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Dermatology

Free Subscription Articles published in PLoS Genet Retrieve available abstracts of 24 articles: HTML format Text format

Single Articles

May 2018
1. WU X, Tommasi di Vignano A, Zhou Q, Michel-Dziunycz PJ, et al
   The ARE-binding protein Tristetraprolin (TTP) is a novel target and mediator of calcineurin tumor suppressing function in the skin.
   PLoS Genet. 2018;14:e1007366.
   PubMed     Text format     Abstract available
   
   
   April 2018
2. PAULO P, Maia S, Pinto C, Pinto P, et al
   Targeted next generation sequencing identifies functionally deleterious germline mutations in novel genes in early-onset/familial prostate cancer.
   PLoS Genet. 2018;14:e1007355.
   PubMed     Text format     Abstract available
   
   
   March 2018
3. BAUER A, Jagannathan V, Hogler S, Richter B, et al
   MKLN1 splicing defect in dogs with lethal acrodermatitis.
   PLoS Genet. 2018;14:e1007264.
   PubMed     Text format     Abstract available
   
   
   
4. CHAN WL, Steiner M, Witkos T, Egerer J, et al
   Impaired proteoglycan glycosylation, elevated TGF-beta signaling, and abnormal osteoblast differentiation as the basis for bone fragility in a mouse model for gerodermia osteodysplastica.
   PLoS Genet. 2018;14:e1007242.
   PubMed     Text format     Abstract available
   
   
   February 2018
5. ENG KH, Szender JB, Etter JL, Kaur J, et al
   Paternal lineage early onset hereditary ovarian cancers: A Familial Ovarian Cancer Registry study.
   PLoS Genet. 2018;14:e1007194.
   PubMed     Text format     Abstract available
   
   
   January 2018
6. DUVERGER O, Carlson JC, Karacz CM, Schwartz ME, et al
   Genetic variants in pachyonychia congenita-associated keratins increase susceptibility to tooth decay.
   PLoS Genet. 2018;14:e1007168.
   PubMed     Text format     Abstract available
   
   
   
7. HOLLERN DP, Swiatnicki MR, Andrechek ER
   Histological subtypes of mouse mammary tumors reveal conserved relationships to human cancers.
   PLoS Genet. 2018;14:e1007135.
   PubMed     Text format     Abstract available
   
   
   October 2017
8. CAIRNS J, Ingle JN, Wickerham LD, Weinshilboum R, et al
   SNPs near the cysteine proteinase cathepsin O gene (CTSO) determine tamoxifen sensitivity in ERalpha-positive breast cancer through regulation of BRCA1.
   PLoS Genet. 2017;13:e1007031.
   PubMed     Text format     Abstract available
   
   
   September 2017
9. GAO G, Pierce BL, Olopade OI, Im HK, et al
   Trans-ethnic predicted expression genome-wide association analysis identifies a gene for estrogen receptor-negative breast cancer.
   PLoS Genet. 2017;13:e1006727.
   PubMed     Text format     Abstract available
   
   
   
10. LIU Y, Walavalkar NM, Dozmorov MG, Rich SS, et al
    Identification of breast cancer associated variants that modulate transcription factor binding.
    PLoS Genet. 2017;13:e1006761.
    PubMed     Text format     Abstract available
    
    
    
11. WANG W, Xu ZZ, Costanzo M, Boone C, et al
    Pathway-based discovery of genetic interactions in breast cancer.
    PLoS Genet. 2017;13:e1006973.
    PubMed     Text format     Abstract available
    
    
    
12. MECHANIC LE, Lindstrom S, Daily KM, Sieberts SK, et al
    Up For A Challenge (U4C): Stimulating innovation in breast cancer genetic epidemiology.
    PLoS Genet. 2017;13:e1006945.
    PubMed     Text format    
    
    
    July 2017
13. KLAR J, Piontek J, Milatz S, Tariq M, et al
    Altered paracellular cation permeability due to a rare CLDN10B variant causes anhidrosis and kidney damage.
    PLoS Genet. 2017;13:e1006897.
    PubMed     Text format     Abstract available
    
    
    June 2017
14. KAWAZU M, Kojima S, Ueno T, Totoki Y, et al
    Integrative analysis of genomic alterations in triple-negative breast cancer in association with homologous recombination deficiency.
    PLoS Genet. 2017;13:e1006853.
    PubMed     Text format     Abstract available
    
    
    March 2017
15. HOFFMAN JD, Graff RE, Emami NC, Tai CG, et al
    Cis-eQTL-based trans-ethnic meta-analysis reveals novel genes associated with breast cancer risk.
    PLoS Genet. 2017;13:e1006690.
    PubMed     Text format     Abstract available
    
    
    
16. STRICKER TP, Brown CD, Bandlamudi C, McNerney M, et al
    Robust stratification of breast cancer subtypes using differential patterns of transcript isoform expression.
    PLoS Genet. 2017;13:e1006589.
    PubMed     Text format     Abstract available
    
    
    February 2017
17. HAGENAARS SP, Hill WD, Harris SE, Ritchie SJ, et al
    Genetic prediction of male pattern baldness.
    PLoS Genet. 2017;13:e1006594.
    PubMed     Text format     Abstract available
    
    
    
18. EVANS JM, Noorai RE, Tsai KL, Starr-Moss AN, et al
    Beyond the MHC: A canine model of dermatomyositis shows a complex pattern of genetic risk involving novel loci.
    PLoS Genet. 2017;13:e1006604.
    PubMed     Text format     Abstract available
    
    
    January 2017
19. KASPAREK P, Ileninova Z, Zbodakova O, Kanchev I, et al
    KLK5 and KLK7 Ablation Fully Rescues Lethality of Netherton Syndrome-Like Phenotype.
    PLoS Genet. 2017;13:e1006566.
    PubMed     Text format     Abstract available
    
    
    September 2016
20. MAIR B, Konopka T, Kerzendorfer C, Sleiman K, et al
    Gain- and Loss-of-Function Mutations in the Breast Cancer Gene GATA3 Result in Differential Drug Sensitivity.
    PLoS Genet. 2016;12:e1006279.
    PubMed     Text format     Abstract available
    
    
    August 2016
21. RUMP A, Benet-Pages A, Schubert S, Kuhlmann JD, et al
    Identification and Functional Testing of ERCC2 Mutations in a Multi-national Cohort of Patients with Familial Breast- and Ovarian Cancer.
    PLoS Genet. 2016;12:e1006248.
    PubMed     Text format     Abstract available
    
    
    June 2016
22. THOUVENOT P, Ben Yamin B, Fourriere L, Lescure A, et al
    Functional Assessment of Genetic Variants with Outcomes Adapted to Clinical Decision-Making.
    PLoS Genet. 2016;12:e1006096.
    PubMed     Text format     Abstract available
    
    
    January 2016
23. MANTERE T, Winqvist R, Kauppila S, Grip M, et al
    Targeted Next-Generation Sequencing Identifies a Recurrent Mutation in MCPH1 Associating with Hereditary Breast Cancer Susceptibility.
    PLoS Genet. 2016;12:e1005816.
    PubMed     Text format     Abstract available
    
    
    
24. FARAJI F, Hu Y, Yang HH, Lee MP, et al
    Post-transcriptional Control of Tumor Cell Autonomous Metastatic Potential by CCR4-NOT Deadenylase CNOT7.
    PLoS Genet. 2016;12:e1005820.
    PubMed     Text format     Abstract available
    
    

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