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Results: 1-11 |
Results: 11
STRL22 IS A RECEPTOR FOR THE CC-CHEMOKINE-MIP-3-ALPHA
Authors: LIAO F ALDERSON R SU J ULLRICH SJ KREIDER BL FARBER JM
Citation: F. Liao et al., STRL22 IS A RECEPTOR FOR THE CC-CHEMOKINE-MIP-3-ALPHA, Biochemical and biophysical research communications, 236(1), 1997, pp. 212-217
FUNCTIONAL INACTIVATION BUT NOT STRUCTURAL MUTATION OF P53 CAUSES LIVER-CANCER
Authors: UEDA H ULLRICH SJ GANGEMI JD KAPPEL CA NGO L FEITELSON MA JAY G
Citation: H. Ueda et al., FUNCTIONAL INACTIVATION BUT NOT STRUCTURAL MUTATION OF P53 CAUSES LIVER-CANCER, Nature genetics, 9(1), 1995, pp. 41-47
TRANSGENIC MOUSE MODELS OF HUMAN GASTRIC AND HEPATIC CARCINOMAS
Authors: ULLRICH SJ ZENG ZZ JAY G
Citation: Sj. Ullrich et al., TRANSGENIC MOUSE MODELS OF HUMAN GASTRIC AND HEPATIC CARCINOMAS, Seminars in cancer biology, 5(1), 1994, pp. 61-68
THE CARBOXY-TERMINAL SERINE-392 PHOSPHORYLATION SITE OF HUMAN P53 IS NOT REQUIRED FOR WILD-TYPE ACTIVITIES
Authors: FISCELLA M ZAMBRANO N ULLRICH SJ UNGER T LIN D CHO B MERCER WE ANDERSON CW APPELLA E
Citation: M. Fiscella et al., THE CARBOXY-TERMINAL SERINE-392 PHOSPHORYLATION SITE OF HUMAN P53 IS NOT REQUIRED FOR WILD-TYPE ACTIVITIES, Oncogene, 9(11), 1994, pp. 3249-3257
SPECIFIC CROSS-REACTIVITY OF ANTIBODIES RAISED AGAINST 2 MAJOR STRESSPROTEINS, STRESS-70 AND CHAPERONIN-60, IN DIVERSE SPECIES
Authors: SANDERS BM MARTIN LS NAKAGAWA PA HUNTER DA MILLER S ULLRICH SJ
Citation: Bm. Sanders et al., SPECIFIC CROSS-REACTIVITY OF ANTIBODIES RAISED AGAINST 2 MAJOR STRESSPROTEINS, STRESS-70 AND CHAPERONIN-60, IN DIVERSE SPECIES, Environmental toxicology and chemistry, 13(8), 1994, pp. 1241-1249
STRUCTURE AND POSTTRANSLATIONAL MODIFICATION OF THE HUMAN P53 PROTEIN
Authors: APPELLA E FISCELLA M ZAMBRANO N ULLRICH SJ SAKAGUCHI K SAKAMOTO H LEWIS MS LIN D MERCER WE ANDERSON CW
Citation: E. Appella et al., STRUCTURE AND POSTTRANSLATIONAL MODIFICATION OF THE HUMAN P53 PROTEIN, Journal of protein chemistry, 13(5), 1994, pp. 499-500
THE HUMAN DNA-ACTIVATED PROTEIN-KINASE, DNA-PK, IS ACTIVATED BY DNA BREAKS AND PHOSPHORYLATES NUCLEAR DNA-BINDING PROTEIN SUBSTRATES ON SERINES AND THREONINES FOLLOWING BY GLUTAMINE
Authors: ANDERSON CW CONNELLY MA ZHANG H SIPLEY JD LEESMILLER SP SAKAGUCHI K ULLRICH SJ JACKSON SP APPELLA E
Citation: Cw. Anderson et al., THE HUMAN DNA-ACTIVATED PROTEIN-KINASE, DNA-PK, IS ACTIVATED BY DNA BREAKS AND PHOSPHORYLATES NUCLEAR DNA-BINDING PROTEIN SUBSTRATES ON SERINES AND THREONINES FOLLOWING BY GLUTAMINE, Journal of protein chemistry, 13(5), 1994, pp. 500-501
MUTATION OF THE SERINE 15 PHOSPHORYLATION SITE OF HUMAN P53 REDUCES THE ABILITY OF P53 TO INHIBIT CELL-CYCLE PROGRESSION
Authors: FISCELLA M ULLRICH SJ ZAMBRANO N SHIELDS MT LIN D LEESMILLER SP ANDERSON CW MERCER WE APPELLA E
Citation: M. Fiscella et al., MUTATION OF THE SERINE 15 PHOSPHORYLATION SITE OF HUMAN P53 REDUCES THE ABILITY OF P53 TO INHIBIT CELL-CYCLE PROGRESSION, Oncogene, 8(6), 1993, pp. 1519-1528
THE EZRIN-LIKE FAMILY OF TYROSINE KINASE SUBSTRATES - RECEPTOR-SPECIFIC PATTERN OF TYROSINE PHOSPHORYLATION AND RELATIONSHIP TO MALIGNANT TRANSFORMATION
Authors: FAZIOLI F WONG WT ULLRICH SJ SAKAGUCHI K APPELLA E DIFIORE PP
Citation: F. Fazioli et al., THE EZRIN-LIKE FAMILY OF TYROSINE KINASE SUBSTRATES - RECEPTOR-SPECIFIC PATTERN OF TYROSINE PHOSPHORYLATION AND RELATIONSHIP TO MALIGNANT TRANSFORMATION, Oncogene, 8(5), 1993, pp. 1335-1345
RELATIONSHIP BETWEEN 90-KILODALTON HEAT-SHOCK PROTEIN, ESTROGEN-RECEPTOR, AND PROGESTERONE-RECEPTOR IN HUMAN MAMMARY-TUMORS
Authors: SHYAMALA G SCHWEITZER M ULLRICH SJ
Citation: G. Shyamala et al., RELATIONSHIP BETWEEN 90-KILODALTON HEAT-SHOCK PROTEIN, ESTROGEN-RECEPTOR, AND PROGESTERONE-RECEPTOR IN HUMAN MAMMARY-TUMORS, Breast cancer research and treatment, 26(1), 1993, pp. 95-100
PHOSPHORYLATION AT SER-15 AND SER-392 IN MUTANT P53-MOLECULES FROM HUMAN TUMORS IS ALTERED COMPARED TO WILD-TYPE P53
Authors: ULLRICH SJ SAKAGUCHI K LEESMILLER SP FISCELLA M MERCER WE ANDERSON CW APPELLA E
Citation: Sj. Ullrich et al., PHOSPHORYLATION AT SER-15 AND SER-392 IN MUTANT P53-MOLECULES FROM HUMAN TUMORS IS ALTERED COMPARED TO WILD-TYPE P53, Proceedings of the National Academy of Sciences of the United Statesof America, 90(13), 1993, pp. 5954-5958
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