| Amyloid and nonfibrillar deposits in mice transgenic for wild-type human transthyretin: a possible model for senile systemic amyloidosis. Teng M.H., Yin J.Y., Vidal R., Ghiso J., Kumar A., Rabenou R., Shah A., Jacobson D.R., Tagoe C., Gallo G. et al.
Lab. Invest. 81:385-396(2001) · Mapped (3) |
| Transthyretin amyloidosis (serine 44) with headache, hearing loss, and peripheral neuropathy. Klein C.J., Nakumura M., Jacobson D.R., Lacy M.Q., Benson M.D., Petersen R.C.
Neurology 51:1462-1464(1998) · UniProtKB (1) |
| Novel transthyretin missense mutation (Thr34) in an Italian family with hereditary amyloidosis. Patrosso M.C., Salvi F., De Grandis D., Vezzoni P., Jacobson D.R., Ferlini A.
Am. J. Med. Genet. 77:135-138(1998) · UniProtKB (1) |
| Transthyretin ILE20, a new variant associated with late-onset cardiac amyloidosis. Jacobson D.R., Pan T., Kyle R.A., Buxbaum J.N.
Hum. Mutat. 9:83-85(1997) · UniProtKB (1) |
| A double-variant transthyretin allele (Ser 6, Ile 33) in the Israeli patient 'SKO' with familial amyloidotic polyneuropathy. Jacobson D.R., Buxbaum J.N.
Hum. Mutat. 3:254-260(1994) · UniProtKB (1) |
| Amyloid fibril composition and transthyretin gene structure in senile systemic amyloidosis. Gustavsson A., Jahr H., Tobiassen R., Jacobson D.R., Sletten K., Westermark P.
Lab. Invest. 73:703-708(1995) · UniProtKB (1) |
| Transthyretin Pro55, a variant associated with early-onset, aggressive, diffuse amyloidosis with cardiac and neurologic involvement. Jacobson D.R., McFarlin D.E., Kane I., Buxbaum J.N.
Hum. Genet. 89:353-356(1992) · UniProtKB (1) · Mapped (5) |
