Results 131 to 140 of about 5,584 (206)

TBX1 Preferentially Binds and Regulates Transcription of Downstream Targets Via a Tandem T-site Repeat

, 2014
Haploinsufficiency of TBX1 is largely responsible for the etiology of physical malformations in individuals with velo-cardio-facial syndrome/DiGeorge syndrome/ 22q11 deletion syndrome.
Castellanos, Raquel
core  

T-Box Transcription Factor TBX1 [PDF]

, 2020
openaire   +1 more source

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

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

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

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