Results 101 to 110 of about 4,652 (175)

Aberrant expression of MAPK1 and MCTS1 in chronic myeloid leukemia (CML). [PDF]

MicroPubl Biol
Kortendick L, Meyer C, Nagel S.
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

Cell cycle-driven transcriptome maturation confers multilineage competence to cardiopharyngeal progenitors. [PDF]

EMBO J
Bernadskaya YY, Kuan A, Tjärnberg A, Brandenburg J, Zhang P, Wiechecki K, Kaplan N, Failla M, Bikou M, Madilian O, Bruderer N, Wang W, Christiaen L.   +12 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

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

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