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Journal Cilia

2. A high-throughput genome-wide siRNA screen for ciliogenesis identifies new ciliary functional components and ciliopathy genes. Issue 1 (December 2015)

Authors:
Szymanska, K; Wheway, G; Doherty, D; Schmidts, M; Mans, D; Nguyen, TMT; Boldt, K; Tödt, G; Abdelhamed, Z; Wunderlich, K; Natarajan, S; Parry, DA; Logan, CV; Herridge, W; Sorusch, N; Wolfrum, U; Ueffing, M; Roepman, R; Mitchison, H; Johnson, C
Journal:
Cilia
Issue:
Volume 4:Issue 1(2015)
Page Start:
1
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

5. A novel ICK mutation causes ciliary disruption and lethal endocrine-cerebro-osteodysplasia syndrome. Issue 1 (December 2016)

Authors:
Oud, Machteld; Bonnard, Carine; Mans, Dorus; Altunoglu, Umut; Tohari, Sumanty; Ng, Alvin; Eskin, Ascia; Lee, Hane; Rupar, C.; Wagenaar, Nathalie; Wu, Ka; Lahiry, Piya; Pazour, Gregory; Nelson, Stanley; Hegele, Robert; Roepman, Ronald; Kayserili, Hülya; Venkatesh, Byrappa; Siu, Victoria; Reversade...
Journal:
Cilia
Issue:
Volume 5:Issue 1(2016)
Page Start:
1
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

9. A study of new NEK8 mutations in patients with severe renal cystic hypodysplasia and ciliopathy-associated defects. Issue 1 (December 2015)

Authors:
Grampa, V; Delous, M; Silbermann, F; Oyde, G; Krug, P; Filhol, E; Alessandri, JL; Sigaudy, S; Bouvier, R; Zabot, MT; Antignac, C; Gubler, M; Attié-Bitach, T; Benmerah, A; Jeanpierre, C; Saunier, S
Journal:
Cilia
Issue:
Volume 4:Issue 1(2015)
Page Start:
1
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

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