1 - 25 of 32 results for author:"Kopp P." in Literature citations
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| New isoform-specific monoclonal antibodies reveal different sub-cellular localisations for talin1 and talin2. Praekelt U., Kopp P.M., Rehm K., Linder S., Bate N., Patel B., Debrand E., Manso A.M., Ross R.S., Conti F. et al. Eur. J. Cell Biol. 91:180-191(2012) · Mapped (16) |
| Identification of allelic variants of pendrin (SLC26A4) with loss and gain of function. Dossena S., Bizhanova A., Nofziger C., Bernardinelli E., Ramsauer J., Kopp P., Paulmichl M. Cell. Physiol. Biochem. 28:467-476(2011) · Mapped (5) |
| Analysis of cellular localization and function of carboxy-terminal mutants of pendrin. Bizhanova A., Chew T.L., Khuon S., Kopp P. Cell. Physiol. Biochem. 28:423-434(2011) · Mapped (5) |
| Tetraspanin CD9 in cell migration. Powner D., Kopp P.M., Monkley S.J., Critchley D.R., Berditchevski F. Biochem. Soc. Trans. 39:563-567(2011) · Mapped (5) |
| The kinesin KIF9 and reggie/flotillin proteins regulate matrix degradation by macrophage podosomes. Cornfine S., Himmel M., Kopp P., El Azzouzi K., Wiesner C., Kruger M., Rudel T., Linder S. Mol. Biol. Cell 22:202-215(2011) · Mapped (8) |
| The Structure of the talin head reveals a novel extended conformation of the FERM domain. Elliott P.R., Goult B.T., Kopp P.M., Bate N., Grossmann J.G., Roberts G.C., Critchley D.R., Barsukov I.L. Structure 18:1289-1299(2010) · Mapped (6) |
| Molecular analysis of the PROP1 and HESX1 genes in patients with septo-optic dysplasia and/or pituitary hormone deficiency. Cruz J.B., Nunes V.S., Clara S.A., Perone D., Kopp P., Nogueira C.R. Arq Bras Endocrinol Metabol 54:482-487(2010) · Mapped (1) |
| Central region of talin has a unique fold that binds vinculin and actin. Gingras A.R., Bate N., Goult B.T., Patel B., Kopp P.M., Emsley J., Barsukov I.L., Roberts G.C., Critchley D.R. J. Biol. Chem. 285:29577-29587(2010) · Mapped (8) |
| 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) |
| The p.A2215D thyroglobulin gene mutation leads to deficient synthesis and secretion of the mutated protein and congenital hypothyroidism with wide phenotype variation. Pardo V., Vono-Toniolo J., Rubio I.G., Knobel M., Possato R.F., Targovnik H.M., Kopp P., Medeiros-Neto G. J. Clin. Endocrinol. Metab. 94:2938-2944(2009) · UniProtKB (1) · Mapped (8) |
| Minireview: The sodium-iodide symporter NIS and pendrin in iodide homeostasis of the thyroid. Bizhanova A., Kopp P. Endocrinology 150:1084-1090(2009) · Mapped (7) |
| Serum IGF-I and C-reactive protein in healthy black and white young men: the CARDIA male hormone study. Colangelo L.A., Chiu B., Kopp P., Liu K., Gapstur S.M. Growth Horm. IGF Res. 19:420-425(2009) · Mapped (19) |
| Pendred syndrome and iodide transport in the thyroid. Kopp P., Pesce L., Solis-S J.C. Trends Endocrinol. Metab. 19:260-268(2008) · Mapped (5) |
| Associations of serum sex hormone binding globulin (SHBG) levels with SHBG gene polymorphisms in the CARDIA Male Hormone Study. Turk A., Kopp P., Colangelo L.A., Urbanek M., Wood K., Liu K., Skinner H.G., Gapstur S.M. Am. J. Epidemiol. 167:412-418(2008) · Mapped (8) |
| Total testosterone, androgen receptor polymorphism, and depressive symptoms in young black and white men: the CARDIA Male Hormone Study. Colangelo L.A., Sharp L., Kopp P., Scholtens D., Chiu B.C., Liu K., Gapstur S.M. Psychoneuroendocrinology 32:951-958(2007) · Mapped (11) |
| PAK4 and alphaPIX determine podosome size and number in macrophages through localized actin regulation. Gringel A., Walz D., Rosenberger G., Minden A., Kutsche K., Kopp P., Linder S. J. Cell. Physiol. 209:568-579(2006) · Mapped (4) |
| Goitrous congenital hypothyroidism and hearing impairment associated with mutations in the TPO and SLC26A4/PDS genes. Pfarr N., Borck G., Turk A., Napiontek U., Keilmann A., Mueller-Forell W., Kopp P., Pohlenz J. J. Clin. Endocrinol. Metab. 91:2678-2681(2006) · UniProtKB (2) |
| The kinesin KIF1C and microtubule plus ends regulate podosome dynamics in macrophages. Kopp P., Lammers R., Aepfelbacher M., Woehlke G., Rudel T., Machuy N., Steffen W., Linder S. Mol. Biol. Cell 17:2811-2823(2006) · Mapped (1) |
| Functional characterization of pendrin in a polarized cell system. Evidence for pendrin-mediated apical iodide efflux. Gillam M.P., Sidhaye A.R., Lee E.J., Rutishauser J., Stephan C.W., Kopp P. J. Biol. Chem. 279:13004-13010(2004) · Mapped (5) |
| Familial combined pituitary hormone deficiency due to a novel mutation R99Q in the hot spot region of Prophet of Pit-1 presenting as constitutional growth delay. Vieira T.C., Dias da Silva M.R., Cerutti J.M., Brunner E., Borges M., Arnaldi L.T., Kopp P., Abucham J. J. Clin. Endocrinol. Metab. 88:38-44(2003) · UniProtKB (1) |
| Clinical and molecular analysis of three families with autosomal dominant neurohypophyseal diabetes insipidus associated with a novel and recurrent mutations in the vasopressin-neurophysin II gene. Rutishauser J., Kopp P., Gaskill M.B., Kotlar T.J., Robertson G.L. Eur. J. Endocrinol. 146:649-656(2002) · UniProtKB (1) · Mapped (2) |
| Cloning of the cat TSH receptor and evidence against an autoimmune etiology of feline hyperthyroidism. Nguyen L.Q., Arseven O.K., Gerber H., Stein B.S., Jameson J.L., Kopp P. Endocrinology 143:395-402(2002) · UniProtKB (1) · Mapped (2) |
| Aggressive metastatic follicular thyroid carcinoma with anaplastic transformation arising from a long-standing goiter in a patient with Pendred's syndrome. Camargo R., Limbert E., Gillam M., Henriques M.M., Fernandes C., Catarino A.L., Soares J., Alves V.A., Kopp P., Medeiros-Neto G. Thyroid 11:981-988(2001) · Mapped (5) |
| A novel mutation (Q40P) in PAX8 associated with congenital hypothyroidism and thyroid hypoplasia: evidence for phenotypic variability in mother and child. Congdon T., Nguyen L.Q., Nogueira C.R., Habiby R.L., Medeiros-Neto G., Kopp P. J. Clin. Endocrinol. Metab. 86:3962-3967(2001) · UniProtKB (1) |
| Clinical and molecular analysis of three Mexican families with Pendred's syndrome. Gonzalez Trevino O., Karamanoglu Arseven O., Ceballos C.J., Vives V.I., Ramirez R.C., Gomez V.V., Medeiros-Neto G., Kopp P. Eur. J. Endocrinol. 144:585-593(2001) · UniProtKB (1) |