Muller M - Search Results

1

Antitumor activity of a phosphorothioate antisense oligodeoxynucleotide targeted against C-raf kinase.

Monia BP, Johnston JF, Geiger T, Muller M, Fabbro D. Monia BP, et al. Among authors: muller m. Nat Med. 1996 Jun;2(6):668-75. doi: 10.1038/nm0696-668. Nat Med. 1996. PMID: 8640558

2

Inhibition of growth of human tumor cell lines in nude mice by an antisense of oligonucleotide inhibitor of protein kinase C-alpha expression.

Dean N, McKay R, Miraglia L, Howard R, Cooper S, Giddings J, Nicklin P, Meister L, Ziel R, Geiger T, Muller M, Fabbro D. Dean N, et al. Among authors: muller m. Cancer Res. 1996 Aug 1;56(15):3499-507. Cancer Res. 1996. PMID: 8758918

3

Sequence-specific antitumor activity of a phosphorothioate oligodeoxyribonucleotide targeted to human C-raf kinase supports an antisense mechanism of action in vivo.

Monia BP, Sasmor H, Johnston JF, Freier SM, Lesnik EA, Muller M, Geiger T, Altmann KH, Moser H, Fabbro D. Monia BP, et al. Among authors: muller m. Proc Natl Acad Sci U S A. 1996 Dec 24;93(26):15481-4. doi: 10.1073/pnas.93.26.15481. Proc Natl Acad Sci U S A. 1996. PMID: 8986837 Free PMC article.

4

Antisense oligonucleotide inhibitors of isozymes of protein kinase C: in vitro and in vivo activity, and clinical development as anti-cancer therapeutics.

McGraw K, McKay R, Miraglia L, Boggs RT, Pribble JP, Muller M, Geiger T, Fabbro D, Dean NM. McGraw K, et al. Among authors: muller m. Anticancer Drug Des. 1997 Jul;12(5):315-26. Anticancer Drug Des. 1997. PMID: 9236849 Review. No abstract available.

5

Antisense oligonucleotides as inhibitors of signal transduction: development from research tools to therapeutic agents.

Dean NM, McKay R, Miraglia L, Geiger T, Müller M, Fabbro D, Bennett CF. Dean NM, et al. Among authors: muller m. Biochem Soc Trans. 1996 Aug;24(3):623-9. doi: 10.1042/bst0240623. Biochem Soc Trans. 1996. PMID: 8878816 Review. No abstract available.

6

Second-generation antisense oligonucleotides: structure-activity relationships and the design of improved signal-transduction inhibitors.

Altmann KH, Fabbro D, Dean NM, Geiger T, Monia BP, Müller M, Nicklin P. Altmann KH, et al. Among authors: muller m. Biochem Soc Trans. 1996 Aug;24(3):630-7. doi: 10.1042/bst0240630. Biochem Soc Trans. 1996. PMID: 8878817 Review. No abstract available.

7

Antitumor activity of a PKC-alpha antisense oligonucleotide in combination with standard chemotherapeutic agents against various human tumors transplanted into nude mice.

Geiger T, Müller M, Dean NM, Fabbro D. Geiger T, et al. Among authors: muller m. Anticancer Drug Des. 1998 Jan;13(1):35-45. Anticancer Drug Des. 1998. PMID: 9474241

8

Antitumor activity of a C-raf antisense oligonucleotide in combination with standard chemotherapeutic agents against various human tumors transplanted subcutaneously into nude mice.

Geiger T, Müller M, Monia BP, Fabbro D. Geiger T, et al. Among authors: muller m. Clin Cancer Res. 1997 Jul;3(7):1179-85. Clin Cancer Res. 1997. PMID: 9815797

9

Phenylamino-pyrimidine (PAP) derivatives: a new class of potent and selective inhibitors of protein kinase C (PKC).

Zimmermann J, Caravatti G, Mett H, Meyer T, Müller M, Lydon NB, Fabbro D. Zimmermann J, et al. Among authors: muller m. Arch Pharm (Weinheim). 1996 Jul;329(7):371-6. doi: 10.1002/ardp.19963290707. Arch Pharm (Weinheim). 1996. PMID: 8764886

10

A derivative of staurosporine (CGP 41 251) shows selectivity for protein kinase C inhibition and in vitro anti-proliferative as well as in vivo anti-tumor activity.

Meyer T, Regenass U, Fabbro D, Alteri E, Rösel J, Müller M, Caravatti G, Matter A. Meyer T, et al. Among authors: muller m. Int J Cancer. 1989 May 15;43(5):851-6. doi: 10.1002/ijc.2910430519. Int J Cancer. 1989. Retraction in: Int J Cancer. 1999 May 17;81(4):669. doi: 10.1002/(sici)1097-0215(19990517)81:4<669::aid-ijc26>3.0.co;2-f PMID: 2714889 Retracted.

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