Sort by
Items per page

Send to

Choose Destination

Links from Gene

Items: 1 to 20 of 112


Genetic Variation in Choline-Metabolizing Enzymes Alters Choline Metabolism in Young Women Consuming Choline Intakes Meeting Current Recommendations.

Ganz AB, Cohen VV, Swersky CC, Stover J, Vitiello GA, Lovesky J, Chuang JC, Shields K, Fomin VG, Lopez YS, Mohan S, Ganti A, Carrier B, Malysheva OV, Caudill MA.

Int J Mol Sci. 2017 Jan 26;18(2). pii: E252. doi: 10.3390/ijms18020252.


Program and Abstracts from the Canadian Digestive Diseases Week™ 2016.

Gastroenterology CA, For The Study Of The Liver CA.

Can J Gastroenterol Hepatol. 2016;2016:4792898. doi: 10.1155/2016/4792898. No abstract available.


Design of a protocol for obtaining genomic DNA from saliva using mouthwash: Samples taken from patients with periodontal disease.

Mendoza ÁC, Volante BB, Hernández ME, Mendoza CC, Pliego AF, Baptista Gonzalez HA, Juárez HE.

J Oral Biol Craniofac Res. 2016 May-Aug;6(2):129-34. doi: 10.1016/j.jobcr.2016.01.002.


Genetic and Functional Sequence Variants of the SIRT3 Gene Promoter in Myocardial Infarction.

Yin X, Pang S, Huang J, Cui Y, Yan B.

PLoS One. 2016 Apr 14;11(4):e0153815. doi: 10.1371/journal.pone.0153815.


The influence of genetic polymorphisms in TLR4 and TIRAP, and their expression levels in peripheral blood, on susceptibility to sepsis.

Zhang J, Yang J, Xu X, Liang L, Sun H, Liu G, Zhang L, Su Y.

Exp Ther Med. 2016 Jan;11(1):131-139.


Variant rs2237892 of KCNQ1 Is Potentially Associated with Hypertension and Macrovascular Complications in Type 2 Diabetes Mellitus in A Chinese Han Population.

Zhang W, Wang H, Guan X, Niu Q, Li W.

Genomics Proteomics Bioinformatics. 2015 Dec;13(6):364-70. doi: 10.1016/j.gpb.2015.05.004.


Variations in Antioxidant Genes and Male Infertility.

Yu B, Huang Z.

Biomed Res Int. 2015;2015:513196. doi: 10.1155/2015/513196. Review.


Variants Near CCK Receptors are Associated With Electrophysiological Responses to Pre-pulse Startle Stimuli in a Mexican American Cohort.

Norden-Krichmar TM, Gizer IR, Phillips E, Wilhelmsen KC, Schork NJ, Ehlers CL.

Twin Res Hum Genet. 2015 Dec;18(6):727-37. doi: 10.1017/thg.2015.77.


Inactivation of SDH and FH cause loss of 5hmC and increased H3K9me3 in paraganglioma/pheochromocytoma and smooth muscle tumors.

Hoekstra AS, de Graaff MA, Briaire-de Bruijn IH, Ras C, Seifar RM, van Minderhout I, Cornelisse CJ, Hogendoorn PC, Breuning MH, Suijker J, Korpershoek E, Kunst HP, Frizzell N, Devilee P, Bayley JP, Bovée JV.

Oncotarget. 2015 Nov 17;6(36):38777-88. doi: 10.18632/oncotarget.6091.


Contribution of BDNF and DRD2 genetic polymorphisms to continued opioid use in patients receiving methadone treatment for opioid use disorder: an observational study.

Bawor M, Dennis BB, Tan C, Pare G, Varenbut M, Daiter J, Plater C, Worster A, Marsh DC, Steiner M, Anglin R, Desai D, Thabane L, Samaan Z.

Addict Sci Clin Pract. 2015 Oct 6;10:19. doi: 10.1186/s13722-015-0040-7.


CRISPR/Cas9 System as an Agent for Eliminating Polyomavirus JC Infection.

Wollebo HS, Bellizzi A, Kaminski R, Hu W, White MK, Khalili K.

PLoS One. 2015 Sep 11;10(9):e0136046. doi: 10.1371/journal.pone.0136046.


Recombination of chl-fus gene (Plastid Origin) downstream of hop: a locus of chromosomal instability.

Salinas Castellanos LC, Chomilier J, Hernández-Torres J.

BMC Genomics. 2015 Aug 4;16:573. doi: 10.1186/s12864-015-1780-1.


Data supporting the design and evaluation of a universal primer pair for pseudogene-free amplification of HPRT1 in real-time PCR.

Valadan R, Hedayatizadeh-Omran A, Alhosseini-Abyazani MN, Amjadi O, Rafiei A, Tehrani M, Alizadeh-Navaei R.

Data Brief. 2015 Jul 6;4:384-9. doi: 10.1016/j.dib.2015.06.009.


An exploratory study of the association between SORL1 polymorphisms and sporadic Alzheimer's disease in the Han Chinese population.

Zhang F, Liu X, Wang B, Cheng Z, Zhao X, Zhu J, Wang D, Wang Y, Dong A, Li P, Jin C.

Neuropsychiatr Dis Treat. 2015 Jun 12;11:1443-8. doi: 10.2147/NDT.S85370.


A recessive homozygous p.Asp92Gly SDHD mutation causes prenatal cardiomyopathy and a severe mitochondrial complex II deficiency.

Alston CL, Ceccatelli Berti C, Blakely EL, Oláhová M, He L, McMahon CJ, Olpin SE, Hargreaves IP, Nolli C, McFarland R, Goffrini P, O'Sullivan MJ, Taylor RW.

Hum Genet. 2015 Aug;134(8):869-79. doi: 10.1007/s00439-015-1568-z.


Do housekeeping genes exist?

Zhang Y, Li D, Sun B.

PLoS One. 2015 May 13;10(5):e0123691. doi: 10.1371/journal.pone.0123691.

Supplemental Content

Support Center