Search Results - "Schoell, B"

Multicolor Spectral Karyotyping of Human Chromosomes by Schröck, E., du Manoir, S., Veldman, T., Schoell, B., Wienberg, J., Ferguson-Smith, M. A., Ning, Y., Ledbetter, D. H., Bar-Am, I., Soenksen, D., Garini, Y., Ried, T.

“…The simultaneous and unequivocal discernment of all human chromosomes in different colors would be of significant clinical and biologic importance…”
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Overexpression of the anti-apoptotic protein AVEN contributes to increased malignancy in hematopoietic neoplasms by Eißmann, M, Melzer, I M, Fernández, S B M, Michel, G, Hrabě de Angelis, M, Hoefler, G, Finkenwirth, P, Jauch, A, Schoell, B, Grez, M, Schmidt, M, Bartholomae, C C, Newrzela, S, Haetscher, N, Rieger, M A, Zachskorn, C, Mittelbronn, M, Zörnig, M

“…AVEN has been identified as an inhibitor of apoptosis, which binds to the adaptor protein, APAF-1, and thereby prevents apoptosome formation and mitochondrial…”
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Specific loss of chromosomes 1, 2, 6, 10, 13, 17, and 21 in chromophobe renal cell carcinomas revealed by comparative genomic hybridization by Speicher, MR, Schoell, B, du Manoir, S, Schrock, E, Ried, T, Cremer, T, Storkel, S, Kovacs, A, Kovacs, G

“…We analyzed 19 chromophobe renal cell carcinomas by means of comparative genomic hybridization. Two tumors revealed no numerical abnormalities. In the…”
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Mapping the Gene Causing Hereditary Primary Hyperparathyroidism in a Portuguese Kindred to Chromosome 1q22‐q31 by Williamson, C., Cavaco, B. M., Jauch, A., Dixon, P. H., Forbes, S., Harding, B., Holtgreve‐Grez, H., Schoell, B., Pereira, M. C., Font, A. P., Loureiro, M. M., Sobrinho, L. G., Santos, M. A., Thakker, R. V.

“…A Portuguese kindred with autosomal dominant isolated primary hyperparathyroidism (HPT) that was associated with parathyroid adenomas and carcinomas was…”
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Topokaryotyping demonstrates single cell variability and stress dependent variations in nuclear envelope associated domains by Jurisic, Anamarija, Robin, Chloé, Tarlykov, Pavel, Siggens, Lee, Schoell, Brigitte, Jauch, Anna, Ekwall, Karl, Sørensen, Claus Storgaard, Lipinski, Marc, Shoaib, Muhammad, Ogryzko, Vasily

“…Abstract Analysis of large-scale interphase genome positioning with reference to a nuclear landmark has recently been studied using sequencing-based single…”
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Initial field evaluation of the Harvard active ozone sampler for personal ozone monitoring by Geyh, A S, Roberts, P T, Lurmann, F W, Schoell, B M, Avol, E L

“…Assessing personal exposure to ozone has only been feasible recently with the introduction of passive ozone samplers. These devices are easy to use, but…”
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Comparison of genomic abnormalities between BRCAX and sporadic breast cancers studied by comparative genomic hybridization by Gronwald, Jacek, Jauch, Anna, Cybulski, Cezary, Schoell, Brigitte, Böhm‐Steuer, Barbara, Lener, Marcin, Grabowska, Ewa, Górski, Bohdan, Jakubowska, Anna, Domagała, Wenancjusz, Chosia, Maria, Scott, Rodney J., Lubiński, Jan

“…Very little is known about the chromosomal regions harbouring genes involved in initiation and progression of BRCAX‐associated breast cancers. We applied…”
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Molecular cytogenetic analysis of formalin-fixed, paraffin-embedded solid tumors by comparative genomic hybridization after universal DNA-amplification by Speicher, M R, du Manoir, S, Schröck, E, Holtgreve-Grez, H, Schoell, B, Lengauer, C, Cremer, T, Ried, T

“…We present a technique which allows the detection and chromosomal localization of DNA sequence copy number changes in solid tumor genomes from frozen sections…”
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Study of 30 patients with unexplained developmental delay and dysmorphic features or congenital abnormalities using conventional cytogenetics and multiplex FISH telomere (M-TEL) integrity assay by POPP, Susanne, SCHULZE, Birgit, KEARNEY, Lyndal, JAUCH, Anna, GRANZOW, Martin, KELLER, Monika, HOLTGREVE-GREZ, Heidi, SCHOELL, Brigitte, BROUGH, Michaela, HAGER, Hans-Dieter, TARIVERDIAN, Gholamali, BROWN, Jill

“…Cryptic subtelomeric chromosome rearrangements are a major cause of mild to severe mental retardation pointing out the necessity of sensitive screening…”
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MULTICOLOR KARYOTYPE ANALYSES OF MOUSE EMBRYONIC STEM CELLS by GUO, JIANLI, JAUCH, ANNA, HEIDI, HOLTGREVE-GREZ, SCHOELL, BRIGITTE, ERZ, DOROTHEE, SCHRANK, MARTINA, JANSSEN, JOHANNES W. G

“…The manipulation of embryonic stem (ES) cells to introduce directional genetic changes into the genome of mice has become an important tool in biomedical…”
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Multiplex FISH telomere integrity assay identifies an unbalanced cryptic translocation der(5)t(3;5)(q27;p15.3) in a family with three mentally retarded individuals by GRANZOW, M, POPP, S, KELLER, M, HOLTGREVE-GREZ, H, BROUGH, M, SCHOELL, B, RAUTERBERG-RULAND, I, HAGER, H.-D, TARIVERDIAN, G, JAUCH, A

“…Cryptic rearrangements involving the terminal regions of chromosomes are suspected to be the cause of idiopathic mental retardation in a significant number of…”
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Multicolor spectral karotyping of human chromosomes by Schrock, E, du Manoir, S, Veldman, T, Schoell, B

“…The simultaneous and unequivocal discernment of all human chromosomes in different colors would be of significant clinical and biologic importance…”
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A response to a commentary by Dr. Daniel J. Cher by Schoell, Kyle, BA, Buser, Zorica, PhD, Jakoi, Andre, MD, Pham, Martin, MD, Patel, Neil N., MD, Hsieh, Patrick C., MD, Liu, John C., MD, Wang, Jeffrey C., MD

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Specific loss of chromosomes 1, 2, 6, 10, 13, 17, and 21 in chromophobe renal cell carcinomas revealed by comparative genomic hydridization by SPEICHER, M. R, SCHOELL, B, DU MANOIR, S, SCHRÖCK, E, RIED, T, CREMER, T, STÖRKEL, S, KOVACS, A, KOVACS, G

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Einfluss der inflammatorischen, intraperitonealen Cytokine auf die Schmerzsymptomatik von Endometriose-Patientinnen by Scholl, B, Bersinger, NA, Mueller, MA

“…Abstract only…”
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Angiogenesis of liver metastases: role of sinusoidal endothelial cells by Gervaz, P, Scholl, B, Mainguene, C, Poitry, S, Gillet, M, Wexner, S

“…Tumor-induced angiogenesis requires migration and remodeling of endothelial cells derived from pre-existing blood vessels. Vascular endothelial growth factor…”
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Isochromosome 1q as an early genetic event in a child with intracranial ependymoma characterized by molecular cytogenetics by Granzow, Martin, Popp, Susanne, Weber, Susanne, Schoell, Brigitte, Holtgreve-Grez, Heidi, Senf, Leonore, Hager, Dieter, Boschert, Jürgen, Scheurlen, Wolfram, Jauch, Anna

“…Data concerning cytogenetic features of childhood ependymoma are rare. In this article, a gain of 1q was identified as the sole alteration in a primary…”
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Comparative genomic hybridization in childhood acute lymphoblastic leukemia: correlation with interphase cytogenetics and loss of heterozygosity analysis by Scholz, Inka, Popp, Susanne, Granzow, Martin, Schoell, Brigitte, Holtgreve-Grez, Heidi, Takeuchi, Seisho, Schrappe, Martin, Harbott, Jochen, Teigler-Schlegel, Andrea, Zimmermann, Martin, Fischer, Christine, Koeffler, H.Phillip, Bartram, Claus R, Jauch, Anna

“…We used comparative genomic hybridization (CGH) to study DNA copy number changes in 71 children with acute lymphoblastic leukemia (ALL) including 50 B-lineage…”
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Attenuated Change Blindness for Exogenously Attended Items in a Flicker Paradigm by Scholl, Brian J.

“…When two scenes are alternately displayed, separated by a mask, even large, repeated changes between the scenes often go unnoticed for surprisingly long…”
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Cecum volvulus by Halkic, N, Scholl, B

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