Methods of use of compounds which inhibit the stem cell...

Chemistry: molecular biology and microbiology – Micro-organism – tissue cell culture or enzyme using process... – Recombinant dna technique included in method of making a...

Reexamination Certificate

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C530S389200

Reexamination Certificate

active

06989248

ABSTRACT:
This invention provides a method of preventing or treating in a subject contact dermatitis which comprises administering to the subject an amount of a compound capable of inhibiting the stem cell factor signaling pathway effective to prevent or treat contact dermatitis so as to thereby prevent or treat contact dermatitis in the subject. This invention also provides a methods of preventing or treating in a subject hyperpigmentation, asthma, cutaneous inflammation, anaphylaxis and bronchospasm, mastocytosis, tumors which express activated kit, and conception.

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patent: 6576812 (2003-06-01), Longley
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Furitsu T, Tsujimura T, Tono T, Ikeda H, Kitayama H, et al: Identification of mutations in the coding sequence of the proto-oncogenec-kitin a human mast cell leukemia cell line causing ligand-independent activation ofc-kitproduct.J. Clin Invest92: 1736-1744, 1993. (Exhibit 5).
Hirota S, Isozaki K, Moriyama Y, Hashimoto K, Nishida T, et al: Gain-of-function mutations of c-kitin human gastrointestinal stromal tumors.Science279: 577-580, 1998. (Exhibit 6).
Kitayama H, Kanakura Y, Furitsu T, Tsujimura T, Oritani K, et al: Constitutively activating mutations of c-kitreceptor tyrosine kinase confer factor-independent growth and tumorigenicity of factor-dependent hematopoietic cell lines.Blood85: 790-798, 1995. (Exhibit 7).
Longley BJ, Metcalfe DD, Tharp M, Wang X, Tyrrell L, et al: Activating and dominant inactivatingc-KITcatalytic domain mutations in distinct clinical forms of human mastocytosisProc Natl Acad Sci USA96: 1609-1614, 1999. (Exhibit 8).
Longley BJ, Tyrrell L, Lu S, Ma Y, Langley K, et al: Somatic c-KITactivating mutation in urticaria pigmentosa and aggressive mastocytosis: establishment of clonality in a human mast cell neoplasm.Nature Genet12: 312-314, 1996.(Exhibit 9).
Ma Y, Cunningham ME, Wang X, Ghosh I, Regan L, Longley BJ: Inhibition of spontaneous receptor phosphorylation by residues in a putative α-helix in the KIT intracellular juxtamembrane region.J Biol Chem274: 13399-13402, 1999b. (Exhibit 10).
Ma Y, Longley BJ, Wang X, Blount JL, Langley K, Caughey GH: Clustering of activating mutations in c-KIT's juxtamembrane coding region in canine mast cell neoplasms.J Invest Dermatol112: 165-170, 1999a. (Exhibit 11).
Nagata H, Worobec AS, Oh CK, Chowdhury BA, Tannenbaum S, et al: Identification of a point of mutation in the catalytic domain of the proctooncogenec-kitin peripheral blood mononuclear cells patients who have mastocytosis with an associated hematologic disorder.Proc Natl Acad Sci USA92: 10560-10564, 1995. (Exhibit 12).
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Tsujimura T, Morimoto M, Hashimoto K, Moriyama Y, Kitayama H, et al: Constitutive activation ofc-kitin FMA3 murine mastocytoma cells caused by deletion of seven amino acids at the juxtamembrane domain.Blood87: 273-283, 1996 (Exhibit 14).
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Devinney R, Gold WV: Establishment of two dog mastocyt

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