HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Forrest A Wright Selected Research

Autosomal Dominant Sensory Ataxia

5/2015A Point Mutation in the Ubiquitin Ligase RNF170 That Causes Autosomal Dominant Sensory Ataxia Destabilizes the Protein and Impairs Inositol 1,4,5-Trisphosphate Receptor-mediated Ca2+ Signaling.

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown:


Forrest A Wright Research Topics

Disease

1Paraplegia (Spastic Paraplegia)
10/2018
1Multiple Myeloma
01/2017
1Neoplasms (Cancer)
01/2017
1Ovarian Neoplasms (Ovarian Cancer)
01/2017
1Autosomal Dominant Sensory Ataxia
05/2015

Drug/Important Bio-Agent (IBA)

1Isoleucine (L-Isoleucine)FDA Link
10/2018
1Threonine (L-Threonine)FDA Link
10/2018
1liposomal doxorubicin (Doxil)FDA Link
01/2017
1Bortezomib (Velcade)FDA Link
01/2017
1Doxorubicin (Adriamycin)FDA LinkGeneric
01/2017
1UbiquitinIBA
05/2015
1Inositol 1,4,5-Trisphosphate Receptors (Inositol Triphosphate Receptor)IBA
05/2015
1Arginine (L-Arginine)FDA Link
05/2015
1Proteins (Proteins, Gene)FDA Link
05/2015
1Cysteine (L-Cysteine)FDA Link
05/2015
1Ligases (Synthetase)IBA
05/2015
1Inositol 1,4,5-TrisphosphateIBA
05/2015