Familial glucocorticoid deficiency syndromes Friedrich C. Luft Clinical Implications 12 June 2002 Pages: 385 - 386
Depletion of the other genome-mitochondrial DNA depletion syndromes in humans Orly ElpelegHanna MandelAnn Saada Review 24 May 2002 Pages: 389 - 396
CD4+ T helper cells and the role they play in viral control Philip J. NorrisEric S. Rosenberg Review 12 April 2002 Pages: 397 - 405
Functional relationships between three novel homozygous mutations in the ACTH receptor gene and familial glucocorticoid deficiency A. PenhoatD. NavilleM. Bégeot Original Article 11 April 2002 Pages: 406 - 411
Mutations in the cardiac myosin-binding protein C gene are the predominant cause of familial hypertrophic cardiomyopathy in eastern Finland Pertti JääskeläinenJohanna KuusistoMarkku Laakso Original Article 11 April 2002 Pages: 412 - 422
Mutations in hepatocyte nuclear factor 4α (HNF4α) gene associated with diabetes result in greater loss of HNF4α function in pancreatic β-cells than in nonpancreatic β-cells and in reduced activation of the apolipoprotein CIII promoter in hepatic cells Bénédicte OxombreEricka MoermanBernard Laine Original Article 08 May 2002 Pages: 423 - 430
Expression and mutation analysis of BRUNOL3, a candidate gene for heart and thymus developmental defects associated with partial monosomy 10p P. LichtnerT. Attié-BitachM. Vekemans Original Article 04 April 2002 Pages: 431 - 442
Stimulation of human natural interferon-α response via paramyxovirus hemagglutinin lectin-cell interaction Jinyang ZengPhilippe FournierVolker Schirrmacher Original Article 07 May 2002 Pages: 443 - 451
Association of polymorphisms of the estrogen receptor α gene with bone mineral density of the femoral neck in elderly Japanese women Yoshiji YamadaFujiko AndoHiroshi Shimokata Original Article 04 June 2002 Pages: 452 - 460
