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Title: US6465627: DAX-1 protein, methods for production and use thereof
[ Derwent Title ]


Country: US United States of America

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71 pages

 
Inventor: McCabe, Edward R. B.; Pacific Palisades, CA
Guo, Weiwen; Los Angeles, CA
Burris, Thomas P.; Woodland Hills, CA
Vilain, Eric; Los Angeles, CA

Assignee: The Regents of the University of California, Oakland, CA
other patents from UNIVERSITY OF CALIFORNIA, THE REGENTS OF (599425) (approx. 4,840)
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Published / Filed: 2002-10-15 / 1996-07-26

Application Number: US1996000687691

IPC Code: Advanced: C07K 14/705; C07K 14/72;
Core: C07K 14/435;
IPC-7: C12N 15/11;

ECLA Code: C07K14/705G; C07K14/72A;

U.S. Class: 536/023.1; 536/024.1;

Field of Search: 435/69.1,320.1,172.3,325,6 536/23.1,23.5,24.1 436/015 514/044

Government Interest:     This invention was made with support under Grant Numbers RO1 HD22563, P30 HD24064, P30 HD27823, and P50 HG00210 from the National Institute of Health, U.S. Department of Health and Human Resources and ACS PF-4074. Accordingly, the U.S. Government may have certain rights in the invention.

Priority Number:
1996-07-26  US1996000687691
1995-07-28  US1995000001713P

Abstract: The invention provides a DAX-1 protein molecule having the amino acid sequence beginning with methionine at position 1 and ending with isoleucine at position 470 as shown in FIG. 12. The invention further provides the genomic nucleic acid sequence for DAX-1, including intron, exons and a promoter region. Additionally, the invention provides methods for using and making the DAX-1 protein and DAX-1 nucleic acid molecules.

Attorney, Agent or Firm: Mandel & Adriano ;

Primary / Asst. Examiners: Martinell, James;

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Parent Case:     This application is based on a provisional application, U.S. Serial No. 60/001,713, filed Jul. 28, 1995.

Designated Country: AU CA EP JP 

Family: Show 4 known family members

First Claim:
Show all 3 claims
What is claimed is:     1. A nucleic acid molecule consisting of a nucleotide sequence beginning with position 1 and ending with position 1579 of SEQ ID NO.: 1.

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Description: Show description

Forward References: Show 1 U.S. patent(s) that reference this one

       
U.S. References: Go to Result Set: All U.S. references   |  Forward references (1)   |   Backward references (1)   |   Citation Link

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Patent  Pub.Date  Inventor Assignee   Title
Buy PDF- 14pp US5310662  1994-05 Evans et al.  The Salk Institute for Biological Studies Receptors: their identification, characterization, preparation and use
       
Foreign References: None

Other Abstract Info: CHEMABS 126(16)208222B DERABS C1997-145382

Other References:
  • Stanesh, Dictionary of Biochemistry and Molecular Biology, 2nd Edition, 1989, p. 490.*
  • Guo et al, Biochemical and Molecular Medicine 56: 8 (1995).* (6 pages) [ISI abstract]
  • Arn, P. et al. (1994) SRYX, A sex reversing locus in Xp21.2 to p22.11, Hum. Genet. 93:389-393 (Exhibit 2). (5 pages) [ISI abstract]
  • Baniahmad, A. et al. (Jun. 1994) The nuclear hormone receptor superfamily in: M.-J. Tsai and B.W. O'Malley, eds., Mechanism of Steroid Hormone Regulation of Gene Transcription, Austin: R.G. Landis, 1-24 (Exhibit 3).
  • Bardoni, B. et al. (1994) A dosage sensitive locus at chromosome Xp21 is involved in male to female sex reversal, Nat. Genet. 7:497-501 (Exhibit 4). (5 pages) [ISI abstract]
  • Brown, T. R. et al. (1990) Mol. Endocrinol. 4:1759-1772 (Exhibit 5). (14 pages)
  • Evans, R. M. (1988) The steroid and thyroid hormone receptor superfamily, Science 240:889-895 (Exhibit 6). (7 pages) Cited by 207 patents
  • Gazder, A. F. et al. (1990) Establishment and characterization of a human adrenocortical carcinoma cell line that expresses multiple pathways of steroid biosynthesis, Cancer Res. 50:5488-5496 (Exhibit 7).
  • Golden, M. P. et al. (1977) Congenital adrenal hypoplasia and hypogonadotropic hypogonadism, Am. J. Dis. Child. 131:1117-1118 (Exhibit 8). (2 pages)
  • Goonewardena, P. et al. (1989) Molecular Xp deletion in a male: suggestion of a locus for hypogonadotropic hypogonadism distal to the glycerol kinase and adrenal hypoplasia loci, Clin. Genet. 35:5-12 (Exhibit 9). (8 pages)
  • Guo, W. et al. (1993) Genomic scanning for expressed sequences in Xp21 identifies the glycerol kinase gene, Nature Genet. 4:367-372 (Exhibit 10). (6 pages) [ISI abstract]
  • Guo, W. et al.
  • Hay, I.D. et al. (1981) Familial cytomegalic adrenocortical hypoplasia: an X-linked syndrome of pubertal failure, Arch Dis. Child. 56:715-721 (Exhibit 12). (7 pages)
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  • Laudet, V. et al. (1992) Evolution of the nuclear receptor gene superfamily, EMBO J. 11:1003-1013 (Exhibit 15). (11 pages) Cited by 8 patents [ISI abstract]
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  • Luo, X. et al. (1994) A cell-specific nuclear receptor is essential for adrenal and gonadal development and sexual differentiation, Cell 77:481-490 (Exhibit 17). (10 pages) [ISI abstract]
  • Marcelli, M. et al. (1990A) J. Clin. Invest. 85:1522-1528 (Exhibit 18).
  • Marcelli, M. et al. (1990B) Mol. Endocrinol. 4:1105-1116 (Exhibit 19).
  • Marcelli, M. et al. (1991) J. Clin. Invest. 87:1123-1126 (Exhibit 20). (4 pages) [ISI abstract]
  • McCabe, E.R.B. (1995) Disorders of glycerol metabolism. In: Scriver CR, Beaudet AL, Sly WS, Valle D, eds. The Metabolic Basis of Inherited Disease, 7th ed., New York, McGraw-Hill, 1631-1652 (Exhibit 21).
  • McPhaul, M. J. et al. (1991) FASEB J. 5:2910-2915 (Exhibit 22). (6 pages) [ISI abstract]
  • McPhaul, M. J. et al. (1994) In: M. Parker, ed. Steroid Hormone Action, New York IRL Press, New York 186-208 (Exhibit 23).
  • Migeon, C.J., Donohoue P. (1994) in: M.S. Kappy et al., eds. Wilkins--The Diagnosis and Treatment of Endocrine Disorders in Childhood and Adolescence, 4th ed.,Springfield: Thomas 717-856 (Exhibit 24).
  • Mullen, C.A. (1994) Pharmac. Ther. 63:199-207 (Exhibit 25). (9 pages) Cited by 30 patents [ISI abstract]
  • Partsch, C-J, Sippell, W. G. (1989) Hypothalamic hypogonadism in congenital adrenal hypoplasia, Horm. Metabol. Res. 21:623-625 (Exhibit 26). (3 pages)
  • Rosenfeld, M. et al. (1991) Adenovirus-mediated transfer of a recombinant α1 -antitrypsin gene to the lung epithelium in vivo, Science 252:431 (Exhibit 27). (4 pages) Cited by 194 patents [ISI abstract]
  • Schena, M. and Yamamoto, K. R. (1988) Mammalian glucocorticoid receptor derivatives enhance transcription in yeast, Science 241:965-967 (Exhibit 28). (3 pages) Cited by 6 patents
  • Seltzer, W.K. et al. (1985) Adrenal dysfunction in glycerol kinase deficiency, Biochem. Med. 33:189-199 (Exhibit 29). (11 pages)
  • Walker, A. P. et al. (1993) Isolation of the human Xp21 glycerol kinase gene by positional cloning, Hum. Mol. Genet. 2:107-114 (Exhibit 30). (8 pages) [ISI abstract]
  • Wang, L. H. et al. (1989) COUP transcription factor is a member of the steroid receptor superfamily, Nature 340:163-166 (Exhibit 31). (4 pages) Cited by 29 patents
  • Worley, K.C. et al. (1992) Identification of the three new markers in Xp21 between DXS28 (C7) and DMD, Genomics 13:957-961 (Exhibit 32). (5 pages) [ISI abstract]
  • Worley, K.C. et al. (1993) Yeast artificial chromosome cloning in the glycerol kinase and adrenal hypoplasia congenita region of Xp21, Genomics 16:407-416 (Exhibit 33). (10 pages) [ISI abstract]
  • Yates, J.R.W. et al. (1987) A deletion of Xp21 maps congenital adrenal hypoplasia distal to glycerol kinase deficiency, Cytogenet. Cell Genet. 46:723 (Exhibit 34). (2 pages)
  • Zanaria, E. et al. (1994) An unusual member of the nuclear hormone receptor superfamily responsible for X-linked adrenal hypoplasia congenita, Nature 372:635-641 (Exhibit 35). (7 pages) Cited by 3 patents [ISI abstract]
  • Guo et al., "Diagnosis of X-linked Adrenal Hypoplasia Congenita By Mutation Analysis off the DAX1 Gene", Journal of the American Medical Association, vol. 274, No. 04, Jul. 26, 1995; pp. 324-330. (7 pages) Cited by 3 patents [ISI abstract]
  • Muscatelli et al., "Mutations in the DAX-1 Gene Give Rise to Both X-linked Adrenal Hypoplasia Congenita and Hypogonadotropic Hypogonadism", Nature, vol. 372, Dec. 15, 1994, pp. 672-676. (5 pages) Cited by 3 patents [ISI abstract]


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