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Journal Abstract Search
105 related items for PubMed ID: 6391574
1. Craniofacial consequences of connective tissue disorders in mice. Brown KS, Hetzel SC, Harne LC. Birth Defects Orig Artic Ser; 1984; 20(3):113-36. PubMed ID: 6391574 [No Abstract] [Full Text] [Related]
2. [Gene errors as a cause of rare and common connective tissue diseases]. Ala-Kokko L, Kuivaniemi H. Duodecim; 1994; 110(7):731-9. PubMed ID: 8542828 [No Abstract] [Full Text] [Related]
3. Renal dysplasia and chondrodysplasia in the ch hydrocephalic mouse: a cellular model of defective differentiation and organization. Richardson RR, Reyes MG. Mt Sinai J Med; 1984 Apr; 51(2):188-96. PubMed ID: 6427604 [No Abstract] [Full Text] [Related]
4. Scanning electron microscopy of cartilage in mice with hereditary chondrodysplasia. Seegmiller RE, Monson CB. Scan Electron Microsc; 1982 Apr; (Pt 3):1259-67. PubMed ID: 6820573 [Abstract] [Full Text] [Related]
5. A microanalytical study of bone mineral in a transgenic mouse model for brittle bone disease. Cassella JP, Ali SY. Cell Biol Int; 1993 Jul; 17(7):693-4. PubMed ID: 8374602 [No Abstract] [Full Text] [Related]
6. Mineral changes in a transgenic mouse model for osteogenesis imperfecta. Cassella JP, Pereira R, Prockop DJ, Ali SY. Br J Biomed Sci; 1996 Jun; 53(2):108-15. PubMed ID: 8757687 [Abstract] [Full Text] [Related]
7. [Current problems pertaining to the histochemistry of various normal and pathologic calcifying matrices]. Bonucci E. Riv Istochim Norm Patol; 1972 Jun; 17(3):153-234. PubMed ID: 4345656 [No Abstract] [Full Text] [Related]
8. Calcification mechanisms. Howell DS. Isr J Med Sci; 1976 Feb; 12(2):91-7. PubMed ID: 770394 [No Abstract] [Full Text] [Related]
9. Connective tissue disease: closing on the threshold. Robinson A. CMAJ; 1993 Oct 01; 149(7):988-91. PubMed ID: 8402427 [No Abstract] [Full Text] [Related]
10. Disorders of connective tissue metabolism as related to the skin. Byers PH, Barsh GS, Holbrook KA. Birth Defects Orig Artic Ser; 1981 Oct 01; 17(2):147-72. PubMed ID: 7039715 [No Abstract] [Full Text] [Related]
11. [Cytological aspects of bone formation]. Knese KH. Internist (Berl); 1966 Nov 01; 7(11):581-90. PubMed ID: 4229859 [No Abstract] [Full Text] [Related]
12. Mice lacking link protein develop dwarfism and craniofacial abnormalities. Watanabe H, Yamada Y. Nat Genet; 1999 Feb 01; 21(2):225-9. PubMed ID: 9988279 [Abstract] [Full Text] [Related]
13. VEGFA is necessary for chondrocyte survival during bone development. Zelzer E, Mamluk R, Ferrara N, Johnson RS, Schipani E, Olsen BR. Development; 2004 May 01; 131(9):2161-71. PubMed ID: 15073147 [Abstract] [Full Text] [Related]
14. Merging the old skeletal biology with the new. I. Intramembranous ossification, endochondral ossification, ectopic bone, secondary cartilage, and pathologic considerations. Cohen MM. J Craniofac Genet Dev Biol; 2000 May 01; 20(2):84-93. PubMed ID: 11100738 [Abstract] [Full Text] [Related]
15. Variability of embryonic development among three inbred strains of mice. Miyake T, Cameron AM, Hall BK. Growth Dev Aging; 1997 May 01; 61(3-4):141-55. PubMed ID: 9546105 [Abstract] [Full Text] [Related]
16. Regulatory mechanisms in the development of bone and cartilage: the use of tissue culture techniques in the study of the development of embryonic bone and cartilage: a perspective. Nijweide PJ, Burger EH, Hekkelman JW, Herrmann-Erlee MP, Gaillard PJ. Prog Clin Biol Res; 1982 May 01; 101():457-80. PubMed ID: 7156153 [Abstract] [Full Text] [Related]
19. Effect of ultrastructural changes on the toughness of bone. Nyman JS, Reyes M, Wang X. Micron; 2005 Jun 09; 36(7-8):566-82. PubMed ID: 16169742 [Abstract] [Full Text] [Related]
20. Cellular analysis of limb development in the mouse mutant hypodactyly. Robertson KE, Chapman MH, Adams A, Tickle C, Darling SM. Dev Genet; 1996 Jun 09; 19(1):9-25. PubMed ID: 8792605 [Abstract] [Full Text] [Related] Page: [Next] [New Search]