Results
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Absence of stearoyl-CoA desaturase-1 ameliorates features of the metabolic syndrome in LDLR-deficient mice. [electronic resource] by
- MacDonald, Marcia L E
- Singaraja, Roshni R
- Bissada, Nagat
- Ruddle, Piers
- Watts, Russell
- Karasinska, Joanna M
- Gibson, William T
- Fievet, Catherine
- Vance, Jean E
- Staels, Bart
- Hayden, Michael R
Producer: 20080307
In:
Journal of lipid research vol. 49
Availability: No items available.
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Despite antiatherogenic metabolic characteristics, SCD1-deficient mice have increased inflammation and atherosclerosis. [electronic resource] by
- MacDonald, Marcia L E
- van Eck, Miranda
- Hildebrand, Reeni B
- Wong, Brian W C
- Bissada, Nagat
- Ruddle, Piers
- Kontush, Anatol
- Hussein, Hala
- Pouladi, Mahmoud A
- Chapman, M John
- Fievet, Catherine
- van Berkel, Theo J C
- Staels, Bart
- McManus, Bruce M
- Hayden, Michael R
Producer: 20090305
In:
Arteriosclerosis, thrombosis, and vascular biology vol. 29
Availability: No items available.
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5.
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Identification and functional analysis of a naturally occurring E89K mutation in the ABCA1 gene of the WHAM chicken. [electronic resource] by
- Attie, Alan D
- Hamon, Yannick
- Brooks-Wilson, Angela R
- Gray-Keller, Mark P
- MacDonald, Marcia L E
- Rigot, Veronique
- Tebon, Angie
- Zhang, Lin-Hua
- Mulligan, Jacob D
- Singaraja, Roshni R
- Bitgood, J James
- Cook, Mark E
- Kastelein, John J P
- Chimini, Giovanna
- Hayden, Michael R
Producer: 20030320
In:
Journal of lipid research vol. 43
Availability: No items available.
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Mutant frizzled-4 disrupts retinal angiogenesis in familial exudative vitreoretinopathy. [electronic resource] by
- Robitaille, Johane
- MacDonald, Marcia L E
- Kaykas, Ajamete
- Sheldahl, Laird C
- Zeisler, Jutta
- Dubé, Marie-Pierre
- Zhang, Lin-Hua
- Singaraja, Roshni R
- Guernsey, Duane L
- Zheng, Binyou
- Siebert, Lee F
- Hoskin-Mott, Ann
- Trese, Michael T
- Pimstone, Simon N
- Shastry, Barkur S
- Moon, Randall T
- Hayden, Michael R
- Goldberg, Y Paul
- Samuels, Mark E
Producer: 20021104
In:
Nature genetics vol. 32
Availability: No items available.
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Mutations in HFE2 cause iron overload in chromosome 1q-linked juvenile hemochromatosis. [electronic resource] by
- Papanikolaou, George
- Samuels, Mark E
- Ludwig, Erwin H
- MacDonald, Marcia L E
- Franchini, Patrick L
- Dubé, Marie-Pierre
- Andres, Lisa
- MacFarlane, Julie
- Sakellaropoulos, Nikos
- Politou, Marianna
- Nemeth, Elizabeta
- Thompson, Jay
- Risler, Jenni K
- Zaborowska, Catherine
- Babakaiff, Ryan
- Radomski, Christopher C
- Pape, Terry D
- Davidas, Owen
- Christakis, John
- Brissot, Pierre
- Lockitch, Gillian
- Ganz, Tomas
- Hayden, Michael R
- Goldberg, Y Paul
Producer: 20040202
In:
Nature genetics vol. 36
Availability: No items available.
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8.
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Identification of a novel gene (HSN2) causing hereditary sensory and autonomic neuropathy type II through the Study of Canadian Genetic Isolates. [electronic resource] by
- Lafreniere, Ronald G
- MacDonald, Marcia L E
- Dube, Marie-Pierre
- MacFarlane, Julie
- O'Driscoll, Mary
- Brais, Bernard
- Meilleur, Sebastien
- Brinkman, Ryan R
- Dadivas, Owen
- Pape, Terry
- Platon, Christele
- Radomski, Chris
- Risler, Jenni
- Thompson, Jay
- Guerra-Escobio, Ana-Maria
- Davar, Gudarz
- Breakefield, Xandra O
- Pimstone, Simon N
- Green, Roger
- Pryse-Phillips, William
- Goldberg, Y Paul
- Younghusband, H Banfield
- Hayden, Michael R
- Sherrington, Robin
- Rouleau, Guy A
- Samuels, Mark E
Producer: 20040603
In:
American journal of human genetics vol. 74
Availability: No items available.
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