováno v: PLoS ONE
PLoS ONE, Vol 15, Iss 8, p e0237361 (2020)
Normal aging involves changes in the ability to acquire, consolidate and recall new information. It has been recently proposed that the reconsolidation process is also affected in older adults. Reconsolidation is triggered after reminder presentation
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1711f6eda85d6a30afbfbe2cd8774c3a
https://pubmed.ncbi.nlm.nih.gov/32764815
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4
Nevoid Basal Cell Carcinoma Syndrome: PTCH1 Mutation Profile and Expression of Genes Involved in the Hedgehog Pathway in Argentinian Patients
Autor: Luis Daniel Mazzuoccolo, Carolina Muchnik, Pablo Javier Azurmendi, Fernando Stengel, Maria Vanesa Romano, Abel González, Maria Florencia Martinez, Alfredo Pedro Martinez
Publikováno v: Cells
Volume 8
Issue 2
Cells, Vol 8, Iss 2, p 144 (2019)
Nevoid basal cell carcinoma syndrome (NBCCS) is an autosomal dominant disorder characterized by multiple basal cell carcinomas (BCC), mainly caused by PTCH1 gene mutations. Our current study aimed to establish (1) PTCH1 germinal and somatic mutationa
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a94583969a8504e2fe8e88dd4d1c6c9d
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5
Transethnic meta-analysis of rare coding variants in PLCG2, ABI3, and TREM2 supports their general contribution to Alzheimer's disease
Autor: Florentino Sanchez-Garcia, Jean-Charles Lambert, Horacio Scaro, Zulma Sevillano, Paolo Bosco, Wolfgang Maier, Silvia Kochen, Alfredo Ramirez, Laura Morelli, Julieta Lisso, Mariana Soledad Sanchez Avalos, Carlos A Mangone, Cynthia Liberczuk, Paolo Caffarra, Frank Jessen, Daniel Gustavo Politis, Eduardo M. Castaño, Guillermo Jemar, Eliecer Coto, Claudia Kairiyama, Daniela Galimberti, Cristina Fezza, Patrizia Mecocci, Per Hoffmann, Jordi Clarimón, Luis I. Brusco, Claudia Hanses, Paola Bossù, Sandro Sorbi, Benedetta Nacmias, Nancy Medel, Mariana Estela Carulla, Michelangelo Mancuso, Federico A. Prestia, Maria Carolina Dalmasso, Pascual Sánchez-Juan, Pablo Galeano, María J. Bullido, Carolina Muchnik, Martin Ingelsson, Luis Eduardo Martinez, Pablo Javier Azurmendi, Caroline Graff, J Becker, Alberto Pilotto, Marcelo Sampaño, Céline Bellenguez, Maria Fierens, Francesco Panza, Natividad Olivar, Esther Milz, Stefanie Heilmann-Heimbach, Gianfranco Spalletta, Patricia Solís
Publikováno v: Translational Psychiatry 9(1), 55 (2019). doi:10.1038/s41398-019-0394-9
Transl Psychiatry . 2019 Jan 31;9(1):55
Digital.CSIC. Repositorio Institucional del CSIC
instname
UCrea Repositorio Abierto de la Universidad de Cantabria
Universidad de Cantabria (UC)
Biblos-e Archivo. Repositorio Institucional de la UAM
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Translational Psychiatry, Vol 9, Iss 1, Pp 1-6 (2019)
Translational Psychiatry
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Rare coding variants in TREM2, PLCG2, and ABI3 were recently associated with the susceptibility to Alzheimer’s disease (AD) in Caucasians. Frequencies and AD-associated effects of variants differ across ethnicities. To start filling the gap on AD g
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3dc3bc4c554424fafcf97959ff45c091
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6
Nevoid Basal Cell Carcinoma Syndrome
Autor: Maria Florencia, Martinez, Maria Vanesa, Romano, Alfredo Pedro, Martinez, Abel, González, Carolina, Muchnik, Fernando Miguel, Stengel, Luis Daniel, Mazzuoccolo, Pablo Javier, Azurmendi
Publikováno v: Cells
Nevoid basal cell carcinoma syndrome (NBCCS) is an autosomal dominant disorder characterized by multiple basal cell carcinomas (BCC), mainly caused by PTCH1 gene mutations. Our current study aimed to establish (1) PTCH1 germinal and somatic mutationa
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::14bda964b7403166828f1a2cd92506d6
https://pubmed.ncbi.nlm.nih.gov/30754660
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8
Co-Inheritance of Autosomal Dominant Polycystic Kidney Disease and Naevoid Basal Cell Carcinoma Syndrome: Effects on Renal Progression
Autor: Hartmut P. H. Neumann, Carolina Muchnik, Paula Virginia Iscoff, Maria Florencia Martinez, Adriana Fraga, Pablo Javier Azurmendi, Elisabet M. Oddo, Luis Daniel Mazzuoccolo, Rodolfo S. Martin
Publikováno v: Nephron. 140(4)
The calcium signalling and hedgehog (HH) signalling pathways operate in the primary cilium. Abnormalities in these pathways cause autosomal dominant polycystic kidney disease (ADPKD) and naevoid basal cell carcinoma syndrome (NBCCS) respectively. Sev
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0bcc48670b83b093e38e4ffbbaa31069
https://pubmed.ncbi.nlm.nih.gov/30368514
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9
Síndrome de carcinoma basocelular nevoide con agenesia de cuerpo calloso, mutación en PTCH1 y ausencia de carcinoma basocelular
Autor: Luis D Mazzuoccolo, María Florencia Martínez, Carolina Muchnik, Pablo J Azurmendi, Fernando Stengel
Publikováno v: Medicina (Buenos Aires), Vol 74, Iss 4, Pp 307-310 (2014)
El síndrome del carcinoma basocelular nevoide (SCBCN) o de Gorlin-Goltz es un raro desorden autosómico dominante con un amplio espectro de manifestaciones clínicas. El signo cardinal es la presencia de múltiples carcinomas basocelulares (CBCs) y
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::6b1b8ed7b75411edefe006e217173a9c
http://www.scielo.org.ar/scielo.php?script=sci_arttext&pid=S0025-76802014000400008&lng=en&tlng=en
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