A novel transgenic line of mice exhibiting autosomal recessive male-specific lethality and non-alcoholic fatty liver disease (English)
- New search for: Sollars, Vincent E.
- New search for: McEntee, Benjamin J.
- New search for: Engiles, Julie B.
- New search for: Rothstein, Jay L.
- New search for: Buchberg, Arthur M.
- New search for: Sollars, Vincent E.
- New search for: McEntee, Benjamin J.
- New search for: Engiles, Julie B.
- New search for: Rothstein, Jay L.
- New search for: Buchberg, Arthur M.
In:
Human molecular genetics
;
11
, 22
;
2777-
;
2002
- Article (Journal) / Electronic Resource
-
Title:A novel transgenic line of mice exhibiting autosomal recessive male-specific lethality and non-alcoholic fatty liver disease
-
Contributors:Sollars, Vincent E. ( author ) / McEntee, Benjamin J. ( author ) / Engiles, Julie B. ( author ) / Rothstein, Jay L. ( author ) / Buchberg, Arthur M. ( author )
-
Published in:Human molecular genetics ; 11, 22 ; 2777-
-
Publisher:
- New search for: Oxford University Press
-
Publication date:2002-10-15
-
ISSN:
-
DOI:
-
Type of media:Article (Journal)
-
Type of material:Electronic Resource
-
Language:English
-
Source:
Table of contents – Volume 11, Issue 22
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 2689
-
Aggregate formation inhibits proteasomal degradation of polyglutamine proteinsVerhoef, Lisette G.G.C. / Lindsten, Kristina / Masucci, Maria G. / Dantuma, Nico P. et al. | 2002
- 2701
-
Cholesterol regulates ABCD2 expression: implications for the therapy of X-linked adrenoleukodystrophyWeinhofer, Isabelle / Forss-Petter, Sonja / Zigman, Mihaela / Berger, Johannes et al. | 2002
- 2709
-
Cln3 {Delta}ex7/8 knock-in mice with the common JNCL mutation exhibit progressive neurologic disease that begins before birthCotman, Susan L. / Vrbanac, Vladimir / Lebel, Lori-Anne / Lee, Richard L. / Johnson, Kevin A. / Donahue, Leah-Rae / Teed, Allison M. / Antonellis, Kristen / Bronson, Roderick T. / Lerner, Terry J. et al. | 2002
- 2723
-
The inherited blindness associated protein AIPL1 interacts with the cell cycle regulator protein NUB1Akey, Dayna T. / Zhu, Xuemei / Dyer, Michael / Li, Aimin / Sorensen, Adam / Blackshaw, Seth / Fukuda-Kamitani, Taeko / Daiger, Stephen P. / Craft, Cheryl M. / Kamitani, Tetsu et al. | 2002
- 2735
-
Domain-specific mutations in sequestosome 1 (SQSTM1) cause familial and sporadic Paget's diseaseHocking, Lynne J. / Lucas, Gavin J.A. / Daroszewska, Anna / Mangion, Jon / Olavesen, Mark / Cundy, Tim / Nicholson, Geoff C. / Ward, Lynley / Bennett, Simon T. / Wuyts, Wim et al. | 2002
- 2741
-
Pseudohypoparathyroidism type Ib with disturbed imprinting in the GNAS1 cluster and Gs{alpha} deficiency in plateletsFreson, Kathleen / Thys, Chantal / Wittevrongel, Christine / Proesmans, Willem / Hoylaerts, Marc F. / Vermylen, Jos / Van Geet, Chris et al. | 2002
- 2751
-
Involvement of survival motor neuron (SMN) protein in cell deathVyas, Sheela / Béchade, Catherine / Riveau, Béatrice / Downward, Julian / Triller, Antoine et al. | 2002
- 2765
-
Molecular and pathological effects of a modifier gene on deficiency of the sodium channel Scn8a (Nav1.6)Kearney, Jennifer A. / Buchner, David A. / de Haan, Georgius / Adamska, Maja / Levin, Stephen I. / Furay, Amy R. / Albin, Roger L. / Jones, Julie M. / Montal, Mauricio / Stevens, Martin J. et al. | 2002
- 2777
-
A novel transgenic line of mice exhibiting autosomal recessive male-specific lethality and non-alcoholic fatty liver diseaseSollars, Vincent E. / McEntee, Benjamin J. / Engiles, Julie B. / Rothstein, Jay L. / Buchberg, Arthur M. et al. | 2002
- 2787
-
Functional association of the parkin gene promoter with idiopathic Parkinson's diseaseWest, Andrew B. / Maraganore, Demetrius / Crook, Julia / Lesnick, Tim / Lockhart, Paul J. / Wilkes, Kristen M. / Kapatos, Gregory / Hardy, John A. / Farrer, Matt J. et al. | 2002
- 2793
-
Craniofacial expression of human and murine TBX22 correlates with the cleft palate and ankyloglossia phenotype observed in CPX patientsBraybrook, Claire / Lisgo, Steven / Doudney, Kit / Henderson, Deborah / Marçano, Ana Carolina B. / Strachan, Tom / Patton, Michael A. / Villard, Laurent / Moore, Gudrun E. / Stanier, Philip et al. | 2002