List of bibliographic references indexed by Technique FISH
Number of relevant bibliographic references: 21.
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| Ident. | Authors (with country if any) | Title |
|---|
| 000402 (2017) |
David Harker [États-Unis] ; Michael Jennings [États-Unis] ; Patrick Mcdonough [États-Unis] ; Melissa Mauskar [États-Unis] ; Stephanie Savory [États-Unis] ; Gregory A. Hosler [États-Unis] ; Travis Vandergriff [États-Unis] | MYC amplification in angiosarcomas arising in the setting of chronic lymphedema of morbid obesity. |
| 002178 (2015) |
Shuhei Yoshida [Japon] ; Rodrigo Hamuy [Japon] ; Yuuichi Hamada [Japon] ; Hiroshi Yoshimoto [Japon] ; Akiyoshi Hirano [Japon] ; Sadanori Akita [Japon] | Adipose-derived stem cell transplantation for therapeutic lymphangiogenesis in a mouse secondary lymphedema model. |
| 002B72 (2014) |
Paula S. Ginter [États-Unis] ; Juan Miguel Mosquera [États-Unis] ; Theresa Y. Macdonald [États-Unis] ; Timothy M. D'Alfonso [États-Unis] ; Mark A. Rubin [États-Unis] ; Sandra J. Shin [États-Unis] | Diagnostic utility of MYC amplification and anti-MYC immunohistochemistry in atypical vascular lesions, primary or radiation-induced mammary angiosarcomas, and primary angiosarcomas of other sites. |
| 002F16 (2013) |
John K. Feller [États-Unis] ; Meera Mahalingam | c-myc and cutaneous vascular neoplasms. |
| 003800 (2013) |
H T El-Bassyouni [Égypte] ; A. El-Gerzawy ; O. Eid ; M O El-Ruby | Clinical and cytogenetic study of a non mosaic 46, X, isodicentric Yq in an Egyptian patient with Turner syndrome. |
| 004645 (2012) |
Antoine Italiano [États-Unis, France] ; Rachael Thomas [États-Unis] ; Matthew Breen [États-Unis] ; Lei Zhang [États-Unis] ; Aimee M. Crago [États-Unis] ; Samuel Singer [États-Unis] ; Raya Khanin [États-Unis] ; Robert G. Maki [États-Unis] ; Aleksandra Mihailovic [États-Unis] ; Markus Hafner [États-Unis] ; Tom Tuschl [États-Unis] ; Cristina R. Antonescu [États-Unis] | The miR‐17‐92 cluster and its target THBS1 are differentially expressed in angiosarcomas dependent on MYC amplification |
| 004789 (2012) |
Anthony P. Fernandez [États-Unis] ; Yang Sun [États-Unis] ; Raymond R. Tubbs [États-Unis] ; John R. Goldblum [États-Unis] ; Steven D. Billings [États-Unis] | FISH for MYC amplification and anti‐MYC immunohistochemistry: useful diagnostic tools in the assessment of secondary angiosarcoma and atypical vascular proliferations |
| 004D30 (2011) |
Agata M. Bogusz [États-Unis] ; Sean M. Hussey ; Payal Kapur ; Yan Peng ; S Tunc Gokaslan | Massive localized lymphedema with unusual presentations: report of 2 cases and review of the literature. |
| 005591 (2010) |
Rosa Fernandez [Espagne] ; Eduardo Pasaro | Tall stature and gonadal dysgenesis in a non-mosaic girl 45,X. |
| 005A84 (2010) |
Johanna Manner [Allemagne] ; Bernhard Radlwimmer [Allemagne] ; Peter Hohenberger [Allemagne] ; Katharina Mössinger [Allemagne] ; Stefan Küffer [Allemagne] ; Christian Sauer [Allemagne] ; Djeda Belharazem [Allemagne] ; Andreas Zettl [Suisse] ; Jean-Michel Coindre [France] ; Christian Hallermann [Allemagne] ; Jörg Thomas Hartmann [Allemagne] ; Detlef Katenkamp [Allemagne] ; Kathrin Katenkamp [Allemagne] ; Patrick Schöffski [Belgique] ; Raf Sciot [Belgique] ; Agnieszka Wozniak [Belgique] ; Peter Lichter [Allemagne] ; Alexander Marx [Allemagne] ; Philipp Ströbel [Allemagne] | MYC High Level Gene Amplification Is a Distinctive Feature of Angiosarcomas after Irradiation or Chronic Lymphedema |
| 007258 (2007) |
Mylène Béri-Deixheimer [France] ; Marie-José Gregoire ; Annick Toutain ; Karène Brochet ; Sylvain Briault ; Jean-Luc Schaff ; Bruno Leheup ; Philippe Jonveaux | Genotype-phenotype correlations to aid in the prognosis of individuals with uncommon 20q13.33 subtelomere deletions: a collaborative study on behalf of the 'association des Cytogénéticiens de langue Française'. |
| 007644 (2007) |
Anita Rauch [Allemagne] ; Helmuth-Günther Dörr | Chromosome 5q subtelomeric deletion syndrome |
| 009226 (2003) |
Anita Rauch [Allemagne] ; Maike Beese [Allemagne] ; Ertan Mayatepek [Allemagne] ; Helmut-Günther Dörr [Allemagne] ; Dieter Wenzel [Allemagne] ; André Reis [Allemagne] ; Udo Trautmann [Allemagne] | A novel 5q35.3 subtelomeric deletion syndrome |
| 009723 (2002) |
P. H. Kvist ; E. S. Jensen ; B. Aalbaek [Danemark] ; H. E. Jensen [Danemark] | Evaluation of the Pathology, Pathogenesis and Aetiology of Auricular Elephantiasis in Slaughter Pigs |
| 00A031 (2001) |
Catherine A. Boucher ; Carole A. Sargent ; Tsutomu Ogata ; Nabeel A. Affara | Breakpoint analysis of Turner patients with partial Xp deletions: implications for the lymphoedema gene location [Original article] [Original article] |
| 00A211 (2000) |
Jianming Fang ; Susan L. Dagenais ; Robert P. Erickson ; Martin F. Arlt ; Michael W. Glynn ; Jerome L. Gorski ; Laurie H. Seaver [États-Unis] ; Thomas W. Glover | Mutations in FOXC2 (MFH-1), a Forkhead Family Transcription Factor, Are Responsible for the Hereditary Lymphedema-Distichiasis Syndrome |
| 00AE54 (1999) |
David Mowat [Australie] ; Anna Jauch [Allemagne] ; Lisa Robson [Australie] ; Arabella Smith [Australie] | Duplication within chromosome 5q characterized by fluorescence in situ hybridization |
| 00B524 (1998) |
Andrew R. Zinn [États-Unis] ; Vijay S. Tonk ; Zhong Chen ; Wendy L. Flejter ; H. Allen Gardner ; Rudy Guerra ; Harvey Kushner [États-Unis] ; Stuart Schwartz ; Virginia P. Sybert ; Daniel L. Van Dyke ; Judith L. Ross [États-Unis] | Evidence for a Turner Syndrome Locus or Loci at Xp11.2-p22.1 |
| 00C327 (1995) |
R P Erickson [États-Unis] ; L. Hudgins ; J F Stone ; S. Schmidt ; C. Wilke ; T W Glover | A "balanced" Y;16 translocation associated with Turner-like neonatal lymphedema suggests the location of a potential anti-Turner gene on the Y chromosome. |
| 012790 (????) |
D. Simm [Allemagne] ; K. Degenhardt ; C. Gerdemann ; T M K. Völkl ; A. Rauch ; H G Dörr | [Chronological age of patients with Turner syndrome at diagnosis]. |
| 012F87 (????) |
Konrad Oexle [Allemagne] ; Maja Hempel ; Anna Jauch ; Thomas Meitinger ; Núria Rivera-Brugués ; Sabine Stengel-Rutkowski ; Tim Strom | 3.7 Mb tandem microduplication in chromosome 5p13.1-p13.2 associated with developmental delay, macrocephaly, obesity, and lymphedema. Further characterization of the dup(5p13) syndrome. |
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