Search Results - "Lindner, T. H."

easyLINKAGE-Plus—automated linkage analyses using large-scale SNP data by Hoffmann, K., Lindner, T. H.

“…We extended the original easyLINKAGE program by enabling linkage analyses for large-scale SNP data in addition to those of microsatellites. We implemented new…”
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German genome-wide linkage scan for type 2 diabetes supports the existence of a metabolic syndrome locus on chromosome 1p36.13 and a type 2 diabetes locus on chromosome 16p12.2 by Hoffmann, K, Mattheisen, M, Dahm, S, Nürnberg, P, Roe, C, Johnson, J, Cox, N. J, Wichmann, H. E, Wienker, T. F, Schulze, J, Schwarz, P. E, Lindner, T. H

“…Aims/hypothesis The aim was to identify type 2 diabetes susceptibility regions in 250 German families. Subjects and methods We conducted a genome-wide linkage…”
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Parameterization of the Optical Properties for Water Clouds in the Infrared by Lindner, T. H., Li, J.

“…A parameterization is presented for the optical properties of water clouds in the infrared spectrum. The cloud optical properties are parameterized in terms of…”
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Molecular genetics of MODY in Germany by Lindner, T H, Cockburn, B N, Bell, G I

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Hydronephrosis Resulting from Bilateral Ureteral Stenosis: A Late Complication of Polyoma BK Virus Cystitis? by Lindner, T. H., Ivovic, J., Maier, M., Niederwieser, D., Wickenhauser, C., Schwalenberg, T., Basara, N., Rasche, F.-M.

“…We report here a case of acute lymphoblastic leukemia in remission presenting a late-onset bilateral hydronephrosis probably due to polyoma BK virus-induced…”
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Diabetes und Nieren by Lindner, T. H.

“…Zusammenfassung Häufigkeit diabetischer Nierenerkrankungen In einigen europäischen Ländern blieb die Inzidenz der terminalen Niereninsuffizienz (ESRD…”
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Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus by Oda, Naohisa, Li, Xiangquan, Baier, Leslie J, Cox, Nancy J, Concannon, Patrick, Lindner, Tom H, Wei, Shan, Schwarz, Peter E.H, Hara, Manami, Bell, Graeme I, Colilla, Susan, Oda, Yukie, del Bosque-Plata, Laura, Iwasaki, Naoko, Bogardus, Clifton, Mashima, Hirosato, Schulze, Jan, Yoshiuchi, Issei, Boerwinkle, Eric, Horikawa, Yohko, Hanis, Craig L, Horikawa, Yukio, Orho-Melander, Marju, Groop, Leif, Hinokio, Yoshinori, Polonsky, Kenneth S

“…Type 2 or non-insulin-dependent diabetes mellitus (NIDDM) is the most common form of diabetes worldwide, affecting approximately 4% of the world's adult…”
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A Novel Syndrome of Diabetes Mellitus, Renal Dysfunction and Genital Malformation Associated with a Partial Deletion of the Pseudo-POU Domain of Hepatocyte Nuclear Factor-1β by Lindner, Tom H., Njølstad, Pål R., Horikawa, Yukio, Bostad, Leif, Bell, Graeme I., Søvik, Oddmund

“…Mutations in the homeodomain-containing transcription factor hepatocyte nuclear factor (HNF)-1β are the cause of one form of maturity-onset diabetes of the…”
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Evaluation of the BACTEC radiometric method for recovery of mycobacteria and drug susceptibility testing of Mycobacterium tuberculosis from acid-fast smear-positive specimens by ROBERTS, G. D, GOODMAN, N. L, HEIFETS, L, LARSH, H. W, LINDNER, T. H, MCCLATCHY, J. K, MCGINNIS, M. R, SIDDIQI, S. H, WRIGHT, P

“…Article Usage Stats Services JCM Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley…”
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Mutations in the coding region of the insulin promoter factor 1 gene are not a common cause of maturity-onset diabetes of the young in japanese subjects by HARA, M, LINDNER, T. H, PAZ, V. P, WANG, X, IWASAKI, N, OGATA, M, IWAMOTO, Y, BELL, G. I

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Molecular genetics of diabetes mellitus in Chinese subjects: identification of mutations in glucokinase and hepatocyte nuclear factor-1α genes in patients with early-onset Type 2 diabetes mellitus/MODY by Ng, M. C. Y., Cockburn, B. N., Lindner, T. H., Yeung, V. T. F., Chow, C. -C., So, W. -Y., Li, J. K. Y., Lo, Y. M. D., Lee, Z. S. K., Cockram, C. S., Critchley, J. A. J. H., Bell, G. I., Chan, J. C. N.

“…Summary Aims To examine the prevalence of identified MODY‐related genes in Chinese subjects with early onset Type 2 diabetes mellitus and a positive family…”
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Hemolytic kidney failure and transient ischemic attack in a 32-year-old female by Anders, R, Grohmann, M, Lindner, T H, Bergmann, C, Halbritter, J

“…We report on the case of a 32-year-old female patient who initially presented with oliguric acute renal failure, hemolytic anemia with moderate…”
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easyLINKAGE: a PERL script for easy and automated two-/multi-point linkage analyses by Lindner, Tom H., Hoffmann, K.

“…We have generated the program easyLINKAGE that combines automated setup and performance of linkage analyses and simulation under an easy to handle graphical…”
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The Author's Reply by Lindner, T. H.

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MPA: A treatment option for lymphocytic colitis and mesalamine‐induced interstitial nephritis by Halbritter, J., Wittenburg, H., Schiefke, I., Amann, K., Lindner, T., Rasche, F.M.

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Interstitial nephritis by Halbritter, J, Mayer, C, Rasche, F M, Amann, K, Lindner, T H

“…Drugs such as antibiotics, non-steroidal anti-inflammatory drugs and proton pump inhibitors, infections and systemic diseases can trigger interstitial…”
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Escobar Syndrome Is a Prenatal Myasthenia Caused by Disruption of the Acetylcholine Receptor Fetal γ Subunit by Hoffmann, Katrin, Müller, Juliane S., Stricker, Sigmar, Megarbane, Andre, Rajab, Anna, Lindner, Tom H., Cohen, Monika, Chouery, Eliane, Adaimy, Lynn, Ghanem, Ismat, Delague, Valerie, Boltshauser, Eugen, Talim, Beril, Horvath, Rita, Robinson, Peter N., Lochmüller, Hanns, Hübner, Christoph, Mundlos, Stefan

“…Escobar syndrome is a form of arthrogryposis multiplex congenita and features joint contractures, pterygia, and respiratory distress. Similar findings occur in…”
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A German genome-wide linkage scan for type 2 diabetes supports the existence of a metabolic syndrome locus on chromosome lp36.13 and a type 2 diabetes locus on chromosome 16p12.2 by HOFFMANN, K, MATTHEISEN, M, SCHWARZ, P. E, LINDNER, T. H, DAHM, S, NIIRNBERG, P, ROE, C, JOHNSON, J, COX, N. J, WICHMANN, H. E, WIENKER, T. F, SHUIZE, J

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Mutations in the gene encoding the lamin B receptor produce an altered nuclear morphology in granulocytes (Pelger-Huët anomaly) by Kaps, Reinhard, Sperling, Karl, Reis, André, Müller, Dietmar, Cruz, Norberto Sotelo, Olins, Donald E, Lucke, Barbara, Karl, Hartmut, Lindner, Tom H, Herrmann, Harald, Olins, Ada L, Ware, Russell E, Hoffmann, Katrin, Aznar, Justo, Vayá, Amparo, Dreger, Christine K, Shultz, Leonard D

“…Pelger-Huët anomaly (PHA; OMIM *169400) is an autosomal dominant disorder characterized by abnormal nuclear shape and chromatin organization in blood…”
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To: Lindner T, Cockburn BN, Bell GI (1999). Molecular genetics of MODY in Germany. Diabetologia 42: 121-123 by Ziemssen, F, Bellanné-Chantelot, C, Osterhoff, M, Schatz, H, Pfeiffer, A F H

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