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NATURE REVIEWS MOLECULAR CELL BIOLOGY, ISSN 1471-0072, 11/2007, Volume 8, Issue 11, pp. 880 - 893
Defects in the function of cellular organelles such as peroxisomes, lysosomes and mitochondria are well-known causes of human diseases. Recently, another... 
INTRAFLAGELLAR TRANSPORT PROTEINS | NIMA-RELATED KINASE | MAMMALIAN PHOTORECEPTOR CELLS | CHLAMYDOMONAS-REINHARDTII | POLYCYSTIC KIDNEY-DISEASE | PLANAR CELL POLARITY | BARDET-BIEDL-SYNDROME | TUMOR-SUPPRESSOR PROTEIN | LEFT-RIGHT ASYMMETRY | REPRODUCTIVE-ORGANS | CELL BIOLOGY
Journal Article
NATURE GENETICS, ISSN 1061-4036, 11/2007, Volume 39, Issue 11, pp. 1350 - 1360
Primary cilia and basal bodies are evolutionarily conserved organelles that mediate communication between the intracellular and extracellular environments.... 
INTRAFLAGELLAR TRANSPORT PROTEINS | TRANSCRIPTION FACTORS | SIGNALING PATHWAYS | NEURAL-TUBE DEFECTS | LOOP-TAIL | MOUSE | GENETICS & HEREDITY | BARDET-BIEDL-SYNDROME | PLANAR CELL POLARITY | CONVERGENT EXTENSION | BETA-CATENIN
Journal Article
Experimental Eye Research, ISSN 0014-4835, 09/2019, Volume 186, pp. 107721 - 107721
Cilia are highly conserved and ubiquitously expressed organelles. Ciliary defects of genetic origins lead to ciliopathies, in which retinal degeneration (RD)... 
Ciliopathies | Leber congenital amaurosis | Bardet-biedl syndrome | Retinitis pigmentosa | Alström syndrome | Unfolded protein response | Index Medicus
Journal Article
Chinese Journal of Medical Genetics, ISSN 1003-9406, 04/2018, Volume 35, Issue 2, pp. 288 - 292
Journal Article
Indian Pediatrics, ISSN 0019-6061, 06/2013, Volume 50, Issue 6, pp. 599 - 601
Bardet-Biedl syndrome (BBS) is a rare autosomal recessive condition characterized by retinitis pigmentosa, polydactyly, obesity, learning disabilities,... 
Cardiomyopathy | Bardet-Biedl syndrome | PEDIATRICS
Journal Article
Giornale italiano di nefrologia : organo ufficiale della Societa italiana di nefrologia, 09/2017, Volume 34, Issue 5, pp. 62 - 72
Journal Article
Nature Genetics, ISSN 1061-4036, 03/2011, Volume 43, Issue 3, pp. 189 - 196
Journal Article
Nigerian Journal of Clinical Practice, ISSN 1119-3077, 07/2019, Volume 22, Issue 7, p. 1026
Journal Article
Journal of Cell Science, ISSN 0021-9533, 2014, Volume 127, Issue 11, pp. 2391 - 2400
Journal Article
Pediatric Obesity, ISSN 2047-6302, 10/2013, Volume 8, Issue 5, pp. E64 - E67
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 12/2010, Volume 107, Issue 50, pp. 21517 - 21522
Journal Article
Sheng wu gong cheng xue bao = Chinese journal of biotechnology, ISSN 1000-3061, 01/2019, Volume 35, Issue 1, pp. 133 - 141
Journal Article
by We, Q and Chen, YX and Gui, YF and Zhao, WH
FRONTIERS IN PHYSIOLOGY, ISSN 1664-042X, 06/2019, Volume 10
Leucine zipper transcription factor like 1 (LZTFL1) is a member of the Bardet-Biedl syndrome gene family. LZTFL1-null mice show the phenotype of obesity,... 
ACTIVATION | PHYSIOLOGY | GENETICS | tumor suppressor | sequence analysis | zebrafish | BARDET-BIEDL SYNDROME | CILIA | LZTFL1 | DEGENERATION
Journal Article
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