Results 111 to 120 of about 4,653 (175)

Multiscale Convergence of Signaling, Epigenetic, and Environmental Networks in Mammalian Palatogenesis and Cleft Palate Pathogenesis. [PDF]

Int J Stem Cells
Won HJ, Song B, Song Y, Shin JO.
europepmc   +1 more source

Fibroblast-driven collagen expansion and altered thymic medullary niches in 22q11.2 deletion syndrome. [PDF]

J Hum Immun
Hennings V, Lingman Framme J, Thörn K, Lundqvist C, Lemarquis A, Oskarsdottir S, Telemo E, Björklund Å, Ekwall O.   +8 more
europepmc   +1 more source

T-Box Transcription Factor TBX1 [PDF]

, 2020
openaire   +1 more source

From DGCR8 expression analysis to diseased pathways in 22q11.2 deletion syndrome. [PDF]

Front Immunol
Boz V, Di Rosa M, Pin A, De Martino E, Faletra F, Baldo F, Magnolato A, Valencic E.   +7 more
europepmc   +1 more source

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

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

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