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See also: WDR60 WD repeat domain 60 in the Gene database

wdr60 in Homo sapiensMus musculusRattus norvegicusAll 272 Gene records

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Items: 1 to 20 of 22


Interactions of the dynein-2 intermediate chain WDR34 with the light chains are required for ciliary retrograde protein trafficking.

Tsurumi Y, Hamada Y, Katoh Y, Nakayama K.

Mol Biol Cell. 2019 Mar 1;30(5):658-670. doi: 10.1091/mbc.E18-10-0678. Epub 2019 Jan 16.


Dynein-2 intermediate chains play crucial but distinct roles in primary cilia formation and function.

Vuolo L, Stevenson NL, Heesom KJ, Stephens DJ.

Elife. 2018 Oct 16;7. pii: e39655. doi: 10.7554/eLife.39655.


Interaction of WDR60 intermediate chain with TCTEX1D2 light chain of the dynein-2 complex is crucial for ciliary protein trafficking.

Hamada Y, Tsurumi Y, Nozaki S, Katoh Y, Nakayama K.

Mol Biol Cell. 2018 Jul 1;29(13):1628-1639. doi: 10.1091/mbc.E18-03-0173. Epub 2018 May 9.


Prenatal diagnosis of short-rib polydactyly syndrome type III or short-rib thoracic dysplasia 3 with or without polydactyly (SRTD3) associated with compound heterozygous mutations in DYNC2H1 in a fetus.

Chen CP, Ko TM, Chang TY, Chern SR, Chen SW, Lai ST, Chuang TY, Wang W.

Taiwan J Obstet Gynecol. 2018 Feb;57(1):123-127. doi: 10.1016/j.tjog.2017.12.021.


Expanding the phenotype associated with biallelic WDR60 mutations: Siblings with retinal degeneration and polydactyly lacking other features of short rib thoracic dystrophies.

Kakar N, Horn D, Decker E, Sowada N, Kubisch C, Ahmad J, Borck G, Bergmann C.

Am J Med Genet A. 2018 Feb;176(2):438-442. doi: 10.1002/ajmg.a.38562. Epub 2017 Dec 22.


Genetic Variants Within Key Nodes of the Cascade of Antipsychotic Mechanisms: Effects on Antipsychotic Response and Schizophrenia Psychopathology in a Naturalistic Treatment Setting in Two Independent Korean and Italian Samples.

Calabrò M, Porcelli S, Crisafulli C, Wang SM, Lee SJ, Han C, Patkar AA, Masand PS, Albani D, Raimondi I, Forloni G, Bin S, Mattiaccio A, Mantovani V, Jun TY, Pae CU, Serretti A.

Adv Ther. 2017 Jun;34(6):1482-1497. doi: 10.1007/s12325-017-0555-2. Epub 2017 May 16.


Homozygous variant in C21orf2 in a case of Jeune syndrome with severe thoracic involvement: Extending the phenotypic spectrum.

McInerney-Leo AM, Wheeler L, Marshall MS, Anderson LK, Zankl A, Brown MA, Leo PJ, Wicking C, Duncan EL.

Am J Med Genet A. 2017 Jun;173(6):1698-1704. doi: 10.1002/ajmg.a.38215. Epub 2017 Apr 19.


An investigation of obesity susceptibility genes in Northern Han Chinese by targeted resequencing.

Wu Y, Wang W, Jiang W, Yao J, Zhang D.

Medicine (Baltimore). 2017 Feb;96(7):e6117. doi: 10.1097/MD.0000000000006117.


Role of neurodevelopment involved genes in psychiatric comorbidities and modulation of inflammatory processes in Alzheimer's disease.

Porcelli S, Crisafulli C, Donato L, Calabrò M, Politis A, Liappas I, Albani D, Atti AR, Salfi R, Raimondi I, Forloni G, Papadimitriou GN, De Ronchi D, Serretti A.

J Neurol Sci. 2016 Nov 15;370:162-166. doi: 10.1016/j.jns.2016.09.053. Epub 2016 Sep 28. Erratum in: J Neurol Sci. 2017 Jan 15;372:49.


New mutations in DYNC2H1 and WDR60 genes revealed by whole-exome sequencing in two unrelated Sardinian families with Jeune asphyxiating thoracic dystrophy.

Cossu C, Incani F, Serra ML, Coiana A, Crisponi G, Boccone L, Rosatelli MC.

Clin Chim Acta. 2016 Apr 1;455:172-80. doi: 10.1016/j.cca.2016.02.006. Epub 2016 Feb 11.


DYNC2LI1 mutations broaden the clinical spectrum of dynein-2 defects.

Kessler K, Wunderlich I, Uebe S, Falk NS, Gießl A, Brandstätter JH, Popp B, Klinger P, Ekici AB, Sticht H, Dörr HG, Reis A, Roepman R, Seemanová E, Thiel CT.

Sci Rep. 2015 Jul 1;5:11649. doi: 10.1038/srep11649.


Tctex1d2 associates with short-rib polydactyly syndrome proteins and is required for ciliogenesis.

Gholkar AA, Senese S, Lo YC, Capri J, Deardorff WJ, Dharmarajan H, Contreras E, Hodara E, Whitelegge JP, Jackson PK, Torres JZ.

Cell Cycle. 2015;14(7):1116-25. doi: 10.4161/15384101.2014.985066.


Borderline personality disorder and childhood maltreatment: a genome-wide methylation analysis.

Prados J, Stenz L, Courtet P, Prada P, Nicastro R, Adouan W, Guillaume S, Olié E, Aubry JM, Dayer A, Perroud N.

Genes Brain Behav. 2015 Feb;14(2):177-88. doi: 10.1111/gbb.12197. Epub 2015 Feb 1.


Whole exome sequencing is an efficient, sensitive and specific method for determining the genetic cause of short-rib thoracic dystrophies.

McInerney-Leo AM, Harris JE, Leo PJ, Marshall MS, Gardiner B, Kinning E, Leong HY, McKenzie F, Ong WP, Vodopiutz J, Wicking C, Brown MA, Zankl A, Duncan EL.

Clin Genet. 2015 Dec;88(6):550-7. doi: 10.1111/cge.12550. Epub 2015 Feb 17.


Subunit composition of the human cytoplasmic dynein-2 complex.

Asante D, Stevenson NL, Stephens DJ.

J Cell Sci. 2014 Nov 1;127(Pt 21):4774-87. doi: 10.1242/jcs.159038. Epub 2014 Sep 9.


Exome sequencing of extended families with autism reveals genes shared across neurodevelopmental and neuropsychiatric disorders.

Cukier HN, Dueker ND, Slifer SH, Lee JM, Whitehead PL, Lalanne E, Leyva N, Konidari I, Gentry RC, Hulme WF, Booven DV, Mayo V, Hofmann NK, Schmidt MA, Martin ER, Haines JL, Cuccaro ML, Gilbert JR, Pericak-Vance MA.

Mol Autism. 2014 Jan 10;5(1):1. doi: 10.1186/2040-2392-5-1.


Genome-wide association study of bipolar disorder in Canadian and UK populations corroborates disease loci including SYNE1 and CSMD1.

Xu W, Cohen-Woods S, Chen Q, Noor A, Knight J, Hosang G, Parikh SV, De Luca V, Tozzi F, Muglia P, Forte J, McQuillin A, Hu P, Gurling HM, Kennedy JL, McGuffin P, Farmer A, Strauss J, Vincent JB.

BMC Med Genet. 2014 Jan 4;15:2. doi: 10.1186/1471-2350-15-2.


A patient with partial trisomy 21 and 7q deletion expresses mild Down syndrome phenotype.

Papoulidis I, Papageorgiou E, Siomou E, Oikonomidou E, Thomaidis L, Vetro A, Zuffardi O, Liehr T, Manolakos E, Vassilis P.

Gene. 2014 Feb 25;536(2):441-3. doi: 10.1016/j.gene.2013.11.078. Epub 2013 Dec 13.


Siblings with opposite chromosome constitutions, dup(2q)/del(7q) and del(2q)/dup(7q).

Shim SH, Shim JS, Min K, Lee HS, Park JE, Park SH, Hwang E, Kim M.

Gene. 2014 Jan 15;534(1):100-6. doi: 10.1016/j.gene.2013.09.093. Epub 2013 Oct 2.


Combined deletion of two Condensin II system genes (NCAPG2 and MCPH1) in a case of severe microcephaly and mental deficiency.

Perche O, Menuet A, Marcos M, Liu L, Pâris A, Utami KH, Kervran D, Cacheux V, Laudier B, Briault S.

Eur J Med Genet. 2013 Nov;56(11):635-41. doi: 10.1016/j.ejmg.2013.07.007. Epub 2013 Sep 4.


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