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Krause, R.; Hemberger, M.; Himmelbauer, H.; Kalscheuer, V.; Fundele, R. H.: Identification and characterization of G90, a novel mouse RNA that lacks an extensive open reading frame. Gene 232 (1), pp. 35 - 42 (1999)
1242.
Journal Article
van de Wetering, R. A.; Gabreels-Festen, A. A.; Kremer, H.; Kalscheuer, V. M.; Gabreels, F. J.; Mariman, E. C.: Regulation and expression of the murine PMP22 gene. Mamm Genome 10 (4), pp. 419 - 22 (1999)
1243.
Journal Article
Neitzel, H.; Kalscheuer, V.; Henschel, S.; Digweed, M.; Sperling, K.: Beta-heterochromatin in mammals: evidence from studies in Microtus agrestis based on the extensive accumulation of L1 and non-L1 retroposons in the heterochromatin. Cytogenet Cell Genet 80 (1-4), pp. 165 - 72 (1998)
1244.
Journal Article
Riesewijk, A. M.; Blagitko, N.; Schinzel, A. A.; Hu, L.; Schulz, U.; Hamel, B. C.; Ropers, H. H.; Kalscheuer, V. M.: Evidence against a major role of PEG1/MEST in Silver-Russell syndrome. Eur J Hum Genet 6 (2), pp. 114 - 20 (1998)
1245.
Journal Article
Riesewijk, A. M.; Xu, Y. Q.; Schepens, M. T.; Mariman, E. M.; Polychronakos, C.; Ropers, H. H.; Kalscheuer, V. M.: Absence of an obvious molecular imprinting mechanism in a human fetus with monoallelic IGF2R expression. Biochem Biophys Res Commun 245 (1), pp. 272 - 7 (1998)
1246.
Journal Article
Riesewijk, A. M.; Hu, L.; Schulz, U.; Tariverdian, G.; Hoglund, P.; Kere, J.; Ropers, H. H.; Kalscheuer, V. M.: Monoallelic expression of human PEG1/MEST is paralleled by parent-specific methylation in fetuses. Genomics 42 (2), pp. 236 - 44 (1997)
1247.
Journal Article
Kalscheuer, V.; Singh, A. P.; Nanda, I.; Sperling, K.; Neitzel, H.: Evolution of the gonosomal heterochromatin of Microtus agrestis: rapid amplification of a large, multimeric, repeat unit containing a 3.0-kb (GATA)11-positive, middle repetitive element. Cytogenet Cell Genet 73 (3), pp. 171 - 8 (1996)
1248.
Journal Article
Riesewijk, A. M.; Schepens, M. T.; Mariman, E. M.; Ropers, H. H.; Kalscheuer, V. M.: The MAS proto-oncogene is not imprinted in humans. Genomics 35 (2), pp. 380 - 2 (1996)
1249.
Journal Article
Riesewijk, A. M.; Schepens, M. T.; Welch, T. R.; van den Berg-Loonen, E. M.; Mariman, E. M.; Ropers, H. H.; Kalscheuer, V. M.: Maternal-specific methylation of the human IGF2R gene is not accompanied by allele-specific transcription. Genomics 31 (2), pp. 158 - 66 (1996)

Book (2)

1250.
Book
Daskalaki, A.: Medical Advancements in Aging and Regenerative Technologies: Clinical Tools and Applications. IGI Global (2012)
1251.
Book
Lazakidou , A.; Daskalaki, A.: Quality Assurance in Healthcare Service Delivery, Nursing and personalized Medicine: Technologies and Processes. IGI Global, Hershey PA (2012), 302 pp.

Book Chapter (24)

1252.
Book Chapter
Jourdain, C.; Eichstädt, B.; Schubert, D.: A Method for Characterizing Protein-Histone Peptide Interactions In Vitro. In: Methods for Plant Nucleus and Chromatin Studies. Methods in Molecular Biology., Vol. 2873, pp. 167 - 184. Humana Press, New York, NY (2024)
1253.
Book Chapter
Zi, Z.; Li, Y.: Optogenetic Control of TGF-β Signaling. In: TGF-Beta Signaling, pp. 113 - 124 (Eds. Zi, Z.; Liu, Xuedong). Humana Press, Totowa. New Jersey (2022)
1254.
Book Chapter
Deng, D.; Zi, Z.: Absolute Quantification of TGF-β Signaling Proteins Using Quantitative Western Blot. In: Methods in Molecular Biology 2488: TGF-Beta Signaling, Vol. 2488, pp. 1 - 12 (Ed. Walker, J. M.). Humana Press, Totowa, New Jersey (2022)
1255.
Book Chapter
Genolet, O.; Ravid-Lustig, L.; Schulz, E. G.: Dissecting molecular phenotypes through FACS-based pooled CRISPR screens. In: Embryonic Stem Cell Protocols. Methods in Molecular Biology, 2520., Vol. 2520, pp. 1 - 24 (Ed. Turksen, K.). Humana Press, New York, NY (2022)
1256.
Book Chapter
Hoehe, M. R.; Herwig, R.: Analysis of 1276 Haplotype-Resolved Genomes Allows Characterization of Cis- and Trans-Abundant Genes. In: Haplotyping. Methods in Molecular Biology (Springer Protocols), Vol. 2590, pp. 237 - 272 (Eds. Peters, B. A.; Drmanac, R.). Humana Press (Springer Science+Business Media, Springer-Verlag GmbH), New York, NY (2022)
1257.
Book Chapter
Jasnovidova, O.; Arnold, M.; Mayer, A.: Illuminating enhancer transcription at nucleotide resolution with native elongating transcript sequencing (NET-Seq). In: Enhancers and Promoters - Methods and Protocols (Methods in Molecular Biology ; 2351), Vol. 2351, pp. 41 - 65 (Ed. Borggrefe, T.). Humana, New York, NY (2021)
1258.
Book Chapter
Gjaltema, R. A. F.; Schulz, E. G.: CRISPR/dCas9 switch systems for temporal transcriptional control. In: Epigenome Editing. Methods in Molecular Biology., Vol. 1767, pp. 167 - 185 (Eds. Jeltsch , A.; Rots, M.). Humana Press, New York (2018)
1259.
Book Chapter
Mayer, A.; Churchman, L. S.: A detailed protocol for subcellular RNA sequencing (subRNA-seq). In: Current Protocols in Molecular Biology, Vol. Suppl. 120, pp. 4.29.1 - 4.29.18 (Ed. Ausubel, F. M.). John Wiley & Sons, Inc., Hoboken, NJ (2017)
1260.
Book Chapter
Suk, E. K.; Schulz , S.; Mentrup, B.; Huebsch, T.; Duitama, J.; Hoehe, M. R.: A Fosmid Pool-Based Next Generation Sequencing Approach to Haplotype-Resolve Whole Genomes. In: Haplotyping: Methods and Protocols (Eds. Tiemann-Boege, I.; Betancourt, A.) (2017)
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