Tangphatsornruang(S),Sangsrakru(D),Chanpra... DNA Res 2010-05-03

...rps19/rps8. We detected sequence length polymorphism in the cp homopolymeric regions at the intra- and inter-specific le...

Fröjmark(Anne-Sophie),Badhai(Jitendra),Kla... J Mol Med (Berl) 2010-03-25

...RPS19) gene in a subgroup of patients. One of the interacting partners with RPS19 is the oncoprotein PIM-1 kinase. We in...

Doherty(Leana),Sheen(Mee Rie),Vlachos(Adri... Am J Hum Genet 2010-03-19

...RPS19, RPS24, RPS17, RPL35A, RPL5, RPL11, and RPS7, in about 43% of patients. To continue our large-scale screen of RP g...

Crétien(Aurore),Proust(Alexis),Delaunay(Je... Am J Hematol 2010-02-24

Mutations in the RPS19 gene have been identified in 25% of individuals affected by Diamond-Blackfan anemia (DBA), a cong...

Quarello(Paola),Garelli(Emanuela),Carando(... Haematologica 2010-05-13

...RPS19 gene, encoding the ribosomal protein S19, are the main known cause of Diamond-Blackfan anemia and account for more...

Haque(Absarul),Mir(Mohammad A) J Virol 2010-12-20

...RPS19), located at the head region of the 40S subunit. We suggest that this N-RPS19 interaction facilitates ribosome loa...

Gazda(Hanna T),Sheen(Mee Rie),Vlachos(Adri... Am J Hum Genet 2009-01-06

...RPS19, RPS24, RPS17, and RPL35A, in about 30% of patients. However, the genetic basis of the remaining 70% of cases is s...

Malan(V),Raoul(O),Firth(H V),Royer(G),Turl... J Med Genet 2009-12-31

...RPS19 gene. Such a paucity of patients might be due to the difficulty in detecting a small rearrangement on this chromos...

Filip(Ana-Maria),Klug(Jörg),Cayli(Sevil),F... J Biol Chem 2009-05-14

...RPS19 were found to strongly inhibit MIF-CD74 interaction. Furthermore, RPS19 significantly compromised CXCR2-dependent ...

Danilova(Nadia),Sakamoto(Kathleen M),Lin(S... Blood 2009-01-12

...RPS19 is the most frequently mutated RP in DBA. RPS19 deficiency impairs ribosomal biogenesis, but how this leads to DBA...