Literature DB >> 1476717

A simple method for DNA extraction from leukocytes for use in PCR.

H A Lewin1, J A Stewart-Haynes.   

Abstract

Mesh：

Substances：

Year:  1992        PMID： 1476717

Source DB:  PubMed          Journal:  Biotechniques        ISSN： 0736-6205            Impact factor:   1.993


× No keyword cloud information.
  19 in total

1.  Mitochondrial genetic background plays a role in increasing risk to asthma.

Authors:  Emily Zifa; Zoe Daniil; Eleutheria Skoumi; Maria Stavrou; Kostantinos Papadimitriou; Marini Terzenidou; Konstantinos Kostikas; Vasileios Bagiatis; Konstantinos I Gourgoulianis; Zissis Mamuris
Journal:  Mol Biol Rep       Date:  2011-09-24       Impact factor: 2.316

2.  The Y-27H39 polymorphism in a Japanese population.

Authors:  W Wang; T Kishida; M Fukuda; Y Tamaki
Journal:  Int J Legal Med       Date:  1996       Impact factor: 2.686

3.  A novel missense mutation in the ABCD1 gene of a Chinese boy diagnosed with X-linked adrenoleukodystrophy: case report.

Authors:  Mengqi Zhang; Shupeng Shi; Haoran Zhang; Lihui Liu; Linchao Wu; Bo Xiao; Weiping Liu
Journal:  Neurol Sci       Date:  2018-10-20       Impact factor: 3.307

4.  A novel frameshift mutation in BLM gene associated with high sister chromatid exchanges (SCE) in heterozygous family members.

Authors:  Ghada Ben Salah; Ikhlas Hadj Salem; Abderrahmen Masmoudi; Fakhri Kallabi; Hamida Turki; Faiza Fakhfakh; Hamadi Ayadi; Hassen Kamoun
Journal:  Mol Biol Rep       Date:  2014-08-17       Impact factor: 2.316

5.  Inter-ethnic differences in genetic polymorphisms of xenobiotic-metabolizing enzymes (CYP1A1, CYP2D6, NAT1 and NAT2) in healthy populations: correlation with the functional in silico prediction.

Authors:  Rim Khlifi; Ghada Ben Salah; Amine Chakroun; Amel Hamza-Chaffai; Ahmed Rebai
Journal:  Mol Biol Rep       Date:  2014-06-17       Impact factor: 2.316

6.  Do GSTM1 and GSTT1 polymorphisms influence the risk of developing mitochondrial diseases in a Tunisian population?

Authors:  Raouia Ghorbel; Ghada Ben Salah; Rania Ghorbel; Afif Ben Mahmoud; Imen Chamkha; Emna Mkaouar-Rebai; Leila Ammar-Keskes; Faiza Fakhfakh
Journal:  Environ Sci Pollut Res Int       Date:  2017-12-12       Impact factor: 4.223

7.  A first description of ataxia with vitamin E deficiency associated with MT-TG gene mutation.

Authors:  Marwa Maalej; Fatma Kammoun; Marwa Kharrat; Wafa Bouchaala; Marwa Ammar; Emna Mkaouar-Rebai; Chahnez Triki; Faiza Fakhfakh
Journal:  Acta Neurol Belg       Date:  2020-09-26       Impact factor: 2.396

8.  Founder effect confirmation of c.241A>G mutation in the L2HGDH gene and characterization of oxidative stress parameters in six Tunisian families with L-2-hydroxyglutaric aciduria.

Authors:  Nadege Kammoun Jellouli; Ikhlass Hadj Salem; Emna Ellouz; Zeineb Kamoun; Fatma kamoun; Abdelaziz tlili; Naziha Kaabachi; Chanez Triki; Faiza Fakhfakh
Journal:  J Hum Genet       Date:  2014-02-27       Impact factor: 3.172

9.  An interethnic variability and a functional prediction of DNA repair gene polymorphisms: the example of XRCC3 (p.Thr241>Met) and XPD (p.Lys751>Gln) in a healthy Tunisian population.

Authors:  Ghada Ben Salah; Nourhene Fendri-Kriaa; Hassen Kamoun; Fakhri Kallabi; Emna Mkaouar-Rebai; Amine Fourati; Hammadi Ayadi; Faiza Fakhfakh
Journal:  Mol Biol Rep       Date:  2012-06-28       Impact factor: 2.316

10.  Impact of polymorphisms of cytochrome-P450 isoenzymes 2C9, 2C19 and 2D6 on plasma concentrations and clinical effects of antidepressants in a naturalistic clinical setting.

Authors:  Katja Grasmäder; Petra Louise Verwohlt; Marcella Rietschel; Aleksandra Dragicevic; Matthias Müller; Christoph Hiemke; Nikolaus Freymann; Astrid Zobel; Wolfgang Maier; Marie Luise Rao
Journal:  Eur J Clin Pharmacol       Date:  2004-05-28       Impact factor: 2.953
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.