Literatur
-
1
de Boer J, Andressoo J O, de Wit J, Huijmans J, Beems R B, van Steeg H, Weeda G, van der Horst G T, van Leeuwen W, Themmen A P, Meradji M, Hoeijmakers J H.
Premature aging in mice deficient in DNA repair and
transcription.
Science.
2002;
296
1276-1279
-
2 Black D M, Bouillon R, Ducy P, Miller P D, Papapoulos S E, Ralston S H, Ross P, Schipani E, Seeman E, Strewler G J, Teti A, Thakker R V, Vanderschueren D. Meeting report from the 24th annual meeting of the American
Society for Bone and Mineral
Research. http//www.bonekey-ibms.org/cgi/content/full/ibmske;2002065v1 2002
-
3
Duncan E L, Brown M A, Sinsheimer J, Bell J, Carr A J, Wordsworth B P, Wass J AH.
Suggestive linkage of the parathyroid receptor type 1 to
osteoporosis.
J Bone Miner
Res.
1999;
14
19 931 999
-
4
Chan G K, Duque G.
Age-related bone loss: old bone, new
facts.
Gerontology.
2002;
48
62-71
-
5
Goto M.
Werner’s syndrome: from clinics to
genetics.
Clin Exp
Rheumatol.
2000;
18
760-766
-
6
Grant S F, Reid D M, Blake G, Herd R, Fogelman I, Ralston S H.
Reduced bone density and osteoporosis associated with a
polymorphic Sp1 binding site in the collagen type I alpha 1 gene.
Nat
Genet.
1996;
14
203-205
-
7
Hock J M, Krishnan V, Onyia J E, Bidwell J P, Milas J, Stanislaus D.
Osteoblast apoptosis and bone turnover.
J Bone
Miner
Res.
2001;
16
975-984
-
8
Inzerillo A, Zaidi M.
Osteoporosis: Trends and Intervention.
Mt Sinai J
Med.
2002;
69
220-231
-
9
Janssens K, VanHul W.
Molecular genetics of too much bone.
Hum Mol
Genet.
2002;
11
2385-2393
-
10
Kronenberg H M.
NPT2a - The key to phosphate homeostasis.
N
Engl J
Med.
2002;
347
1022-1024
-
11
Mohaghegh P, Hickson.
Premature aging in RecQ helicase-deficient human
syndromes.
Int J Biochem Cell
Biol.
2002;
34
1496-1501
-
12
Obermayer-Pietsch B, Chararas C, Kotschan S, Walter D, Leb G.
Genetic background of osteoporosis.
Acta Med
Austriaca.
2000;
27
18-22
-
13
Peacock M, Turner C H, Econs M J, Foroud T.
Genetics of osteoporosis.
Endocrine
Rev.
2002;
23
303-326
-
14
Prie D, Huart V, Bakouh N, Planelles G, Dellis O, Gerard B, Hulin P, Benque-Blanchet F, Silve C, Grandchamp B, Friedlander G.
Nephrolithiasis and osteoporosis associated with
hypophosphatemia caused by mutations in the type 2a sodium-phosphate
cotransporter.
N Engl J
Med.
2002;
347
983-991
-
15
Ralston S H.
Genetic control of susceptibility to
osteoporosis.
J Clin Endocrinol
Metab.
2002;
87
2460-2466
-
16
Tyner S D, Venkatachalam S, Choi J, Jones S, Ghebranious N, Igelmann H, Lu X, Soron G, Cooper B, Brayton C, Hee, Park S, Thompson T, Karsenty G, Bradley A, Donehower L A.
p53 mutant mice that display early ageing-associated
phenotypes.
Nature.
2002;
415
45-53
-
17
Uitterlinden A G, Pols H AP, Burger H, Huang Q, VanDaele P LA, VanDujn C M, Hofman A, Birkenhäger J C, VanLeuwen J PTM.
A large-scale population-based study of the association of
vitamin D receptor gene polymorphisms with bone mineral density.
J
Bone Miner
Res.
1996;
11
1241-1248
Prof. Dr. F. Jakob
Lehrstuhl für Orthopädie, Universität
Würzburg
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97074 Würzburg
