Hakutulokset - Dan Doherty
- Näytetään 1 - 20 yhteensä 49 tuloksesta
- Siirry seuraavalle sivulle
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Joubert Syndrome: Insights Into Brain Development, Cilium Biology, and Complex Disease Tekijä Dan Doherty
Julkaistu 2009Revisão -
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The genetics of cerebellar malformations Tekijä Kimberly A. Aldinger, Dan Doherty
Julkaistu 2016Revisão -
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Cerebellar hypoplasia: Differential diagnosis and diagnostic approach Tekijä Andrea Poretti, Eugen Boltshauser, Dan Doherty
Julkaistu 2014Artigo -
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The Joubert–Meckel–Nephronophthisis Spectrum of Ciliopathies Tekijä Julie C. Van De Weghe, Arianna Gómez, Dan Doherty
Julkaistu 2022Revisão -
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Joubert syndrome (and related disorders) (OMIM 213300) Tekijä Melissa A. Parisi, Dan Doherty, Phillip F. Chance, Ian Glass
Julkaistu 2007Artigo -
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The ciliopathy gene cc2d2a controls zebrafish photoreceptor outer segment development through a role in Rab8-dependent vesicle trafficking Tekijä Ruxandra Bachmann‐Gagescu, Ian G. Phelps, George Stearns, Brian A. Link, Susan E. Brockerhoff, Cecilia B. Moens, Dan Doherty
Julkaistu 2011Artigo -
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Pontine Tegmental Cap Dysplasia: MR Imaging and Diffusion Tensor Imaging Features of Impaired Axonal Navigation Tekijä Patrice Jissendi‐Tchofo, Dan Doherty, George McGillivray, Robert F. Hevner, Dennis Shaw, Gisele E. Ishak, Richard J. Leventer, A. James Barkovich
Julkaistu 2008Artigo -
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Hypomorphism for RPGRIP1L, a Ciliary Gene Vicinal to the FTO Locus, Causes Increased Adiposity in Mice Tekijä George Stratigopoulos, Jayne F. Martin Carli, Diana R. O’Day, Liheng Wang, Charles A. LeDuc, Patricia Lanzano, Wendy K. Chung, Michael Rosenbaum, Dieter Egli, Dan Doherty, Rudolph L. Leibel
Julkaistu 2014Artigo -
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Rhombencephalosynapsis: a hindbrain malformation associated with incomplete separation of midbrain and forebrain, hydrocephalus and a broad spectrum of severity Tekijä Gisele E. Ishak, Jennifer C. Dempsey, Dennis Shaw, Hannah M. Tully, Margaret P Adam, Pedro A. Sanchez‐Lara, Ian Glass, Tessa Rue, Kathleen J. Millen, William B. Dobyns, Dan Doherty
Julkaistu 2012Artigo -
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Joubert Syndrome: Ophthalmological Findings in Correlation with Genotype and Hepatorenal Disease in 99 Patients Prospectively Evaluated at a Single Center Tekijä Brian P. Brooks, Wadih M. Zein, A. Thompson, Maryam Mokhtarzadeh, Dan Doherty, Melissa A. Parisi, Ian Glass, May Christine V. Malicdan, Thierry Vilboux, Meghana Vemulapalli, James C. Mullikin, William A. Gahl, Meral Gunay‐Aygun
Julkaistu 2018Artigo -
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Mutations in TRAPPC12 Manifest in Progressive Childhood Encephalopathy and Golgi Dysfunction Tekijä Miroslav P. Milev, Megan E. Grout, Djenann Saint‐Dic, Yong-Han Hank Cheng, Ian Glass, Christopher J. Hale, D. Hanna, Michael O. Dorschner, Keshika Prematilake, Avraham Shaag, Orly Elpeleg, Michael Sacher, Dan Doherty, Simon Edvardson
Julkaistu 2017Artigo -
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Recognizable cerebellar dysplasia associated with mutations in multiple tubulin genes Tekijä Renske Oegema, Thomas D. Cushion, Ian G. Phelps, Seo‐Kyung Chung, Jennifer C. Dempsey, Sarah Collins, Jonathan G.L. Mullins, Tracy Dudding, Harinder Gill, Andrew Green, William B. Dobyns, Gisele E. Ishak, Mark I. Rees, Dan Doherty
Julkaistu 2015Artigo -
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Large-scale targeted sequencing comparison highlights extreme genetic heterogeneity in nephronophthisis-related ciliopathies Tekijä Markus Schueler, Jan Halbritter, Ian G. Phelps, Daniela A. Braun, Edgar A. Otto, Jonathan D. Porath, Heon Yung Gee, Jay Shendure, Brian J. O’Roak, Jennifer A. Lawson, Marwa M. Nabhan, Neveen A. Soliman, Dan Doherty, Friedhelm Hildebrandt
Julkaistu 2015Artigo -
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A human cell atlas of fetal chromatin accessibility Tekijä Silvia Domcke, Andrew J. Hill, Riza M. Daza, Junyue Cao, Diana R. O’Day, Hannah A. Pliner, Kimberly A. Aldinger, Dmitry Pokholok, Fan Zhang, Jennifer H. Milbank, Michael Zager, Ian Glass, Frank J. Steemers, Dan Doherty, Cole Trapnell, Darren A. Cusanovich, Jay Shendure
Julkaistu 2020Artigo -
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A human cell atlas of fetal gene expression Tekijä Junyue Cao, Diana R. O’Day, Hannah A. Pliner, Paul D. Kingsley, Mei Deng, Riza M. Daza, Michael Zager, Kimberly A. Aldinger, Ronnie Blecher‐Gonen, Fan Zhang, Malte Spielmann, James Palis, Dan Doherty, Frank J. Steemers, Ian Glass, Cole Trapnell, Jay Shendure
Julkaistu 2020Artigo
Työkalut:
Liittyvät aiheet
Biology
Genetics
Gene
Phenotype
Joubert syndrome
Medicine
Cilium
Neuroscience
Ciliopathy
Cell biology
Ciliopathies
Mutation
Pathology
Anatomy
Cerebellum
Ciliogenesis
Computational biology
Exome sequencing
Nephronophthisis
Psychology
Internal medicine
Zebrafish
Bioinformatics
Disease
Epilepsy
Intraflagellar transport
Mutant
Neuroimaging
Polymicrogyria
Cerebellar vermis