Pages that link to "Q38354296"

The following pages link to Prevalence of mutations in AGPAT2 among human lipodystrophies (Q38354296):

Displaying 37 items.

• Cloning and characterization of murine 1-acyl-sn-glycerol 3-phosphate acyltransferases and their regulation by PPARalpha in murine heart (Q24303951) (← links)
• Seipin deficiency alters fatty acid Delta9 desaturation and lipid droplet formation in Berardinelli-Seip congenital lipodystrophy (Q24320010) (← links)
• Clinical review#: Lipodystrophies: genetic and acquired body fat disorders (Q28246346) (← links)
• Agpat6 deficiency causes subdermal lipodystrophy and resistance to obesity (Q28504549) (← links)
• Agpat6--a novel lipid biosynthetic gene required for triacylglycerol production in mammary epithelium (Q28513321) (← links)
• Fat poetry: a kingdom for PPAR gamma (Q33437489) (← links)
• What's the matter with MAT? Marrow adipose tissue, metabolism, and skeletal health (Q33726338) (← links)
• Towards a mechanistic understanding of lipodystrophy and seipin functions (Q34278915) (← links)
• Phenotypic heterogeneity in biochemical parameters correlates with mutations in AGPAT2 or Seipin genes among Berardinelli-Seip congenital lipodystrophy patients (Q34487883) (← links)
• The human obesity gene map: the 2005 update (Q34567973) (← links)
• Sequential regulation of diacylglycerol acyltransferase 2 expression by CAAT/enhancer-binding protein beta (C/EBPbeta) and C/EBPalpha during adipogenesis (Q34628676) (← links)
• Mammalian triacylglycerol metabolism: synthesis, lipolysis, and signaling (Q35235426) (← links)
• Berardinelli-Seip syndrome and achalasia: a shared pathomechanism? (Q35762169) (← links)
• Barraquer-Simons syndrome: a rare form of acquired lipodystrophy. (Q35961396) (← links)
• Clinical Features and Management of Non-HIV-Related Lipodystrophy in Children: A Systematic Review (Q36223346) (← links)
• Leptin therapy for partial lipodystrophy linked to a PPAR-gamma mutation (Q36962898) (← links)
• Lipodystrophies: disorders of adipose tissue biology (Q37219869) (← links)
• The human lipodystrophy gene product Berardinelli-Seip congenital lipodystrophy 2/seipin plays a key role in adipocyte differentiation (Q37369119) (← links)
• Divergent metabolic phenotype between two sisters with congenital generalized lipodystrophy due to double AGPAT2 homozygous mutations. a clinical, genetic and in silico study. (Q37538539) (← links)
• Exploring the pathophysiology behind the more common genetic and acquired lipodystrophies (Q38155007) (← links)
• Congenital lipodystrophies and dyslipidemias (Q38232357) (← links)
• Congenital generalized lipodystrophies--new insights into metabolic dysfunction (Q38560271) (← links)
• Identification of a novel nonsense mutation and a missense substitution in the AGPAT2 gene causing congenital generalized lipodystrophy type 1. (Q42426413) (← links)
• Type II nuclear hormone receptors, coactivator, and target gene repression in adipose tissue in the acute-phase response (Q42798829) (← links)
• Congenital generalized lipodystrophy: identification of novel variants and expansion of clinical spectrum. (Q50442875) (← links)
• Description of an AGPAT2 pathologic allelic variant in a 54-year-old Caucasian woman with Berardinelli-Seip syndrome (Q51439894) (← links)
• Transcriptomic characterization of the long-term dihydrotestosterone effects in adipose tissue. (Q53553914) (← links)
• Síndrome de Berardinelli-Seip: descrição genética e metabólica de cinco pacientes (Q57234963) (← links)
• A Single Complex Allele in a Patient With Partial Lipodystrophy (Q57491600) (← links)
• Membrane topology of the human seipin protein (Q57567852) (← links)
• Current literature in diabetes (Q73891900) (← links)
• Genetic basis of congenital generalized lipodystrophy (Q79162420) (← links)
• A Taiwanese boy with congenital generalized lipodystrophy caused by homozygous Ile262fs mutation in the BSCL2 gene (Q82711794) (← links)
• Acromegaly with congenital generalized lipodystrophy - two rare insulin resistance conditions in one patient: a case report (Q89807409) (← links)
• Congenital Generalized Lipoatrophy (Berardinelli-Seip Syndrome) Type 1: Description of Novel AGPAT2 Homozygous Variants Showing the Highly Heterogeneous Presentation of the Disease (Q89965097) (← links)
• A New Compound Heterozygous Mutation Of BSCL2 In A Chinese Zhuang Ethnic Family With Congenital Generalized Lipodystrophy (Q91866383) (← links)
• The Structure and Function of Acylglycerophosphate Acyltransferase 4/ Lysophosphatidic Acid Acyltransferase Delta (AGPAT4/LPAATδ) (Q92715789) (← links)