Retinal degeneration caused by mutations in TULP1.
Retinal degeneration caused by mutations in TULP1.
复制标题
TULP1 突变引起的视网膜变性。
DOI:
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发表时间:
2003
影响因子:
--
通讯作者:
S. Hagstrom
中科院分区:
文献类型:
--
作者:
Q. Xi;G. Pauer;K. West;J. Crabb;S. Hagstrom
TULP1 is a member of a family of four proteins named TULPs for tubby-like proteins, defined by the highly conserved C-terminal half of their primary sequences (60 ia 90% amino acid identity). This protein family includes TUB, TULP1, TULP2, and TULP3, all of which have different N-termini and different cellular expression patterns (North et al., 1997). Other than members of the TULP family, database searches do not reveal any significant homology with known proteins or functional motifs. Their physiological functions are unknown but two have been linked to photoreceptor degeneration. Mutations in the human TULPI gene were found to be a cause of retinitis pigmentosa (Hagstrom et al., 1998; Banerjee et al., 1998). Loss of Tulp1 function in mice, introduced by gene knockout, also causes photoreceptor degeneration (Hagstrom et al., 1999; Ikeda et al., 2000). A naturally occurring recessive null mutation in the tubby gene in mice causes photoreceptor and cochlear degeneration and adult-onset obesity (Ohlemiller et al., 1995).
影响因子:
4.4
作者:
S. Hagstrom;M. Adamian;Michael S. Scimeca;B. Pawlyk;Guohua Yue;Tiansen Li
通讯作者:
S. Hagstrom;M. Adamian;Michael S. Scimeca;B. Pawlyk;Guohua Yue;Tiansen Li
影响因子:
3.3
作者:
Lopes VS;Jimeno D;Khanobdee K;Song X;Chen B;Nusinowitz S;Williams DS
通讯作者:
Williams DS
DOI:
10.1073/pnas.94.7.3128
发表时间:
1997-04-01
影响因子:
11.1
作者:
North, MA;Naggert, JK;Nishina, PM
通讯作者:
Nishina, PM