Pavan WJ - Search Results

1

A mouse model of Waardenburg syndrome type IV resulting from an ENU-induced mutation in endothelin 3.

Matera I, Cockroft JL, Moran JL, Beier DR, Goldowitz D, Pavan WJ. Matera I, et al. Among authors: pavan wj. Pigment Cell Res. 2007 Jun;20(3):210-5. doi: 10.1111/j.1600-0749.2007.00371.x. Pigment Cell Res. 2007. PMID: 17516928

2

Sox10 mutation disrupts neural crest development in Dom Hirschsprung mouse model.

Southard-Smith EM, Kos L, Pavan WJ. Southard-Smith EM, et al. Among authors: pavan wj. Nat Genet. 1998 Jan;18(1):60-4. doi: 10.1038/ng0198-60. Nat Genet. 1998. PMID: 9425902

3

The Sox10(Dom) mouse: modeling the genetic variation of Waardenburg-Shah (WS4) syndrome.

Southard-Smith EM, Angrist M, Ellison JS, Agarwala R, Baxevanis AD, Chakravarti A, Pavan WJ. Southard-Smith EM, et al. Among authors: pavan wj. Genome Res. 1999 Mar;9(3):215-25. Genome Res. 1999. PMID: 10077527 Free article.

4

Hepatocyte growth factor/scatter factor-MET signaling in neural crest-derived melanocyte development.

Kos L, Aronzon A, Takayama H, Maina F, Ponzetto C, Merlino G, Pavan W. Kos L, et al. Pigment Cell Res. 1999 Feb;12(1):13-21. doi: 10.1111/j.1600-0749.1999.tb00503.x. Pigment Cell Res. 1999. PMID: 10193678

5

Spatially restricted hypopigmentation associated with an Ednrbs-modifying locus on mouse chromosome 10.

Rhim H, Dunn KJ, Aronzon A, Mac S, Cheng M, Lamoreux ML, Tilghman SM, Pavan WJ. Rhim H, et al. Among authors: pavan wj. Genome Res. 2000 Jan;10(1):17-29. Genome Res. 2000. PMID: 10645946 Free article.

6

The use of expression profiling to study pigment cell biology and dysfunction.

Loftus SK, Pavan WJ. Loftus SK, et al. Among authors: pavan wj. Pigment Cell Res. 2000 Jun;13(3):141-6. doi: 10.1034/j.1600-0749.2000.130304.x. Pigment Cell Res. 2000. PMID: 10885671 Review.

7

A defect in a novel ADAMTS family member is the cause of the belted white-spotting mutation.

Rao C, Foernzler D, Loftus SK, Liu S, McPherson JD, Jungers KA, Apte SS, Pavan WJ, Beier DR. Rao C, et al. Among authors: pavan wj. Development. 2003 Oct;130(19):4665-72. doi: 10.1242/dev.00668. Development. 2003. PMID: 12925592

8

Spotlight on spotted mice: a review of white spotting mouse mutants and associated human pigmentation disorders.

Baxter LL, Hou L, Loftus SK, Pavan WJ. Baxter LL, et al. Among authors: pavan wj. Pigment Cell Res. 2004 Jun;17(3):215-24. doi: 10.1111/j.1600-0749.2004.00147.x. Pigment Cell Res. 2004. PMID: 15140066 Review.

9

WNT1 and WNT3a promote expansion of melanocytes through distinct modes of action.

Dunn KJ, Brady M, Ochsenbauer-Jambor C, Snyder S, Incao A, Pavan WJ. Dunn KJ, et al. Among authors: pavan wj. Pigment Cell Res. 2005 Jun;18(3):167-80. doi: 10.1111/j.1600-0749.2005.00226.x. Pigment Cell Res. 2005. PMID: 15892713

10

Deletion of long-range sequences at Sox10 compromises developmental expression in a mouse model of Waardenburg-Shah (WS4) syndrome.

Antonellis A, Bennett WR, Menheniott TR, Prasad AB, Lee-Lin SQ; NISC Comparative Sequencing Program; Green ED, Paisley D, Kelsh RN, Pavan WJ, Ward A. Antonellis A, et al. Among authors: pavan wj. Hum Mol Genet. 2006 Jan 15;15(2):259-71. doi: 10.1093/hmg/ddi442. Epub 2005 Dec 5. Hum Mol Genet. 2006. PMID: 16330480

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