Hecht JT - Search Results

1

Pseudoachondroplasia/COMP - translating from the bench to the bedside.

Posey KL, Alcorn JL, Hecht JT. Posey KL, et al. Among authors: hecht jt. Matrix Biol. 2014 Jul;37:167-73. doi: 10.1016/j.matbio.2014.05.006. Epub 2014 Jun 2. Matrix Biol. 2014. PMID: 24892720 Free PMC article. Review.

2

Mutations in exon 17B of cartilage oligomeric matrix protein (COMP) cause pseudoachondroplasia.

Hecht JT, Nelson LD, Crowder E, Wang Y, Elder FF, Harrison WR, Francomano CA, Prange CK, Lennon GG, Deere M, et al. Hecht JT, et al. Nat Genet. 1995 Jul;10(3):325-9. doi: 10.1038/ng0795-325. Nat Genet. 1995. PMID: 7670471

3

Linkage of typical pseudoachondroplasia to chromosome 19.

Hecht JT, Francomano CA, Briggs MD, Deere M, Conner B, Horton WA, Warman M, Cohn DH, Blanton SH. Hecht JT, et al. Genomics. 1993 Dec;18(3):661-6. doi: 10.1016/s0888-7543(05)80370-2. Genomics. 1993. PMID: 8307577

4

Mosaicism in pseudoachondroplasia.

Ferguson HL, Deere M, Evans R, Rotta J, Hall JG, Hecht JT. Ferguson HL, et al. Among authors: hecht jt. Am J Med Genet. 1997 Jun 13;70(3):287-91. Am J Med Genet. 1997. PMID: 9188668

5

The fate of cartilage oligomeric matrix protein is determined by the cell type in the case of a novel mutation in pseudoachondroplasia.

Maddox BK, Keene DR, Sakai LY, Charbonneau NL, Morris NP, Ridgway CC, Boswell BA, Sussman MD, Horton WA, Bächinger HP, Hecht JT. Maddox BK, et al. Among authors: hecht jt. J Biol Chem. 1997 Dec 5;272(49):30993-7. doi: 10.1074/jbc.272.49.30993. J Biol Chem. 1997. PMID: 9388247 Free article.

6

Characterization of cartilage oligomeric matrix protein (COMP) in human normal and pseudoachondroplasia musculoskeletal tissues.

Hecht JT, Deere M, Putnam E, Cole W, Vertel B, Chen H, Lawler J. Hecht JT, et al. Matrix Biol. 1998 Aug;17(4):269-78. doi: 10.1016/s0945-053x(98)90080-4. Matrix Biol. 1998. PMID: 9749943

7

Identification of twelve mutations in cartilage oligomeric matrix protein (COMP) in patients with pseudoachondroplasia.

Deere M, Sanford T, Ferguson HL, Daniels K, Hecht JT. Deere M, et al. Among authors: hecht jt. Am J Med Genet. 1998 Dec 28;80(5):510-3. doi: 10.1002/(sici)1096-8628(19981228)80:5<510::aid-ajmg14>3.0.co;2-f. Am J Med Genet. 1998. PMID: 9880218

8

Retention of cartilage oligomeric matrix protein (COMP) and cell death in redifferentiated pseudoachondroplasia chondrocytes.

Hecht JT, Montufar-Solis D, Decker G, Lawler J, Daniels K, Duke PJ. Hecht JT, et al. Matrix Biol. 1998 Dec;17(8-9):625-33. doi: 10.1016/s0945-053x(98)90113-5. Matrix Biol. 1998. PMID: 9923655

9

Identification of nine novel mutations in cartilage oligomeric matrix protein in patients with pseudoachondroplasia and multiple epiphyseal dysplasia.

Deere M, Sanford T, Francomano CA, Daniels K, Hecht JT. Deere M, et al. Among authors: hecht jt. Am J Med Genet. 1999 Aug 27;85(5):486-90. doi: 10.1002/(sici)1096-8628(19990827)85:5<486::aid-ajmg10>3.0.co;2-o. Am J Med Genet. 1999. PMID: 10405447

10

Delta 469 mutation in the type 3 repeat calcium binding domain of cartilage oligomeric matrix protein (COMP) disrupts calcium binding.

Hou J, Putkey JA, Hecht JT. Hou J, et al. Among authors: hecht jt. Cell Calcium. 2000 Jun;27(6):309-14. doi: 10.1054/ceca.2000.0125. Cell Calcium. 2000. PMID: 11013461

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