scholarly journals The human mitochondrial transport/carrier protein family. Nonsynonymous single nucleotide polymorphisms (nsSNPs) and mutations that lead to human diseases

2006 ◽  
Vol 1757 (9-10) ◽  
pp. 1263-1270 ◽  
Author(s):  
Hartmut Wohlrab
Keyword(s):  
Single Nucleotide Polymorphisms ◽  
Protein Family ◽  
Human Diseases ◽  
Carrier Protein ◽  
Nucleotide Polymorphisms ◽  
Single Nucleotide ◽  
Mitochondrial Transport ◽  
Transport Carrier

Single nucleotide polymorphisms in piRNA-pathway genes: an insight into genetic determinants of human diseases

2019 ◽  
Vol 295 (1) ◽  
pp. 1-12 ◽  
Author(s):  
Jyoti Roy ◽  
Kalyani Anand ◽  
Swati Mohapatra ◽  
Rojalin Nayak ◽  
Trisha Chattopadhyay ◽  
...  
Keyword(s):  
Single Nucleotide Polymorphisms ◽  
Human Diseases ◽  
Nucleotide Polymorphisms ◽  
Genetic Determinants ◽  
Single Nucleotide ◽  
Pirna Pathway ◽  
Insight Into

Role of single nucleotide polymorphisms in pharmacogenomics and their association with human diseases

2015 ◽  
Vol 47 (3) ◽  
pp. 281-290 ◽  
Author(s):  
Renu Chaudhary ◽  
Bharat Singh ◽  
Manish Kumar ◽  
Surendra K. Gakhar ◽  
Adesh K. Saini ◽  
...  
Keyword(s):  
Single Nucleotide Polymorphisms ◽  
Human Diseases ◽  
Nucleotide Polymorphisms ◽  
Single Nucleotide

Association of single-nucleotide polymorphisms of the KEAP1 gene with the risk of various human diseases and its functional impact using in silico analysis

2018 ◽  
Vol 137 ◽  
pp. 205-218 ◽  
Author(s):  
Umapathy Dhamodharan ◽  
Balashanmugam Ponjayanthi ◽  
Dornadula Sireesh ◽  
Elango Bhakkiyalakshmi ◽  
Kunka Mohanram Ramkumar
Keyword(s):  
Single Nucleotide Polymorphisms ◽  
In Silico ◽  
In Silico Analysis ◽  
Human Diseases ◽  
Nucleotide Polymorphisms ◽  
Single Nucleotide ◽  
Functional Impact ◽  
Silico Analysis

A method for SNP detection using MoS2@AuNPs and SYBR Green I in combination with enzyme digestion

2019 ◽  
Vol 43 (47) ◽  
pp. 18571-18574
Author(s):  
Lirong Yan ◽  
Zebin Deng ◽  
Haixia Shi ◽  
Bing Xie ◽  
Li Gao
Keyword(s):  
Single Nucleotide Polymorphisms ◽  
Gene Sequence ◽  
Enzyme Digestion ◽  
Sybr Green ◽  
Sybr Green I ◽  
Human Diseases ◽  
Nucleotide Polymorphisms ◽  
Snp Detection ◽  
Single Nucleotide

Single-nucleotide polymorphisms (SNPs) in a gene sequence are markers for a variety of human diseases.

Development of a simple method for the determination of single nucleotide polymorphisms

2010 ◽  
Vol 34 (8) ◽  
pp. S75-S75
Author(s):  
Weifeng Zhu ◽  
Zhuoqi Liu ◽  
Daya Luo ◽  
Xinyao Wu ◽  
Fusheng Wan
Keyword(s):  
Single Nucleotide Polymorphisms ◽  
Nucleotide Polymorphisms ◽  
Simple Method ◽  
Single Nucleotide

Sex Differences in Childhood Associations between DNA Markers and General Cognitive Ability

2007 ◽  
Vol 28 (3) ◽  
pp. 161-164 ◽  
Author(s):  
Rosalind Arden ◽  
Nicole Harlaar ◽  
Robert Plomin
Keyword(s):  
Sex Differences ◽  
Single Nucleotide Polymorphisms ◽  
Cognitive Ability ◽  
Dna Markers ◽  
Community Sample ◽  
Nucleotide Polymorphisms ◽  
General Cognitive Ability ◽  
Single Nucleotide ◽  
The Difference

Abstract. An association between intelligence at age 7 and a set of five single-nucleotide polymorphisms (SNPs) has been identified and replicated. We used this composite SNP set to investigate whether the associations differ between boys and girls for general cognitive ability at ages 2, 3, 4, 7, 9, and 10 years. In a longitudinal community sample of British twins aged 2-10 (n > 4,000 individuals), we found that the SNP set is more strongly associated with intelligence in males than in females at ages 7, 9, and 10 and the difference is significant at 10. If this finding replicates in other studies, these results will constitute the first evidence of the same autosomal genes acting differently on intelligence in the two sexes.

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