User:Brian Mark - Revision history

Harry Brumer: added Contributor tag, GH links

2010-04-23T21:18:14Z

added Contributor tag, GH links

Brian Mark at 20:36, 23 April 2010

2010-04-23T20:36:47Z

Brian Mark at 20:35, 23 April 2010

2010-04-23T20:35:50Z

Brian Mark at 20:31, 23 April 2010

2010-04-23T20:31:04Z

Brian Mark at 20:30, 23 April 2010

2010-04-23T20:30:22Z

Brian Mark at 20:26, 23 April 2010

2010-04-23T20:26:14Z

Brian Mark: Created page with ' Normal.dotm 0 0 1 136 776 University of Manitoba 6 1 952 12.0 0 false 18 pt 18 pt 0 0 false false false '''Brian Mark''' obtained hi…'

2010-04-23T20:24:28Z

Created page with ' Normal.dotm 0 0 1 136 776 University of Manitoba 6 1 952 12.0 0 false 18 pt 18 pt 0 0 false false false '''Brian Mark''' obtained hi…'

New page

Normal.dotm 0 0 1 136 776 University of Manitoba 6 1 952 12.0 0 false 18 pt 18 pt 0 0 false false false

'''Brian Mark''' obtained his BSc in Biology from the University of Winnipeg, Canada in 1995, which was followed by an MSc degree in Biochemistry from the University of Manitoba, Canada in 1998. He completed his PhD degree at the University of Alberta with Michael James in 2003, studying the structure and catalytic mechanism of human and bacterial N-acetyl-beta-hexosaminidases (GH20). His postdoctoral research was carried out at Los Alamos National Laboratory, USA, working with Thomas Terwilliger and Geoffrey Waldo to develop new methods to enhance the solubility of recombinant proteins for structural analysis. In 2005, Dr. Mark returned to Canada and joined the Department of Microbiology, University of Manitoba as an Assistant Professor. He investigates the structural biology of enzymes within the Gram-negative peptidoglycan recycling pathway and how their products regulate the inducible expression of chromosomal AmpC beta-lactamase. The glycoside hydrolase NagZ (GH3) is of particular interest in this pathway since it produces a peptidoglycan metabolite that positively regulates AmpC beta-lactamase expression.

← Older revision		Revision as of 21:18, 23 April 2010
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−	'''Brian Mark''' obtained his BSc in Biology from the University of Winnipeg, Canada in 1995, which he followed with an MSc degree in Biochemistry from the University of Manitoba, Canada in 1998. He completed his PhD degree at the University of Alberta with Michael James in 2003, studying the structure and catalytic mechanism of human and bacterial N-acetyl-β-hexosaminidases (GH20). His postdoctoral research was carried out at Los Alamos National Laboratory, USA, working with Thomas Terwilliger and Geoffrey Waldo to develop new methods to enhance the solubility of recombinant proteins for structural analysis. In 2005, Dr. Mark returned to Canada and joined the Department of Microbiology, University of Manitoba as an Assistant Professor. He investigates the structural biology of enzymes within the Gram-negative peptidoglycan recycling pathway and how their products regulate the inducible expression of chromosomal AmpC beta-lactamase. The glycoside hydrolase NagZ (GH3) is of particular interest in this pathway since it produces a peptidoglycan metabolite that positively regulates AmpC beta-lactamase expression.	+	'''Brian Mark''' obtained his BSc in Biology from the University of Winnipeg, Canada in 1995, which he followed with an MSc degree in Biochemistry from the University of Manitoba, Canada in 1998. He completed his PhD degree at the University of Alberta with Michael James in 2003, studying the structure and catalytic mechanism of human and bacterial N-acetyl-β-hexosaminidases ([[GH20]]). His postdoctoral research was carried out at Los Alamos National Laboratory, USA, working with Thomas Terwilliger and Geoffrey Waldo to develop new methods to enhance the solubility of recombinant proteins for structural analysis. In 2005, Dr. Mark returned to Canada and joined the Department of Microbiology, University of Manitoba as an Assistant Professor. He investigates the structural biology of enzymes within the Gram-negative peptidoglycan recycling pathway and how their products regulate the inducible expression of chromosomal AmpC beta-lactamase. The glycoside hydrolase NagZ ([[GH3]]) is of particular interest in this pathway since it produces a peptidoglycan metabolite that positively regulates AmpC beta-lactamase expression.
		+
		+	[[Category:Contributors\|Mark, Brian]]

← Older revision		Revision as of 20:36, 23 April 2010
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−	'''Brian Mark''' obtained his BSc in Biology from the University of Winnipeg, Canada in 1995, which ~~was~~ followed by an MSc degree in Biochemistry from the University of Manitoba, Canada in 1998. He completed his PhD degree at the University of Alberta with Michael James in 2003, studying the structure and catalytic mechanism of human and bacterial N-acetyl-β-hexosaminidases (GH20). His postdoctoral research was carried out at Los Alamos National Laboratory, USA, working with Thomas Terwilliger and Geoffrey Waldo to develop new methods to enhance the solubility of recombinant proteins for structural analysis. In 2005, Dr. Mark returned to Canada and joined the Department of Microbiology, University of Manitoba as an Assistant Professor. He investigates the structural biology of enzymes within the Gram-negative peptidoglycan recycling pathway and how their products regulate the inducible expression of chromosomal AmpC beta-lactamase. The glycoside hydrolase NagZ (GH3) is of particular interest in this pathway since it produces a peptidoglycan metabolite that positively regulates AmpC beta-lactamase expression.	+	'''Brian Mark''' obtained his BSc in Biology from the University of Winnipeg, Canada in 1995, which he followed with an MSc degree in Biochemistry from the University of Manitoba, Canada in 1998. He completed his PhD degree at the University of Alberta with Michael James in 2003, studying the structure and catalytic mechanism of human and bacterial N-acetyl-β-hexosaminidases (GH20). His postdoctoral research was carried out at Los Alamos National Laboratory, USA, working with Thomas Terwilliger and Geoffrey Waldo to develop new methods to enhance the solubility of recombinant proteins for structural analysis. In 2005, Dr. Mark returned to Canada and joined the Department of Microbiology, University of Manitoba as an Assistant Professor. He investigates the structural biology of enzymes within the Gram-negative peptidoglycan recycling pathway and how their products regulate the inducible expression of chromosomal AmpC beta-lactamase. The glycoside hydrolase NagZ (GH3) is of particular interest in this pathway since it produces a peptidoglycan metabolite that positively regulates AmpC beta-lactamase expression.

← Older revision		Revision as of 20:35, 23 April 2010
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−	'''Brian Mark''' obtained his BSc in Biology from the University of Winnipeg, Canada in 1995, which was followed by an MSc degree in Biochemistry from the University of Manitoba, Canada in 1998. He completed his PhD degree at the University of Alberta with Michael James in 2003, studying the structure and catalytic mechanism of human and bacterial N-acetyl-~~beta~~-hexosaminidases (GH20). His postdoctoral research was carried out at Los Alamos National Laboratory, USA, working with Thomas Terwilliger and Geoffrey Waldo to develop new methods to enhance the solubility of recombinant proteins for structural analysis. In 2005, Dr. Mark returned to Canada and joined the Department of Microbiology, University of Manitoba as an Assistant Professor. He investigates the structural biology of enzymes within the Gram-negative peptidoglycan recycling pathway and how their products regulate the inducible expression of chromosomal AmpC beta-lactamase. The glycoside hydrolase NagZ (GH3) is of particular interest in this pathway since it produces a peptidoglycan metabolite that positively regulates AmpC beta-lactamase expression.	+	'''Brian Mark''' obtained his BSc in Biology from the University of Winnipeg, Canada in 1995, which was followed by an MSc degree in Biochemistry from the University of Manitoba, Canada in 1998. He completed his PhD degree at the University of Alberta with Michael James in 2003, studying the structure and catalytic mechanism of human and bacterial N-acetyl-β-hexosaminidases (GH20). His postdoctoral research was carried out at Los Alamos National Laboratory, USA, working with Thomas Terwilliger and Geoffrey Waldo to develop new methods to enhance the solubility of recombinant proteins for structural analysis. In 2005, Dr. Mark returned to Canada and joined the Department of Microbiology, University of Manitoba as an Assistant Professor. He investigates the structural biology of enzymes within the Gram-negative peptidoglycan recycling pathway and how their products regulate the inducible expression of chromosomal AmpC beta-lactamase. The glycoside hydrolase NagZ (GH3) is of particular interest in this pathway since it produces a peptidoglycan metabolite that positively regulates AmpC beta-lactamase expression.

← Older revision		Revision as of 20:31, 23 April 2010
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−	'''Brian Mark''' obtained his BSc in Biology from the University of Winnipeg, Canada in 1995, which was followed by an MSc degree in Biochemistry from the University of Manitoba, Canada in 1998. He completed his PhD degree at the University of Alberta with Michael James in 2003, studying the structure and catalytic mechanism of human and bacterial N-acetyl-&beta-hexosaminidases (GH20). His postdoctoral research was carried out at Los Alamos National Laboratory, USA, working with Thomas Terwilliger and Geoffrey Waldo to develop new methods to enhance the solubility of recombinant proteins for structural analysis. In 2005, Dr. Mark returned to Canada and joined the Department of Microbiology, University of Manitoba as an Assistant Professor. He investigates the structural biology of enzymes within the Gram-negative peptidoglycan recycling pathway and how their products regulate the inducible expression of chromosomal AmpC beta-lactamase. The glycoside hydrolase NagZ (GH3) is of particular interest in this pathway since it produces a peptidoglycan metabolite that positively regulates AmpC beta-lactamase expression.	+	'''Brian Mark''' obtained his BSc in Biology from the University of Winnipeg, Canada in 1995, which was followed by an MSc degree in Biochemistry from the University of Manitoba, Canada in 1998. He completed his PhD degree at the University of Alberta with Michael James in 2003, studying the structure and catalytic mechanism of human and bacterial N-acetyl-beta-hexosaminidases (GH20). His postdoctoral research was carried out at Los Alamos National Laboratory, USA, working with Thomas Terwilliger and Geoffrey Waldo to develop new methods to enhance the solubility of recombinant proteins for structural analysis. In 2005, Dr. Mark returned to Canada and joined the Department of Microbiology, University of Manitoba as an Assistant Professor. He investigates the structural biology of enzymes within the Gram-negative peptidoglycan recycling pathway and how their products regulate the inducible expression of chromosomal AmpC beta-lactamase. The glycoside hydrolase NagZ (GH3) is of particular interest in this pathway since it produces a peptidoglycan metabolite that positively regulates AmpC beta-lactamase expression.

← Older revision		Revision as of 20:30, 23 April 2010
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−	'''Brian Mark''' obtained his BSc in Biology from the University of Winnipeg, Canada in 1995, which was followed by an MSc degree in Biochemistry from the University of Manitoba, Canada in 1998. He completed his PhD degree at the University of Alberta with Michael James in 2003, studying the structure and catalytic mechanism of human and bacterial N-acetyl-beta-hexosaminidases (GH20). His postdoctoral research was carried out at Los Alamos National Laboratory, USA, working with Thomas Terwilliger and Geoffrey Waldo to develop new methods to enhance the solubility of recombinant proteins for structural analysis. In 2005, Dr. Mark returned to Canada and joined the Department of Microbiology, University of Manitoba as an Assistant Professor. He investigates the structural biology of enzymes within the Gram-negative peptidoglycan recycling pathway and how their products regulate the inducible expression of chromosomal AmpC beta-lactamase. The glycoside hydrolase NagZ (GH3) is of particular interest in this pathway since it produces a peptidoglycan metabolite that positively regulates AmpC beta-lactamase expression.	+	'''Brian Mark''' obtained his BSc in Biology from the University of Winnipeg, Canada in 1995, which was followed by an MSc degree in Biochemistry from the University of Manitoba, Canada in 1998. He completed his PhD degree at the University of Alberta with Michael James in 2003, studying the structure and catalytic mechanism of human and bacterial N-acetyl-&beta-hexosaminidases (GH20). His postdoctoral research was carried out at Los Alamos National Laboratory, USA, working with Thomas Terwilliger and Geoffrey Waldo to develop new methods to enhance the solubility of recombinant proteins for structural analysis. In 2005, Dr. Mark returned to Canada and joined the Department of Microbiology, University of Manitoba as an Assistant Professor. He investigates the structural biology of enzymes within the Gram-negative peptidoglycan recycling pathway and how their products regulate the inducible expression of chromosomal AmpC beta-lactamase. The glycoside hydrolase NagZ (GH3) is of particular interest in this pathway since it produces a peptidoglycan metabolite that positively regulates AmpC beta-lactamase expression.

← Older revision		Revision as of 20:26, 23 April 2010
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−	~~Normal.dotm 0 0 1 136 776 University of Manitoba 6 1 952 12.0 0 false 18 pt 18 pt 0 0 false false false~~
−
	'''Brian Mark''' obtained his BSc in Biology from the University of Winnipeg, Canada in 1995, which was followed by an MSc degree in Biochemistry from the University of Manitoba, Canada in 1998. He completed his PhD degree at the University of Alberta with Michael James in 2003, studying the structure and catalytic mechanism of human and bacterial N-acetyl-beta-hexosaminidases (GH20). His postdoctoral research was carried out at Los Alamos National Laboratory, USA, working with Thomas Terwilliger and Geoffrey Waldo to develop new methods to enhance the solubility of recombinant proteins for structural analysis. In 2005, Dr. Mark returned to Canada and joined the Department of Microbiology, University of Manitoba as an Assistant Professor. He investigates the structural biology of enzymes within the Gram-negative peptidoglycan recycling pathway and how their products regulate the inducible expression of chromosomal AmpC beta-lactamase. The glycoside hydrolase NagZ (GH3) is of particular interest in this pathway since it produces a peptidoglycan metabolite that positively regulates AmpC beta-lactamase expression.		'''Brian Mark''' obtained his BSc in Biology from the University of Winnipeg, Canada in 1995, which was followed by an MSc degree in Biochemistry from the University of Manitoba, Canada in 1998. He completed his PhD degree at the University of Alberta with Michael James in 2003, studying the structure and catalytic mechanism of human and bacterial N-acetyl-beta-hexosaminidases (GH20). His postdoctoral research was carried out at Los Alamos National Laboratory, USA, working with Thomas Terwilliger and Geoffrey Waldo to develop new methods to enhance the solubility of recombinant proteins for structural analysis. In 2005, Dr. Mark returned to Canada and joined the Department of Microbiology, University of Manitoba as an Assistant Professor. He investigates the structural biology of enzymes within the Gram-negative peptidoglycan recycling pathway and how their products regulate the inducible expression of chromosomal AmpC beta-lactamase. The glycoside hydrolase NagZ (GH3) is of particular interest in this pathway since it produces a peptidoglycan metabolite that positively regulates AmpC beta-lactamase expression.