Neurology Vascular Neurology Neurological Surgery Psychiatry
Work:
The Emory Clin
1365 Clifton Rd NE, Atlanta, GA 30322 Atlanta Va Medical Center
1670 Clairmont Rd, Decatur, GA 30033 Emory Univ. Neurology
615 Michael St, Atlanta, GA 30322 Emory Medical Care Foundation
80 Jesse Hill Jr Dr SE, Atlanta, GA 30303
Education:
Pontificia Universidad Javeriana (1989)
Us Patents
Brain-Associated Inhibitor Of Tissue-Type Plasminogen Activator
The present invention relates to a novel BAIT protein which is a member of serpin superfamily which is expressed primarily in brain tissue. In particular, isolated nucleic acid molecules are provided encoding the human and recombinant methods for producing the same. The invention further relates to screening methods for identifying agonists and antagonists of BAIT activity. Also provided are diagnostic methods for detecting nervous system-related disorders and therapeutic methods for treating nervous system-related disorders. Additionally, the present invention is related to methods of treating patients with BAIT polynucleotides or polypeptides, wherein said patients have had seizures or epilepsy.
Methods Of Reducing Vascular Permeability In Tissue By Inhibition Of Tissue Plasminogen Activator (Tpa) And Tpa Inhibitors Useful Therein
Daniel A. Lawrence - Derwood MD, US Manuel S. Yepes - Rockville MD, US Dudley Strickland - Brookeville MD, US
Assignee:
The Regents of The University of Michigan - Ann Arbor MI
International Classification:
A61K 38/00
US Classification:
514 2
Abstract:
The present invention is a method of reducing vascular permeability in tissue of a subject comprising inhibiting the activity of serine proteinase tissue-type plasminogen activator (tPA). This tPA activity which increases permeability of the tissue in a subject results in edema in the tissue is separate from tPA's thrombolytic activity. The present invention more specifically relates to administering an amount of a tPA inhibitor sufficient to reduce the vascular permeability increasing activity of tPA in a subject. Useful tPA inhibitors for the present method are neuroserpin, mutant neuroserpin, wild-type PAI-1, mutant PAI-1, an antibody that binds to tPA, an antibody that binds to the low-density lipoprotein (LDL) receptor or a low-density lipoprotein (LDL) receptor family antagonist.
Tweak As A Therapeutic Target For Treating Central Nervous System Diseases Associated With Cerebral Edema And Cell Death
The present invention is directed to compositions and methods for treating cerebral edema and cell death in neurological conditions characterized by disruption of the architecture of the neurovascular unit with increase in the permeability of the NVU, particularly for treating stroke. One aspect of the present invention relates to a composition comprising an agent that interferes with a TWEAK-mediated signaling pathway. Another aspect of the present invention relates to a method of using a composition which comprises an agent that inhibits Fn14 activity or Fn14 expression for the prevention and/or treatment of cerebral edema and cell death occurring in certain neurological conditions such as cerebral ischemia.
Methods And Compositions For Modulation Of Blood-Neural Barrier
Ulf Eriksson - Stockholm, SE Daniel Lawrence - Ann Arbor MI, US Enming Joe Su - Ann Arbor MI, US Dudley Strickland - Brookeville MD, US Manuel Yepes - Atlanta GA, US Linda Fredriksson - Hagersten, SE
Assignee:
Ludwig Institute for Cancer Research - New York NY University of Maryland - Baltimore MD The Regents of the University of Michigan - Ann Arbor MI
International Classification:
A61K 39/395 C07K 16/28 C07K 14/71
US Classification:
4241301, 4241431, 5303871, 53038822
Abstract:
Methods and compositions for modulating blood-neural barrier (BNB) for the treatment of CNS conditions such as edema, and for increased drug delivery efficacy across the BNB. The present invention further relates to improved tPA treatment of ischemic cerebrovascular and related diseases in combination with antagonism of the PDGF signaling pathway. The inventive method and composition is particularly suitable for conjunctive therapy of ischemic stroke using tPA and an anti-PDGF-C antagonist or an anti-PDGFR-α antagonist.
Brain-Associated Inhibitor Of Tissue-Type Plasminogen Activator
Daniel Lawrence - Derwood MD, US Manuel Yepes - Alexandria VA, US Maria Sandkvist - Derwood MD, US Michael Wong - Wexford PA, US Timothy Coleman - Gaithersburg MD, US
Assignee:
Human Genome Sciences, Inc. - Rockville MD
International Classification:
C07H021/02 C07H021/04
US Classification:
536/023100
Abstract:
The present invention relates to a novel BAIT protein which is a member of serpin superfamily which is expressed primarily in brain tissue. In particular, isolated nucleic acid molecules are provided encoding the human and recombinant methods for producing the same. The invention further relates to screening methods for identifying agonists and antagonists of BAIT activity. Also provided are diagnostic methods for detecting nervous system-related disorders and therapeutic methods for treating nervous system-related disorders. Additionally, the present invention is related to methods of treating patients with BAIT polynucleotides or polypeptides, wherein said patients have had a stroke.
Brain-Associated Inhibitor Of Tissue-Type Plasminogen Activator
The present invention relates to a novel BAIT protein which is a member of serpin superfamily which is expressed primarily in brain tissue. In particular, isolated nucleic acid molecules are provided encoding the human and recombinant methods for producing the same. The invention further relates to screening methods for identifying agonists and antagonists of BAIT activity. Also provided are diagnostic methods for detecting nervous system-related disorders and therapeutic methods for treating nervous system-related disorders. Additionally, the present invention is related to methods of treating patients with BAIT polynucleotides or polypeptides, wherein said patients have had seizures or epilepsy.
Brain Associated Inhibitor Of Tissue - Type Plasminogen Activator
Daniel Lawrence - Derwood MD, US Manuel Yepes - Alexandria VA, US Maria Sandkvist - Derwood MD, US Timothy Coleman - Gaithersburg MD, US Michael Wong - Wexford PA, US
International Classification:
A61K038/17
US Classification:
514/012000
Abstract:
The present invention relates to a novel BAIT protein which is a member of serpin superfamily which is expressed primarily in brain tissue. In particular, isolated nucleic acid molecules are provided encoding the human and recombinant methods for producing the same. The invention further relates to screening methods for identifying agonists and antagonists of BAIT activity. Also provided are diagnostic methods for detecting nervous system-related disorders and therapeutic methods for treating nervous system-related disorders. Additionally, the present invention is related to methods of treating patients with BAIT polynucleotides or polypeptides, wherein said patients have had a stroke.
Brain-Associated Inhibitor Of Tissue-Type Plasminogen Activator
Gregg Hastings - Westlake Village CA, US Timothy Coleman - Derwood MD, US Patrick Dillon - Carlsbad CA, US Daniel Lawrence - Derwood MD, US Maria Sandkvist - Ann Arbor MI, US Manuel Yepes - Rockville MD, US Michael Wong - East Amhurst NY, US
Assignee:
Human Genome Sciences, Inc. - Rockville MD The Regents of the University of Michigan - Ann Arbor MI
The present invention relates to a novel BAIT protein which is a member of serpin superfamily which is expressed primarily in brain tissue. In particular, isolated nucleic acid molecules are provided encoding the human and recombinant methods for producing the same. The invention further relates to screening methods for identifying agonists and antagonists of BAIT activity. Also provided are diagnostic methods for detecting nervous system-related disorders and therapeutic methods for treating nervous system-related disorders. Additionally, the present invention is related to methods of treating patients with BAIT polynucleotides or polypeptides, wherein said patients have had seizures or epilepsy.