Search Results - "Buechner, S"

Common skin disorders of the penis by Buechner, S.A.

“…Summary Diseases of the male genitalia range from infectious lesions to inflammatory and neoplastic conditions, including many genital manifestations of more…”
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Homozygous missense mutation in the lamin A/C gene causes autosomal recessive Hutchinson-Gilford progeria syndrome by Plasilova, M, Chattopadhyay, C, Pal, P, Schaub, N A, Buechner, S A, Mueller, Hj, Miny, P, Ghosh, A, Heinimann, K

“…[...]to B-type lamins, which are ubiquitously expressed in all cell types at all developmental stages, A-type lamins are absent in the cells of the early…”
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Perspective tracking in the real world: Gaze angle analysis in a collaborative wayfinding task by Schwarzkopf, S., Büchner, S. J., Hölscher, C., Konieczny, L.

“…In collaborative wayfinding, partners jointly search the environment for task-relevant information. Studies on collaborative search suggest that it is most…”
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T-cadherin loss induces an invasive phenotype in human keratinocytes and squamous cell carcinoma (SCC) cells in vitro and is associated with malignant transformation of cutaneous SCC in vivo by Pfaff, D., Philippova, M., Buechner, S.A., Maslova, K., Mathys, T., Erne, P., Resink, T.J.

“…Summary Background  Cadherins play important roles in controlling keratinocyte growth, differentiation and survival. Atypical…”
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Evolutionary history and species delimitations: a case study of the hazel dormouse, Muscardinus avellanarius by Mouton, A., Mortelliti, A., Grill, A., Sara, M., Kryštufek, B., Juškaitis, R., Latinne, A., Amori, G., Randi, E., Büchner, S., Schulz, B., Ehlers, S., Lang, J., Adamik, P., Verbeylen, G., Dorenbosch, M., Trout, R., Elmeros, M., Aloise, G., Mazzoti, S., Matur, F., Poitevin, F., Michaux, J. R.

“…Robust identification of species and significant evolutionary units (ESUs) is essential to implement appropriate conservation strategies for endangered…”
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Reduced Arousability during sleep in patients with Familial Dysautonomia by Moeller, S, Buechner, S, Czarkowska, H, Koehn, J, Ayappa, I, Axelrod, F.B, Rapoport, D.M, Hilz, M.J

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Delayed onset of graft‐versus‐host disease in immunodeficent human leucocyte antigen‐DQ8 transgenic, murine major histocompatibility complex class II‐deficient mice repopulated by human peripheral blood mononuclear cells by Büchner, S. M., Sliva, K., Bonig, H., Völker, I., Waibler, Z., Kirberg, J., Schnierle, B. S.

“…Summary Haematopoietic humanization of mice is used frequently to study the human immune system and its reaction upon experimental intervention…”
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High T-cadherin expression is a feature of basal cell carcinoma by Buechner, S.A., Philippova, M., Erne, P., Mathys, T., Resink, T.J.

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A young male patient affected by Anderson–Fabry's disease presenting recurrent strokes. A case report by Buechner, S, Borsini, W

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Changes of epidermal mu-opiate receptor expression and nerve endings in chronic atopic dermatitis by Bigliardi-Qi, M, Lipp, B, Sumanovski, L T, Buechner, S A, Bigliardi, P L

“…There is increasing evidence that neuropeptides such as a substance P, neurotrophins or beta-endorphin, an endogenous agonist for mu-opioid receptor, are…”
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Fas-ligand gene silencing in basal cell carcinoma tissue with small interfering RNA by JI, J, WERNLI, M, MIELGO, A, BUECHNER, S. A, ERB, P

“…Basal cell carcinoma (BCC) is the most frequent cancer in the Caucasian population. Cells of BCC strongly express Fas-ligand (FasL), a member of the tumor…”
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Central nervous system involvement in Anderson–Fabry disease: a clinical and MRI retrospective study by Buechner, S, Moretti, M, Burlina, A P, Cei, G, Manara, R, Ricci, R, Mignani, R, Parini, R, Di Vito, R, Giordano, G P, Simonelli, P, Siciliano, G, Borsini, W

“…Background:Anderson–Fabry disease (AFD) is an X-linked lysosomal storage disorder caused by deficiency of alpha-galactosidase A. Central nervous system (CNS)…”
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Pancreatic panniculitis in a patient with an acinar cell cystadenocarcinoma of the pancreas by Beltraminelli, H S, Buechner, S A, Häusermann, P

“…We describe a 60-year-old man with pancreatic panniculitis associated with arthritis and peripheral eosinophilia in whom the skin symptoms led to a diagnosis…”
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Cutaneous plasmablastic lymphoma in an HIV-positive male: an unrecognized cutaneous manifestation by Häusermann, P, Khanna, N, Buess, M, Itin, P H, Battegay, M, Dirnhofer, S, Buechner, S A

“…Plasmablastic lymphoma (PBL) is a rare and relatively new entity originally described in HIV-infected individuals. This subset of Epstein-Barr-virus…”
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Cutaneous myiasis due to Dermatobia hominis by Hohenstein, E J, Buechner, S A

“…Cutaneous myiasis caused by the human botfly Dermatobia hominis involves the infestation of tissue with dipterous fly larvae and is common in the neotropical…”
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At the outer part of the active site in Trypanosoma cruzi glucokinase: The role of phenylalanine 337 by Carey, Shane M., Kearns, Sean P., Millington, Matthew E., Buechner, Gregory S., Alvarez, Beda E., Daneshian, Leily, Abiskaroon, Brendan, Chruszcz, Maksymilian, D'Antonio, Edward L.

“…The hole mutagenesis approach was used to interrogate the importance of F337 in Trypanosoma cruzi glucokinase (TcGlcK) in order to understand the complete set…”
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Papular elastorrhexis. report of five cases by Buechner, S A, Itin, P

“…Papular elastorrhexis is a rare disorder that occurs predominantly during adolescence. We report 5 patients with asymptomatic white, nonfollicular, firm…”
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The crystal structure of glucokinase from Leishmania braziliensis by Buechner, Gregory S., Millington, Matthew E., Perry, Kay, D’Antonio, Edward L.

“…•The X-ray crystal structure of L. braziliensis glucokinase was solved at 1.85 Å resolution.•L. braziliensis glucokinase crystallized in the apo form and open…”
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Advanced electrocardiographic predictors of mortality in familial dysautonomia by Solaimanzadeh, I, Schlegel, T.T, Feiveson, A.H, Greco, E.C, DePalma, J.L, Starc, V, Marthol, H, Tutaj, M, Buechner, S, Axelrod, F.B, Hilz, M.J

“…Abstract Objective To identify electrocardiographic predictors of mortality in patients with familial dysautonomia (FD). Methods Ten-minute resting…”
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Circumscribed juvenile pityriasis rubra pilaris by Arnold, AW, Buechner, SA

“…ABSTRACT We report the case of a 20‐year‐old woman with a 10‐year history of circumscribed juvenile‐onset pityriasis rubra pilaris (PRP, type IV). Our patient…”
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