Ngā hua rapu - Nicholas Katsanis
- E whakaatu ana i te 1 - 20 hua o te 181
- Haere ki te Whārangi Whai Ake
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1
The oligogenic properties of Bardet-Biedl syndrome mā Nicholas Katsanis
I whakaputaina 2004Revisão -
2
The continuum of causality in human genetic disorders mā Nicholas Katsanis
I whakaputaina 2016Artigo -
3
Molecular genetic testing and the future of clinical genomics mā Sara Huston, Nicholas Katsanis
I whakaputaina 2013Revisão -
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Genetic architecture of reciprocal CNVs mā Christelle Golzio, Nicholas Katsanis
I whakaputaina 2013Revisão -
5
Genetic Modifiers and Oligogenic Inheritance mā Maria Kousi, Nicholas Katsanis
I whakaputaina 2015Revisão -
6
The Genetic Basis of Hydrocephalus mā Maria Kousi, Nicholas Katsanis
I whakaputaina 2016Revisão -
7
Mechanistic insights into Bardet-Biedl syndrome, a model ciliopathy mā Norann A. Zaghloul, Nicholas Katsanis
I whakaputaina 2009Revisão -
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Functional modules, mutational load and human genetic disease mā Norann A. Zaghloul, Nicholas Katsanis
I whakaputaina 2010Revisão -
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The ciliopathies: a transitional model into systems biology of human genetic disease mā Erica E. Davis, Nicholas Katsanis
I whakaputaina 2012Revisão -
10
Cilia in vertebrate development and disease mā Edwin C. Oh, Nicholas Katsanis
I whakaputaina 2012Revisão -
11
Context-Dependent Regulation of Wnt Signaling through the Primary Cilium mā Edwin C. Oh, Nicholas Katsanis
I whakaputaina 2012Revisão -
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Ciliopathies mā Friedhelm Hildebrandt, Thomas Benzing, Nicholas Katsanis
I whakaputaina 2011Revisão -
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Cystic diseases of the kidney: ciliary dysfunction and cystogenic mechanisms mā Cecilia Gascue, Nicholas Katsanis, José L. Badano
I whakaputaina 2010Revisão -
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Exploring the molecular basis of Bardet-Biedl syndrome mā Nicholas Katsanis, James R. Lupski, Philip L. Beales
I whakaputaina 2001Revisão -
19
Interpreting human genetic variation with in vivo zebrafish assays mā Erica E. Davis, Stephan G. Frangakis, Nicholas Katsanis
I whakaputaina 2014Revisão -
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Ngā utauta rapu:
Ngā marau whai pānga
Biology
Genetics
Gene
Phenotype
Medicine
Cell biology
Cilium
Mutation
Allele
Neuroscience
Ciliopathy
Zebrafish
Computational biology
Bardet–Biedl syndrome
Ciliopathies
Internal medicine
Exome sequencing
Missense mutation
Disease
Genotype
Pathology
Genome
Intraflagellar transport
Locus (genetics)
Ophthalmology
Evolutionary biology
Gene expression
Single-nucleotide polymorphism
Genetic heterogeneity
Mutant