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1
Genome-wide Association Study of Vitamin B6, Vitamin B12, Folate, and Homocysteine Blood Concentrations
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Artigo
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Genome-wide Association Study of Vitamin B6, Vitamin B12, Folate, and Homocysteine Blood Concentrations

Tanaka, Toshiko ; Scheet, Paul ; Giusti, Betti ; Bandinelli, Stefania ; Piras, Maria Grazia ; Usala, Gianluca ; Lai, Sandra ; Mulas, Antonella ; Corsi, Anna Maria ; Vestrini, Anna ; Sofi, Francesco ; Gori, Anna Maria ; Abbate, Rosanna ; Guralnik, Jack ; Singleton, Andrew ; Abecasis, Goncalo R. ; Schlessinger, David ; Uda, Manuela ; Ferrucci, Luigi

American journal of human genetics, 2009-04, Vol.84 (4), p.477-482 [Periódico revisado por pares]

Cambridge, MA: Elsevier Inc

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2
Prevalence of unknown thyroid disorders in a Sardinian cohort
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Artigo
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Prevalence of unknown thyroid disorders in a Sardinian cohort

Delitala, Alessandro P ; Pilia, Maria Grazia ; Ferreli, Liana ; Loi, Francesco ; Curreli, Nicolò ; Balaci, Lenuta ; Schlessinger, David ; Cucca, Francesco

European journal of endocrinology, 2014-07, Vol.171 (1), p.143-149 [Periódico revisado por pares]

Bristol: Bioscientifica Ltd

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3
Sex-Specific Correlates of Walking Speed in a Wide Age-Ranged Population
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Artigo
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Sex-Specific Correlates of Walking Speed in a Wide Age-Ranged Population

Tolea, Magdalena I. ; Costa, Paul T. ; Terracciano, Antonio ; Griswold, Michael ; Simonsick, Eleanor M. ; Najjar, Samer S. ; Scuteri, Angelo ; Deiana, Barbara ; Orrù, Marco ; Masala, Marco ; Uda, Manuela ; Schlessinger, David ; Ferrucci, Luigi

The journals of gerontology. Series B, Psychological sciences and social sciences, 2010-03, Vol.65B (2), p.174-184 [Periódico revisado por pares]

Cary, NC: Oxford University Press

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4
Independent and additive effects of cytokine patterns and the metabolic syndrome on arterial aging in the SardiNIA Study
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Artigo
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Independent and additive effects of cytokine patterns and the metabolic syndrome on arterial aging in the SardiNIA Study

Scuteri, Angelo ; Orru, Marco ; Morrell, Christopher ; Piras, Maria Grazia ; Taub, Dennis ; Schlessinger, David ; Uda, Manuela ; Lakatta, Edward G

Atherosclerosis, 2011-04, Vol.215 (2), p.459-464 [Periódico revisado por pares]

Amsterdam: Elsevier Ireland Ltd

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5
Prevalence of CKD and Its Relationship to eGFR-Related Genetic Loci and Clinical Risk Factors in the SardiNIA Study Cohort
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Artigo
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Prevalence of CKD and Its Relationship to eGFR-Related Genetic Loci and Clinical Risk Factors in the SardiNIA Study Cohort

PANI, Antonello ; BRAGG-GRESHAM, Jennifer ; LOI, Francesco ; ABECASIS, Gonçalo R ; SCHLESSINGER, David ; CUCCA, Francesco ; MASALA, Marco ; PIRAS, Doloretta ; ATZENI, Alice ; PILIA, Maria G ; FERRELI, Liana ; BALACI, Lenuta ; CURRELI, Nicolò ; DELITALA, Alessandro

Journal of the American Society of Nephrology, 2014-07, Vol.25 (7), p.1533-1544 [Periódico revisado por pares]

Washington, DC: American Society of Nephrology

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6
Personality Traits Prospectively Predict Verbal Fluency in a Lifespan Sample
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Artigo
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Personality Traits Prospectively Predict Verbal Fluency in a Lifespan Sample

SUTIN, Angelina R ; TERRACCIANO, Antonio ; KITNER-TRIOLO, Melissa H ; UDA, Manuela ; SCHLESSINGER, David ; ZONDERMAN, Alan B

Psychology and aging, 2011-12, Vol.26 (4), p.994-999 [Periódico revisado por pares]

Washington, DC: American Psychological Association

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7
The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome
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Artigo
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The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome

Marzella, Rosalia ; Uda, Manuela ; Rocchi, Mariano ; Loi, Angela ; Bonneau, Dominique ; Cao, Antonio ; Chiappe, Francesca ; Gasparini, Paolo ; Crisponi, Laura ; Deiana, Manila ; Schlessinger, David ; Porcu, Susanna ; Pilia, Giuseppe ; Nicolino, Marc ; Bisceglia, Luigi ; Amati, Patrizia ; Zelante, Leopoldo ; Nagaraja, Ramaiah ; Serafina Ristaldi, M ; Lienhardt-Roussie, Anne ; Nivelon, Annie ; Verloes, Alain

Nature genetics, 2001-02, Vol.27 (2), p.159-166 [Periódico revisado por pares]

London: Nature Publishing Group

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8
Requirement for Shh and Fox family genes at different stages in sweat gland development
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Artigo
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Requirement for Shh and Fox family genes at different stages in sweat gland development

Kunisada, Makoto ; Cui, Chang-Yi ; Piao, Yulan ; Ko, Minoru S.H. ; Schlessinger, David

Human molecular genetics, 2009-05, Vol.18 (10), p.1769-1778 [Periódico revisado por pares]

Oxford: Oxford University Press

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9
Mutations in GPC3 , a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome
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Artigo
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Mutations in GPC3 , a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome

Pilia, Giuseppe ; Hughes-Benzie, Rhiannon M ; MacKenzie, Alex ; Baybayan, Primo ; Chen, Ellson Y ; Huber, Reid ; Neri, Giovanni ; Cao, Antonio ; Forabosco, Antonino ; Schlessinger, David

Nature genetics, 1996-03, Vol.12 (3), p.241-247 [Periódico revisado por pares]

London: Nature Publishing Group

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10
X-linked situs abnormalities result from mutations in ZIC3
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Artigo
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X-linked situs abnormalities result from mutations in ZIC3

Gebbia, Marinella ; Ferrero, Giovanni B ; Pilia, Giuseppe ; Bassi, Maria T ; Aylsworth, Arthur S ; Penman-Splitt, Miranda ; Bird, Lynne M ; Bamforth, John S ; Burn, John ; Schlessinger, David ; Nelson, David L ; Casey, Brett

Nature genetics, 1997-11, Vol.17 (3), p.305-308 [Periódico revisado por pares]

London: Nature Publishing Group

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