Niederreither K - Search Results

1

[Oral cavity as a target and a marker of environmental exposures: developmental dental defects].

Babajko S, Gayrard V, Houari S, Thu Bui A, Barouki R, Niederreither K, Fini JB, Dursun E, Coumoul X. Babajko S, et al. Among authors: niederreither k. Med Sci (Paris). 2020 Mar;36(3):225-230. doi: 10.1051/medsci/2020024. Epub 2020 Mar 31. Med Sci (Paris). 2020. PMID: 32228840 Free article. Review. French.

2

Enamel and dental anomalies in latent-transforming growth factor beta-binding protein 3 mutant mice.

Morkmued S, Hemmerle J, Mathieu E, Laugel-Haushalter V, Dabovic B, Rifkin DB, Dollé P, Niederreither K, Bloch-Zupan A. Morkmued S, et al. Among authors: niederreither k. Eur J Oral Sci. 2017 Feb;125(1):8-17. doi: 10.1111/eos.12328. Eur J Oral Sci. 2017. PMID: 28084688 Free PMC article.

3

Dental and extra-oral clinical features in 41 patients with WNT10A gene mutations: A multicentric genotype-phenotype study.

Tardieu C, Jung S, Niederreither K, Prasad M, Hadj-Rabia S, Philip N, Mallet A, Consolino E, Sfeir E, Noueiri B, Chassaing N, Dollfus H, Manière MC, Bloch-Zupan A, Clauss F. Tardieu C, et al. Among authors: niederreither k. Clin Genet. 2017 Nov;92(5):477-486. doi: 10.1111/cge.12972. Epub 2017 Mar 19. Clin Genet. 2017. PMID: 28105635

4

Deficiency of the SMOC2 matricellular protein impairs bone healing and produces age-dependent bone loss.

Morkmued S, Clauss F, Schuhbaur B, Fraulob V, Mathieu E, Hemmerlé J, Clevers H, Koo BK, Dollé P, Bloch-Zupan A, Niederreither K. Morkmued S, et al. Among authors: niederreither k. Sci Rep. 2020 Sep 9;10(1):14817. doi: 10.1038/s41598-020-71749-6. Sci Rep. 2020. PMID: 32908163 Free PMC article.

5

Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning.

Laugel-Haushalter V, Morkmued S, Stoetzel C, Geoffroy V, Muller J, Boland A, Deleuze JF, Chennen K, Pitiphat W, Dollfus H, Niederreither K, Bloch-Zupan A, Pungchanchaikul P. Laugel-Haushalter V, et al. Among authors: niederreither k. Front Physiol. 2018 Sep 26;9:1329. doi: 10.3389/fphys.2018.01329. eCollection 2018. Front Physiol. 2018. PMID: 30319441 Free PMC article.

6

In situ hybridization with 35S-labeled probes for retinoid receptors.

Niederreither K, Dollé P. Niederreither K, et al. Methods Mol Biol. 1998;89:247-67. doi: 10.1385/0-89603-438-0:247. Methods Mol Biol. 1998. PMID: 9664333 Review. No abstract available.

7

Decreased embryonic retinoic acid synthesis results in a DiGeorge syndrome phenotype in newborn mice.

Vermot J, Niederreither K, Garnier JM, Chambon P, Dollé P. Vermot J, et al. Among authors: niederreither k. Proc Natl Acad Sci U S A. 2003 Feb 18;100(4):1763-8. doi: 10.1073/pnas.0437920100. Epub 2003 Jan 31. Proc Natl Acad Sci U S A. 2003. PMID: 12563036 Free PMC article.

8

Dorsal pancreas agenesis in retinoic acid-deficient Raldh2 mutant mice.

Martín M, Gallego-Llamas J, Ribes V, Kedinger M, Niederreither K, Chambon P, Dollé P, Gradwohl G. Martín M, et al. Among authors: niederreither k. Dev Biol. 2005 Aug 15;284(2):399-411. doi: 10.1016/j.ydbio.2005.05.035. Dev Biol. 2005. PMID: 16026781 Free article.

9

Retinaldehyde dehydrogenase 2 (RALDH2)-mediated retinoic acid synthesis regulates early mouse embryonic forebrain development by controlling FGF and sonic hedgehog signaling.

Ribes V, Wang Z, Dollé P, Niederreither K. Ribes V, et al. Among authors: niederreither k. Development. 2006 Jan;133(2):351-61. doi: 10.1242/dev.02204. Development. 2006. PMID: 16368932

10

Involvement of retinol dehydrogenase 10 in embryonic patterning and rescue of its loss of function by maternal retinaldehyde treatment.

Rhinn M, Schuhbaur B, Niederreither K, Dollé P. Rhinn M, et al. Among authors: niederreither k. Proc Natl Acad Sci U S A. 2011 Oct 4;108(40):16687-92. doi: 10.1073/pnas.1103877108. Epub 2011 Sep 19. Proc Natl Acad Sci U S A. 2011. PMID: 21930923 Free PMC article.

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