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Marius Ueffing

Showing results (281-290 of 296) with videos related to

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Nature Communications|March 30, 2016
Corrigendum: TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transportMiriam Schmidts, Yuqing Hou, Claudio R Cortés, et al.
Genome Biology|December 31, 2015
KIAA0556 is a novel ciliary basal body component mutated in Joubert syndromeAnna A W M Sanders, Erik de Vrieze, Anas M Alazami, et al.
Molecular & Cellular Proteomics : MCP|August 14, 2009
A community standard format for the representation of protein affinity reagentsDavid E Gloriam, Sandra Orchard, Daniela Bertinetti, et al.
Genome Biology|November 30, 2016
Characterizing the morbid genome of ciliopathiesRanad Shaheen, Katarzyna Szymanska, Basudha Basu, et al.
Nature Genetics|June 5, 2007
Mutations in LCA5, encoding the ciliary protein lebercilin, cause Leber congenital amaurosisAnneke I den Hollander, Robert K Koenekoop, Moin D Mohamed, et al.
Nature Communications|January 26, 2020
Extensive rewiring of the EGFR network in colorectal cancer cells expressing transforming levels of KRAS<sup>G13D</sup>Susan A Kennedy, Mohamed-Ali Jarboui, Sriganesh Srihari, et al.
Nature Methods|December 30, 2006
ProteomeBinders: planning a European resource of affinity reagents for analysis of the human proteomeMichael J Taussig, Oda Stoevesandt, Carl A K Borrebaeck, et al.
American Journal of Respiratory and Critical Care Medicine|April 16, 2024
Recessively Inherited Deficiency of Secreted WFDC2 (HE4) Causes Nasal Polyposis and BronchiectasisGerard W Dougherty, Lawrence E Ostrowski, Tabea Nöthe-Menchen, et al.
Nephron|November 27, 2025
Biallelic <italic>TMEM72</italic> Variants in Patients with a Nephronophthisis-Like PhenotypeLaura R Claus, Rozemarijn Snoek, Siebren Faber, et al.
Nature Genetics|June 25, 2013
ANKS6 is a central component of a nephronophthisis module linking NEK8 to INVS and NPHP3Sylvia Hoff, Jan Halbritter, Daniel Epting, et al.
Pageof 30

Showing results (281-290 of 296) with videos related to

Sort By:
Pageof 30
Nature Communications|March 30, 2016
Corrigendum: TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transportMiriam Schmidts, Yuqing Hou, Claudio R Cortés, et al.
Genome Biology|December 31, 2015
KIAA0556 is a novel ciliary basal body component mutated in Joubert syndromeAnna A W M Sanders, Erik de Vrieze, Anas M Alazami, et al.
Molecular & Cellular Proteomics : MCP|August 14, 2009
A community standard format for the representation of protein affinity reagentsDavid E Gloriam, Sandra Orchard, Daniela Bertinetti, et al.
Genome Biology|November 30, 2016
Characterizing the morbid genome of ciliopathiesRanad Shaheen, Katarzyna Szymanska, Basudha Basu, et al.
Nature Genetics|June 5, 2007
Mutations in LCA5, encoding the ciliary protein lebercilin, cause Leber congenital amaurosisAnneke I den Hollander, Robert K Koenekoop, Moin D Mohamed, et al.
Nature Communications|January 26, 2020
Extensive rewiring of the EGFR network in colorectal cancer cells expressing transforming levels of KRAS<sup>G13D</sup>Susan A Kennedy, Mohamed-Ali Jarboui, Sriganesh Srihari, et al.
Nature Methods|December 30, 2006
ProteomeBinders: planning a European resource of affinity reagents for analysis of the human proteomeMichael J Taussig, Oda Stoevesandt, Carl A K Borrebaeck, et al.
American Journal of Respiratory and Critical Care Medicine|April 16, 2024
Recessively Inherited Deficiency of Secreted WFDC2 (HE4) Causes Nasal Polyposis and BronchiectasisGerard W Dougherty, Lawrence E Ostrowski, Tabea Nöthe-Menchen, et al.
Nephron|November 27, 2025
Biallelic <italic>TMEM72</italic> Variants in Patients with a Nephronophthisis-Like PhenotypeLaura R Claus, Rozemarijn Snoek, Siebren Faber, et al.
Nature Genetics|June 25, 2013
ANKS6 is a central component of a nephronophthisis module linking NEK8 to INVS and NPHP3Sylvia Hoff, Jan Halbritter, Daniel Epting, et al.
Pageof 30