-
1
-
-
25844487690
-
The phenotype of fibrodysplasia ossificans progressiva
-
Kaplan F.S., et al. The phenotype of fibrodysplasia ossificans progressiva. Clin. Rev. Bone Miner. Metab. 3 (2005) 183-188
-
(2005)
Clin. Rev. Bone Miner. Metab.
, vol.3
, pp. 183-188
-
-
Kaplan, F.S.1
-
2
-
-
40149099148
-
Fibrodysplasia ossificans progressiva
-
Kaplan F.S., et al. Fibrodysplasia ossificans progressiva. Best Pract. Res. Clin. Rheumatol. 22 (2008) 191-205
-
(2008)
Best Pract. Res. Clin. Rheumatol.
, vol.22
, pp. 191-205
-
-
Kaplan, F.S.1
-
3
-
-
33646348736
-
A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva
-
Shore E.M., et al. A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva. Nat. Genet. 38 (2006) 525-527
-
(2006)
Nat. Genet.
, vol.38
, pp. 525-527
-
-
Shore, E.M.1
-
4
-
-
0027403045
-
The natural history of heterotopic ossification in patients who have fibrodysplasia ossificans progressiva
-
Cohen R.B., et al. The natural history of heterotopic ossification in patients who have fibrodysplasia ossificans progressiva. J. Bone Joint Surg. 75-A (1993) 215-219
-
(1993)
J. Bone Joint Surg.
, vol.75 -A
, pp. 215-219
-
-
Cohen, R.B.1
-
5
-
-
0028287031
-
Age and joint-specific risk of initial heterotopic ossification in patients who have fibrodysplasia ossificans progressiva
-
Rocke D.M., et al. Age and joint-specific risk of initial heterotopic ossification in patients who have fibrodysplasia ossificans progressiva. Clin. Orthop. Rel. Res. 301 (1994) 243-248
-
(1994)
Clin. Orthop. Rel. Res.
, vol.301
, pp. 243-248
-
-
Rocke, D.M.1
-
6
-
-
0027477670
-
The histopathology of fibrodysplasia ossificans progressiva: an endochondral process
-
Kaplan F.S., and Zasloff M.A. The histopathology of fibrodysplasia ossificans progressiva: an endochondral process. J. Bone Joint Surg. 75-A (1993) 220-230
-
(1993)
J. Bone Joint Surg.
, vol.75 -A
, pp. 220-230
-
-
Kaplan, F.S.1
Zasloff, M.A.2
-
7
-
-
25844456883
-
The fibrodysplasia ossificans progressiva lesion
-
Pignolo R.J., et al. The fibrodysplasia ossificans progressiva lesion. Clin. Rev. Bone Miner. Metab. 3 (2005) 195-200
-
(2005)
Clin. Rev. Bone Miner. Metab.
, vol.3
, pp. 195-200
-
-
Pignolo, R.J.1
-
8
-
-
0031964498
-
Catastrophic falls in patients who have fibrodysplasia ossificans progressiva
-
Glaser D.L., et al. Catastrophic falls in patients who have fibrodysplasia ossificans progressiva. Clin. Orthop. Rel. Res. 346 (1998) 110-116
-
(1998)
Clin. Orthop. Rel. Res.
, vol.346
, pp. 110-116
-
-
Glaser, D.L.1
-
9
-
-
0029915544
-
Submandibular swelling in patients with fibrodysplasia ossificans progressiva
-
Janoff H.B., et al. Submandibular swelling in patients with fibrodysplasia ossificans progressiva. Otolaryngol. Head Neck Surg. 114 (1996) 599-604
-
(1996)
Otolaryngol. Head Neck Surg.
, vol.114
, pp. 599-604
-
-
Janoff, H.B.1
-
10
-
-
0029012733
-
Permanent heterotopic ossification at the injection site after diphtheria-tetanus-pertussis immunizations in children who have fibrodysplasia ossificans progressiva
-
Lanchoney T.F., et al. Permanent heterotopic ossification at the injection site after diphtheria-tetanus-pertussis immunizations in children who have fibrodysplasia ossificans progressiva. J. Pediatr. 126 (1995) 762-764
-
(1995)
J. Pediatr.
, vol.126
, pp. 762-764
-
-
Lanchoney, T.F.1
-
11
-
-
0029678648
-
Severe restriction in jaw movement after routine injection of local anesthetic in patients who have fibrodysplasia ossificans progressiva
-
Luchetti W., et al. Severe restriction in jaw movement after routine injection of local anesthetic in patients who have fibrodysplasia ossificans progressiva. Oral Surg. Oral Med. Oral Pathol. Oral Radiol. Endod. 81 (1995) 21-25
-
(1995)
Oral Surg. Oral Med. Oral Pathol. Oral Radiol. Endod.
, vol.81
, pp. 21-25
-
-
Luchetti, W.1
-
12
-
-
0031044744
-
Limb swelling in patients who have fibrodysplasia ossificans progressiva
-
Moriatis J.M., et al. Limb swelling in patients who have fibrodysplasia ossificans progressiva. Clin. Orthop. Rel. Res. 336 (1997) 247-253
-
(1997)
Clin. Orthop. Rel. Res.
, vol.336
, pp. 247-253
-
-
Moriatis, J.M.1
-
13
-
-
2942750256
-
Influenza-like viral illnesses and flare-ups of fibrodysplasia ossificans progressiva (FOP)
-
Scarlett R.F., et al. Influenza-like viral illnesses and flare-ups of fibrodysplasia ossificans progressiva (FOP). Clin. Orthop. Rel. Res. 423 (2004) 275-279
-
(2004)
Clin. Orthop. Rel. Res.
, vol.423
, pp. 275-279
-
-
Scarlett, R.F.1
-
14
-
-
0028115971
-
Spinal deformity in patients who have fibrodysplasia ossificans progressiva
-
Shah P.B., et al. Spinal deformity in patients who have fibrodysplasia ossificans progressiva. J. Bone Joint Surg. 76-A (1994) 1442-1450
-
(1994)
J. Bone Joint Surg.
, vol.76 -A
, pp. 1442-1450
-
-
Shah, P.B.1
-
15
-
-
0031974285
-
Pulmonary and cardiac function in advanced fibrodysplasia ossificans progressiva
-
Kussmaul W.G., et al. Pulmonary and cardiac function in advanced fibrodysplasia ossificans progressiva. Clin. Orthop. Rel. Res. 346 (1998) 104-109
-
(1998)
Clin. Orthop. Rel. Res.
, vol.346
, pp. 104-109
-
-
Kussmaul, W.G.1
-
16
-
-
25844510176
-
Thoracic insufficiency syndrome in patients with fibrodysplasia ossificans progressiva
-
Kaplan F.S., and Glaser D.L. Thoracic insufficiency syndrome in patients with fibrodysplasia ossificans progressiva. Clin. Rev. Bone Miner. Metab. 3 (2005) 213-216
-
(2005)
Clin. Rev. Bone Miner. Metab.
, vol.3
, pp. 213-216
-
-
Kaplan, F.S.1
Glaser, D.L.2
-
17
-
-
25844453495
-
The genetics of fibrodysplasia ossificans progressiva
-
Shore E.M., et al. The genetics of fibrodysplasia ossificans progressiva. Clin. Rev. Bone Miner. Metab. 3 (2005) 201-204
-
(2005)
Clin. Rev. Bone Miner. Metab.
, vol.3
, pp. 201-204
-
-
Shore, E.M.1
-
18
-
-
25844523629
-
Iatrogenic harm caused by diagnostic errors in fibrodysplasia ossificans progressiva
-
Kitterman J.A., et al. Iatrogenic harm caused by diagnostic errors in fibrodysplasia ossificans progressiva. Pediatrics 116 (2005) 654-661
-
(2005)
Pediatrics
, vol.116
, pp. 654-661
-
-
Kitterman, J.A.1
-
19
-
-
44449166223
-
Early diagnosis of fibrodysplasia ossificans progressiva
-
Kaplan F.S., et al. Early diagnosis of fibrodysplasia ossificans progressiva. Pediatrics 121 (2008) e1295-e1300
-
(2008)
Pediatrics
, vol.121
-
-
Kaplan, F.S.1
-
20
-
-
25844529319
-
Developmental anomalies of the cervical spine in patients with fibrodysplasia ossificans progressiva are distinctly different from those in patients with Klippel-Feil syndrome
-
Schaffer A., et al. Developmental anomalies of the cervical spine in patients with fibrodysplasia ossificans progressiva are distinctly different from those in patients with Klippel-Feil syndrome. Spine 30 (2005) 1379-1385
-
(2005)
Spine
, vol.30
, pp. 1379-1385
-
-
Schaffer, A.1
-
21
-
-
38949093587
-
Proximal tibial osteochondromas in patients with fibrodysplasia ossificans progressiva
-
Deirmengian G.K., et al. Proximal tibial osteochondromas in patients with fibrodysplasia ossificans progressiva. J. Bone Joint Surg. Am. 90 (2008) 366-374
-
(2008)
J. Bone Joint Surg. Am.
, vol.90
, pp. 366-374
-
-
Deirmengian, G.K.1
-
22
-
-
25844516368
-
Three pairs of monozygotic twins with fibrodysplasia ossificans progressiva: the role of environment in the progression of heterotopic ossification
-
Hebela N., et al. Three pairs of monozygotic twins with fibrodysplasia ossificans progressiva: the role of environment in the progression of heterotopic ossification. Clin. Rev. Bone Miner. Metab. 3 (2005) 205-208
-
(2005)
Clin. Rev. Bone Miner. Metab.
, vol.3
, pp. 205-208
-
-
Hebela, N.1
-
23
-
-
0025307333
-
Fibrodysplasia ossificans progressiva: a clue from the fly?
-
Kaplan F.S., et al. Fibrodysplasia ossificans progressiva: a clue from the fly?. Calcif. Tissue Int. 47 (1990) 117-125
-
(1990)
Calcif. Tissue Int.
, vol.47
, pp. 117-125
-
-
Kaplan, F.S.1
-
24
-
-
0038035670
-
Paresis of a bone morphogenetic protein-antagonist response in a genetic disorder of heterotopic skeletogenesis
-
Ahn J., et al. Paresis of a bone morphogenetic protein-antagonist response in a genetic disorder of heterotopic skeletogenesis. J. Bone Joint Surg. 85-A (2003) 667-674
-
(2003)
J. Bone Joint Surg.
, vol.85 -A
, pp. 667-674
-
-
Ahn, J.1
-
25
-
-
37249016863
-
Dysregulated BMP signaling and enhanced osteogenic differentiation of connective tissue progenitor cells from patients with fibrodysplasia ossificans progressiva
-
Billings P.C., et al. Dysregulated BMP signaling and enhanced osteogenic differentiation of connective tissue progenitor cells from patients with fibrodysplasia ossificans progressiva. J. Bone Miner. Res. 23 (2008) 305-313
-
(2008)
J. Bone Miner. Res.
, vol.23
, pp. 305-313
-
-
Billings, P.C.1
-
26
-
-
33646865518
-
Dysregulation of the BMP-p38 MAPK signaling pathway in cells from patients with fibrodysplasia ossificans progressiva (FOP)
-
Fiori J.L., et al. Dysregulation of the BMP-p38 MAPK signaling pathway in cells from patients with fibrodysplasia ossificans progressiva (FOP). J. Bone Miner. Res. 21 (2006) 902-909
-
(2006)
J. Bone Miner. Res.
, vol.21
, pp. 902-909
-
-
Fiori, J.L.1
-
27
-
-
0031059563
-
Bone morphogenetic protein 2/4 in early fibromatous lesions of fibrodysplasia ossificans progressiva
-
Gannon F.H., et al. Bone morphogenetic protein 2/4 in early fibromatous lesions of fibrodysplasia ossificans progressiva. Hum. Pathol. 28 (1997) 339-343
-
(1997)
Hum. Pathol.
, vol.28
, pp. 339-343
-
-
Gannon, F.H.1
-
28
-
-
4644264945
-
Transgenic mice overexpressing BMP4 develop a fibrodysplasia ossificans progressiva (FOP)-like phenotype
-
Kan L., et al. Transgenic mice overexpressing BMP4 develop a fibrodysplasia ossificans progressiva (FOP)-like phenotype. Am. J. Pathol. 165 (2004) 1107-1115
-
(2004)
Am. J. Pathol.
, vol.165
, pp. 1107-1115
-
-
Kan, L.1
-
29
-
-
25844482558
-
Dysregulation of BMP4 receptor trafficking and signaling in fibrodysplasia ossificans progressiva
-
Kaplan F.S., et al. Dysregulation of BMP4 receptor trafficking and signaling in fibrodysplasia ossificans progressiva. Clin. Rev. Bone Miner. Metab. 3 (2005) 217-223
-
(2005)
Clin. Rev. Bone Miner. Metab.
, vol.3
, pp. 217-223
-
-
Kaplan, F.S.1
-
30
-
-
33744773190
-
Dysregulation of the BMP4 signaling pathway in fibrodysplasia ossificans progressiva
-
Kaplan F.S., et al. Dysregulation of the BMP4 signaling pathway in fibrodysplasia ossificans progressiva. Ann. N. Y. Acad. Sci. 1068 (2006) 54-65
-
(2006)
Ann. N. Y. Acad. Sci.
, vol.1068
, pp. 54-65
-
-
Kaplan, F.S.1
-
31
-
-
0037337134
-
Bone morphogenetic protein 4 regulation in fibrodysplasia ossificans progressiva
-
Olmsted E.A., et al. Bone morphogenetic protein 4 regulation in fibrodysplasia ossificans progressiva. Clin. Orthop. Rel. Res. 408 (2003) 331-343
-
(2003)
Clin. Orthop. Rel. Res.
, vol.408
, pp. 331-343
-
-
Olmsted, E.A.1
-
32
-
-
20844450082
-
Fibrodysplasia ossificans progressiva (FOP), a disorder of ectopic osteogenesis, misregulates cell surface expression and trafficking of BMPRIA
-
Serrano de la Peña L., et al. Fibrodysplasia ossificans progressiva (FOP), a disorder of ectopic osteogenesis, misregulates cell surface expression and trafficking of BMPRIA. J. Bone Miner. Res. 20 (2005) 1168-1176
-
(2005)
J. Bone Miner. Res.
, vol.20
, pp. 1168-1176
-
-
Serrano de la Peña, L.1
-
33
-
-
0029746491
-
Over-expression of an osteogenic morphogen in fibrodysplasia ossificans progressiva
-
Shafritz A.B., et al. Over-expression of an osteogenic morphogen in fibrodysplasia ossificans progressiva. N. Engl. J. Med. 335 (1996) 555-561
-
(1996)
N. Engl. J. Med.
, vol.335
, pp. 555-561
-
-
Shafritz, A.B.1
-
34
-
-
37249082497
-
Morphogen receptor genes and metamorphogenes: skeleton keys to metamorphosis
-
Kaplan F.S., and Shore E.M. Morphogen receptor genes and metamorphogenes: skeleton keys to metamorphosis. Ann. N. Y. Acad. Sci. 1116 (2007) 113-133
-
(2007)
Ann. N. Y. Acad. Sci.
, vol.1116
, pp. 113-133
-
-
Kaplan, F.S.1
Shore, E.M.2
-
35
-
-
0031984796
-
Acute lymphocytic infiltration in an extremely early lesion of fibrodysplasia ossificans progressiva
-
Gannon F.H., et al. Acute lymphocytic infiltration in an extremely early lesion of fibrodysplasia ossificans progressiva. Clin. Orthop. Rel. Res. 346 (1998) 19-25
-
(1998)
Clin. Orthop. Rel. Res.
, vol.346
, pp. 19-25
-
-
Gannon, F.H.1
-
36
-
-
0027929950
-
Radiographic and scintigraphic features of modeling and remodeling in the heterotopic skeleton of patients who have fibrodysplasia ossificans progressiva
-
Kaplan F.S., et al. Radiographic and scintigraphic features of modeling and remodeling in the heterotopic skeleton of patients who have fibrodysplasia ossificans progressiva. Clin. Orthop. Rel. Res. 304 (1994) 238-247
-
(1994)
Clin. Orthop. Rel. Res.
, vol.304
, pp. 238-247
-
-
Kaplan, F.S.1
-
37
-
-
0035020150
-
Fibrodysplasia ossificans progressiva
-
Mahboubi S., et al. Fibrodysplasia ossificans progressiva. Pediatr. Radiol. 31 (2001) 307-314
-
(2001)
Pediatr. Radiol.
, vol.31
, pp. 307-314
-
-
Mahboubi, S.1
-
38
-
-
33847717517
-
Heparan sulfate proteoglycans (HSPGs) modulate BMP2 osteogenic bioactivity in C2C12 cells
-
Jiao X., et al. Heparan sulfate proteoglycans (HSPGs) modulate BMP2 osteogenic bioactivity in C2C12 cells. J. Biol. Chem. 282 (2007) 1080-1086
-
(2007)
J. Biol. Chem.
, vol.282
, pp. 1080-1086
-
-
Jiao, X.1
-
39
-
-
34248223174
-
A new era of fibrodysplasia ossificans progressiva (FOP): a druggable target for the second skeleton
-
Kaplan F.S., et al. A new era of fibrodysplasia ossificans progressiva (FOP): a druggable target for the second skeleton. Exp. Opin. Biol. Ther. 7 (2004) 705-712
-
(2004)
Exp. Opin. Biol. Ther.
, vol.7
, pp. 705-712
-
-
Kaplan, F.S.1
-
40
-
-
0042978771
-
ALK2 functions as a type I BMP receptor and induces Indian Hedgehog in chondrocytes during skeletal development
-
Zhang D., et al. ALK2 functions as a type I BMP receptor and induces Indian Hedgehog in chondrocytes during skeletal development. J. Bone Miner. Res. 18 (2003) 1593-1604
-
(2003)
J. Bone Miner. Res.
, vol.18
, pp. 1593-1604
-
-
Zhang, D.1
-
41
-
-
49149097175
-
Activation of BMP signaling by the FOP ACVR1 R206H mutation
-
Shen Q., et al. Activation of BMP signaling by the FOP ACVR1 R206H mutation. J. Bone Miner. Res. 22 Suppl. 1 (2007) S43
-
(2007)
J. Bone Miner. Res.
, vol.22
, Issue.SUPPL. 1
-
-
Shen, Q.1
-
42
-
-
71649097946
-
-
Fukuda, T. et al. Constitutively activated ALK2 and increased smad 1/5 cooperatively induce BMP signaling in fibrodysplasia ossificans progressiva. J. Biol. Chem. 2008 Aug 6 (Epub ahead of print)
-
Fukuda, T. et al. Constitutively activated ALK2 and increased smad 1/5 cooperatively induce BMP signaling in fibrodysplasia ossificans progressiva. J. Biol. Chem. 2008 Aug 6 (Epub ahead of print)
-
-
-
-
43
-
-
34548457296
-
Functional modeling of the ACVR1 (R206H) mutation in FOP
-
Groppe J.C., et al. Functional modeling of the ACVR1 (R206H) mutation in FOP. Clin. Orthop. Rel. Res. 462 (2007) 87-92
-
(2007)
Clin. Orthop. Rel. Res.
, vol.462
, pp. 87-92
-
-
Groppe, J.C.1
-
44
-
-
0030926004
-
Mechanism of TGF-β receptor inhibition by FKBP12
-
Chen Y.-G., et al. Mechanism of TGF-β receptor inhibition by FKBP12. EMBO J. 16 (1997) 3866-3876
-
(1997)
EMBO J.
, vol.16
, pp. 3866-3876
-
-
Chen, Y.-G.1
-
45
-
-
0035918274
-
Smurf 1 interacts with transforming growth factor-β type I receptor through Smad7 and induces receptor degradation
-
Ebisawa T., et al. Smurf 1 interacts with transforming growth factor-β type I receptor through Smad7 and induces receptor degradation. J. Biol. Chem. 276 (2001) 12477-12480
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 12477-12480
-
-
Ebisawa, T.1
-
46
-
-
0033524943
-
Crystal structure of the cytosplasmic domain of the type I TGF-β receptor in complex with FKBP12
-
Huse M., et al. Crystal structure of the cytosplasmic domain of the type I TGF-β receptor in complex with FKBP12. Cell 96 (1999) 425-436
-
(1999)
Cell
, vol.96
, pp. 425-436
-
-
Huse, M.1
-
47
-
-
0034796457
-
The TGF-β receptor activation process: an inhibitor-to-substrate binding switch
-
Huse M., et al. The TGF-β receptor activation process: an inhibitor-to-substrate binding switch. Mol. Cell 8 (2001) 671-682
-
(2001)
Mol. Cell
, vol.8
, pp. 671-682
-
-
Huse, M.1
-
48
-
-
0030576525
-
The immunophilin FKBP12 functions as a common inhibitor of the TGF-β family type I receptors
-
Wang T., et al. The immunophilin FKBP12 functions as a common inhibitor of the TGF-β family type I receptors. Cell 86 (1996) 435-444
-
(1996)
Cell
, vol.86
, pp. 435-444
-
-
Wang, T.1
-
49
-
-
33745197796
-
FKBP12 functions as an adaptor of the Smad7-Smurf1 complex on activin type I receptor
-
Yamaguchi T., et al. FKBP12 functions as an adaptor of the Smad7-Smurf1 complex on activin type I receptor. J. Mol. Endocrinol. 36 (2006) 569-579
-
(2006)
J. Mol. Endocrinol.
, vol.36
, pp. 569-579
-
-
Yamaguchi, T.1
-
50
-
-
25844447735
-
Fibrodysplasia ossificans progressiva: an historical perspective
-
Kaplan F.S. Fibrodysplasia ossificans progressiva: an historical perspective. Clin. Rev. Bone Miner. Metab. 3 (2005) 179-181
-
(2005)
Clin. Rev. Bone Miner. Metab.
, vol.3
, pp. 179-181
-
-
Kaplan, F.S.1
-
51
-
-
0344345444
-
A contribution to the study of myositis ossificans progressiva
-
591-637
-
Rosenstirn J.A. A contribution to the study of myositis ossificans progressiva. Ann. Surg. 68 (1918) 468-520 591-637
-
(1918)
Ann. Surg.
, vol.68
, pp. 468-520
-
-
Rosenstirn, J.A.1
-
52
-
-
25644454404
-
A new grammar for drug discovery
-
Fishman M.C., and Porter J.A. A new grammar for drug discovery. Nature 437 (2005) 491-493
-
(2005)
Nature
, vol.437
, pp. 491-493
-
-
Fishman, M.C.1
Porter, J.A.2
-
53
-
-
37249002233
-
The key to the closet is the key to the kingdom: a common lesson of rare diseases
-
Kaplan F.S. The key to the closet is the key to the kingdom: a common lesson of rare diseases. Orphan Dis. Update 24 (2006) 1-9
-
(2006)
Orphan Dis. Update
, vol.24
, pp. 1-9
-
-
Kaplan, F.S.1
-
54
-
-
37249010753
-
Dorsomorphin inhibits BMP signals required for embryogenesis and iron metabolism
-
Yu P.B., et al. Dorsomorphin inhibits BMP signals required for embryogenesis and iron metabolism. Nat. Chem. Biol. 4 (2008) 33-41
-
(2008)
Nat. Chem. Biol.
, vol.4
, pp. 33-41
-
-
Yu, P.B.1
-
55
-
-
37249079346
-
Small-molecule dissection of BMP signaling
-
Anderson G.J., and Darshan D. Small-molecule dissection of BMP signaling. Nat. Chem. Biol. 4 (2008) 15-16
-
(2008)
Nat. Chem. Biol.
, vol.4
, pp. 15-16
-
-
Anderson, G.J.1
Darshan, D.2
-
56
-
-
57349171954
-
BMP type I receptor inhibition reduces heterotopic ossification
-
Yu P.B., et al. BMP type I receptor inhibition reduces heterotopic ossification. Nat. Med. 14 (2008) 1363-1369
-
(2008)
Nat. Med.
, vol.14
, pp. 1363-1369
-
-
Yu, P.B.1
-
57
-
-
10744229194
-
In vivo somatic cell gene transfer of an engineered noggin mutein prevents BMP4-induced heterotopic ossification
-
Glaser D.L., et al. In vivo somatic cell gene transfer of an engineered noggin mutein prevents BMP4-induced heterotopic ossification. J. Bone Joint Surg. 85-A (2003) 2332-2342
-
(2003)
J. Bone Joint Surg.
, vol.85 -A
, pp. 2332-2342
-
-
Glaser, D.L.1
-
58
-
-
0141626663
-
Stromal cells of fibrodysplasia ossificans progressiva lesions express smooth muscle lineage markers and the osteogenic transcription factor Runx2/Cbfa-1: clues to a vascular origin of heterotopic ossification
-
Hegyi L., et al. Stromal cells of fibrodysplasia ossificans progressiva lesions express smooth muscle lineage markers and the osteogenic transcription factor Runx2/Cbfa-1: clues to a vascular origin of heterotopic ossification. J. Pathol. 201 (2003) 141-148
-
(2003)
J. Pathol.
, vol.201
, pp. 141-148
-
-
Hegyi, L.1
-
59
-
-
25844469044
-
Immunological features of fibrodysplasia ossificans progressiva and the dysregulated BMP4 pathway
-
Kaplan F.S., et al. Immunological features of fibrodysplasia ossificans progressiva and the dysregulated BMP4 pathway. Clin. Rev. Bone Miner. Metab. 3 (2005) 189-193
-
(2005)
Clin. Rev. Bone Miner. Metab.
, vol.3
, pp. 189-193
-
-
Kaplan, F.S.1
-
60
-
-
33846839273
-
Hematopoietic stem-cell contribution to ectopic skeletogenesis
-
Kaplan F.S., et al. Hematopoietic stem-cell contribution to ectopic skeletogenesis. J. Bone Joint Surg. Am. 89 (2007) 347-357
-
(2007)
J. Bone Joint Surg. Am.
, vol.89
, pp. 347-357
-
-
Kaplan, F.S.1
-
61
-
-
3042701421
-
Heterotopic ossification
-
Kaplan F.S., et al. Heterotopic ossification. J. Am. Acad. Orthop. Surg. 12 (2004) 116-125
-
(2004)
J. Am. Acad. Orthop. Surg.
, vol.12
, pp. 116-125
-
-
Kaplan, F.S.1
-
62
-
-
71649088580
-
Identification of progenitor cells that contribute to heterotopic skeletogenesis
-
in press
-
Lounev, V. et al. Identification of progenitor cells that contribute to heterotopic skeletogenesis. J. Bone Joint Surg. Am. (in press)
-
J. Bone Joint Surg. Am
-
-
Lounev, V.1
-
63
-
-
70649102232
-
ACVR1 knock-in mouse model for fibrodysplasia ossificans progressiva
-
Chakkalakal S.A., et al. ACVR1 knock-in mouse model for fibrodysplasia ossificans progressiva. J. Bone Miner. Res. 23 Suppl. 1 (2008) S57
-
(2008)
J. Bone Miner. Res.
, vol.23
, Issue.SUPPL. 1
-
-
Chakkalakal, S.A.1
-
64
-
-
33947509956
-
Hypoxic adipocytes pattern early heterotopic bone formation
-
Olmsted-Davis E., et al. Hypoxic adipocytes pattern early heterotopic bone formation. Am. J. Pathol. 170 (2007) 620-632
-
(2007)
Am. J. Pathol.
, vol.170
, pp. 620-632
-
-
Olmsted-Davis, E.1
-
65
-
-
0029789409
-
Protein builds second skeleton
-
Roush W. Protein builds second skeleton. Science 273 (1996) 1170
-
(1996)
Science
, vol.273
, pp. 1170
-
-
Roush, W.1
|