| TSHR is the main causative locus in autosomal recessively inherited thyroid dysgenesis. Cangul H., Aycan Z., Saglam H., Forman J.R., Cetinkaya S., Tarim O., Bober E., Cesur Y., Kurtoglu S., Darendeliler F. et al.
J. Pediatr. Endocrinol. Metab. 25:419-426(2012) · Mapped (6) |
| The exon 3-deleted/full-length growth hormone receptor polymorphism and response to growth hormone therapy in growth hormone deficiency and Turner syndrome: a multicenter study. Bas F., Darendeliler F., Aycan Z., Cetinkaya E., Berberoglu M., Sıklar Z., Ocal G., Timirci O., Cetinkaya S., Darcan S. et al.
Horm Res Paediatr 77:85-93(2012) · Mapped (4) |
| Novel TSHR mutations in consanguineous families with congenital nongoitrous hypothyroidism. Cangul H., Morgan N.V., Forman J.R., Saglam H., Aycan Z., Yakut T., Gulten T., Tarim O., Bober E., Cesur Y. et al.
Clin. Endocrinol. (Oxf) 73:671-677(2010) · Mapped (6) |
| A mother and son with Noonan syndrome resulting from a PTPN11 mutation: first report of molecularly proven cases from Turkey. Demir K., Yntema H.G., Altincik A., Bober E.
Turk. J. Pediatr. 52:321-324(2010) · Mapped (6) |
| A novel mutation in the AVPR2 gene (222delA) associated with X-linked nephrogenic diabetes insipidus in a boy with growth failure. Abaci A., Wood K., Demir K., Buyukgebiz A., Bober E., Kopp P.
Endocr Pract 16:231-236(2010) · Mapped (1) |
| Different extent of cardiac malfunction and resistance to oxidative stress in heterozygous and homozygous manganese-dependent superoxide dismutase-mutant mice. Loch T., Vakhrusheva O., Piotrowska I., Ziolkowski W., Ebelt H., Braun T., Bober E.
Cardiovasc. Res. 82:448-457(2009) · Mapped (4) |
| Sirt7-dependent inhibition of cell growth and proliferation might be instrumental to mediate tissue integrity during aging. Vakhrusheva O., Braeuer D., Liu Z., Braun T., Bober E.
J. Physiol. Pharmacol. 59 Suppl 9:201-212(2008) · Mapped (2) |
| Sirt7 increases stress resistance of cardiomyocytes and prevents apoptosis and inflammatory cardiomyopathy in mice. Vakhrusheva O., Smolka C., Gajawada P., Kostin S., Boettger T., Kubin T., Braun T., Bober E.
Circ. Res. 102:703-710(2008) · UniProtKB (1) · Mapped (3) |
| Functional redundancy of NSCL-1 and NeuroD during development of the petrosal and vestibulocochlear ganglia. Kruger M., Schmid T., Kruger S., Bober E., Braun T.
Eur. J. Neurosci. 24:1581-1590(2006) · Mapped (16) |
| Paracellin-1 gene mutation with multiple congenital abnormalities. Turkmen M., Kasap B., Soylu A., Bober E., Konrad M., Kavukcu S.
Pediatr. Nephrol. 21:1776-1778(2006) · Mapped (2) |
| Reduced mobility of fibroblast growth factor (FGF)-deficient myoblasts might contribute to dystrophic changes in the musculature of FGF2/FGF6/mdx triple-mutant mice. Neuhaus P., Oustanina S., Loch T., Kruger M., Bober E., Dono R., Zeller R., Braun T.
Mol. Cell. Biol. 23:6037-6048(2003) · Mapped (20) |
| The Dlx5 homeobox gene is essential for vestibular morphogenesis in the mouse embryo through a BMP4-mediated pathway. Merlo G.R., Paleari L., Mantero S., Zerega B., Adamska M., Rinkwitz S., Bober E., Levi G.
Dev. Biol. 248:157-169(2002) · Mapped (22) |
| FGFs control the patterning of the inner ear but are not able to induce the full ear program. Adamska M., Herbrand H., Adamski M., Krueger M., Braun T., Bober E.
Mech. Dev. 109:303-313(2001) · UniProtKB (1) |
| Five Nkx5 genes show differential expression patterns in anlagen of sensory organs in medaka: insight into the evolution of the gene family. Adamska M., Wolff A., Kreusler M., Wittbrodt J., Braun T., Bober E.
Dev. Genes Evol. 211:338-349(2001) · UniProtKB (5) |
| Inner ear and lateral line expression of a zebrafish Nkx5-1 gene and its downregulation in the ears of FGF8 mutant, ace. Adamska M., Leger S., Brand M., Hadrys T., Braun T., Bober E.
Mech. Dev. 97:161-165(2000) · UniProtKB (1) |
| Netrin 1 is required for semicircular canal formation in the mouse inner ear. Salminen M., Meyer B.I., Bober E., Gruss P.
Development 127:13-22(2000) · Mapped (4) |
| Two highly related homeodomain proteins, Nkx5-1 and Nkx5-2, display different DNA binding specificities. Mennerich D., Hoffmann S., Hadrys T., Arnold H.H., Bober E.
Biol. Chem. 380:1041-1048(1999) · UniProtKB (1) |
| Craniofacial, vestibular and bone defects in mice lacking the Distal-less-related gene Dlx5. Acampora D., Merlo G.R., Paleari L., Zerega B., Postiglione M.P., Mantero S., Bober E., Barbieri O., Simeone A., Levi G.
Development 126:3795-3809(1999) · Mapped (43) |
| Two regulatory genes, cNkx5-1 and cPax2, show different responses to local signals during otic placode and vesicle formation in the chick embryo. Herbrand H., Guthrie S., Hadrys T., Hoffmann S., Arnold H.H., Rinkwitz-Brandt S., Bober E.
Development 125:645-654(1998) · UniProtKB (1) |
| Nkx5-1 controls semicircular canal formation in the mouse inner ear. Hadrys T., Braun T., Rinkwitz-Brandt S., Arnold H.-H., Bober E.
Development 125:33-39(1998) · UniProtKB (1) · Mapped (6) |
| Regionalized expression of Nkx5-1, Nkx5-2, Pax2 and sek genes during mouse inner ear development. Rinkwitz-Brandt S., Arnold H.H., Bober E.
Hear. Res. 99:129-138(1996) · UniProtKB (1) · Mapped (8) |
| Gene targeting the myf-5 locus with nlacZ reveals expression of this myogenic factor in mature skeletal muscle fibres as well as early embryonic muscle. Tajbakhsh S., Bober E., Babinet C., Pournin S., Arnold H., Buckingham M.
Dev. Dyn. 206:291-300(1996) · Mapped (3) |
| Distinct temporal expression of mouse Nkx-5.1 and Nkx-5.2 homeobox genes during brain and ear development. Rinkwitz-Brandt S., Justus M., Oldenettel I., Arnold H.-H., Bober E.
Mech. Dev. 52:371-381(1995) · UniProtKB (2) · Mapped (7) |
| Early skeletal muscle development proceeds normally in parthenogenetic mouse embryos. Fundele R., Bober E., Arnold H.H., Grim M., Bender R., Wilting J., Christ B.
Dev. Biol. 161:30-36(1994) · Mapped (9) |
| Pax-3 is required for the development of limb muscles: a possible role for the migration of dermomyotomal muscle progenitor cells. Bober E., Franz T., Arnold H.H., Gruss P., Tremblay P.
Development 120:603-612(1994) · Mapped (10) |
