Search Results - "IMM, A"

Establishing an algorithm for molecular genetic diagnostics in 127 families with juvenile nephronophthisis by Hildebrandt, Friedhelm, Rensing, Cornelia, Betz, Regina C., Sommer, Ulrike, Birnbaum, Stefanie, Imm, Anita, Omran, Heymut, Leipoldt, Michael, Otto, Edgar, the Arbeitsgemeinschaft Für Paediatrische Nephrologie (APN) Study Group

“…Establishing an algorithm for molecular genetic diagnostics in 127 families with juvenile nephronophthisis. Juvenile nephronophthisis (NPH1), an autosomal…”
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Fluid resuscitation in circulatory shock by Imm, A, Carlson, R W

“…Over the past century, the treatment of various forms of circulatory shock has included fluid resuscitation with either crystalloidal or colloidal solutions…”
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Patients with mutations in NPHS2 (Podocin) do not respond to standard steroid treatment of nephrotic syndrome by RUF, Rainer G, LICHTENBERGER, Anne, BAGGA, Arvind, NEUHAUS, Thomas, FUCHSHUBER, Arno, BAKKALOGLU, Aysin, HILDEBRANDT, Friedhelm, KARLE, Stephanie M, HAAS, Johannes P, ANACLETO, Franzisco E, SCHULTHEISS, Michael, ZALEWSKI, Isabella, IMM, Anita, RUF, Eva-Maria, MUCHA, Bettina

“…Nephrotic syndrome (NS) represents the association of proteinuria, hypoalbuminemia, edema, and hyperlipidemia. Steroid-resistant NS (SRNS) is defined by…”
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Nephrocystin-5, a ciliary IQ domain protein, is mutated in Senior-Loken syndrome and interacts with RPGR and calmodulin by Hildebrandt, Friedhelm, Otto, Edgar A, Loeys, Bart, Khanna, Hemant, Hellemans, Jan, Sudbrak, Ralf, Fan, Shuling, Muerb, Ulla, O'Toole, John F, Helou, Juliana, Attanasio, Massimo, Utsch, Boris, Sayer, John A, Lillo, Concepcion, Jimeno, David, Coucke, Paul, Paepe, Anne De, Reinhardt, Richard, Klages, Sven, Tsuda, Motoyuki, Kawakami, Isao, Kusakabe, Takehiro, Omran, Heymut, Imm, Anita, Tippens, Melissa, Raymond, Pamela A, Hill, Jo, Beales, Phil, He, Shirley, Kispert, Andreas, Margolis, Benjamin, Williams, David S, Swaroop, Anand

“…Nephronophthisis (NPHP) is the most frequent genetic cause of chronic renal failure in children. Identification of four genes mutated in NPHP subtypes 1-4…”
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Serotyping and electron microscopy studies of Staphylococcus aureus clinical isolates with monoclonal antibodies to capsular polysaccharide types 5 and 8 by HOCHKEPPEL, H. K, BRAUN, D. G, VISCHER, W, IMM, A, SUTTER, S, STAEUBLI, U, GUGGENHEIM, R, KAPLAN, E. L, BOUTONNIER, A, FOURNIER, J. M

“…Article Usage Stats Services JCM Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley…”
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Prevalence of WT1 mutations in a large cohort of patients with steroid-resistant and steroid-sensitive nephrotic syndrome by Ruf, Rainer G., Schultheiss, Michael, Lichtenberger, Anne, Karle, Stephanie M., Zalewski, Isabella, Mucha, Bettina, Everding, Anne Schulze, Neuhaus, Thomas, Patzer, Ludwig, Plank, Christian, Haas, Johannes P., Ozaltin, Fatih, Imm, Anita, Fuchshuber, Arno, Bakkaloglu, Aysin, Hildebrandt, Friedhelm

“…Prevalence of WT1 mutations in a large cohort of patients with steroid-resistant and steroid-sensitive nephrotic syndrome. Nephrotic syndrome (NS) represents…”
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Specificity of H-2-linked Ir gene control in mice: demonstration of T helper cells recognizing branched synthetic polypeptides in low responder mice by Stotter, H, Imm, A, Meyer-Delius, M, Rude, E

“…This report provides evidence for the presence of T helper cells capable of recognizing the polypeptide antigens T6-A--L and (H,G)-A--L in low responder mice…”
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Mapping a new suggestive gene locus for autosomal dominant nephrolithiasis to chromosome 9q33.2–q34.2 by total genome search for linkage by Wolf, Matthias T. F., Zalewski, Isabella, Martin, Félix Claverie, Ruf, Rainer, Müller, Dominik, Hennies, Hans C., Schwarz, Stella, Panther, Franziska, Attanasio, Massimo, Acosta, Hilaria G., Imm, Anita, Lucke, Barbara, Utsch, Boris, Otto, Edgar, Nurnberg, Peter, Nieto, Victor Garcia, Hildebrandt, Friedhelm

“…Background. Nephrolithiasis is a complex, multifactorial disease resulting from genetic and environmental interaction. The pathogenesis of nephrolithiasis is…”
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Improved strategy for molecular genetic diagnostics in juvenile nephronophthisis by Heninger, Erika, Otto, Edgar, Imm, Anita, Caridi, Gianluca, Hildebrandt, Friedhelm

“…Juvenile or type 1 nephronophthisis (NPH1), an autosomal recessive cystic kidney disease, represents the most common genetic cause of end-stage renal disease…”
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Evidence for a B-cell memory-forming factor (BMFF) able to reconstitute cyclosporin-A-induced suppression of the secondary response by Jurado, A, Imm, A, Heusser, C

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Card sorting as a measure of learning and serial action by Tinker, M. A, Imm, A. J, Swanson, C. A

“…The problem involves the determination of the reliability of performance, the relation between performances, and progress in learning for five different…”
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A gene locus for steroid-resistant nephrotic syndrome with deafness maps to chromosome 14q24.2 by RUF, Rainer G, WOLF, Matthias T. F, LENNERT, Thomas, FUCHSHUBER, Arno, NURNBERG, Peter, HILDEBRANDT, Friedhelm, HENNIES, Hans C, LUCKE, Barbara, ZINN, Christina, VARNHOLT, Verena, LICHTENBERGER, Anne, PASCH, Andreas, IMM, Anita, BRIESE, Sonia

“…Steroid-resistant nephrotic syndrome (SRNS) leads to end-stage renal disease (ESRD) in childhood or young adulthood. Positional cloning for genes causing SRNS…”
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A deletion distinct from the classical homologous recombination of juvenile nephronophthisis type 1 (NPH1) allows exact molecular definition of deletion breakpoints by Otto, Edgar, Betz, Regina, Rensing, Cornelia, Schätzle, Silvia, Kuntzen, Thomas, Vetsi, Thalia, Imm, Anita, Hildebrandt, Friedhelm

“…Juvenile nephronophthisis, an autosomal recessive cystic kidney disease, is the most common genetic cause of end‐stage renal disease in children and young…”
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Specificity of H-2-linked Ir gene control in mice: recognition of the core structure A--L in defined sequence analogues of (T,G,)-A--L by Stötter, H, Imm, A, Meyer-Delius, M, Rüde, E

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Roles of Milk Fat Globule Membrane on Fat Digestion and Infant Nutrition by Chai, Changhoon, Oh, Sejong, Imm, Jee-Young

“…Milk fats are present as globules emulsified in the aqueous phase of milk and stabilized by a delicate membrane architecture called milk fat globule membrane…”
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Ecklonia cava Extract Containing Dieckol Suppresses RANKL-Induced Osteoclastogenesis via MAP Kinase/NF-κB Pathway Inhibition and Heme Oxygenase-1 Induction by Kim, Seonyoung, Kang, Seok-Seong, Choi, Soo-Im, Kim, Gun-Hee, Imm, Jee-Young

“…Ecklonia cava, an edible marine brown alga (Laminariaceae), is a rich source of bioactive compounds such as fucoidan and phlorotannins. Ecklonia cava extract…”
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Combination of Milk Polar Lipids and Casein Hydrolysate as a Healthy Emulsifier for Ice Cream by Ji-Hwa Park, Yu Bin Lee, Sung Ho Lee, Eunkyung Ko, Jee-Young Imm

“…The demand for healthy ingredients in food products including ice cream, is continuously increasing. The potential of a combination of milk polar lipids (MPL)…”
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Effect of Modified Casein to Whey Protein Ratio on Dispersion Stability, Protein Quality and Body Composition in Rats by Jeong, Eun Woo, Park, Gyu Ri, Kim, Jiyun, Yun, So-Yul, Imm, Jee-Young, Lee, Hyeon Gyu

“…The present study was designed to investigate the effects of protein formula with different casein (C) to whey protein (W) ratios on dispersion stability,…”
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Effects of Lactobacillus reuteri MG5346 on Receptor Activator of Nuclear Factor-Kappa B Ligand (RANKL)-Induced Osteoclastogenesis and Ligature-Induced Experimental Periodontitis Rats by Yu-Jin Jeong, Jae-In Jung, YongGyeong Kim, Chang-Ho Kang, Jee-Young Imm

“…Effects of culture supernatants of Lactobacillus reuteri MG5346 (CS-MG5346) on receptor activator of nuclear factor-kappa B ligand (RANKL)-induced…”
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Erratum to: Effect of Modified Casein to Whey Protein Ratio on Dispersion Stability, Protein Quality and Body Composition in Rats by Eun Woo Jeong, Gyu Ri Park, Jiyun Kim, So-Yul Yun, Jee-Young Imm, Hyeon Gyu Lee

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