SEARCH

SEARCH BY CITATION

LITERATURE CITED

  • Aase K,Abramsson A,Karlsson L,Betsholtz C,Eriksson U. 2002. Expression analysis of PDGF-C in adult and developing mouse tissues. Mech Dev 110: 187191.
  • Ahlgren SC,Bronner-Fraser M. 1999. Inhibition of sonic hedgehog signaling in vivo results in craniofacial neural crest cell death. Curr Biol 9: 13041314.
  • Arts HH,Doherty D,van Beersum SE,Parisi MA,Letteboer SJ,Gorden NT,Peters TA,Marker T,Voesenek K,Kartono A,Ozyurek H,Farin FM,Kroes HY,Wolfrum U,Brunner HG,Cremers FP,Glass IA,Knoers NV,Roepman R. 2007. Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome. Nat Genet 39: 882888.
  • Bachler M,Neubuser A. 2001. Expression of members of the Fgf family and their receptors during midfacial development. Mech Dev 100: 313316.
  • Badano JL,Mitsuma N,Beales PL,Katsanis N. 2006. The ciliopathies: An emerging class of human genetic disorders. Annu Rev Genomics Hum Genet 7: 125148.
  • Baker K,Beales P. 2009. Making sense of cilia in disease: The human ciliopathies. Am J Med Genet 151C: 281295.
  • Balk K,Biesecker LG. 2008. The clinical atlas of Greig cephalopolysyndactyly syndrome. Am J Med Genet A 146A: 548557.
  • Basch ML,Bronner-Fraser M. 2006. Neural crest inducing signals. Adv Exp Med Biol 589: 2431.
  • Belloni E,Muenke M,Roessler E,Traverso G,Siegel- Bartelt J,Frumkin A,Mitchell HF,Donis-Keller H,Helms C,Hing AV,Heng HH,Koop B,Martindale D,Rommens JM,Tsui LC,Scherer SW. 1996. Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly. Nat Genet 14: 353356.
  • Berbari NF,Johnson AD,Lewis JS,Askwith CC,Mykytyn K. 2008. Identification of ciliary localization sequences within the third intracellular loop of G protein-coupled receptors. Mol Biol Cell 19: 15401547.
  • Bimonte S,De Angelis A,Quagliata L,Giusti F,Tammaro R,Dallai R,Ascenzi MG,Diez-Roux G,Franco B. 2010. Ofd1 is required in limb bud patterning and endochondral bone development. Dev Biol 349(2): 179191.
  • Bluestone CD. 2003. Surgical Atlas of Pediatric Otolaryngology. Pediatr Otolaryngol 4: 979995.
  • Brugmann SA,Allen NC,James AW,Mekonnen Z,Madan E,Helms JA. 2010. A primary cilia dependent etiology for midline facial disorders. Hum Mol Genet 19(8): 15771592.
  • Brugmann SA,Goodnough LH,Gregorieff A,Leucht P,Ten Berge D,Fuerer C,Clevers H,Nusse R,Helms JA. 2007. Wnt signaling mediates regional specification in the vertebrate face. Development 134: 32833295.
  • Cadigan KM,Nusse R. 1997. Wnt signaling: A common theme in animal development. Genes Dev 11: 32863305.
  • Caspary T,Larkins CE,Anderson KV. 2007. The graded response to Sonic Hedgehog depends on cilia architecture. Dev Cell 12: 767778.
  • Chiang C,Litingtung Y,Lee E,Young KE,Corden JL,Westphal H,Beachy PA. 1996. Cyclopia and defective axial patterning in mice lacking Sonic hedgehog gene function. Nature 383: 407413.
  • Chiquet BT,Blanton SH,Burt A,Ma D,Stal S,Mulliken JB,Hecht JT. 2008. Variation in WNT genes is associated with non-syndromic cleft lip with or without cleft palate. Hum Mol Genet 17: 22122218.
  • Chuong CM,Noveen A. 1999. Phenotypic determination of epithelial appendages: Genes, developmental pathways, and evolution. J Investig Dermatol Symp Proc 4: 307311.
  • Cohen MM. 2005. Editorial: Perspectives on craniosynostosis. Am J Med Genet A 136: 313326.
  • Cohen MMJr,Sulik KK. 1992. Perspectives on holoprosencephaly: Part II. Central nervous system, craniofacial anatomy, syndrome commentary, diagnostic approach, and experimental studies. J Craniofac Genet Dev Biol 12: 196244.
  • Corbit KC,Aanstad P,Singla V,Norman AR,Stainier DY,Reiter JF. 2005. Vertebrate smoothened functions at the primary cilium. Nature 437: 10181021.
  • Corbit KC,Shyer AE,Dowdle WE,Gaulden J,Singla V,Chen MH,Chuang PT,Reiter JF. 2008. Kif3a constrains beta-catenin-dependent Wnt signaling through dual ciliary and non-ciliary mechanisms. Nat Cell Biol 10: 7076.
  • Cordero D,Marcucio R,Hu D,Gaffield W,Tapadia M,Helms JA. 2004. Temporal perturbations in sonic hedgehog signaling elicit the spectrum of holoprosencephaly phenotypes. J Clin Invest 114: 485494.
  • Cortellino S,Wang C,Wang B,Bassi MR,Caretti E,Champeval D,Calmont A,Jarnik M,Burch J,Zaret KS,Larue L,Bellacosa A. 2009. Defective ciliogenesis, embryonic lethality and severe impairment of the Sonic Hedgehog pathway caused by inactivation of the mouse complex A intraflagellar transport gene Ift122/Wdr10, partially overlapping with the DNA repair gene Med1/Mbd4. Dev Biol 325: 225237.
  • Creuzet S,Schuler B,Couly G,Le Douarin NM. 2004. Reciprocal relationships between Fgf8 and neural crest cells in facial and forebrain development. Proc Natl Acad Sci USA 101: 48434847.
  • D'Angelo A,Franco B. 2010. The primary cilium in different tissues—Lessons from patients and animal models. Pediatr Nephrol. [Epub ahead of print].
  • DasGupta R,Fuchs E. 1999. Multiple roles for activated LEF/TCF transcription complexes during hair follicle development and differentiation. Development 126: 45574568.
  • Delous M,Baala L,Salomon R,Laclef C,Vierkotten J,Tory K,Golzio C,Lacoste T,Besse L,Ozilou C,Moutkine I,Hellman NE,Anselme I,Silbermann F,Vesque C,Gerhardt C,Rattenberry E,Wolf MT,Gubler MC,Martinovic J,Encha-Razavi F,Boddaert N,Gonzales M,Macher MA,Nivet H,Champion G,Bertheleme JP,Niaudet P,McDonald F,Hildebrandt F,Johnson CA,Vekemans M,Antignac C,Ruther U,Schneider-Maunoury S,Attie-Bitach T,Saunier S. 2007. The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome. Nat Genet 39: 875881.
  • DeMyer W. 1964. The face predicts the brain: Diagnostic significance of median facial anomialies for holoprosencephaly (arhinencephay). Pediatrics August: 256263.
  • Ding H,Wu X,Bostrom H,Kim I,Wong N,Tsoi B,O'Rourke M,Koh GY,Soriano P,Betsholtz C,Hart TC,Marazita ML,Field LL,Tam PP,Nagy A. 2004. A specific requirement for PDGF-C in palate formation and PDGFR-alpha signaling. Nat Genet 36: 11111116.
  • Eggenschwiler JT,Anderson KV. 2007. Cilia and developmental signaling. Annu Rev Cell Dev Biol 23: 345373.
  • Fath MA,Mullins RF,Searby C,Nishimura DY,Wei J,Rahmouni K,Davis RE,Tayeh MK,Andrews M,Yang B,Sigmund CD,Stone EM,Sheffield VC. 2005. Mkks-null mice have a phenotype resembling Bardet-Biedl syndrome. Hum Mol Genet 14: 11091118.
  • Ferrante MI,Romio L,Castro S,Collins JE,Goulding DA,Stemple DL,Woolf AS,Wilson SW. 2009. Convergent extension movements and ciliary function are mediated by ofd1, a zebrafish orthologue of the human oral-facial-digital type 1 syndrome gene. Hum Mol Genet 18: 289303.
  • Ferrante MI,Zullo A,Barra A,Bimonte S,Messaddeq N,Studer M,Dolle P,Franco B. 2006. Oral-facial-digital type I protein is required for primary cilia formation and left-right axis specification. Nat Genet 38: 112117.
  • Geetha-Loganathan P,Nimmagadda S,Antoni L,Fu K,Whiting CJ,Francis-West P,Richman JM. 2009. Expression of WNT signalling pathway genes during chicken craniofacial development. Dev Dyn 238: 11501165.
  • Gerdes JM,Davis EE,Katsanis N. 2009. The vertebrate primary cilium in development, homeostasis, and disease. Cell 137: 3245.
  • Gerdes JM,Liu Y,Zaghloul NA,Leitch CC,Lawson SS,Kato M,Beachy PA,Beales PL,DeMartino GN,Fisher S,Badano JL,Katsanis N. 2007. Disruption of the basal body compromises proteasomal function and perturbs intracellular Wnt response. Nat Genet 39: 13501360.
  • Goetz SC,Anderson KV. 2010. The primary cilium: A signaling centre during vertebrate development. Nat Rev Genet 11: 331344.
  • Graham A,Smith A. 2001. Patterning the pharyngeal arches. Bioessays 23: 5461.
  • Hoch RV,Soriano P. 2003. Roles of PDGF in animal development. Development 130: 47694784.
  • Hu D,Helms JA. 1999. The role of sonic hedgehog in normal and abnormal craniofacial morphogenesis. Development 126: 48734884.
  • Hu D,Marcucio RS. 2009. A SHH-responsive signaling center in the forebrain regulates craniofacial morphogenesis via the facial ectoderm. Development 136: 107116.
  • Hu D,Marcucio RS,Helms JA. 2003. A zone of frontonasal ectoderm regulates patterning and growth in the face. Development 130: 17491758.
  • Huang B,Masyuk T,LaRusso N. 2009. Isolation of primary cilia for morphological analysis. Methods Cell Biol 94: 103115.
  • Huang P,Schier AF. 2009. Dampened Hedgehog signaling but normal Wnt signaling in zebrafish without cilia. Development 136: 30893098.
  • Huangfu D,Anderson KV. 2005. Cilia and Hedgehog responsiveness in the mouse. Proc Natl Acad Sci USA 102: 1132511330.
  • Huangfu D,Liu A,Rakeman AS,Murcia NS,Niswander L,Anderson KV. 2003. Hedgehog signalling in the mouse requires intraflagellar transport proteins. Nature 426: 8387.
  • Humke EW,Dorn KV,Milenkovic L,Scott MP,Rohatgi R. 2010. The output of Hedgehog signaling is controlled by the dynamic association between Suppressor of Fused and the Gli proteins. Genes Dev 24: 670682.
  • Ishii M,Ishii Y,Moriyama T,Enomoto S,Ono T,Ohyama K,Kuroda T. 2002. Seventeen-year follow-up of a patient with median cleft of the lower lip, mandible, and tongue with flexion contracture: A case report. Cleft Palate Craniofac J 39: 555559.
  • Jeong J,Mao J,Tenzen T,Kottmann AH,McMahon AP. 2004. Hedgehog signaling in the neural crest cells regulates the patterning and growth of facial primordia. Genes Dev 18: 937951.
  • Jin H,White SR,Shida T,Schulz S,Aguiar M,Gygi SP,Bazan JF,Nachury MV. 2010. The conserved Bardet-Biedl syndrome proteins assemble a coat that traffics membrane proteins to cilia. Cell 141: 12081219.
  • Juriloff DM,Harris MJ,Brown CJ. 2001. Unravelling the complex genetics of cleft lip in the mouse model. Mamm Genome 12: 426435.
  • Juriloff DM,Harris MJ,Dewell SL,Brown CJ,Mager DL,Gagnier L,Mah DG. 2005. Investigations of the genomic region that contains the clf1 mutation, a causal gene in multifactorial cleft lip and palate in mice. Birth Defects Res A Clin Mol Teratol 73: 103113.
  • Juriloff DM,Harris MJ,Mah DG. 1996. The clf1 gene maps to a 2- to 3-cM region of distal mouse chromosome 11. Mamm Genome 7: 789.
  • Khanna H,Davis EE,Murga-Zamalloa CA,Estrada- Cuzcano A, Lopez I,den Hollander AI,Zonneveld MN,Othman MI,Waseem N,Chakarova CF,Maubaret C,Diaz-Font A,MacDonald I,Muzny DM,Wheeler DA,Morgan M,Lewis LR,Logan CV,Tan PL,Beer MA,Inglehearn CF,Lewis RA,Jacobson SG,Bergmann C,Beales PL,Attie-Bitach T,Johnson CA,Otto EA,Bhattacharya SS,Hildebrandt F,Gibbs RA,Koenekoop RK,Swaroop A,Katsanis N. 2009. A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies. Nat Genet 41: 739745.
  • Kim J,Krishnaswami SR,Gleeson JG. 2008. CEP290 interacts with the centriolar satellite component PCM-1 and is required for Rab8 localization to the primary cilium. Hum Mol Genet 17: 37963805.
  • Kolpakova-Hart E,Jinnin M,Hou B,Fukai N,Olsen BR. 2007. Kinesin-2 controls development and patterning of the vertebrate skeleton by Hedgehog- and Gli3-dependent mechanisms. Dev Biol 309: 273284.
  • Konstantinidou AE,Fryssira H,Sifakis S,Karadimas C,Kaminopetros P,Agrogiannis G,Velonis S,Nikkels PG,Patsouris E. 2009. Cranioectodermal dysplasia: A probable ciliopathy. Am J Med Genet A 149A: 22062211.
  • Lan Y,Ryan RC,Zhang Z,Bullard SA,Bush JO,Maltby KM,Lidral AC,Jiang R. 2006. Expression of Wnt9b and activation of canonical Wnt signaling during midfacial morphogenesis in mice. Dev Dyn 235: 14481454.
  • Lenton KA,Nacamuli RP,Wan DC,Helms JA,Longaker MT. 2005a. Cranial suture biology. Curr Top Dev Biol 66: 287328.
  • Lenton KA,Nacamuli RP,Wan DC,Helms JA,Longaker MT,Gerald PS. 2005b. Cranial suture biology. Curr Top Dev Biol 66: 287328.
  • Lunt SC,Haynes T,Perkins BD. 2009. Zebrafish ift57, ift88, and ift172 intraflagellar transport mutants disrupt cilia but do not affect hedgehog signaling. Dev Dyn 238: 17441759.
  • Macatee TL,Hammond BP,Arenkiel BR,Francis L,Frank DU,Moon AM. 2003. Ablation of specific expression domains reveals discrete functions of ectoderm- and endoderm-derived FGF8 during cardiovascular and pharyngeal development. Development 130: 63616374.
  • Marchac D,Renier D. 1989. Craniosynostosis. World J Surg 13: 358365.
  • Marcucio RS,Cordero DR,Hu D,Helms JA. 2005. Molecular interactions coordinating development of the forebrain and face. Dev Biol 284: 4861.
  • Maretto S,Cordenonsi M,Dupont S,Braghetta P,Broccoli V,Hassan AB,Volpin D,Bressan GM,Piccolo S. 2003. Mapping Wnt/beta-catenin signaling during mouse development and in colorectal tumors. Proc Natl Acad Sci USA. 100(6): 32993304.
  • Marshall WF. 2008. Basal bodies platforms for building cilia. Curr Top Dev Biol 85: 122.
  • Marszalek JR,Ruiz-Lozano P,Roberts E,Chien KR,Goldstein LS. 1999. Situs inversus and embryonic ciliary morphogenesis defects in mouse mutants lacking the KIF3A subunit of kinesin-II. Proc Natl Acad Sci USA 96: 50435048.
  • Marti E,Takada R,Bumcrot DA,Sasaki H,McMahon AP. 1995. Distribution of Sonic hedgehog peptides in the developing chick and mouse embryo. Development 121: 25372547.
  • May SR,Ashique AM,Karlen M,Wang B,Shen Y,Zarbalis K,Reiter J,Ericson J,Peterson AS. 2005. Loss of the retrograde motor for IFT disrupts localization of Smo to cilia and prevents the expression of both activator and repressor functions of Gli. Dev Biol 287: 378389.
  • McCabe KL,Bronner-Fraser M. 2008. Essential role for PDGF signaling in ophthalmic trigeminal placode induction. Development 135: 18631874.
  • McGlashan SR,Jensen CG,Poole CA. 2006. Localization of extracellular matrix receptors on the chondrocyte primary cilium. J Histochem Cytochem 54: 10051014.
  • Ming JE,Roessler E,Muenke M. 1998. Human developmental disorders and the Sonic hedgehog pathway. Mol Med Today 4: 343349.
  • Mooney MD,Siegel MI. 2002. Understanding craniofacial anomalies: The etiopathogenesis of craniosynotoses and facial clefting. New York: Wiley-Liss.
  • Morrison-Graham K,Schatteman GC,Bork T,Bowen-Pope DF,Weston JA. 1992. A PDGF receptor mutation in the mouse (Patch) perturbs the development of a non-neuronal subset of neural crest-derived cells. Development 115: 133142.
  • Muenke M. 1994. Holoprosencephaly as a genetic model for normal craniofacial development. Semin Dev Biol 5: 293301.
  • Mykytyn K,Mullins RF,Andrews M,Chiang AP,Swiderski RE,Yang B,Braun T,Casavant T,Stone EM,Sheffield VC. 2004. Bardet-Biedl syndrome type 4 (BBS4)-null mice implicate Bbs4 in flagella formation but not global cilia assembly. Proc Natl Acad Sci USA 101: 86648669.
  • Nachury MV,Loktev AV,Zhang Q,Westlake CJ,Peranen J,Merdes A,Slusarski DC,Scheller RH,Bazan JF,Sheffield VC,Jackson PK. 2007. A core complex of BBS proteins cooperates with the GTPase Rab8 to promote ciliary membrane biogenesis. Cell 129: 12011213.
  • Neugebauer JM,Amack JD,Peterson AG,Bisgrove BW,Yost HJ. 2009. FGF signaling during embryo development regulates cilia length in diverse epithelia. Nature 458: 651654.
  • Nishimura DY,Fath M,Mullins RF,Searby C,Andrews M,Davis R,Andorf JL,Mykytyn K,Swiderski RE,Yang B,Carmi R,Stone EM,Sheffield VC. 2004. Bbs2-null mice have neurosensory deficits, a defect in social dominance, and retinopathy associated with mislocalization of rhodopsin. Proc Natl Acad Sci USA 101: 1658816593.
  • Ocbina PJ,Tuson M,Anderson KV. 2009. Primary cilia are not required for normal canonical Wnt signaling in the mouse embryo. PLoS One 4: e6839.
  • Ohazama A,Haycraft CJ,Seppala M,Blackburn J,Ghafoor S,Cobourne M,Martinelli DC,Fan CM,Peterkova R,Lesot H,Yoder BK,Sharpe PT. 2009. Primary cilia regulate Shh activity in the control of molar tooth number. Development 136: 897903.
  • Oosterwegel M,van de Wetering M,Timmerman J,Kruisbeek A,Destree O,Meijlink F,Clevers H. 1993. Differential expression of the HMG box factors TCF-1 and LEF-1 during murine embryogenesis. Development 118: 439448.
  • Orr-Urtreger A,Lonai P. 1992. Platelet-derived growth factor-A and its receptor are expressed in separate, but adjacent cell layers of the mouse embryo. Development 115: 10451058.
  • Posnick JC. 2000. Craniofacial syndromes and anomalies. In: PosnickJC, editor. Craniofacial and maxillofacial surgery in children and young adults. Philadelphia: W.B. Saunders. pp 391527.
  • Rice D. 2008. Developmental anatomy of craniofacial sutures. In: RiceD, editor. Craniofacial sutures. Development, disease and treatment. vol 12. Basel: Karger. pp 2240.
  • Roessler E,Belloni E,Gaudenz K,Jay P,Berta P,Scherer SW,Tsui LC,Muenke M. 1996. Mutations in the human Sonic Hedgehog gene cause holoprosencephaly. Nat Genet 14: 357360.
  • Rohatgi R,Milenkovic L,Scott MP. 2007. Patched1 regulates hedgehog signaling at the primary cilium. Science 317: 372376.
  • Ross AJ,May-Simera H,Eichers ER,Kai M,Hill J,Jagger DJ,Leitch CC,Chapple JP,Munro PM,Fisher S,Tan PL,Phillips HM,Leroux MR,Henderson DJ,Murdoch JN,Copp AJ,Eliot MM,Lupski JR,Kemp DT,Dollfus H,Tada M,Katsanis N,Forge A,Beales PL. 2005. Disruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebrates. Nat Genet 37: 11351140.
  • Ruiz-Perez VL,Blair HJ,Rodriguez-Andres ME,Blanco MJ,Wilson A,Liu YN,Miles C,Peters H,Goodship JA. 2007. Evc is a positive mediator of Ihh-regulated bone growth that localizes at the base of chondrocyte cilia. Development 134: 29032912.
  • Schmidt C,Patel K. 2005. Wnts and the neural crest. Anat Embryol (Berl) 209: 349355.
  • Schneider L,Cammer M,Lehman J,Nielsen SK,Guerra CF,Veland IR,Stock C,Hoffmann EK,Yoder BK,Schwab A,Satir P,Christensen ST. 2010. Directional cell migration and chemotaxis in wound healing response to PDGF-AA are coordinated by the primary cilium in fibroblasts. Cell Physiol Biochem 25: 279292.
  • Schneider L,Clement CA,Teilmann SC,Pazour GJ,Hoffmann EK,Satir P,Christensen ST. 2005. PDGFRalphaalpha signaling is regulated through the primary cilium in fibroblasts. Curr Biol 15: 18611866.
  • Selleck MAJ,Bronner-Fraser M. 1995. Origins of the avian neural crest: The role of neural plate-epidermal interactions. Development (Cambridge) 121: 525538.
  • Simons M,Gloy J,Ganner A,Bullerkotte A,Bashkurov M,Kronig C,Schermer B,Benzing T,Cabello OA,Jenny A,Mlodzik M,Polok B,Driever W,Obara T,Walz G. 2005. Inversin, the gene product mutated in nephronophthisis type II, functions as a molecular switch between Wnt signaling pathways. Nat Genet 37: 537543.
  • Song L,Li Y,Wang K,Wang YZ,Molotkov A,Gao L,Zhao T,Yamagami T,Wang Y,Gan Q,Pleasure DE,Zhou CJ. 2009. Lrp6-mediated canonical Wnt signaling is required for lip formation and fusion. Development 136: 31613171.
  • Soriano P. 1997. The PDGF alpha receptor is required for neural crest cell development and for normal patterning of the somites. Development 124: 26912700.
  • Szabo-Rogers HL,Geetha-Loganathan P,Nimmagadda S,Fu KK,Richman JM. 2008. FGF signals from the nasal pit are necessary for normal facial morphogenesis. Dev Biol 318: 289302.
  • Tallquist MD,Soriano P. 2003. Cell autonomous requirement for PDGFRalpha in populations of cranial and cardiac neural crest cells. Development 130: 507518.
  • Tobin JL,Di Franco M,Eichers E,May-Simera H,Garcia M,Yan J,Quinlan R,Justice MJ,Hennekam RC,Briscoe J,Tada M,Mayor R,Burns AJ,Lupski JR,Hammond P,Beales PL. 2008. Inhibition of neural crest migration underlies craniofacial dysmorphology and Hirschsprung's disease in Bardet-Biedl syndrome. Proc Natl Acad Sci USA 105: 67146719.
  • Tran PV,Haycraft CJ,Besschetnova TY,Turbe-Doan A,Stottmann RW,Herron BJ,Chesebro AL,Qiu H,Scherz PJ,Shah JV,Yoder BK,Beier DR. 2008. THM1 negatively modulates mouse sonic hedgehog signal transduction and affects retrograde intraflagellar transport in cilia. Nat Genet 40: 403410.
  • Trumpp A,Depew MJ,Rubenstein JL,Bishop JM,Martin GR. 1999. Cre-mediated gene inactivation demonstrates that FGF8 is required for cell survival and patterning of the first branchial arch. Genes Dev 13: 31363148.
  • Veeman MT,Slusarski DC,Kaykas A,Louie SH,Moon RT. 2003. Zebrafish prickle, a modulator of noncanonical Wnt/Fz signaling, regulates gastrulation movements. Curr Biol 13: 680685.
  • Vierkotten J,Dildrop R,Peters T,Wang B,Ruther U. 2007. Ftm is a novel basal body protein of cilia involved in Shh signaling. Development 134: 25692577.
  • Vortkamp A,Gessler M,Grzeschik KH. 1991. GLI3 zinc-finger gene interrupted by translocations in Greig syndrome families. Nature 352: 539540.
  • Walczak-Sztulpa J,Eggenschwiler J,Osborn D,Brown DA,Emma F,Klingenberg C,Hennekam RC,Torre G,Garshasbi M,Tzschach A,Szczepanska M,Krawczynski M,Zachwieja J,Zwolinska D,Beales PL,Ropers HH,Latos-Bielenska A,Kuss AW. 2010. Cranioectodermal Dysplasia. Sensenbrenner syndrome is a ciliopathy caused by mutations in the IFT122 gene. Am J Hum Genet 86: 949956.
  • Wang J,Shackleford GM. 1996. Murine Wnt10a and Wnt10b: Cloning and expression in developing limbs, face and skin of embryos and in adults. Oncogene 13: 15371544.
  • Weatherbee SD,Niswander LA,Anderson KV. 2009. A mouse model for Meckel syndrome reveals Mks1 is required for ciliogenesis and Hedgehog signaling. Hum Mol Genet 18: 45654575.
  • Young NM,Chong HJ,Hu D,Hallgrimsson B,Marcucio RS. 2010. Quantitative analyses link modulation of sonic hedgehog signaling to continuous variation in facial growth and shape. Development 137: 34053409.
  • Zaghloul NA,Katsanis N. 2010. Functional modules, mutational load and human genetic disease. Trends Genet 26: 168176.
  • Zimmermann KW. 1898. Beitrage zur Kenntnis einiger Drusen und Epithelien. Arch Mikr Anat u Entwick 52: 552.