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1,25-Dihydroxyvitamin D sub(3) Regulation of c-myc) protooncogene transcription. Possible involvement of protein kinase C
1,25-Dihydroxyvitamin D sub(3) Regulation of c-myc) protooncogene transcription. Possible involvement of protein kinase C
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1,25-Dihydroxyvitamin D sub(3) Regulation of c-myc) protooncogene transcription. Possible involvement of protein kinase C

Simpson, RU ; Hsu, Todd ; Wendt, MD ; Taylor, J M

The Journal of biological chemistry, 1989-01, Vol.264 (33), p.19710-19715 [Periódico revisado por pares]

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2
ABO(H) Blood Group A and B Glycosyltransferases Recognize Substrate via Specific Conformational Changes
ABO(H) Blood Group A and B Glycosyltransferases Recognize Substrate via Specific Conformational Changes
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ABO(H) Blood Group A and B Glycosyltransferases Recognize Substrate via Specific Conformational Changes

Alfaro, Javier A. ; Zheng, Ruixiang Blake ; Persson, Mattias ; Letts, James A. ; Polakowski, Robert ; Bai, Yu ; Borisova, Svetlana N. ; Seto, Nina O.L. ; Lowary, Todd L. ; Palcic, Monica M. ; Evans, Stephen V.

The Journal of biological chemistry, 2008-04, Vol.283 (15), p.10097-10108 [Periódico revisado por pares]

United States: Elsevier Inc

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3
Acid-activatable Cysteine Proteinases in the Cellular Slime Mold Dictyostelium discoideum
Acid-activatable Cysteine Proteinases in the Cellular Slime Mold Dictyostelium discoideum
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Acid-activatable Cysteine Proteinases in the Cellular Slime Mold Dictyostelium discoideum

North, M J ; Nicol, K ; Sands, T W ; Cotter, D A

The Journal of biological chemistry, 1996-06, Vol.271 (24), p.14462-14467 [Periódico revisado por pares]

United States: American Society for Biochemistry and Molecular Biology

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4
Actin-latrunculin A structure and function. Differential modulation of actin-binding protein function by latrunculin A
Actin-latrunculin A structure and function. Differential modulation of actin-binding protein function by latrunculin A
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Actin-latrunculin A structure and function. Differential modulation of actin-binding protein function by latrunculin A

Yarmola, E G ; Somasundaram, T ; Boring, T A ; Spector, I ; Bubb, M R

The Journal of biological chemistry, 2000-09, Vol.275 (36), p.28120 [Periódico revisado por pares]

United States

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5
Activation of Archaeal Transcription Mediated by Recruitment of Transcription Factor B
Activation of Archaeal Transcription Mediated by Recruitment of Transcription Factor B
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Activation of Archaeal Transcription Mediated by Recruitment of Transcription Factor B

Ochs, Simon M. ; Thumann, Sybille ; Richau, Renate ; Weirauch, Matt T. ; Lowe, Todd M. ; Thomm, Michael ; Hausner, Winfried

The Journal of biological chemistry, 2012-05, Vol.287 (22), p.18863-18871 [Periódico revisado por pares]

United States: Elsevier Inc

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6
Adenylyl cyclase G, an osmosensor controlling germination of Dictyostelium spores
Adenylyl cyclase G, an osmosensor controlling germination of Dictyostelium spores
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Adenylyl cyclase G, an osmosensor controlling germination of Dictyostelium spores

Es, S. van (University of Leiden, Leiden, The Netherlands.) ; Virdy, K.J ; Pitt, G.S ; Meima, M ; Sands, T.W ; Devreotes, P.N ; Cotter, D.A ; Schaap, P

The Journal of biological chemistry, 1996-09, Vol.271 (39), p.23623-23625 [Periódico revisado por pares]

United States: American Society for Biochemistry and Molecular Biology

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7
Aim18p and Aim46p are chalcone isomerase domain–containing mitochondrial hemoproteins in Saccharomyces cerevisiae
Aim18p and Aim46p are chalcone isomerase domain–containing mitochondrial hemoproteins in Saccharomyces cerevisiae
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Aim18p and Aim46p are chalcone isomerase domain–containing mitochondrial hemoproteins in Saccharomyces cerevisiae

Schmitz, Jonathan M. ; Wolters, John F. ; Murray, Nathan H. ; Guerra, Rachel M. ; Bingman, Craig A. ; Hittinger, Chris Todd ; Pagliarini, David J.

The Journal of biological chemistry, 2023-03, Vol.299 (3), p.102981-102981, Article 102981 [Periódico revisado por pares]

United States: Elsevier Inc

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8
alpha -Conotoxin OmIA Is a Potent Ligand for the Acetylcholine-binding Protein as Well as alpha 3 beta 2 and alpha 7 Nicotinic Acetylcholine Receptors
alpha -Conotoxin OmIA Is a Potent Ligand for the Acetylcholine-binding Protein as Well as alpha 3 beta 2 and alpha 7 Nicotinic Acetylcholine Receptors
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alpha -Conotoxin OmIA Is a Potent Ligand for the Acetylcholine-binding Protein as Well as alpha 3 beta 2 and alpha 7 Nicotinic Acetylcholine Receptors

Talley, Todd T ; Olivera, Baldomero M ; Han, Kyou-Hoon ; Christensen, Sean B ; Dowell, Cheryl ; Tsigelny, Igor ; Ho, Kwok-Yiu ; Taylor, Palmer ; McIntosh, JMichael

The Journal of biological chemistry, 2006-08, Vol.281 (34), p.24678-24686 [Periódico revisado por pares]

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9
Alpha-conotoxin OmIA is a potent ligand for the acetylcholine-binding protein as well as alpha3beta2 and alpha7 nicotinic acetylcholine receptors
Alpha-conotoxin OmIA is a potent ligand for the acetylcholine-binding protein as well as alpha3beta2 and alpha7 nicotinic acetylcholine receptors
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Alpha-conotoxin OmIA is a potent ligand for the acetylcholine-binding protein as well as alpha3beta2 and alpha7 nicotinic acetylcholine receptors

Talley, Todd T ; Olivera, Baldomero M ; Han, Kyou-Hoon ; Christensen, Sean B ; Dowell, Cheryl ; Tsigelny, Igor ; Ho, Kwok-Yiu ; Taylor, Palmer ; McIntosh, J Michael

The Journal of biological chemistry, 2006-08, Vol.281 (34), p.24678 [Periódico revisado por pares]

United States

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10
Amyloid-binding Small Molecules Efficiently Block SEVI (Semen-derived Enhancer of Virus Infection)- and Semen-mediated Enhancement of HIV-1 Infection
Amyloid-binding Small Molecules Efficiently Block SEVI (Semen-derived Enhancer of Virus Infection)- and Semen-mediated Enhancement of HIV-1 Infection
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Amyloid-binding Small Molecules Efficiently Block SEVI (Semen-derived Enhancer of Virus Infection)- and Semen-mediated Enhancement of HIV-1 Infection

Olsen, Joanna S. ; Brown, Caitlin ; Capule, Christina C. ; Rubinshtein, Mark ; Doran, Todd M. ; Srivastava, Rajesh K. ; Feng, Changyong ; Nilsson, Bradley L. ; Yang, Jerry ; Dewhurst, Stephen

The Journal of biological chemistry, 2010-11, Vol.285 (46), p.35488-35496 [Periódico revisado por pares]

United States: Elsevier Inc

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