RUBIACEAE by N. Hahn

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RUBIACEAE by N. Hahn

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LAMIACEAE by N. Hahn, G. J. Bredenkamp

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Transcription factor genetics and biology in predisposition to bone marrow failure and hematological malignancy by Jiarna R. Zerella, Jiarna R. Zerella, Claire C. Homan, Claire C. Homan, Peer Arts, Peer Arts, Anna L. Brown, Anna L. Brown, Anna L. Brown, Hamish S. Scott, Hamish S. Scott, Hamish S. Scott, Christopher N. Hahn, Christopher N. Hahn, Christopher N. Hahn

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The 10th Barossa meeting: Cell Signalling to Cancer Medicine by Winnie L. Kan, Barbara J. McClure, Christopher N. Hahn, Jason A. Powell

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A study of residual lesions in horses that recovered from clinical signs of chronic equine dysautonomia by Elspeth M. Milne, R. Scott Pirie, Caroline N. Hahn, Jorge del‐Pozo, Dawn Drummond, Sharon Moss, Bruce C. McGorum

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Reducing the lipase LIPE in mutant α-synuclein mice improves Parkinson-like deficits and reveals sex differences in fatty acid metabolism by M.A. Adom, W.N. Hahn, T.D. McCaffery, T.E. Moors, X. Zhang, P. Svenningsson, D.J. Selkoe, S. Fanning, S. Nuber

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10.04 Spatial transcriptomics identifies metabolic dysregulation as a key driver of T cell exclusion in esophageal adenocarcinoma by J Sanders, TD de Gruijl, HWM van Laarhoven, J Van den Bossche, S Derks, EN Bos, N Hahn, I Nijman, DL van der Peet

Laser pulse-length dependent ablation and shock generation in silicon at 5×10^{14} W/cm^{2} intensities by M. Bailly-Grandvaux, E. N. Hahn, T. R. Joshi, K. Werellapatha, T. Cordova, R. E. Turner, J. E. Garay, R. B. Spielman, J. K. Wicks, F. N. Beg

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Genome-wide gene expression profiling identifies overlap with malignant adrenocortical tumours and novel mechanisms of inefficient steroidogenesis in familial ACTH-independent macr... by Gagliardi, Lucia, Ling, King Hwa, Chung, Hoow Kok, Carolan, Joseph, Brautigan, Peter, Kenyon, Rosalie, J. D'Andrea, Richard, Van der Hoek, Mark, N. Hahn, Christopher, Torpy, David

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Two monogenic disorders masquerading as one: severe congenital neutropenia with monocytosis and non-syndromic sensorineural hearing loss by Parvathy Venugopal, Lucia Gagliardi, Cecily Forsyth, Jinghua Feng, Kerry Phillips, Milena Babic, Nicola K. Poplawski, Hugh Young Rienhoff, Andreas W. Schreiber, Christopher N. Hahn, Anna L. Brown, Hamish S. Scott

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Generation of G51D and 3D mice reveals decreased α-synuclein tetramer-monomer ratios promote Parkinson’s disease phenotypes by Silke Nuber, Xiaoqun Zhang, Thomas D. McCaffery, Tim E. Moors, Marie-Alexandre Adom, Wolf N. Hahn, Dylan Martin, Maria Ericsson, Arati Tripathi, Ulf Dettmer, Per Svenningsson, Dennis J. Selkoe

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Author Correction: Generation of G51D and 3D mice reveals decreased α-synuclein tetramer-monomer ratios promote Parkinson’s disease phenotypes by Silke Nuber, Xiaoqun Zhang, Thomas D. McCaffery, Tim E. Moors, Marie-Alexandre Adom, Wolf N. Hahn, Dylan Martin, Maria Ericsson, Arati Tripathi, Ulf Dettmer, Per Svenningsson, Dennis J. Selkoe

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A novel germline SAMD9L mutation in a family with ataxia-pancytopenia syndrome and pediatric acute lymphoblastic leukemia by Jesse J.C. Cheah, Anna L. Brown, Andreas W. Schreiber, Jinghua Feng, Milena Babic, Sarah Moore, Chun-Chun Young, Miriam Fine, Kerry Phillips, Michael Guandalini, Peter Wilson, Nicola Poplawski, Christopher N. Hahn, Hamish S. Scott

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Self-reverting mutations partially correct the blood phenotype in a Diamond Blackfan anemia patient by Parvathy Venugopal, Sarah Moore, David M. Lawrence, Amee J. George, Ross D. Hannan, Sarah CE Bray, Luen Bik To, Richard J. D’Andrea, Jinghua Feng, Amanda Tirimacco, Alexandra L Yeoman, Chun Chun Young, Miriam Fine, Andreas W Schreiber, Christopher N. Hahn, Christopher Barnett, Ben Saxon, Hamish S. Scott

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A novel, somatic, transforming mutation in the extracellular domain of Epidermal Growth Factor Receptor identified in myeloproliferative neoplasm by D. A. Casolari, T. Nguyen, C. M. Butcher, D. G. Iarossi, C. N. Hahn, S. C. Bray, P. Neufing, W. T. Parker, J. Feng, K. Z. Y. Maung, A. Wee, L. Vidovic, C. H. Kok, P. G. Bardy, S. Branford, I. D. Lewis, S. W. Lane, H. S. Scott, D. M. Ross, R. J. D’Andrea

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TP53 mutation variant allele frequency of ≥10% is associated with poor prognosis in therapy-related myeloid neoplasms by Mithun Vinod Shah, Elizabeth Ngoc Hoa Tran, Syed Shah, Rakchha Chhetri, Anmol Baranwal, Dariusz Ladon, Carl Shultz, Aref Al-Kali, Anna L. Brown, Dong Chen, Hamish S. Scott, Patricia Greipp, Daniel Thomas, Hassan B. Alkhateeb, Deepak Singhal, Naseema Gangat, Sharad Kumar, Mrinal M. Patnaik, Christopher N. Hahn, Chung Hoow Kok, Ayalew Tefferi, Devendra K. Hiwase

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The RUNX1 database (RUNX1db): establishment of an expert curated RUNX1 registry and genomics database as a public resource for familial platelet disorder with myeloid malignancy by Claire C. Homan, Sarah L. King-Smith, David M. Lawrence, Peer Arts, Jinghua Feng, James Andrews, Mark Armstrong, Thuong Ha, Julia Dobbins, Michael W. Drazer, Kai Yu, Csaba Bödör, Alan Cantor, Mario Cazzola, Erin Degelman, Courtney D. DiNardo, Nicolas Duployez, Remi Favier, Stefan Fröhling, Jude Fitzgibbon, Jeffery M. Klco, Alwin Krämer, Mineo Kurokawa, Joanne Lee, Luca Malcovati, Neil V. Morgan, Georges Natsoulis, Carolyn Owen, Keyur P. Patel, Claude Preudhomme, Hana Raslova, Hugh Rienhoff, Tim Ripperger, Rachael Schulte, Kiran Tawana, Elvira Velloso, Benedict Yan, Paul Liu, Lucy A. Godley, Andreas W. Schreiber, Christopher N. Hahn, Hamish S. Scott, Anna L. Brown

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