Pillow with retractable umbrella
A pillow assembly having a supporting assembly and a retractable umbrella assembly that is easily transportable and allows a user to support his/her head while covering their face from sunlight.
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| Number | Title | Issue Date |
| 6187548 | Methods using human calcium sensor protein, fragments thereof and DNA encoding same The present invention relates to the isolation of a cDNA clone encoding the calcium sensor in human placenta and subsequent Northern blots confirming the mRNA expression also in human parathyroid and kidney tubule cells. Close sequence similarity is demon... | 02/13/2001 |
| 6143508 | Device and process for cell capture and recovery Devices, processes and compositions are provided for effective separation of cells from a mixture of cells, where depletion or positive selection may be employed to provide a cellular population of interest. Of particular utility is the separation of cell... | 11/07/2000 |
| 6127550 | Stereospecific preparation of chiral 1-aryl-and 1-heteroaryl-2-substituted ethyl-2-amines This invention is directed to methods for stereospecifically preparing [(1-optionally substituted aryl)- or (1-optionally substituted heteroaryl)]-2-substituted ethyl-2-amines, having chirality at the 2-position, and to intermediates to the substituted et... | 10/03/2000 |
| 6057369 | Substituted (aryl, heteroaryl, arylmethyl or heteroarylmethyl) hydroxamic acid compounds This invention is directed to compounds of formula I: ##STR1## wherein the variables are as described herein. Compounds within the scope of the present invention possess useful properties, more particularly pharmaceutical properties. They are especia... | 05/02/2000 |
| 6034093 | Substituted sulfonic acid N-[(aminoiminomethyl)phenylalkyl]-azaheterocyclylamide compounds The compounds of formula I exhibit useful pharmacological activity and accordingly are incorporated into pharmaceutical compositions and used in the treatment of patients suffering from certain medical disorders. More specifically, they are inhibitors of ... | 03/07/2000 |
| 5866685 | Antithrombotic azacycloalkylalkanoyl peptides and pseudopeptides The present invention relates to azacycloalkylalkanoyl peptides and pseudopeptides which inhibit platelet aggregation and thrombus formation thereby being useful in the prevention and treatment of thrombosis associated with disease states such as myocardi... | 02/02/1999 |
| 5863888 | Human Bek Fibroblast growth factor receptor The complete cDNA cloning of two human genes previously designated flg and bek is disclosed. These genes encode for two similar but distinct surface receptors comprised of an extracellular domain with three immunoglobulin-like regions, a single transmembr... | 01/26/1999 |
| 5861314 | Adeno-associated viral (AAV) liposomes and methods related thereto A composition for genetic manipulation which comprises a liposome comprised of lipid material, and adeno-associated viral (AAV) material. Typically, the AAV material is plasmid, and comprises a terminal repeat of the AAV genome. Methods are disclosed for ... | 01/19/1999 |
| 5861171 | Adeno-associated viral (AAV) liposomes and methods related thereto A composition for genetic manipulation which comprises a liposome comprised of lipid material, and adeno-associated viral (AAV) material. Typically, the AAV material is plasmid, and comprises a terminal repeat of the AAV genome. Methods are disclosed for ... | 01/19/1999 |
| 5849538 | DNA encoding human endothelial cell growth factors and plasmids comprising said DNA The present invention is directed to DNA encoding human endothelial cell growth factors, and to plasmids comprising said DNA. In particular, the invention relates to DNA encoding a cleavable signal peptide and an endothelial cell growth factor, wherein re... | 12/15/1998 |
| 5834441 | Adeno-associated viral (AAV) liposomes and methods related thereto A composition for genetic manipulation which comprises a liposome comprised of lipid material, and adeno-associated viral (AAV) material. Typically, the AAV material is plasmid, and comprises a terminal repeat of the AAV genome. Methods are disclosed for ... | 11/10/1998 |
| 5827826 | Compositions of human endothelial cell growth factor The present invention is directed to compositions comprising endothelial cell growth factor, an acceptable carrier and, optionally, an extracellular matrix protein, a glycosaminoglycan or serum albumin. The compositions are useful for wound repair.... | 10/27/1998 |
| 5807686 | Pluripotential quiescent stem cell population A cell population which is composed of cells bearing the stem cell marker CD34 and which are small in size and have little granulation are obtained by separating low density mononuclear hematopoietic cells according to size and then selecting for CD34 | 09/15/1998 |
| 5795889 | Bis mono- and bicyclic aryl and heteroaryl compounds which inhibit EGF and/or PDGF receptor tyrosine kinase This invention relates to bis mono- and/or bicyclic aryl and/or heteroaryl compounds exhibiting protein tyrosine kinase inhibition activity. More specifically, it relates to the method of inhibiting abnormal cell proliferation in a patient suffering from ... | 08/18/1998 |
| 5780590 | Antithrombotic azacycloalkylalkanoyl peptides and pseudopeptides The invention is directed to a non-hygroscopic stable crystalline form of the antithrombotic compound N-N-N-(4-piperdin-4-yl)butanoyl)-N-ethylglycyl!-(L)-aspartyl!-(L)-ଲ -cyclohexyl-alanine amide, to processes for preparing said stable cryst... | 07/14/1998 |
| 5780280 | Recombinant adeno-associated virus vectors Simplified methods to produce recombinant adeno-associated virus (rAAV) vectors are described. The methods involve the use of chimeric plasmids which incorporate the Epstein Barr nuclear antigen (EBNA) gene, the latent origin of replication of Epstein Bar... | 07/14/1998 |
| 5736554 | Compounds having antihypertensive, cardioprotective, anti-ischemic and antilipolytic properties Compounds of the Formula ##STR1## wherein: K is N or N.fwdarw.O; Q is CH2 or O; T is ##STR2## or R3 O--CH2 ; X is a straight or branched chain alkylene, cycloalkylene or cycloalkenylene group, each of which is op... | 04/07/1998 |
| 5730713 | Removal of selected factors from whole blood or its components This invention provides a composition, device and method for the removal of selected factors, such as cytokines or pharmaceuticals, from a substance such as whole blood or plasma. Advantageously, the invention provides for the treatment or prevention of s... | 03/24/1998 |
| 5731315 | Substituted sulfonic acid n-(aminoiminomethyl)phenylalkyl!-azaheterocyclamide compounds The compounds of formula I exhibit useful pharmacological activity and accordingly are incorporated into pharmaceutical compositions and used in the treatment of patients suffering from certain medical disorders. More specifically, they are inhibitors of ... | 03/24/1998 |
| 5721237 | Protein tyrosine kinase aryl and heteroaryl quinazoline compounds having selective inhibition of HER-2 autophosphorylation properties This invention relates to a method for the selective treatment of cell growth and differentiation characterized by activity of the human epidermal growth factor receptor type 2 (HER2). More specifically, this invention relates to the use of substituted or... | 02/24/1998 |
| 5714493 | Aryl and heteroaryl quinazoline compounds which inhibit CSF-1R receptor tyrosine kinase This invention relates to the treatment of intimation in a patient suffering from such disorder. More specifically, the invention relates to mono- and/or bicyclic aryl or heteroaryl quinazoline compounds in the treatment of inflammation.... | 02/03/1998 |
| 5710158 | Aryl and heteroaryl quinazoline compounds which inhibit EGF and/or PDGF receptor tyrosine kinase This invention relates to the modulation and/or inhibition of cell signaling, cell proliferation, cell inflammatory response, the control of abnormal cell growth and cell reproduction. More specifically, this invention relates to the use of mono- and/or b... | 01/20/1998 |
| 5710254 | Purification of von Willebrand factor by affinity chromatography A method of improving the therapeutic activity of von Willebrand Factor obtained from materials comprising on Willebrand Factor comprising incubating said Factor at a temperature of about 20° C. to about 55° C. for about 1 to about 30 hours, most prefer... | 01/20/1998 |
| 5677329 | Styryl-substituted monocyclic and bicyclic heteroaryl compounds which inhibit EGF receptor tyrosine kinase Methods of inhibiting cell proliferation in a patient suffering from such disorder comprising the use of a styryl-substituted heteroaryl compound wherein the heteroaryl group is a monocyclic ring with 1 or 2 heteroatoms, or a bicyclic ring with 1 to about... | 10/14/1997 |
| 5674482 | Polymers with alkyl- or heteroalkyl -aryl backbone and pharmaceutical compositions incorporating same A biologically active polymeric compound comprising an alkylaryl or heteroalkylaryl backbone having about 5 to about 50 repeating aromatic ring-containing units and which, according to the computer program marketed as SYBYL.RTM. version 5.2 running on a D... | 10/07/1997 |
| 5656643 | Bis mono-and bicyclic aryl and heteroaryl compounds which inhibit EGF and/or PDGF receptor tyrosine kinase This invention relates to bis mono- and/or bicyclic aryl and/or heteroaryl compounds exhibiting protein tyrosine kinase inhibition activity. More specifically, it relates to the method of inhibiting abnormal cell proliferation in a patient suffering from ... | 08/12/1997 |
| 5656598 | Use of fibroblast growth factors to stimulate bone growth The present invention provides therapeutic compositions for the prevention and treatment of pathological conditions involving bone and dental tissue. The present invention also provides a method to promote bone repair and/or growth for the treatment of pa... | 08/12/1997 |
| 5656655 | Styryl-substituted heteroaryl compounds which inhibit EGF receptor tyrosine kinase A method of inhibiting cell proliferation in a patient suffering from such disorder comprising the administration to the patient of a pharmaceutically effective amount of a pharmaceutical composition containing, in admixture with a pharmaceutically accept... | 08/12/1997 |
| 5652366 | DI (1R)-(-)camphosulfonic acid) salt, preparation thereof and use thereof This invention relates to di[(1 R)-(-)-camphosulfonic acid) salt of [1S-[1,2ଲ,3ଲ,4,(S*)]]-4-[7-[[2-(3-chloro-2-thienyl )-1-ethylethyl]amino]3 H-imidazo[4,5-b]pyridin-3-yl]-N-ethyl-2,3-dihydroxycyclopentanecarboxamide , and a p... | 07/29/1997 |
| 5648243 | Human serum albumin expression construct The present invention provides DNA constructs comprising a promoter DNA sequence and a DNA sequence coding for human serum albumin. In one embodiment the human serum albumin sequence comprises at least one, but not all, of the introns in the naturally occ... | 07/15/1997 |
| 5646153 | Bis mono- and bicyclic aryl and heteroaryl compounds which inhibit EGF and/or PDGF receptor tyrosine kinase This invention relates to bis mono- and/or bicyclic aryl and/or heteroaryl compounds exhibiting protein tyrosine kinase inhibition activity. More specifically, it relates to the method of inhibiting abnormal cell proliferation in a patient suffering from ... | 07/08/1997 |
| 5614496 | Use of fibroblast growth factors to stimulate bone growth The present invention provides therapeutic compositions for the prevention and treatment of pathological conditions involving bone and dental tissue. The present invention also provides a method to promote bone repair and/or growth for the treatment of pa... | 03/25/1997 |
| 5612353 | Substituted (sulfinic acid, sulfonic acid, sulfonylamino or sulfinylamino) N-[(aminoiminomethyl)phenylalkyl]-azaheterocyclylamide compounds The compounds of formula I exhibit useful pharmacological activity and accordingly are incorporated into pharmaceutical compositions and used in the treatment of patients suffering from certain medical disorders. More especially, they are Factor Xa inhibi... | 03/18/1997 |
| 5605884 | Factor VIII formulations in high ionic strength media Stable, highly purified Factor VIII protein formulations are provided in high ionic strength media which comprises: sodium chloride, potassium chloride or mixtures thereof; calcium chloride; and histidine as the buffering agent.... | 02/25/1997 |
| 5596020 | Amino bi- and tri-carbocyclic alkane bis-aryl squalene synthase inhibitors This invention relates to a class of novel amino bi- and tri-carbocyclic alkane compounds having bis-aryl substitution which exhibit squalene synthase inhibition properties. The bi- and tri-carbocyclic alkane ring contains an amino group and the ring is f... | 01/21/1997 |
| 5589377 | Recombinant adeno-associated virus vectors Simplified methods to produce recombinant adeno-associated virus (rAAV) vectors are described. The AAV rep and cap genes are combined in a single recombinant adenovirus vector, i.e., a rep/cap adenovirus vector which combines in a single vector all comple... | 12/31/1996 |
| 5571506 | Aromatic oligomeric compounds useful as mimics of bioactive macromolecules This invention relates to aromatic oligomeric compounds useful in the treatment of cardiovascular, bone metabolic, hypolipidaemic, neuronal, gastrointestinal and elastase-mediated connective tissue degradation disorders and disorders which may be treated ... | 11/05/1996 |
| 5571790 | Recombinant human endothelial cell growth factor Endothelial cell growth factor is achieved through the application of recombinant DNA technology to prepare cloning vehicles encoding the ECGF protein and procedures are disclosed for recovering ECGF protein essentially free of other proteins of human ori... | 11/05/1996 |
| 5563128 | Phosphonate derivatives of lipophilic amines This invention relates to a class of novel phosphonate derivatives of lipophilic amines which exhibit squalene synthase inhibition properties. More specifically the compounds are bis aryl cycloalkylamino and azacycloalkyl phosphonates. Compounds of this i... | 10/08/1996 |
| 5561134 | Compounds having antihypertensive, cardioprotective, anti-ischemic and antilipolytic properties Compounds of the Formula ##STR1## wherein: K is N or N.fwdarw.O; Q is CH2 or O; T is ##STR2## or R3 O--CH2 ; X is a straight or branched chain alkylene, cycloalkylene or cycloalkenylene group, each of which is op... | 10/01/1996 |