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Refinado por: assunto: Medical Sciences remover
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Gain-of-Function Mutations of ARHGAP31, a Cdc42/Rac1 GTPase Regulator, Cause Syndromic Cutis Aplasia and Limb Anomalies
Gain-of-Function Mutations of ARHGAP31, a Cdc42/Rac1 GTPase Regulator, Cause Syndromic Cutis Aplasia and Limb Anomalies
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Gain-of-Function Mutations of ARHGAP31, a Cdc42/Rac1 GTPase Regulator, Cause Syndromic Cutis Aplasia and Limb Anomalies

Southgate, Laura ; Machado, Rajiv D. ; Snape, Katie M. ; Primeau, Martin ; Dafou, Dimitra ; Ruddy, Deborah M. ; Branney, Peter A. ; Fisher, Malcolm ; Lee, Grace J. ; Simpson, Michael A. ; He, Yi ; Bradshaw, Teisha Y. ; Blaumeiser, Bettina ; Winship, William S. ; Reardon, Willie ; Maher, Eamonn R. ; FitzPatrick, David R. ; Wuyts, Wim ; Zenker, Martin ; Lamarche-Vane, Nathalie ; Trembath, Richard C.

American journal of human genetics, 2011-05, Vol.88 (5), p.574-585 [Periódico revisado por pares]

Cambridge, MA: Elsevier Inc

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2
The protective effects of guaraná extract (Paullinia cupana) on fibroblast NIH-3T3 cells exposed to sodium nitroprusside
The protective effects of guaraná extract (Paullinia cupana) on fibroblast NIH-3T3 cells exposed to sodium nitroprusside
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The protective effects of guaraná extract (Paullinia cupana) on fibroblast NIH-3T3 cells exposed to sodium nitroprusside

Bittencourt, L.S. ; Machado, D.C. ; Machado, M.M. ; Dos Santos, G.F.F. ; Algarve, T.D. ; Marinowic, D.R. ; Ribeiro, E.E. ; Soares, F.A.A. ; Barbisan, F. ; Athayde, M.L. ; Cruz, I.B.M.

Food and chemical toxicology, 2013-03, Vol.53, p.119-125 [Periódico revisado por pares]

Oxford: Elsevier Ltd

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3
High-performance liquid chromatography with fluorescence detection for quantitation of tryptophan and tyrosine in a shrimp waste protein concentrate
High-performance liquid chromatography with fluorescence detection for quantitation of tryptophan and tyrosine in a shrimp waste protein concentrate
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High-performance liquid chromatography with fluorescence detection for quantitation of tryptophan and tyrosine in a shrimp waste protein concentrate

Sánchez-Machado, D.I. ; Chavira-Willys, B. ; López-Cervantes, J.

Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 2008-02, Vol.863 (1), p.88-93 [Periódico revisado por pares]

Amsterdam: Elsevier B.V

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4
Synthesis, biological evaluation and molecular docking studies of 3-(triazolyl)-coumarin derivatives: Effect on inducible nitric oxide synthase
Synthesis, biological evaluation and molecular docking studies of 3-(triazolyl)-coumarin derivatives: Effect on inducible nitric oxide synthase
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Synthesis, biological evaluation and molecular docking studies of 3-(triazolyl)-coumarin derivatives: Effect on inducible nitric oxide synthase

Stefani, Hélio A. ; Gueogjan, Karina ; Manarin, Flávia ; Farsky, Sandra H.P. ; Zukerman-Schpector, Julio ; Caracelli, Ignez ; Pizano Rodrigues, Sergio R. ; Muscará, Marcelo N. ; Teixeira, Simone A. ; Santin, José R. ; Machado, Isabel D. ; Bolonheis, Simone M. ; Curi, Rui ; Vinolo, Marco A.

European journal of medicinal chemistry, 2012-12, Vol.58, p.117-127 [Periódico revisado por pares]

Kidlington: Elsevier Masson SAS

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5
BMPR2 Haploinsufficiency as the Inherited Molecular Mechanism for Primary Pulmonary Hypertension
BMPR2 Haploinsufficiency as the Inherited Molecular Mechanism for Primary Pulmonary Hypertension
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BMPR2 Haploinsufficiency as the Inherited Molecular Mechanism for Primary Pulmonary Hypertension

Machado, Rajiv D ; Pauciulo, Michael W. ; Thomson, Jennifer R. ; Lane, Kirk B. ; Morgan, Neil V. ; Wheeler, Lisa ; Phillips III, John A. ; Newman, John ; Williams, Denise ; Galiè, Nazzareno ; Manes, Alessandra ; McNeil, Keith ; Yacoub, Magdi ; Mikhail, Ghada ; Rogers, Paula ; Corris, Paul ; Humbert, Marc ; Donnai, Dian ; Martensson, Gunnar ; Tranebjaerg, Lisbeth ; Loyd, James E. ; Trembath, Richard C. ; Nichols, William C.

American journal of human genetics, 2001-01, Vol.68 (1), p.92-102 [Periódico revisado por pares]

Chicago, IL: Elsevier Inc

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6
De Novo Thrombotic Microangiopathy After Kidney Transplantation: Clinical Features, Treatment, and Long-Term Patient and Graft Survival
De Novo Thrombotic Microangiopathy After Kidney Transplantation: Clinical Features, Treatment, and Long-Term Patient and Graft Survival
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De Novo Thrombotic Microangiopathy After Kidney Transplantation: Clinical Features, Treatment, and Long-Term Patient and Graft Survival

Caires, R.A ; Marques, I.D.B ; Repizo, L.P ; Sato, V.A.H ; Carmo, L.P.F ; Machado, D.J.B ; de Paula, F.J ; Nahas, W.C ; David-Neto, E

Transplantation proceedings, 2012-10, Vol.44 (8), p.2388-2390 [Periódico revisado por pares]

Amsterdam: Elsevier Inc

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7
Heterozygous germline mutations in BMPR2 , encoding a TGF-β receptor, cause familial primary pulmonary hypertension
Heterozygous germline mutations in BMPR2 , encoding a TGF-β receptor, cause familial primary pulmonary hypertension
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Heterozygous germline mutations in BMPR2 , encoding a TGF-β receptor, cause familial primary pulmonary hypertension

Lane, Kirk B ; Machado, Rajiv D ; Pauciulo, Michael W ; Thomson, Jennifer R ; Phillips, John A ; Loyd, James E ; Nichols, William C ; Trembath, Richard C

Nature genetics, 2000-09, Vol.26 (1), p.81-84 [Periódico revisado por pares]

London: Nature Publishing Group

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8
Clinical and Molecular Genetic Features of Pulmonary Hypertension in Patients with Hereditary Hemorrhagic Telangiectasia
Clinical and Molecular Genetic Features of Pulmonary Hypertension in Patients with Hereditary Hemorrhagic Telangiectasia
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Clinical and Molecular Genetic Features of Pulmonary Hypertension in Patients with Hereditary Hemorrhagic Telangiectasia

Trembath, Richard C ; Thomson, Jennifer R ; Machado, Rajiv D ; Morgan, Neil V ; Atkinson, Carl ; Winship, Ingrid ; Simonneau, Gerald ; Galie, Nazzareno ; Loyd, James E ; Humbert, Marc ; Nichols, William C ; Berg, Jonathan ; Manes, Alessandra ; McGaughran, Julie ; Pauciulo, Michael ; Wheeler, Lisa ; Morrell, Nicholas W

The New England journal of medicine, 2001-08, Vol.345 (5), p.325-334 [Periódico revisado por pares]

Boston, MA: Massachusetts Medical Society

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9
Molecular and functional analysis identifies ALK-1 as the predominant cause of pulmonary hypertension related to hereditary haemorrhagic telangiectasia
Molecular and functional analysis identifies ALK-1 as the predominant cause of pulmonary hypertension related to hereditary haemorrhagic telangiectasia
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Molecular and functional analysis identifies ALK-1 as the predominant cause of pulmonary hypertension related to hereditary haemorrhagic telangiectasia

Harrison, R E ; Flanagan, J A ; Sankelo, M ; Abdalla, S A ; Rowell, J ; Machado, R D ; Elliott, C G ; Robbins, I M ; Olschewski, H ; McLaughlin, V ; Gruenig, E ; Kermeen, F ; Laitinen, T ; Morrell, N W ; Trembath, R C

Journal of medical genetics, 2003-12, Vol.40 (12), p.865-871 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd

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10
Identification of nontuberculous mycobacteria in clinical samples using molecular methods: a 3-year study
Identification of nontuberculous mycobacteria in clinical samples using molecular methods: a 3-year study
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Identification of nontuberculous mycobacteria in clinical samples using molecular methods: a 3-year study

Couto, I. ; Machado, D. ; Viveiros, M. ; Rodrigues, L. ; Amaral, L.

Clinical microbiology and infection, 2010-08, Vol.16 (8), p.1161-1164 [Periódico revisado por pares]

Oxford, UK: Elsevier Ltd

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