AG08467
                                                
                                                Fibroblast from Gingival, Gum
                                                
                                                
                                             
                                            
                                                
                                                    
                                                         Description:
                                                    
                                                    
                                                         
                                                            
                                                            HUTCHINSON-GILFORD PROGERIA SYNDROME; HGPS 
                                                            
                                                    
                                                 
                                                
                                                
                                                
                                                
                                             
                                         
                                     
                                    
                                        
                                            
                                            
                                            
                                            
                                                
                                                    
                                                        
                                                            
                                                            
                                                                
                                                                    
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                                                                            Repository
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                                                                            NIA Aging Cell Culture Repository
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	| Subcollection | 
	Heritable Diseases | 
 
                                                                
                                                                
                                                                
                                                                
                                                                
                                                                
                                                                
                                                                    
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                                                                            Biopsy Source
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                                                                            Gum
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                                                                            Cell Type
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                                                                            Fibroblast
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                                                                            Tissue Type
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                                                                            Gingival
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                                                                            Transformant
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                                                                            Untransformed
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                                                                            Sample Source
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                                                                            Fibroblast from Gingival, Gum
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                                                                        | 
                                                                            Race
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                                                                            White
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                                                                            Family Member
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                                                                            1
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                                                                            Relation to Proband
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                                                                            proband
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                                                                            Confirmation
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                                                                            Clinical summary/Case history
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                                                                            Species
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                                                                            Homo sapiens
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                                                                            Common Name
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                                                                            Human
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                                                                            Remarks
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	| Remarks | 
	Donor showed loss of subcutaneous fat, a beak nose, osteoarthritis, venous prominence, and an elevated urinary glucosaminoglycan level, but no alopecia. Low weight and dislocated hips present at birth. Marfan features have also developed. The biopsy was taken ante-mortem on 10/25/85. The culture was initiated using explants of minced gingival tissue. The cell morphology is fibroblast-like.  A skin fibroblast culture from same donor is AG08466. | 
 
                                                                
                                                             
                                                            
                                                            
                                                         
                                                     
                                                 
                                                
                                                    
                                                        
                                                            
                                                            
                                                            
                                                                
	| Csoka AB, Cao H, Sammak PJ, Constantinescu D, Schatten GP, Hegele RA, Novel lamin A/C gene (LMNA) mutations in atypical progeroid syndromes. J Med Genet41(4):304-8 2004 | 
 
	| PubMed ID: 15060110 | 
 
                                                                
                                                             
                                                            
                                                         
                                                     
                                                 
                                                
                                                
                                                
                                                    
                                                        
                                                            
                                                            
                                                                
	| Passage Frozen | 
	3 | 
 
	| Split Ratio | 
	1:3 | 
 
	| Temperature | 
	37 C | 
 
	| Percent CO2 | 
	5% | 
 
	| Medium | 
	Eagle's Minimum Essential Medium with Earle's salts and non-essential amino acids with 2mM L-glutamine or equivalent | 
 
	| Serum | 
	15% fetal bovine serum Not inactivated           | 
 
	| Substrate | 
	None specified | 
 
	| Subcultivation Method | 
	trypsin-EDTA | 
 
	| Supplement | 
	- | 
 
                                                                
                                                                
                                                             
                                                         
                                                     
                                                 
                                             
                                         
                                     
                                 
                                
                             
                         
                     
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