Results 151 to 160 of about 5,637 (202)

Genome-wide identification and functional validation of the WW domain containing oxidoreductase gene associated with sleep duration. [PDF]

Sci Rep
Kim S, Kang SW, Kim SE, Kim HJ, Kim SA, Lee YW, Kim EY, Shin C, Lee HW.   +8 more
europepmc   +1 more source

Maintaining the unmethylated state [PDF]

, 2013

core   +1 more source

Hyaluronan: An Architect and Integrator for Cancer and Neural Diseases. [PDF]

Int J Mol Sci
Hsu CY, Nguyen-Tran HH, Chen YA, Lee KT, Juang TY, Chiang MF, Liu SY, Chang NS.   +7 more
europepmc   +1 more source

Identifying individuals with rare disease variants by inferring shared ancestral haplotypes from SNP array data. [PDF]

NAR Genom Bioinform
Robertson E, Grinton BE, Oliver KL, Fearnley LG, Hildebrand MS, Sadleir LG, Scheffer IE, Berkovic SF, Bennett MF, Bahlo M.   +9 more
europepmc   +1 more source

Case report: Adult patient with WWOX developmental and epileptic encephalopathy: 40 years of observation. [PDF]

Front Genet
Teplyshova A, Sharkov A.
europepmc   +1 more source

Karakterisering av regulatoriske regioner oppstrøms for WWOX

, 2005
Det humane genet WWOX har blitt identifisert av flere uavhengige forskningsgrupper i forbindelse med studier av strukturelle abnormaliteter av kromosom 16q i ulike krefttyper. Dette genet er lokalisert innenfor kromosom 16q23.3-24.1, et område hvor det er observert høy frekvens av tap av heterozygositet (LOH) i en rekke tumorer og tumorcellelinjer. Det
openaire   +1 more source

Dissociation of the nuclear WWOX/TRAF2 switch renders UV/cold shock-mediated nuclear bubbling cell death at low temperatures. [PDF]

Cell Commun Signal
Chen SJ, Tsai CC, Lin SR, Lee MH, Huang SS, Zeng HY, Wang LH, Chiang MF, Sheu HM, Chang NS.   +9 more
europepmc   +1 more source

miRNA as a Prognostic Marker in Small Lung Cell Carcinoma. [PDF]

Genes (Basel)
Bednarz M, Osińska A, Durda J, Kędra M, Boruch M, Gontarz J, Petniak A, Kocki J, Gil-Kulik P.   +8 more
europepmc   +1 more source

Parkinson's disease-associated alterations in DNA methylation and hydroxymethylation in human brain. [PDF]

NPJ Parkinsons Dis
Choza JI, Virani M, Kuhn NC, Adams M, Kochmanski J, Bernstein AI.   +5 more
europepmc   +1 more source

Developmental epileptic encephalopathy caused by homozygosity of a c.172+1G>C variant in the WWOX gene. [PDF]

Mol Genet Genomic Med
You Y, Wu W, Du Y, Hu J, Li B.
europepmc   +1 more source