Skip Header

5 results for author:"Laurier V." in Literature citations

Page 1 of 1

to top of page·  

Results Customize

› Repeat search in UniProtKB (8)

Identification of a novel BBS gene (BBS12) highlights the major role of a vertebrate-specific branch of chaperonin-related proteins in Bardet-Biedl syndrome.

Stoetzel C., Muller J., Laurier V., Davis E.E., Zaghloul N.A., Vicaire S., Jacquelin C., Plewniak F., Leitch C.C., Sarda P. et al.

Am. J. Hum. Genet. 80:1-11(2007) · UniProtKB (1) · Mapped (8)

Bardet-Biedl syndrome: a unique family for a major gene (BBS10).

Dollfus H., Muller J., Stoetzel C., Laurier V., Bonneau D., Megarbane A., Poch O., Mandel J.L.

Med Sci (Paris) 22:901-904(2006) · Mapped (2)

BBS10 encodes a vertebrate-specific chaperonin-like protein and is a major BBS locus.

Stoetzel C., Laurier V., Davis E.E., Muller J., Rix S., Badano J.L., Leitch C.C., Salem N., Chouery E., Corbani S. et al.

Nat. Genet. 38:521-524(2006) · UniProtKB (1) · Mapped (12)

BBS8 is rarely mutated in a cohort of 128 Bardet-Biedl syndrome families.

Stoetzel C., Laurier V., Faivre L., Megarbane A., Perrin-Schmitt F., Verloes A., Bonneau D., Mandel J.-L., Cossee M., Dollfus H.

J. Hum. Genet. 51:81-84(2006) · UniProtKB (1)

Testing for triallelism: analysis of six BBS genes in a Bardet-Biedl syndrome family cohort.

Hichri H., Stoetzel C., Laurier V., Caron S., Sigaudy S., Sarda P., Hamel C., Martin-Coignard D., Gilles M., Leheup B. et al.

Eur. J. Hum. Genet. 13:607-616(2005) · UniProtKB (5)

to top of page·

Page 1 of 1