Search Results - "Höppner, W"

Two-Dimensional Mapping of the Electrostatic Potential in Transistors by Electron Holography by Rau, W. D., Schwander, P., Baumann, F. H., Höppner, W., Ourmazd, A.

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A new hot spot for mutations in the ret protooncogene causing familial medullary thyroid carcinoma and multiple endocrine neoplasia type 2A by BERNDT, I, REUTER, M, SALLER, B, FRANK-RAUE, K, GROTH, P, GRUSSENDORF, M, RAUE, F, RITTER, M. M, HÖPPNER, W

“…One hundred and eighty-one families with multiple endocrine neoplasia type 2A (MEN-2A) or familial medullary thyroid carcinoma (FMTC) have been investigated…”
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Fabrication of MEMS actuators from the BEOL of a 0.25μm BiCMOS technology platform by Kulse, P., Birkholz, M., Ehwald, K.-E., Bauer, J., Drews, J., Haak, U., Höppner, W., Katzer, J., Schulz, K., Wolansky, D.

“…[Display omitted] ► Preparation of monolithic integrated 50nm thin TiN actuator. ► Using a standard BEOL module of a 0.25 BiCMOS technology. ► Introducing a…”
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A RET double mutation in the germline of a kindred with FMTC by Bartsch, D K, Hasse, C, Schug, C, Barth, P, Rothmund, M, Höppner, W

“…Activating germline mutations of the RET proto-oncogene are found in more than 90% of families with multiple endocrine neoplasia type 2a (MEN 2a) and familial…”
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Developing effective screening strategies in multiple endocrine neoplasia type 1 (MEN 1) on the basis of clinical and sequencing data of German patients with MEN 1 by Schaaf, L, Pickel, J, Zinner, K, Hering, U, Höfler, M, Goretzki, P E, Spelsberg, F, Raue, F, von zur Mühlen, A, Gerl, H, Hensen, J, Bartsch, D K, Rothmund, M, Schneyer, U, Dralle, H, Engelbach, M, Karges, W, Stalla, G K, Höppner, W

“…Multiple-endocrine-neoplasia-type-1 (MEN1) is an autosomal-dominant inherited disorder characterized by the combined occurrence of primary hyperparathyroidism…”
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Long-term outcome in 46 gene carriers of hereditary medullary thyroid carcinoma after prophylactic thyroidectomy: impact of individual RET genotype by Frank-Raue, K, Buhr, H, Dralle, H, Klar, E, Senninger, N, Weber, T, Rondot, S, Höppner, W, Raue, F

“…Objective: In children with RET proto-oncogene mutation, curative treatment of medullary thyroid carcinoma (MTC) is possible by prophylactic thyroidectomy…”
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A novel type of mutation in the cysteine rich domain of the RET receptor causes ligand independent activation by ARLT, D. H, BAUR, B, WAGNER, B, HÖPPNER, W

“…Multiple endocrine neoplasia type 2A (MEN 2A) is a dominantly inherited cancer syndrome, which involves the triad of MTC, pheochromocytoma, and…”
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Lack of MEN1 gene mutations in 27 sporadic insulinomas by Cupisti, Höppner, Dotzenrath, Simon, Berndt, Röher, Goretzki

“…Background Multiple endocrine neoplasia type 1 (MEN 1) is an autosomal dominant familial cancer syndrome characterized by tumours of the parathyroids, anterior…”
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Effect of in vivo thyroid hormone status on insulin signalling and GLUT1 and GLUT4 glucose transport systems in rat adipocytes by Matthaei, S, Trost, B, Hamann, A, Kausch, C, Benecke, H, Greten, H, Höppner, W, Klein, H H

“…To examine the effect of thyroid hormone status on insulin action in isolated rat adipocytes, age- and weight-matched Sprague-Dawley rats were rendered…”
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Renal cell carcinoma in a transplanted kidney: successful organ-preserving procedure by Höppner, W, Grosse, K, Dreikorn, K

“…We report a case of a de novo renal cell carcinoma in a transplanted kidney, which was detected 3 years after the transplantation. The tumor was excised under…”
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Molecular pathophysiology of the pituitary-gonadal axis by Simoni, M, Gromoll, J, Höppner, W, Nieschlag, E

“…Mutations of gonadotropin beta subunits or gonadotropin receptors are involved in some reproductive diseases leading to alterations of pubertal maturation or…”
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Genotype-phenotype correlations in hereditary medullary thyroid carcinoma : Oncological features and biochemical properties by MACHENS, Andreas, GIMM, Oliver, HINZE, Raoul, HÖPPNER, Wolfgang, BOEHM, Bernhard O, DRALLE, Henning

“…In hereditary medullary thyroid carcinoma (MTC), few genotype-phenotype correlations have been established. RET genotypes (exons 10, 11, 13, and 14) of 63…”
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Mutational analysis of the follicle-stimulating hormone (FSH) receptor in normal and infertile men : Identification and characterization of two discrete FSH receptor isoforms by SIMONI, M, GROMOLL, J, HÖPPNER, W, KAMISCHKE, A, KRAFFT, T, STÄHLE, D, NIESCHLAG, E

“…In a search for pathophysiological causes of idiopathic male infertility we investigated the occurrence of mutations of the FSH receptor in 48 men with this…”
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Results and follow-up in eleven MEN 2A gene carriers after prophylactic thyroidectomy by Frank-Raue, K, Höppner, W, Buhr, H, Herfarth, C, Raue, F

“…In 11 MEN 2A gene carriers prophylactic thyroidectomy was carried out between the age of 4 to 17 years. All gene carriers had pathological basal and/or…”
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Prognostic value of codon 918 (ATG→ACG) RET proto‐oncogene mutations in sporadic medullary thyroid carcinoma by Schilling, Tobias, Bürck, Julia, Sinn, Hans‐Peter, Clemens, Andreas, Otto, Herwart F., Höppner, Wolfgang, Herfarth, Christian, Ziegler, Reinhard, Schwab, Manfred, Raue, Friedhelm

“…We have determined the frequency of 918 RET proto‐oncogene mutations (ATG→ACG) in primary MTC tumors and metastases and correlated the presence or absence of…”
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Fabry disease: reduced activities of respiratory chain enzymes with decreased levels of energy-rich phosphates in fibroblasts by Lücke, Thomas, Höppner, Wiebke, Schmidt, Esther, Illsinger, Sabine, Das, Anibh M

“…Fabry disease (FD, MIM 301500) caused by a deficient activity of α-galactosidase A is characterized by intralysosomal storage of glycosphingolipids. Main…”
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Ultra sharp crystalline silicon tip array used as field emitter by Mehr, W., Wolff, A., Frankenfeld, H., Skaloud, T., Höppner, W., Bugiel, E., Lärz, J., Hunger, B.

“…This article describes the fabrication of single crystal silicon field emission tip arrays. Each array consists of 2500 tips. We used 4 in. (100) oriented n…”
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Mutation screening and isoform prevalence of the follicle stimulating hormone receptor gene in women with premature ovarian failure, resistant ovary syndrome and polycystic ovary syndrome by Conway, Gerard S., Conway, Emily, Walker, Caroline, Hoppner, Gromoll, Simoni

“…OBJECTIVE To determine whether mutations in the FSH receptor gene are associated with premature ovarian failure (POF) or resistant ovary syndrome (ROS) in…”
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Presymptomatic genetic screening in families with multiple endocrine neoplasia type 2 by FRILLING, A, HÖPPNER, W, ENG, C, MULLIGAN, L, RAUE, F, BROELSCH, C. E

“…Medullary thyroid carcinoma occurs sporadically or as a part of the inherited cancer syndrome multiple endocrine neoplasia (MEN) type 2. The MEN 2 gene has…”
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Molecular genetic alterations on chromosomes 11 and 22 in ependymomas by Lamszus, Katrin, Lachenmayer, Lenard, Heinemann, Uta, Kluwe, Lan, Finckh, Ulrich, Höppner, Wolfgang, Stavrou, Dimitrios, Fillbrandt, Regina, Westphal, Manfred

“…Ependymomas arise from the ependymal cells at different locations throughout the brain and spinal cord. These tumors have a broad age distribution with a range…”
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