Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Manoj, Valluru"'
Publikováno v:
Nephrology Dialysis Transplantation. 37
BACKGROUND AND AIMS ADTKD–UMOD (Autosomal dominant tubulointerstitial kidney disease–UMOD) is a rare genetic disease due to a heterozygous mutation in the UMOD gene encoding uromodulin. It is classically characterized by minimal proteinuria, slow
Autor:
Sara, Simonini, Joyita, Deb, Laila, Moubayidin, Pauline, Stephenson, Manoj, Valluru, Alejandra, Freire-Rios, Karim, Sorefan, Dolf, Weijers, Jiří, Friml, Lars, Østergaard
Publikováno v:
Genesdevelopment. 31(17)
Simonini et al. present an alternative auxin-sensing mechanism in which the auxin response factor ARF3/ETTIN controls gene expression through interactions with process-specific transcription factors.
Autor:
Carolyn A, Staton, Lucy A, Shaw, Manoj, Valluru, Leslie, Hoh, Ivan, Koay, Simon S, Cross, Malcolm W, Reed, Nicola J, Brown
Publikováno v:
Histopathology. 59(2)
This study aimed to identify the involvement of class 3 semaphorins (Sema3) and receptors, neuropilins (Np1 and Np2) and plexins (A1-A4) in breast cancer development and angiogenesis.We quantified and correlated Sema3A, Sema3B, Sema3F and their known