1. A Homozygous Mutation in the TUB Gene Associated with Retinal Dystrophy and Obesity. Issue 3 (20th December 2013) Authors: Borman, Arundhati Dev; Pearce, Laura R.; Mackay, Donna S.; Nagel‐Wolfrum, Kerstin; Davidson, Alice E.; Henderson, Robert; Garg, Sumedha; Waseem, Naushin H.; Webster, Andrew R.; Plagnol, Vincent; Wolfrum, Uwe; Farooqi, I. Sadaf; Moore, Anthony T. Journal: Human mutation Issue: Volume 35:Issue 3(2014:Mar.) Page Start: 289 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Adhesion Class GPCRs in GtoPdb v.2021.3. (2021) Authors: Arac-Ozkan, Demet; Aust, Gabriela; Bonner, Tom I.; Cappallo-Obermann, Heike; Formstone, Caroline; Hamann, Jörg; Harty, Breanne; Heyne, Henrike; Kirchhoff, Christiane; Knapp, Barbara; Krishnan, Arunkumar; Langenhan, Tobias; Duc, Diana Le; Lin, Hsi-Hsien; Martinelli, David C.; Monk, Kelly; Piao, Xi... Journal: IUPHAR/BPS guide to pharmacology CITE Issue: Number 3(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Affinity proteomics identifies novel functional modules related to adhesion GPCRs. Issue 1 (22nd August 2019) Authors: Knapp, Barbara; Roedig, Jens; Boldt, Karsten; Krzysko, Jacek; Horn, Nicola; Ueffing, Marius; Wolfrum, Uwe Journal: Annals of the New York Academy of Sciences Issue: Volume 1456:Issue 1(2019) Page Start: 144 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Autophagy interferes with human cytomegalovirus genome replication, morphogenesis, and progeny release. Issue 3 (4th March 2021) Authors: Zimmermann, Christine; Krämer, Nadine; Krauter, Steffi; Strand, Dennis; Sehn, Elisabeth; Wolfrum, Uwe; Freiwald, Anja; Butter, Falk; Plachter, Bodo Journal: Autophagy Issue: Volume 17:Issue 3(2021) Page Start: 779 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. C21orf2 is mutated in recessive early-onset retinal dystrophy with macular staphyloma and encodes a protein that localises to the photoreceptor primary cilium. Issue 12 (20th August 2015) Authors: Khan, Arif O; Eisenberger, Tobias; Nagel-Wolfrum, Kerstin; Wolfrum, Uwe; Bolz, Hanno J Journal: British journal of ophthalmology Issue: Volume 99:Issue 12(2015) Page Start: 1725 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Characterization of the ternary Usher syndrome SANS/ush2a/whirlin protein complex. (30th January 2017) Authors: Sorusch, Nasrin; Bauß, Katharina; Plutniok, Janet; Samanta, Ananya; Knapp, Barbara; Nagel-Wolfrum, Kerstin; Wolfrum, Uwe Journal: Human molecular genetics Issue: Volume 26:Number 6(2017:Mar. 15) Page Start: 1157 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Cilia - The sensory antennae in the eye. (September 2017) Authors: May-Simera, Helen; Nagel-Wolfrum, Kerstin; Wolfrum, Uwe Journal: Progress in retinal and eye research Issue: Volume 60(2017:Sep.) Page Start: 144 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Early disruption of photoreceptor cell architecture and loss of vision in a humanized pig model of usher syndromes. Issue 4 (7th March 2022) Authors: Grotz, Sophia; Schäfer, Jessica; Wunderlich, Kirsten A; Ellederova, Zdenka; Auch, Hannah; Bähr, Andrea; Runa‐Vochozkova, Petra; Fadl, Janet; Arnold, Vanessa; Ardan, Taras; Veith, Miroslav; Santamaria, Gianluca; Dhom, Georg; Hitzl, Wolfgang; Kessler, Barbara; Eckardt, Christian; Klein, Joshua; Bry... Journal: EMBO molecular medicine Issue: Volume 14:Issue 4(2022) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Expression and subcellular localization of USH1C/harmonin in human retina provides insights into pathomechanisms and therapy. Issue 3 (23rd August 2022) Authors: Nagel-Wolfrum, Kerstin; Fadl, Benjamin R; Becker, Mirjana M; Wunderlich, Kirsten A; Schäfer, Jessica; Sturm, Daniel; Fritze, Jacques; Gür, Burcu; Kaplan, Lew; Andreani, Tommaso; Goldmann, Tobias; Brooks, Matthew; Starostik, Margaret R; Lokhande, Anagha; Apel, Melissa; Fath, Karl R; Stingl, Katari... Journal: Human molecular genetics Issue: Volume 32:Issue 3(2023) Page Start: 431 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. KIAA0556 is a novel ciliary basal body component mutated in Joubert syndrome. Issue 1 (December 2015) Authors: Sanders, Anna; de Vrieze, Erik; Alazami, Anas; Alzahrani, Fatema; Malarkey, Erik; Sorusch, Nasrin; Tebbe, Lars; Kuhns, Stefanie; van Dam, Teunis; Alhashem, Amal; Tabarki, Brahim; Lu, Qianhao; Lambacher, Nils; Kennedy, Julie; Bowie, Rachel; Hetterschijt, Lisette; van Beersum, Sylvia; van Reeuwijk,... Journal: Genome biology Issue: Volume 16:Issue 1(2015) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗