OpenURL Connection Search

Select item for more details and to access through your institution.

Wnt-5/pipetail functions in vertebrate axis formation as a negative regulator of Wnt/β-catenin activity.
Published in:
Journal of Cell Biology, 2003, v. 162, n. 5, p. 889, doi. 10.1083/jcb.200303107
By:
- Westfall, Trudi A.;
- Brimeyer, Ryan;
- Twedt, Jen;
- Gladon, Jean;
- Olberding, Andrea;
- Furutani-Seiki, Makoto;
- Slusarski, Diane C.
Publication type:
Article
A splice site mutation in the TSEN2 causes a new syndrome with craniofacial and central nervous system malformations, and atypical hemolytic uremic syndrome.
Published in:
Clinical Genetics, 2022, v. 101, n. 3, p. 346, doi. 10.1111/cge.14105
By:
- Canpolat, Nur;
- Liu, Dingxiao;
- Atayar, Emine;
- Saygili, Seha;
- Kara, Nazli Sila;
- Westfall, Trudi A.;
- Ding, Qiong;
- Brown, Bartley J.;
- Braun, Terry A.;
- Slusarski, Diane;
- Karli Oguz, Kader;
- Ozluk, Yasemin;
- Tuysuz, Beyhan;
- Tastemel Ozturk, Tugba;
- Sever, Lale;
- Sezerman, Osman Ugur;
- Topaloglu, Rezan;
- Caliskan, Salim;
- Attanasio, Massimo;
- Ozaltin, Fatih
Publication type:
Article
Wnt5b-Ryk pathway provides directional signals to regulate gastrulation movement.
Published in:
Journal of Cell Biology, 2010, v. 190, n. 2, p. 263, doi. 10.1083/jcb.200912128
By:
- Lin, Shengda;
- Baye, Lisa M.;
- Westfall, Trudi A.;
- Slusarski, Diane C.
Publication type:
Article
Hypomorphic mutations in TRNT1 cause retinitis pigmentosa with erythrocytic microcytosis.
Published in:
Human Molecular Genetics, 2016, v. 25, n. 1, p. 44, doi. 10.1093/hmg/ddv446
By:
- DeLuca, Adam P.;
- Whitmore, S. Scott;
- Barnes, Jenna;
- Sharma, Tasneem P.;
- Westfall, Trudi A.;
- Scott, C. Anthony;
- Weed, Matthew C.;
- Wiley, Jill S.;
- Wiley, Luke A.;
- Johnston, Rebecca M.;
- Schnieders, Michael J.;
- Lentz, Steven R.;
- Tucker, Budd A.;
- Mullins, Robert F.;
- Scheetz, Todd E.;
- Stone, Edwin M.;
- Slusarski, Diane C.
Publication type:
Article
Genetic interaction between Bardet-Biedl syndrome genes and implications for limb patterning.
Published in:
Human Molecular Genetics, 2008, v. 17, n. 13, p. 1956, doi. 10.1093/hmg/ddn093
By:
- Tayeh, Marwan K.;
- Yen, Hsan-Jan;
- Beck, John S.;
- Searby, Charles C.;
- Westfall, Trudi A.;
- Griesbach, Hilary;
- Sheffield, Val C.;
- Slusarski, Diane C.
Publication type:
Article

Found: 5

Wnt-5/pipetail functions in vertebrate axis formation as a negative regulator of Wnt/β-catenin activity.

A splice site mutation in the TSEN2 causes a new syndrome with craniofacial and central nervous system malformations, and atypical hemolytic uremic syndrome.

Wnt5b-Ryk pathway provides directional signals to regulate gastrulation movement.

Hypomorphic mutations in TRNT1 cause retinitis pigmentosa with erythrocytic microcytosis.

Genetic interaction between Bardet-Biedl syndrome genes and implications for limb patterning.