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A Jauch

Showing results (91-100 of 109) with videos related to

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Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1993
Role of chromosome territories in the functional compartmentalization of the cell nucleusT Cremer, A Kurz, R Zirbel, et al.
European Journal of Cancer (Oxford, England : 1990)|March 28, 1998
Sensitive and reliable detection of genomic imbalances in human neuroblastomas using comparative genomic hybridisation analysisM Van Gele, N Van Roy, A Jauch, et al.
Leukemia|February 19, 2014
Predictive value of longitudinal whole-body magnetic resonance imaging in patients with smoldering multiple myelomaM Merz, T Hielscher, B Wagner, et al.
Blood|February 7, 2001
Concurrent activation of a novel putative transforming gene, myeov, and cyclin D1 in a subset of multiple myeloma cell lines with t(11;14)(q13;q32)J W Janssen, J W Vaandrager, T Heuser, et al.
Oncogene|August 16, 2006
Frequent loss of chromosome 9, homozygous CDKN2A/p14(ARF)/CDKN2B deletion and low TSC1 mRNA expression in pleomorphic xanthoastrocytomasR G Weber, A Hoischen, M Ehrler, et al.
Cancer Genetics and Cytogenetics|February 15, 2001
Comparative genomic hybridization in childhood acute lymphoblastic leukemia: correlation with interphase cytogenetics and loss of heterozygosity analysisI Scholz, S Popp, M Granzow, et al.
Leukemia|July 4, 2014
Immunoglobulin light-chain amyloidosis shares genetic susceptibility with multiple myelomaN Weinhold, A Försti, M I da Silva Filho, et al.
Neurogenetics|March 25, 2000
The human small conductance calcium-regulated potassium channel gene (hSKCa3) contains two CAG repeats in exon 1, is on chromosome 1q21.3, and shows a possible association with schizophreniaO Wittekindt, A Jauch, E Burgert, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|February 5, 1999
Mapping the gene causing hereditary primary hyperparathyroidism in a Portuguese kindred to chromosome 1q22-q31C Williamson, B M Cavaco, A Jauch, et al.
Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde|July 27, 1999
Topical lomefloxacin 0.3% twice daily versus tobramycin 0.3% in acute bacterial conjunctivitis: A multicenter double-blind phase III studyP E Gallenga, L Lobefalo, L Colangelo, et al.
Pageof 11

Showing results (91-100 of 109) with videos related to

Sort By:
Pageof 11
Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1993
Role of chromosome territories in the functional compartmentalization of the cell nucleusT Cremer, A Kurz, R Zirbel, et al.
European Journal of Cancer (Oxford, England : 1990)|March 28, 1998
Sensitive and reliable detection of genomic imbalances in human neuroblastomas using comparative genomic hybridisation analysisM Van Gele, N Van Roy, A Jauch, et al.
Leukemia|February 19, 2014
Predictive value of longitudinal whole-body magnetic resonance imaging in patients with smoldering multiple myelomaM Merz, T Hielscher, B Wagner, et al.
Blood|February 7, 2001
Concurrent activation of a novel putative transforming gene, myeov, and cyclin D1 in a subset of multiple myeloma cell lines with t(11;14)(q13;q32)J W Janssen, J W Vaandrager, T Heuser, et al.
Oncogene|August 16, 2006
Frequent loss of chromosome 9, homozygous CDKN2A/p14(ARF)/CDKN2B deletion and low TSC1 mRNA expression in pleomorphic xanthoastrocytomasR G Weber, A Hoischen, M Ehrler, et al.
Cancer Genetics and Cytogenetics|February 15, 2001
Comparative genomic hybridization in childhood acute lymphoblastic leukemia: correlation with interphase cytogenetics and loss of heterozygosity analysisI Scholz, S Popp, M Granzow, et al.
Leukemia|July 4, 2014
Immunoglobulin light-chain amyloidosis shares genetic susceptibility with multiple myelomaN Weinhold, A Försti, M I da Silva Filho, et al.
Neurogenetics|March 25, 2000
The human small conductance calcium-regulated potassium channel gene (hSKCa3) contains two CAG repeats in exon 1, is on chromosome 1q21.3, and shows a possible association with schizophreniaO Wittekindt, A Jauch, E Burgert, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|February 5, 1999
Mapping the gene causing hereditary primary hyperparathyroidism in a Portuguese kindred to chromosome 1q22-q31C Williamson, B M Cavaco, A Jauch, et al.
Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde|July 27, 1999
Topical lomefloxacin 0.3% twice daily versus tobramycin 0.3% in acute bacterial conjunctivitis: A multicenter double-blind phase III studyP E Gallenga, L Lobefalo, L Colangelo, et al.
Pageof 11