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51
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Influence of Food Choices on Lipids and Lipoproteins in African Americans : 759 May 29 1:45 PM - 2:00 PM
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Brandon, L. Jerome;
;
(Medicine and science in sports and exercise,
v.40,
2008,
pp.S57)
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52
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Serotonin Receptor 2C -759C/T Polymorphism and Weight Change or Treatment Response to Mirtazapine in Korean Depressive Patients
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Pae, Chi-Un;
Department of Psychiatry, Bucheon St. Mary's Hospital, The Catholic University of Korea College of Medicine, Bucheon, Republic of Korea.;
(Psychiatry investigation,
v.11,
2014,
pp.342-343)
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53
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Corrigendum to “Investigation into the neural correlates of emotional augmentation of clinical pain” [Neuroimage 40/2 (2008) 759–766]
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Schweinhardt, Petra;
Kalk, Nicola;
Wartolowska, Karolina;
Chessell, Iain;
Wordsworth, Paul;
Tracey, Irene;
;
(NeuroImage,
v.56,
2011,
pp.384-384)
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54
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Eclampsia, <i>in vitro</i> fertilization and the risk of preterm birth: a retrospective cohort study based on 2,880,759 samples
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Wang, Jing;
Yin, Jiansong;
Xue, Mei;
Sun, Wenhui;
Wan, Yu;
Department of Neonatology , Changzhou No. 2 People’s Hospital , The Affiliated Hospital of Nanjing Medical University , Changzhou , China;
(Translational pediatrics,
v.12,
2023,
pp.1017-1027)
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55
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[Association of HTR2C-759C/T and -697G/C polymorphisms with antipsychotic agent-induced weight gain]
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Shao, Ping;
Zhao, Jing-ping;
Chen, Jin-dong;
Wu, Ren-rong;
He, Yi-qun;
;
(中南大學學報. Journal of Central South University. 醫學版,
v.33,
2008,
pp.312-315)
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56
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759 Mitral regurgitation assessment before revascularization after myocardial infarction - comparison of 3D real time vs 2D transthoracic echocardiography
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;
;
(European journal of echocardiography : journal of the Working Group on Echocardiography of the European Society of Cardiology,
v.6,
2005,
pp.S116)
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57
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Investigating the disease association of <i>USH2A</i> p.C759F variant by leveraging large retinitis pigmentosa cohort data
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DuPont, Mariana;
Jones, Evan M.;
Xu, Mingchu;
Chen, Rui;
College of Arts and Sciences, Dillard University, New Orleans, LA, USA;
Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA;
Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA;
Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA;
(Ophthalmic genetics,
v.39,
2018,
pp.291-292)
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58
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Polygenic scores, diet quality, and type 2 diabetes risk: An observational study among 35,759 adults from 3 US cohorts
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Merino, Jordi;
Guasch-Ferré
, Marta;
Li, Jun;
Chung, Wonil;
Hu, Yang;
Ma, Baoshan;
Li, Yanping;
Kang, Jae H.;
Kraft, Peter;
Liang, Liming;
Sun, Qi;
Franks, Paul W.;
Manson, JoAnn E.;
Willet, Walter C.;
Florez, Jose C.;
Hu, Frank B.;
Diabetes Unit and Center for Genomic Medicine, Massachusetts General Hospital, Boston, Massachusetts, United States of America;
Department of Nutrition, Harvard TH Chan School of Public Health, Boston, Massachusetts, United States of America;
Department of Nutrition, Harvard TH Chan School of Public Health, Boston, Massachusetts, United States of America;
Department of Epidemiology, Harvard TH Chan School of Public Health, Boston, Massachusetts, United States of America;
Department of Nutrition, Harvard TH Chan School of Public Health, Boston, Massachusetts, United States of America;
Department of Epidemiology, Harvard TH Chan School of Public Health, Boston, Massachusetts, United States of America;
Department of Nutrition, Harvard TH Chan School of Public Health, Boston, Massachusetts, United States of America;
Channing Division of Network Medicine, Department of Medicine, Brigham and Women’s Hospital and Harvard Medical School, Boston, Massachusetts, United States of America;
(PLoS medicine,
v.19,
2022,
pp.e1003972)
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59
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Genetic analysis of 2299delG and C759F mutations (USH2A) in patients with visual and/or auditory impairments
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Aller, Elena;
Ná
jera, Carmen;
Millá
n, José
Ma;
Oltra, Juan S;
Pé
rez-Garrigues, Herminio;
Vilela, Concepció
n;
Navea, Amparo;
Beneyto, Magdalena;
[1] 1Departamento de Gené
tica, Facultad de C Bioló
gicas, Universidad de Valencia, Valencia, Spain [2] 2Unidad de Gené
tica y Diagnó
stico Prenatal, Hospital La Fe, Valencia, Spain;
1Departamento de Gené
tica, Facultad de C Bioló
gicas, Universidad de Valencia, Valencia, Spain;
2Unidad de Gené
tica y Diagnó
stico Prenatal, Hospital La Fe, Valencia, Spain;
2Unidad de Gené
tica y Diagnó
stico Prenatal, Hospital La Fe, Valencia, Spain;
3Servicio de Otorrinolaringologí
a, Hospital La Fe, Valencia, Spain;
4Unidad de Neurofisiologí
a, Hospital La Fe, Valencia, Spain;
5Servicio de Oftalmologí
a, Hospital La Fe, Valencia, Spain;
2Unidad de Gené
tica y Diagnó
stico Prenatal, Hospital La Fe, Valencia, Spain;
(European journal of human genetics : EJHG,
v.12,
2004,
pp.407-410)
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60
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Unravelling the pathogenic role and genotype-phenotype correlation of the <i>USH2A</i> p.(Cys759Phe) variant among Spanish families
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Pé
rez-Carro, Raquel;
Blanco-Kelly, Fiona;
Galbis-Martí
nez, Liliá
n;
Garcí
a-Garcí
a, Gema;
Aller, Elena;
Garcí
a-Sandoval, Blanca;
Mí
nguez, Pablo;
Corton, Marta;
Mahí
llo-Ferná
ndez, Ignacio;
Martí
n-Mé
rida, Inmaculada;
Avila-Ferná
ndez, Almudena;
Millá
n, José
M.;
Ayuso, Carmen;
Department of Genetics, Instituto de Investigació
n Sanitaria-Fundació
n Jimenez Diaz University Hospital-Universidad Autó
noma de Madrid (IIS-FJD, UAM), Madrid, Spain;
Department of Genetics, Instituto de Investigació
n Sanitaria-Fundació
n Jimenez Diaz University Hospital-Universidad Autó
noma de Madrid (IIS-FJD, UAM), Madrid, Spain;
Department of Genetics, Instituto de Investigació
n Sanitaria-Fundació
n Jimenez Diaz University Hospital-Universidad Autó
noma de Madrid (IIS-FJD, UAM), Madrid, Spain;
Center for Biomedical Network Research on Rare Diseases (CIBERER), ISCIII, Madrid, Spain;
Center for Biomedical Network Research on Rare Diseases (CIBERER), ISCIII, Madrid, Spain;
Center for Biomedical Network Research on Rare Diseases (CIBERER), ISCIII, Madrid, Spain;
Department of Genetics, Instituto de Investigació
n Sanitaria-Fundació
n Jimenez Diaz University Hospital-Universidad Aut&o;
(PloS one,
v.13,
2018,
pp.e0199048)