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Scholar Results 1 - 10 of about 101 related to Goldfine: Necdin and E2F4 are modulated by rosiglitazone therapy in diabetic human adipose.... (0.12 sec) 

Necdin and E2F4 are modulated by rosiglitazone therapy in diabetic human …

- diabetesjournals.org
AB Goldfine, S Crunkhorn, M Costello, H Gami, EJ … - Diabetes, 2006 - Am Diabetes Assoc
To identify novel pathways mediating molecular mechanisms of thiazolidinediones (TZDs) in
humans, we assessed gene expression in adipose and muscle tissue from six subjects with type
2 diabetes before and after 8 weeks of treatment with rosiglitazone. mRNA was analyzed ...
Cited by 4 - Related articles - BL Direct - All 5 versions

Evolutionary genomic remodelling of the human 4 q subtelomere(4 q 35. 2)


B Bodega, MF Cardone, S Müller, M Neusser … - BMC Evolutionary …, 2007 - biomedcentral.com
A basic block consisting of short D4Z4 arrays (10–15 repeats), 4q35.2 specific sequences, and
approximately 35 kb of interspersed repeats from different LINE subfamilies was repeated at
least twice in the gorilla 4qter. This genomic organisation has undergone evolutionary ...
Cited by 5 - Related articles - Cached - All 7 versions

Intrinsic phenotypic diversity of embryonic and fetal myoblasts is revealed by …


S Biressi, E Tagliafico, G Lamorte, S Monteverde, E … - Developmental Biology, 2007 - Elsevier
Skeletal muscle development occurs asynchronously and it has been proposed to be dependent
upon the generation of temporally distinct populations of myogenic cells. This long-held hypothesis
has not been tested directly due to the inability to isolate and analyze purified populations ...
Cited by 8 - Related articles - All 3 versions

The Prader-Willi syndrome murine imprinting center is not involved in the spatio- …


F Watrin, E Le Meur, N Roeckel, MA Ripoche, L … - BMC genetics, 2005 - biomedcentral.com
The human Prader-Willi syndrome (PWS) domain and its mouse orthologue include a cluster
of paternally expressed genes which imprinted expression is co-ordinately regulated by an imprinting
center (IC) closely associated to the Snurf-Snrpn gene. Besides their co-regulated ...
Cited by 8 - Related articles - Cached - All 7 versions

Relationships of maternal and paternal birthweights to features of the metabolic …

- nih.gov
SR Veena, S Geetha, SD Leary, J Saperia, DJ Fisher, K … - Diabetologia, 2007 - Springer
Abstract Aims/hypothesis The association between lower birth- weight and metabolic syndrome
may result from fetal undernutrition (fetal programming hypothesis) and/or genes causing both
low birthweight and insulin resistance (fetal insulin hypothesis). We studied associations ...
Cited by 2 - Related articles - BL Direct - All 10 versions

Cold-induced expression of the VEGF gene in brown adipose tissue is …


JM Fredriksson, H Nikami, J Nedergaard - FEBS letters, 2005 - Elsevier
To examine whether cold-induced vascular endothelial growth factor (VEGF) gene expression
in brown adipose tissue involved generation of hypoxic oxygen levels by thermogenic
processes, we cold-exposed wild-type mice, as well as uncoupling protein-1 (UCP1)- ...
Cited by 3 - Related articles - All 5 versions

Diabetes risk begins in utero


M Woo, ME Patti - Cell metabolism, 2008 - Elsevier
The association between low birth weight and adult disease was first reported by David Barker
(Barker et al., 1989). Barker accessed the records of 15,000 men and women born before 1930
whose medical history was meticulously documented by nurses in Hertfordshire, ...
Cited by 3 - Related articles - All 5 versions

Necdin acts as a transcriptional repressor that interacts with multiple guanosine …


K Matsumoto, H Taniura, T Uetsuki, K Yoshikawa - Gene, 2001 - Elsevier
Necdin is a growth suppressor expressed predominantly in postmitotic neurons, and ectopic
expression of this protein suppresses cell growth. Here we report that Necdin directly binds to
specific DNA sequences and serves as a transcriptional repressor. Polyhistidine-tagged ...
Cited by 20 - Related articles - All 3 versions

Targeted deletion of the MLC1f/3f downstream enhancer results in precocious MLC …


P Jiang, J Song, G Gu, E Slonimsky, E Li, N Rosenthal - Developmental Biology, 2002 - Elsevier
The expression of skeletal muscle contractile proteins is tightly regulated during embryonic
development. In the mouse, the myosin light chain (MLC) 1f/3f gene locus is not activated until
E9.5, exclusively in skeletal muscle precursor cells. A potent enhancer downstream of the ...
Cited by 12 - Related articles - BL Direct - All 4 versions

Myogenic progenitor cells in the mouse embryo are marked by the expression of …


M Buckingham, L Bajard, P Daubas, M Esner, M … - Anatomy and …, 2006 - Springer
Abstract The transcription factors Pax3 and Pax7 are important regulators of myogenic cell
fate, as demon- strated by genetic manipulations in the mouse embryo. Pax3 lies genetically
upstream of MyoD and has also been shown recently to directly control Myf5 tran- ...
Cited by 12 - Related articles - BL Direct - All 4 versions


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