Results 191 to 200 of about 548,182 (236)

De novo transcriptome assembly of the Moroccan fir, Abies marocana Trab. [PDF]

Sci Data
Méndez-Cea B, García-García I, Pavesio-Toledano M, Horreo JL, Seco JI, Gallego FJ, Linares JC.   +6 more
europepmc   +1 more source

Erratum. [PDF]

Biol Psychiatry Glob Open Sci
europepmc   +1 more source

Correction: An integrative approach to identify novel miRNA-mRNA interaction networks in LMNA-cardiomyopathy. [PDF]

Sci Rep
Córdoba-Caballero J, Bonet F, Campuzano O, Sarquella-Brugada G, Perez de Castro I, Vilaplana-Martí B, Seoane-Zonjic P, Mangas A, Ranea JAG, Toro R.   +9 more
europepmc   +1 more source

RBFOX1 association with age at onset of Alzheimer's disease. [PDF]

Alzheimers Dement
Xicota L, Cheng R, Andersen SL, Zmuda JM, Wojczynski M, Feitosa MF, Bradley J, Cruchaga C, Contreras AG, Hohman TJ, Reyes-Dumeyer D, Vardarajan BV, Cosentino S, Mayeux R, Lee JH, Barral S, Long‐Life Family Study (LLFS), Estudio Familiar de Influencia Genetica en Alzheimer (EFIGA), and The National Institute on Aging Alzheimer's Disease Family Based Study (NIA‐LOAD FBS).   +18 more
europepmc   +1 more source

[Genetic ancestry and the SNP RS4988235 of lactose tolerance in the population of Lima]. [PDF]

Rev Peru Med Exp Salud Publica
Vladimir Flores S, Roco-Videla Á, Montaña RM.   +2 more
europepmc   +1 more source

GENETIC DETERMINANTS OF ANTIBIOTIC RESISTANCE AND VIRULENCE IN <i>Staphylococcus aureus</i> ISOLATES FROM HOSPITAL SURFACES IN HIGH-RISK AREAS OF LOJA, ECUADOR. [PDF]

Afr J Infect Dis
Cristina LQ, Carlos AT, Jonnathan OT, Paola OB, Karla TA.   +4 more
europepmc   +1 more source

Issue Information: (Advanced Genetics 2/07)

Advanced Genetics, Volume 7, Issue 2, June 2026.
wiley   +1 more source

Correction: Torres-Arroyo et al. Immunoblotting Analysis of Fruit Proteins in Mexican Pediatric Patients Suggests the Existence of New Allergens. Diseases 2025, 13, 284. [PDF]

Diseases
Torres-Arroyo A, Suárez-Gutiérrez M, Iglesias-Amaya A, López-Durán A, Díaz-García L, Reyes-Vivas H, Mendoza-Hernández DA.   +6 more
europepmc   +1 more source

Identification of a variant in the USH1G gene in a family with Usher syndrome [PDF]

Biomedica
Gélvez N, López G, Tamayo ML.
europepmc   +1 more source

Erratum in: Abnormal Splicing in the Final Intron of PRX Results in Dominant Congenital Cataract Without Neurological Phenotype. [PDF]

Invest Ophthalmol Vis Sci
europepmc   +1 more source