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MicroRNA‐27b is a regulatory hub in lipid metabolism and is altered in dyslipidemiaVickers, Kasey C. ; Shoucri, Bassem M. ; Levin, Michael G. ; Wu, Han ; Pearson, Daniel S. ; Osei‐Hwedieh, David ; Collins, Francis S. ; Remaley, Alan T. ; Sethupathy, PraveenHepatology (Baltimore, Md.), 2013-02, Vol.57 (2), p.533-542 [Periódico revisado por pares]Hoboken: Wiley Subscription Services, Inc., A Wiley CompanyTexto completo disponível |
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Material Type: Artigo
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Genetic reduction of mTOR extends lifespan in a mouse model of Hutchinson‐Gilford Progeria syndromeCabral, Wayne A. ; Tavarez, Urraca L. ; Beeram, Indeevar ; Yeritsyan, Diana ; Boku, Yoseph D. ; Eckhaus, Michael A. ; Nazarian, Ara ; Erdos, Michael R. ; Collins, Francis S.Aging cell, 2021-09, Vol.20 (9), p.e13457-n/a [Periódico revisado por pares]England: John Wiley & Sons, IncTexto completo disponível |
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Material Type: Artigo
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Bone dysplasia in Hutchinson-Gilford progeria syndrome is associated with dysregulated differentiation and function of bone cell populationsCabral, Wayne A ; Stephan, Chris ; Terajima, Masahiko ; Thaivalappil, Abhirami A ; Blanchard, Owen ; Tavarez, Urraca L ; Narisu, Narisu ; Yan, Tingfen ; Wincovitch, Stephen M ; Taga, Yuki ; Yamauchi, Mitsuo ; Kozloff, Kenneth M ; Erdos, Michael R ; Collins, Francis SAging cell, 2023-09, Vol.22 (9), p.e13903-e13903 [Periódico revisado por pares]England: John Wiley & Sons, IncTexto completo disponível |
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Differentiating Moebius syndrome and other congenital facial weakness disorders with electrodiagnostic studiesLehky, Tanya ; Joseph, Reversa ; Toro, Camilo ; Wu, Tianxia ; Van Ryzin, Carol ; Gropman, Andrea ; Facio, Flavia M. ; Webb, Bryn D. ; Jabs, Ethylin W. ; Barry, Brenda S. ; Engle, Elizabeth C. ; Collins, Francis S. ; Manoli, IriniMuscle & nerve, 2021-04, Vol.63 (4), p.516-524 [Periódico revisado por pares]Hoboken, USA: John Wiley & Sons, IncTexto completo disponível |
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Material Type: Artigo
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Analysis of somatic mutations identifies signs of selection during in vitro aging of primary dermal fibroblastsNarisu, Narisu ; Rothwell, Rebecca ; Vrtačnik, Peter ; Rodríguez, Sofía ; Didion, John ; Zöllner, Sebastian ; Erdos, Michael R. ; Collins, Francis S. ; Eriksson, MariaAging cell, 2019-12, Vol.18 (6), p.e13010-n/a [Periódico revisado por pares]England: John Wiley & Sons, IncTexto completo disponível |
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Material Type: Artigo
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Tag SNP selection for Finnish individuals based on the CEPH Utah HapMap databaseWiller, Cristen J. ; Scott, Laura J. ; Bonnycastle, Lori L. ; Jackson, Anne U. ; Chines, Peter ; Pruim, Randall ; Bark, Craig W. ; Tsai, Ya-Yu ; Pugh, Elizabeth W. ; Doheny, Kimberly F. ; Kinnunen, Leena ; Mohlke, Karen L. ; Valle, Timo T. ; Bergman, Richard N. ; Tuomilehto, Jaakko ; Collins, Francis S. ; Boehnke, MichaelGenetic epidemiology, 2006-02, Vol.30 (2), p.180-190 [Periódico revisado por pares]Hoboken: Wiley Subscription Services, Inc., A Wiley CompanyTexto completo disponível |
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Material Type: Artigo
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Founder Mutation in RSPH4A Identified in Patients of Hispanic Descent with Primary Ciliary DyskinesiaDaniels, M. Leigh Anne ; Leigh, Margaret W. ; Davis, Stephanie D. ; Armstrong, Michael C. ; Carson, Johnny L. ; Hazucha, Milan ; Dell, Sharon D. ; Eriksson, Maria ; Collins, Francis S. ; Knowles, Michael R. ; Zariwala, Maimoona A.Human mutation, 2013-10, Vol.34 (10), p.1352-1356 [Periódico revisado por pares]United States: Blackwell Publishing LtdTexto completo disponível |
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Material Type: Artigo
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Human longevity and common variations in the LMNA gene: a meta‐analysisConneely, Karen N. ; Capell, Brian C. ; Erdos, Michael R. ; Sebastiani, Paola ; Solovieff, Nadia ; Swift, Amy J. ; Baldwin, Clinton T. ; Budagov, Temuri ; Barzilai, Nir ; Atzmon, Gil ; Puca, Annibale A. ; Perls, Thomas T. ; Geesaman, Bard J. ; Boehnke, Michael ; Collins, Francis S.Aging cell, 2012-06, Vol.11 (3), p.475-481 [Periódico revisado por pares]Oxford, UK: Blackwell Publishing LtdTexto completo disponível |
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Material Type: Artigo
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Steering a New Course for Stem Cell Research: NIH's Intramural Center for Regenerative MedicineRao, Mahendra S. ; Collins, Francis S.Stem cells translational medicine, 2012-01, Vol.1 (1), p.15-17 [Periódico revisado por pares]United States: AlphaMed PressTexto completo disponível |
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Material Type: Artigo
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Hyperparathyroidism in hereditary syndromes: Special expressions and special managementsMARX, Stephen J ; SIMONDS, William F ; CHEN, Clara C ; CHANG, Richard ; CHANDRASEKHARAPPA, Settara C ; COLLINS, Francis S ; AGARWAL, Sunita K ; BURNS, A. Lee ; WEINSTEIN, Lee S ; COCHRAN, Craig ; SKARULIS, Monica C ; SPIEGEL, Allen M ; LIBUTTI, Steven K ; ALEXANDER, H. RichardJournal of bone and mineral research, 2002-11, Vol.17, p.N37-N43 [Periódico revisado por pares]Duham, NC: American Society for Bone and Mineral ResearchTexto completo disponível |