Elliot J. Androphy - Natick MA, US Nishita Doshi - Cambridge MA, US Alexandra Belayew - Esneux, BE
Assignee:
New England Medical Center - Boston MA University of Mons-Hainaut - Mons
International Classification:
C12Q 1/68 G01N 33/50
US Classification:
435 6, 435 4, 436 63, 436 64
Abstract:
The invention is based on the elucidation of a mechanism by which HPV promotes oncogenesis and provides a methods of diagnosing malignant tumors and methods of preventing the development of malignancies or inhibiting tumor growth. A method for diagnosing a neoplasm in a mammal is carried out by measuring the level of helicase-like transcription factor (HLTF) in tissue of the mammal. An increase in the level of HLTF in the tissue compared to the level in a normal control tissue indicates the presence of a neoplasm in the tissue.
Spinal Muscular Atrophy (Sma) Treatment Via Targeting Of Splice Site Inhibitory Sequences
Ravindra N. Singh - Shrewsbury MA, US Natalia N. Singh - Shrewsbury MA, US Nirmal K. Singh - Temple TX, US Elliot J. Androphy - Natick MA, US
Assignee:
University of Massachusetts - Boston MA
International Classification:
C07H 21/04 C07H 21/02 A61K 48/00
US Classification:
536 245, 536 231, 536 2431, 536 2433, 514 44
Abstract:
The present invention is directed to methods and compositions capable of blocking the inhibitory effect of a newly-identified intronic inhibitory sequence element, named ISS-N1 (for “intronic splicing silencer”), located in the SMN2 gene. The compositions and methods of the instant invention include oligonucleotide reagents (e. g. , oligoribonucleotides) that effectively target the SMN2 ISS-N1 site in the SMN2 pre-mRNA, thereby modulating the splicing of SMN2 pre-mRNA to include exon 7 in the processed transcript. The ISS-N1 blocking agents of the invention cause elevated expression of SMN protein, thus compensating for the loss of SMN protein expression commonly observed in subjects with spinal muscular atrophy (SMA).
Ravindra N. Singh - Shrewsbury MA, US Natalia N. Singh - Shrewsbury MA, US Nirmal K. Singh - Temple TX, US Elliot J. Androphy - Natick MA, US
Assignee:
University of Massachusetts - Boston MA
International Classification:
A61K 48/00 C07H 21/04 C07H 21/02
US Classification:
514 44, 536 231, 536 2431, 536 2433, 536 245
Abstract:
The present invention is directed to methods and compositions capable of blocking the inhibitory effect of a newly-identified intronic inhibitory sequence element, named ISS-N1 (for “intronic splicing silencer”), located in the SMN2 gene. The compositions and methods of the instant invention include oligonucleotide reagents (e. g. , oligoribonucleotides) that effectively target the SMN2 ISS-N1 site in the SMN2 pre-mRNA, thereby modulating the splicing of SMN2 pre-mRNA to include exon 7 in the processed transcript. The ISS-N1 blocking agents of the invention cause elevated expression of SMN protein, thus compensating for the loss of SMN protein expression commonly observed in subjects with spinal muscular atrophy (SMA).
Spinal Muscular Atrophy (Sma) Treatment Via Targeting Of Smn2 Splice Site Inhibitory Sequences
Ravindra N. Singh - Shrewsbury MA, US Natalia N. Singh - Shrewsbury MA, US Nirmal K. Singh - Temple TX, US Elliot J. Androphy - Natick MA, US
Assignee:
University of Massachusetts - Boston MA
International Classification:
A61K 48/00 C07H 21/04
US Classification:
514 44, 536 234, 536 2431, 536 3433
Abstract:
The present invention is directed to methods and compositions capable of blocking the inhibitory effect of a newly-identified intronic inhibitory sequence element, named ISS-N1 (for “intronic splicing silencer”), located in the SMN2 gene. The compositions and methods of the instant invention include oligonucleotide reagents (e. g. , oligoribonucleotides) that effectively target the SMN2 ISS-N1 site in the SMN2 pre-mRNA, thereby modulating the splicing of SMN2 pre-mRNA to include exon 7 in the processed transcript. The ISS-N1 blocking agents of the invention cause elevated expression of SMN protein, thus compensating for the loss of SMN protein expression commonly observed in subjects with spinal muscular atrophy (SMA).
Juan Jose Marugan - Gaithersburg MD, US Jingbo Xiao - Rockville MD, US Steven A. Titus - Elkridge MD, US Noel Southall - Chevy Chase MD, US Wei Zheng - Potomac MD, US Elliot J. Androphy - Natick MA, US Jonathan Cherry - Worcester MA, US
Assignee:
Secretary, Department of Health and Human Services - Bethesda MD
International Classification:
C07D 417/04
US Classification:
514326, 546209
Abstract:
Aryl substituted thiazol-2-yl-piperidines and related compounds useful as modulators of survival motor neuron (SMN) protein production are provided herein. Without being bound to any particular theory it is believed the aryl substituted thiazol-2-yl-piperidines and related compounds provided herein act to increase production of the SMN2 form of survival motor neuron protein. These compounds are useful for treating spinal muscular atrophy. Pharmaceutical compositions containing a carrier and one or more of the aryl substituted thiazol-2-yl-piperidine or related compounds described herein are also provided. Methods of treating spinal muscular atrophy are also provided by this disclosure.
Spinal Muscular Atrophy (Sma) Treatment Via Targeting Of Smn2 Splice Site Inhibitory Sequences
Natalia N. SINGH - Shrewsbury MA, US Nirmal K. SINGH - Temple TX, US Elliot J. ANDROPHY - Natick MA, US
Assignee:
UNIVERSITY OF MASSACHUSETTS - Boston MA
International Classification:
C12N 15/113
US Classification:
514 44 A, 536 245, 435375
Abstract:
The present invention is directed to methods and compositions capable of blocking the inhibitory effect of a newly-identified intronic inhibitory sequence element, named ISS-N1 (for “intronic splicing silencer”), located in the SMN2 gene. The compositions and methods of the instant invention include oligonucleotide reagents (e.g., oligoribonucleotides) that effectively target the SMN2 ISS-N1 site in the SMN2 pre-mRNA, thereby modulating the splicing of SMN2 pre-mRNA to include exon 7 in the processed transcript. The ISS-N1 blocking agents of the invention cause elevated expression of SMN protein, thus compensating for the loss of SMN protein expression commonly observed in subjects with spinal muscular atrophy (SMA).
License Records
Elliot J Androphy
License #:
MT000075T - Expired
Category:
Medicine
Type:
Graduate Medical Trainee
Medicine Doctors
Dr. Elliot J Androphy, Indianapolis IN - MD (Doctor of Medicine)
Umass Medical School Oct 2001 - Jul 2010
Professor and Vice Chair
Indiana University School of Medicine Oct 2001 - Jul 2010
Professor and Chair, Department of Dermatology