Results
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1741.
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1742.
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A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva. [electronic resource] by
- Shore, Eileen M
- Xu, Meiqi
- Feldman, George J
- Fenstermacher, David A
- Cho, Tae-Joon
- Choi, In Ho
- Connor, J Michael
- Delai, Patricia
- Glaser, David L
- LeMerrer, Martine
- Morhart, Rolf
- Rogers, John G
- Smith, Roger
- Triffitt, James T
- Urtizberea, J Andoni
- Zasloff, Michael
- Brown, Matthew A
- Kaplan, Frederick S
Producer: 20060801
In:
Nature genetics vol. 38
Availability: No items available.
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1743.
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1744.
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NF-κB/MAPK activation underlies ACVR1-mediated inflammation in human heterotopic ossification. [electronic resource] by
- Barruet, Emilie
- Morales, Blanca M
- Cain, Corey J
- Ton, Amy N
- Wentworth, Kelly L
- Chan, Tea V
- Moody, Tania A
- Haks, Mariëlle C
- Ottenhoff, Tom Hm
- Hellman, Judith
- Nakamura, Mary C
- Hsiao, Edward C
Producer: 20191202
In:
JCI insight vol. 3
Availability: No items available.
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1745.
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1746.
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1747.
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1748.
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1749.
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1750.
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1751.
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1752.
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1753.
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1754.
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1755.
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1756.
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1757.
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1758.
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1759.
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1760.
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Neofunction of ACVR1 in fibrodysplasia ossificans progressiva. [electronic resource] by
- Hino, Kyosuke
- Ikeya, Makoto
- Horigome, Kazuhiko
- Matsumoto, Yoshihisa
- Ebise, Hayao
- Nishio, Megumi
- Sekiguchi, Kazuya
- Shibata, Mitsuaki
- Nagata, Sanae
- Matsuda, Shuichi
- Toguchida, Junya
Producer: 20160509
In:
Proceedings of the National Academy of Sciences of the United States of America vol. 112
Availability: No items available.
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