Results 171 to 180 of about 19,199 (198)

Single-cell atlas of the transcriptome and chromatin accessibility in the human retina. [PDF]

Nat Genet
Li J, Wang J, Ibarra IL, Cheng X, Luecken MD, Lu J, Monavarfeshani A, Yan W, Zheng Y, Zuo Z, Colborn SLZ, Cortez BS, Owen LA, Wick B, Bao X, Choi J, Haeussler M, Tran NM, Shekhar K, Sanes JR, Stout JT, Chen S, Li Y, DeAngelis MM, Theis FJ, Chen R.   +25 more
europepmc   +1 more source

Establishment and evaluation of a prognostic model for sodium overload necrosis in acute myeloid leukemia. [PDF]

Transl Cancer Res
Xie K, Wei J.
europepmc   +1 more source

Whole-genome sequencing reveals an East Asian-specific rare variant of INPP5J associated with Alzheimer's disease. [PDF]

Transl Psychiatry
Kimura T, Yamakawa A, Mitsumori R, Niida S, Ozaki K, Shigemizu D.   +5 more
europepmc   +1 more source

Resources and applications of public biomedical data. [PDF]

Front Bioinform
Liu M, Ye Z, Liu H, Ma P, Pang H, Li Y, Wang Q, Shen Y, Xie X, Zhao Y.   +9 more
europepmc   +1 more source

Somatic copy number alterations profiling in non-small cell lung cancer and their correlation with clinical efficacy in first-line treatment. [PDF]

Genome Med
Priano I, Amat R, Carbonell C, Arbusà-Roca A, Iranzo P, Pardo N, Soleda M, Romero-Sola G, Sinigaglia B, Polo-Alonso S, Callejo A, Valdivia A, Rocha P, Hernandez-Losa J, Sese M, Mirallas O, Masfarré L, Cedrés S, Martinez-Marti A, Caro-Consuegra R, Felip E.   +20 more
europepmc   +1 more source

Haplotype-resolved DNA methylation at the <i>APOE</i> locus identifies allele-specific epigenetic signatures relevant to Alzheimer's disease risk. [PDF]

NPJ Dement
Genner RM, Meredith M, Daida K, Moller A, Weller C, Ayuketah A, Jerez PA, Akeson S, Malik L, Baker B, Kouam C, Paquette K, Catching A, Bromberek S, Hu F, Reed X, Marenco S, Auluck P, Mandal A, Paten B, Gibbs JR, Jain M, Cookson MR, Singleton AB, Nalls M, Blauwendraat C, Billingsley KJ.   +26 more
europepmc   +1 more source

A single-cell eQTL atlas of the developing human brain

Cameron D, Tume C, Vinh N, Davies S, Morgan J, Baran Y, Won H, Pardinas A, O'Donovan M, Bray N.   +9 more
europepmc   +1 more source

The insertion of an ATTTC repeat in an Alu element hyperactivates a neurodevelopmental enhancer in spinocerebellar ataxia type 37.

Cell Rep
Loureiro JR, Castro AF, Figueiredo AS, Eufrásio A, Dhingra A, Galhardo M, Marcelino H, Rodrigues CC, Sampaio P, Azevedo M, Sousa M, Dória S, Rizzu P, Heutink P, Bessa J, Silveira I.   +15 more
europepmc   +1 more source

A comprehensive AMR genotype-phenotype database (CABBAGE)

Dickens E, Derelle R, Beardmore R, Suresh A, Uplekar S, Azov AG, Gurbich TA, El Houdaigui B, Keatley J, Ochkalova S, Koci O, Rahman NM, Shivalikanjli A, Winterbottom A, Yordanova G, Parkinson H, Yates AD, Finn RD, Lees JA, Chindelevitch L.   +19 more
europepmc   +1 more source