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15 results for author:"Collin C." in Literature citations

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MOZ regulates the Tbx1 locus, and Moz mutation partially phenocopies DiGeorge syndrome.

Voss A.K., Vanyai H.K., Collin C., Dixon M.P., McLennan T.J., Sheikh B.N., Scambler P., Thomas T.

Dev. Cell 23:652-663(2012) · Mapped (75)

The homeodomain-containing transcription factors Arx and Pax4 control enteroendocrine subtype specification in mice.

Beucher A., Gjernes E., Collin C., Courtney M., Meunier A., Collombat P., Gradwohl G.

PLoS ONE 7:e36449-e36449(2012) · Mapped (6)

Competence of failed endocrine progenitors to give rise to acinar but not ductal cells is restricted to early pancreas development.

Beucher A., Martin M., Spenle C., Poulet M., Collin C., Gradwohl G.

Dev. Biol. 361:277-285(2012) · Mapped (3)

Identification of the Drosophila and Tribolium receptors for the recently discovered insect RYamide neuropeptides.

Collin C., Hauser F., Krogh-Meyer P., Hansen K.K., Gonzalez de Valdivia E., Williamson M., Grimmelikhuijzen C.J.

Biochem. Biophys. Res. Commun. 412:578-583(2011) · UniProtKB (4) · Mapped (5)

ERG dependence distinguishes developmental control of hematopoietic stem cell maintenance from hematopoietic specification.

Taoudi S., Bee T., Hilton A., Knezevic K., Scott J., Willson T.A., Collin C., Thomas T., Voss A.K., Kile B.T. et al.

Genes Dev. 25:251-262(2011) · Mapped (9)

[BRAF V600E mutation in papillary thyroid carcinoma: prevalence and detection in fine needle aspiration specimens].

Dujardin F., Pages J.C., Collin C., de Calan L., Lecomte P., Guyetant S.

Ann Pathol 30:252-262(2010) · Mapped (3)

Moz and retinoic acid coordinately regulate H3K9 acetylation, Hox gene expression, and segment identity.

Voss A.K., Collin C., Dixon M.P., Thomas T.

Dev. Cell 17:674-686(2009) · Mapped (36)

A comparative study of the performance of individuals with fragile X syndrome and Fmr1 knockout mice on Hebb-Williams mazes.

MacLeod L.S., Kogan C.S., Collin C.A., Berry-Kravis E., Messier C., Gandhi R.

Genes Brain Behav. 9:53-64(2010) · Mapped (11)

KCa2.3 channel-dependent hyperpolarization increases melanoma cell motility.

Chantome A., Girault A., Potier M., Collin C., Vaudin P., Pages J.C., Vandier C., Joulin V.

Exp. Cell Res. 315:3620-3630(2009) · Mapped (6)

NHS-A isoform of the NHS gene is a novel interactor of ZO-1.

Sharma S., Koh K.S., Collin C., Dave A., McMellon A., Sugiyama Y., McAvoy J.W., Voss A.K., Gecz J., Craig J.E.

Exp. Cell Res. 315:2358-2372(2009) · UniProtKB (1) · Mapped (7)

C3G regulates cortical neuron migration, preplate splitting and radial glial cell attachment.

Voss A.K., Britto J.M., Dixon M.P., Sheikh B.N., Collin C., Tan S.S., Thomas T.

Development 135:2139-2149(2008) · Mapped (34)

Protein and gene expression analysis of Phf6, the gene mutated in the Borjeson-Forssman-Lehmann Syndrome of intellectual disability and obesity.

Voss A.K., Gamble R., Collin C., Shoubridge C., Corbett M., Gecz J., Thomas T.

Gene Expr. Patterns 7:858-871(2007) · Mapped (7)

The transcriptional coactivator Querkopf controls adult neurogenesis.

Merson T.D., Dixon M.P., Collin C., Rietze R.L., Bartlett P.F., Thomas T., Voss A.K.

J. Neurosci. 26:11359-11370(2006) · Mapped (6)

Characterization of human cytokeratin 2, an epidermal cytoskeletal protein synthesized late during differentiation.

Collin C., Moll R., Kubicka S., Ouhayoun J.-P., Franke W.W.

Exp. Cell Res. 202:132-141(1992) · UniProtKB (1)

Suprabasal marker proteins distinguishing keratinizing squamous epithelia: cytokeratin 2 polypeptides of oral masticatory epithelium and epidermis are different.

Collin C., Ouhayoun J.P., Grund C., Franke W.W.

Differentiation 51:137-148(1992) · UniProtKB (1)

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