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Refinado por: Nome da Publicação: Clinical Biochemistry remover
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1
Single nucleotide polymorphism C/T -13910, located upstream of the lactase gene, associated with adult-type hypolactasia: Validation for clinical practice
Single nucleotide polymorphism C/T -13910, located upstream of the lactase gene, associated with adult-type hypolactasia: Validation for clinical practice
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Single nucleotide polymorphism C/T -13910, located upstream of the lactase gene, associated with adult-type hypolactasia: Validation for clinical practice

Mattar, Rejane ; do Socorro Monteiro, Maria ; Villares, Cibele Aparecida ; dos Santos, Aníbal Ferreira ; Carrilho, Flair José

Clinical biochemistry, 2008-05, Vol.41 (7), p.628-630 [Periódico revisado por pares]

Elsevier Inc

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2
Single nucleotide polymorphism C/T-13910, located upstream of the lactase gene, associated with adult-type hypolactasia: Validation for clinical practice
Single nucleotide polymorphism C/T-13910, located upstream of the lactase gene, associated with adult-type hypolactasia: Validation for clinical practice
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Single nucleotide polymorphism C/T-13910, located upstream of the lactase gene, associated with adult-type hypolactasia: Validation for clinical practice

Rejane Mattar Margia do Socorro Monteiro; Cibele Aparecida Villares; Aníbal Ferreira dos Santos; Flair José Carrilho

Clinical Biochemistry Toronto v. 41, n.7/8, p. 628-630, 2008

Toronto 2008

Acesso online. A biblioteca também possui exemplares impressos.

3
Single nucleotide polymorphism C/T-13910, located upstream of the lactase gene, associated with adult-type hypolactasia: Validation for clinical practice
Single nucleotide polymorphism C/T-13910, located upstream of the lactase gene, associated with adult-type hypolactasia: Validation for clinical practice
Material Type:
Artigo 		Adicionar ao Meu Espaço

Single nucleotide polymorphism C/T-13910, located upstream of the lactase gene, associated with adult-type hypolactasia: Validation for clinical practice

Rejane Mattar Margia do Socorro Monteiro; Cibele Aparecida Villares; Aníbal Ferreira dos Santos; Flair José Carrilho

Clinical Biochemistry Toronto v. 41, n.7/8, p. 628-630, 2008

Toronto 2008

Acesso online. A biblioteca também possui exemplares impressos.

4
Interleukin-18 promoter −137 G/C polymorphism (rs187238) is associated with biochemical markers of renal function and cardiovascular disease in type 2 diabetes patients
Interleukin-18 promoter −137 G/C polymorphism (rs187238) is associated with biochemical markers of renal function and cardiovascular disease in type 2 diabetes patients
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Interleukin-18 promoter −137 G/C polymorphism (rs187238) is associated with biochemical markers of renal function and cardiovascular disease in type 2 diabetes patients

Cavalcante, Jânio Emanuel Andrade ; de Sousa, Ederson Laurindo Holanda ; de Oliveira Rodrigues, Raphael ; de Almeida Viana, Glautemberg ; Duarte Gadelha, Daniel ; de Carvalho, Manoela Montenegro Dias ; Sousa, Duaran Lopes ; Silva, Allysson Jordan Xavier ; Filho, Raimundo Rigoberto Barbosa Xavier ; Fernandes, Virgínia Oliveira ; Montenegro Júnior, Renan Magalhães ; de Sousa Alves, Renata ; Meneses, Gdayllon Cavalcante ; Sampaio, Tiago Lima ; Queiroz, Maria Goretti Rodrigues

Clinical biochemistry, 2020-06, Vol.80, p.1-7 [Periódico revisado por pares]

United States: Elsevier Inc

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5
Apolipoprotein M promoter polymorphisms alter promoter activity and confer the susceptibility to the development of type 1 diabetes
Apolipoprotein M promoter polymorphisms alter promoter activity and confer the susceptibility to the development of type 1 diabetes
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Apolipoprotein M promoter polymorphisms alter promoter activity and confer the susceptibility to the development of type 1 diabetes

Wu, Xiaopan ; Niu, Nifang ; Brismar, Kerstin ; Zhu, Xilin ; Wang, Xin ; Efendic, Suad ; Du, Te ; Liu, Yang ; Gu, Harvest F. ; Liu, Ying

Clinical biochemistry, 2009, Vol.42 (1), p.17-21 [Periódico revisado por pares]

United States: Elsevier Inc

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6
Paraoxonase 2 C311S single nucleotide polymorphism is associated with type C lesions in coronary atherosclerosis
Paraoxonase 2 C311S single nucleotide polymorphism is associated with type C lesions in coronary atherosclerosis
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Paraoxonase 2 C311S single nucleotide polymorphism is associated with type C lesions in coronary atherosclerosis

Paszek, Elżbieta ; Godlewski, Jacek ; Wołkow, Paweł ; Żmudka, Krzysztof ; Słowik, Agnieszka ; Legutko, Jacek ; Kleczyński, Paweł

Clinical biochemistry, 2022-07, Vol.105-106, p.64-69 [Periódico revisado por pares]

United States: Elsevier Inc

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7
Association of single nucleotide polymorphism rs6903956 on chromosome 6p24.1 with coronary artery disease and lipid levels in different ethnic groups of the Singaporean population
Association of single nucleotide polymorphism rs6903956 on chromosome 6p24.1 with coronary artery disease and lipid levels in different ethnic groups of the Singaporean population
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Association of single nucleotide polymorphism rs6903956 on chromosome 6p24.1 with coronary artery disease and lipid levels in different ethnic groups of the Singaporean population

Tayebi, Naeimeh ; Ke, Tingjing ; Foo, Jia Nee ; Friedlander, Yechiel ; Liu, Jianjun ; Heng, Chew-Kiat

Clinical biochemistry, 2013-06, Vol.46 (9), p.755-759 [Periódico revisado por pares]

United States: Elsevier Inc

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8
Genotyping single nucleotide polymorphisms by MALDI mass spectrometry in clinical applications
Genotyping single nucleotide polymorphisms by MALDI mass spectrometry in clinical applications
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Genotyping single nucleotide polymorphisms by MALDI mass spectrometry in clinical applications

Tost, Jörg ; Gut, Ivo Glynne

Clinical biochemistry, 2005-04, Vol.38 (4), p.335-350 [Periódico revisado por pares]

United States: Elsevier Inc

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9
Genetic polymorphisms in the Wnt/β-catenin pathway genes as predictors of tumor development and survival in patients with hepatitis B virus-associated hepatocellular carcinoma
Genetic polymorphisms in the Wnt/β-catenin pathway genes as predictors of tumor development and survival in patients with hepatitis B virus-associated hepatocellular carcinoma
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Genetic polymorphisms in the Wnt/β-catenin pathway genes as predictors of tumor development and survival in patients with hepatitis B virus-associated hepatocellular carcinoma

Kim, Soon Sun ; Cho, Hyo Jung ; Lee, Hyun-Young ; Park, Ju Han ; Noh, Choong Kyun ; Shin, Sung Jae ; Lee, Kee Myung ; Yoo, Byung Moo ; Lee, Kwang Jae ; Cho, Sung Won ; Cheong, Jae Youn

Clinical biochemistry, 2016-07, Vol.49 (10-11), p.792-801 [Periódico revisado por pares]

United States: Elsevier Inc

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10
Paraoxonase 1 (PON1) and stroke; the dilemma of genetic variation
Paraoxonase 1 (PON1) and stroke; the dilemma of genetic variation
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Paraoxonase 1 (PON1) and stroke; the dilemma of genetic variation

Tajbakhsh, Amir ; Rezaee, Mehdi ; Rivandi, Mahdi ; Forouzanfar, Faranak ; Afzaljavan, Fahimeh ; Pasdar, Alireza

Clinical biochemistry, 2017-12, Vol.50 (18), p.1298-1305 [Periódico revisado por pares]

United States: Elsevier Inc

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Deste Autor:

  1. Carrilho, F
  2. Villares, C
  3. Santos, A
  4. Mattar, R
  5. Monteiro, M

Neste Assunto:

  1. Life Sciences & Biomedicine
  2. Science & Technology
  3. Medical Laboratory Technology
  4. Humans
  5. Female

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

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