Appeal No. 2007-0083 Application No. 10/174,574 ID NO:31, which encodes a polypeptide referred to as “PRO270,” which has the amino acid sequence shown in SEQ ID NO:32. Page 8 and Figure 32. The encoded amino acid sequence is disclosed to include a signal sequence, transmembrane domain, sites for various post-translational modifications, and a “Myb DNA-binding domain repeat signature 1.” Figure 32. The present specification does not further characterize the amino acid sequence of SEQ ID NO:32. However, the present application claims priority as follows: This application is a continuation of . . . a continuation of . . . a continuation-in-part of . . . US Application 09/380139 filed 8/25/1999, now abandoned, which is the National Stage filed under 35 USC §371 of PCT Application PCT/US98/19330 filed 9/16/1998, which claims priority under 35 USC § 119 to US provisional application 60/063121 filed 10/24/1997. Preliminary Amendment filed Sept. 18, 2002, pages 1-2. PCT application US98/19330 was published as WO 99/14328 on March 25, 1999. Thus, the contents of that application were known to those of ordinary skill in the art as of that date. WO 99/14328 characterizes PRO270 as follows: Thioredoxins [a]ffect reduction-oxidation (redox) state. Many diseases are potentially related to redox state and reactive oxygen species may play a role in many important biological processes. The transcription factors, NF-kappa-B and AP-1, are regulated by redox state and are known to affect the expression of a large variety of genes thought to be involved in the pathogenesis of AIDS, cancer, atherosclerosis and diabetic complications. Such proteins may also play a role in cellular antioxidant defense, and in pathological conditions involving oxidative stress such as stroke and inflammation in addition to having a role in apoptosis. Therefore, thioredoxins, and 2Page: Previous 1 2 3 4 5 6 7 8 9 10 Next
Last modified: September 9, 2013