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Items: 1 to 20 of 28

1.

Raster3D: photorealistic molecular graphics.

Merritt EA, Bacon DJ.

Methods Enzymol. 1997;277:505-24. No abstract available.

PMID:
18488322
2.

Human capillary morphogenesis protein 2 functions as an anthrax toxin receptor.

Scobie HM, Rainey GJ, Bradley KA, Young JA.

Proc Natl Acad Sci U S A. 2003 Apr 29;100(9):5170-4. Epub 2003 Apr 16.

3.

Buried water molecules contribute to the conformational stability of a protein.

Takano K, Yamagata Y, Yutani K.

Protein Eng. 2003 Jan;16(1):5-9.

PMID:
12646687
4.
6.

The gene for juvenile hyaline fibromatosis maps to chromosome 4q21.

Rahman N, Dunstan M, Teare MD, Hanks S, Edkins SJ, Hughes J, Bignell GR, Mancini G, Kleijer W, Campbell M, Keser G, Black C, Williams N, Arbour L, Warman M, Superti-Furga A, Futreal PA, Pope FM.

Am J Hum Genet. 2002 Oct;71(4):975-80. Epub 2002 Sep 4.

7.

A high-resolution recombination map of the human genome.

Kong A, Gudbjartsson DF, Sainz J, Jonsdottir GM, Gudjonsson SA, Richardsson B, Sigurdardottir S, Barnard J, Hallbeck B, Masson G, Shlien A, Palsson ST, Frigge ML, Thorgeirsson TE, Gulcher JR, Stefansson K.

Nat Genet. 2002 Jul;31(3):241-7. Epub 2002 Jun 10.

PMID:
12053178
8.

Domain structure and organisation in extracellular matrix proteins.

Hohenester E, Engel J.

Matrix Biol. 2002 Mar;21(2):115-28. Review.

PMID:
11852228
10.

Nonmuscle myosin heavy chain IIA mutations define a spectrum of autosomal dominant macrothrombocytopenias: May-Hegglin anomaly and Fechtner, Sebastian, Epstein, and Alport-like syndromes.

Heath KE, Campos-Barros A, Toren A, Rozenfeld-Granot G, Carlsson LE, Savige J, Denison JC, Gregory MC, White JG, Barker DF, Greinacher A, Epstein CJ, Glucksman MJ, Martignetti JA.

Am J Hum Genet. 2001 Nov;69(5):1033-45. Epub 2001 Oct 4.

11.

Mutations in the region encoding the von Willebrand factor A domain of matrilin-3 are associated with multiple epiphyseal dysplasia.

Chapman KL, Mortier GR, Chapman K, Loughlin J, Grant ME, Briggs MD.

Nat Genet. 2001 Aug;28(4):393-6.

PMID:
11479597
12.

Functional interplay between type I collagen and cell surface matrix metalloproteinase activity.

Ellerbroek SM, Wu YI, Overall CM, Stack MS.

J Biol Chem. 2001 Jul 6;276(27):24833-42. Epub 2001 Apr 30.

13.

Infantile systemic hyalinosis in siblings: clinical report, biochemical and ultrastructural findings, and review of the literature.

Stucki U, Spycher MA, Eich G, Rossi A, Sacher P, Steinmann B, Superti-Furga A.

Am J Med Genet. 2001 Apr 22;100(2):122-9.

PMID:
11298373
14.

Two siblings with juvenile hyaline fibromatosis: case reports and review of the literature.

Keser G, Karabulut B, Oksel F, Calli C, Ustün EE, Akalin T, Koçanaoğullari H, Gümüdiş G, Doğanavşargil E.

Clin Rheumatol. 1999;18(3):248-52. Review.

PMID:
11206353
15.

Bone morphogenetic protein-3 is a negative regulator of bone density.

Daluiski A, Engstrand T, Bahamonde ME, Gamer LW, Agius E, Stevenson SL, Cox K, Rosen V, Lyons KM.

Nat Genet. 2001 Jan;27(1):84-8.

PMID:
11138004
16.

Laminins and human disease.

McGowan KA, Marinkovich MP.

Microsc Res Tech. 2000 Nov 1;51(3):262-79. Review.

PMID:
11054876
17.

Laminins: an overview.

Jones JC, Dehart GW, Gonzales M, Goldfinger LE.

Microsc Res Tech. 2000 Nov 1;51(3):211-3. Review. No abstract available.

PMID:
11054871
18.

Form and function: the laminin family of heterotrimers.

Colognato H, Yurchenco PD.

Dev Dyn. 2000 Jun;218(2):213-34. Review.

19.

Mutation analysis and molecular genetics of epidermolysis bullosa.

Pulkkinen L, Uitto J.

Matrix Biol. 1999 Feb;18(1):29-42. Review.

PMID:
10367729
20.

Juvenile hyaline fibromatosis: clinical heterogeneity in three patients.

Mancini GM, Stojanov L, Willemsen R, Kleijer WJ, Huijmans JG, van Diggelen OP, de Klerk JB, Vuzevski VD, Oranje AP.

Dermatology. 1999;198(1):18-25.

PMID:
10026396

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