Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Steve Bobis"'
Autor:
Steve Bobis, Hala Abdalrahman Ahmed, Prashant Bavi, Latifa Al Sharif, Nada Abu Dhaim, Dania S. Khalil, Zainularifeen Abduljaleel, Jameela Shinwari, Amna Magrashi, Nada Al Tassan, Samaher AlAhmed, Saeed Bohlega
Publikováno v:
Human Mutation. 33:351-354
Autosomal recessive ataxias are heterogeneous group of disorders characterized by cerebellar atrophy and peripheral sensorimotor neuropathy. Molecular characterization of this group of disorders identified a number of genes contributing to these over
Autor:
Steve Bobis, Saleh Al-Mesfer, Fowzan S. Alkuraya, Jawahir Y. Mohamed, Hala Abdalrahman Ahmed, Arif O. Khan, Hisham Alkuraya, Mohammed A. Aldahmesh
Publikováno v:
Journal of Medical Genetics. 48:597-601
Background Knobloch syndrome (KS) is a developmental disorder characterised by occipital skull defect, high myopia, and vitreo-retinal degeneration. Although genetic heterogeneity has been suspected, COL18A1 is the only known KS disease gene to date.
Autor:
Ayodele, Alaiya, Jonathan, Fox, Steve, Bobis, Goran, Matic, Zakia, Shinwari, Eman, Barhoush, Marcela, Márquez, Sten, Nilsson, Anders R, Holmberg
Publikováno v:
Cancer genomicsproteomics. 11(1)
Osteodex is a novel bi-functional macromolecular polybisphosphonate developed for treatment of bone metastases in prostate and breast cancer. High efficacy of osteodex has been demonstrated both in vitro and in vivo. The present study investigates wh
Autor:
Steve Bobis, Mais Hashem, Lama Al-Abdi, Abdullah Jarallah, Dilek Colak, Emad B. Abboud, Hisham Alkuraya, Leen Abu-Safieh, Georges Nemer, Fadi Bitar, Hala Ahmad, Hanan E. Shamseldin, Shamsa Al-Enzi, Fowzan S. Alkuraya
Publikováno v:
The American Journal of Human Genetics. (2):313-319
Insulin-like growth factor binding proteins (IGFBPs) play important physiological functions through the modulation of IGF signaling as well as IGF-independent mechanisms. Despite the established role of IGFs in development, a similar role for the sev