Results 141 to 150 of about 5,757 (204)

Sex-specific gonadal transcriptome during early development of Siberian sturgeon. [PDF]

Biol Sex Differ
Lasalle Gerla A, Benech-Correa G, Klopp C, Vizziano-Cantonnet D.   +3 more
europepmc   +1 more source

Prevotella copri promotes white adipose browning and ameliorates adiposity. [PDF]

Nat Commun
Liu S, Li H, Li R, Chang Y, Wang S, Wang Z, Sun Y, Li M, Liu M, Zhou Y, Jiao H, Wang X, Zhao J, Li B, Zhang T, Feng Z, Xu J, Lin H.   +17 more
europepmc   +1 more source

Integrated multiomics profiling of amniotic fluid exosomes reveals dysregulated lipid and protein signatures in fetal 22q11.2 deletion syndrome. [PDF]

Hum Genomics
Xiao H, Li T, Zhang M, Lv X, Gao Y, Guo Q, Guo Z, Wang H, Guo L, Liu H, Liao S, Wu D.   +11 more
europepmc   +1 more source

Mexican Patients With Suspected 22q11.2 Deletion Syndrome: Clinical Characterization and Molecular Findings by Fluorescence In Situ Hybridization and Multiplex Ligation-Dependent Probe Amplification. [PDF]

Mol Genet Genomic Med
Aguayo-Orozco TA, Rivera H, Figuera LE, Esparza-García E, Perea-Díaz FJ, Jaloma-Cruz AR, Rizo-de la Torre LDC, Domínguez-Quezada MG.   +7 more
europepmc   +1 more source

Genetic and epigenetic markers in the METTL21C gene associated with umbilical hernia in pigs. [PDF]

BMC Genomics
Wozniak J, Szabelska-Beresewicz A, Zyprych-Walczak J, Niemyjski R, Dudek K, Stachowiak M, Nowacka-Woszuk J.   +6 more
europepmc   +1 more source

Minoxidil restores thymic growth in 22q11.2 deletion syndrome by limiting Sox9⁺ chondrocyte expansion. [PDF]

J Hum Immun
Bhalla P, Ahuja N, Kumar A, Xing C, Moses A, Shukla A, Boetel K, Evers BM, Shelton JM, de la Morena MT, Wysocki CA, Cleaver OB, van Oers NSC.   +12 more
europepmc   +1 more source

HLH and spinal neurofibroma: a single case report in a patient with DiGeorge syndrome. [PDF]

Front Oncol
Tallone R, Micalizzi C, Faraci M, De Marco P, Capra V, Beccaria A, Livellara V, Arkhangelskaya E, Ramaglia A, Ronchetto P, Ognibene M, Bono M, Muraca M, Vellone VG, Rebuffi C, Marcenaro S, Pelanconi L, Haupt R, Dufour C, Strati MF, Merlo S.   +20 more
europepmc   +1 more source

Phenocopies of 22q11.2DS: revealing genetic diversity in clinically suspected 22q11.2 deletion syndrome. [PDF]

Mol Cell Pediatr
Szumutku F, Lengyel A, Pinti É, Kun I, Németh K, Abonyi T, Gál F, Ryu SW, Song Y, Ujfalusi A, Kádár K, Jávorszky E, Tory K, Kis É, Goda V, Kriván G, Kovács ÁF, Haltrich I.   +17 more
europepmc   +1 more source

Epstein-Barr virus (EBV) -related Hodgkin lymphoma in a 1-year-old child with DiGeorge syndrome. [PDF]

BMC Pediatr
Rao Z, Wang H, Chen S, Yang Y, Liu H, Ma C, Zhou J, Ye Z.   +7 more
europepmc   +1 more source

The Cuproptosis-Associated AL139023.1/miR-139-5p/ELOVL5 ceRNA Axis Regulates Proliferation, Migration, and Cell Cycle in Esophageal Squamous Cell Carcinoma. [PDF]

Cancer Manag Res
Liang K, Gao Y, Zhang X, Yang J.
europepmc   +1 more source