Aristaless-Like Homeobox protein 1 (ALX1) variant associated with craniofacial structure and frontonasal dysplasia in Burmese cats.

[1]  L. Froenicke,et al.  Variation of cats under domestication: genetic assignment of domestic cats to breeds and worldwide random-bred populations. , 2013, Animal Genetics.

[2]  Tokiharu Takahashi,et al.  Defective neural crest migration revealed by a Zebrafish model of Alx1-related frontonasal dysplasia. , 2013, Human molecular genetics.

[3]  J. Mullikin,et al.  Extent of Linkage Disequilibrium in the Domestic Cat, Felis silvestris catus, and Its Breeds , 2013, PloS one.

[4]  G. Erhardt,et al.  First WNK4-Hypokalemia Animal Model Identified by Genome-Wide Association in Burmese Cats , 2012, PloS one.

[5]  Holly C. Beale,et al.  Variation of BMP3 Contributes to Dog Breed Skull Diversity , 2012, PLoS genetics.

[6]  A. Balli,et al.  Proposal for a new radiological index to determine skull conformation in the dog. , 2012, Schweizer Archiv fur Tierheilkunde.

[7]  K. Failing,et al.  Cephalometric measurements and determination of general skull type of Cavalier King Charles Spaniels. , 2011, Veterinary radiology & ultrasound : the official journal of the American College of Veterinary Radiology and the International Veterinary Radiology Association.

[8]  Niki Kruijsen,et al.  [Does the bulldog still have a future?]. , 2011, Tijdschrift voor diergeneeskunde.

[9]  B. Gandolfi,et al.  The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71 , 2010, Mammalian Genome.

[10]  P. McGreevy,et al.  Human Induced Rotation and Reorganization of the Brain of Domestic Dogs , 2010, PloS one.

[11]  G. Oechtering,et al.  Brachyzephalie bei Hund und Katze: eine „menschengemachte” Obstruktion der oberen Atemwege , 2010 .

[12]  E. Uz,et al.  Disruption of ALX1 causes extreme microphthalmia and severe facial clefting: expanding the spectrum of autosomal-recessive ALX-related frontonasal dysplasia. , 2010, American journal of human genetics.

[13]  A. McFadyen,et al.  Feline orofacial pain syndrome (FOPS): A retrospective study of 113 cases , 2010, Journal of Feline Medicine & Surgery.

[14]  G. Oechtering,et al.  [Brachycephaly in dog and cat: a "human induced" obstruction of the upper airways]. , 2010, Pneumologie.

[15]  Jeffrey C Barrett,et al.  Haploview: Visualization and analysis of SNP genotype data. , 2009, Cold Spring Harbor protocols.

[16]  M. Bortolini,et al.  TCOF1 T/Ser variant and brachycephaly in dogs. , 2009, Animal genetics.

[17]  P. Scambler,et al.  Frontorhiny, a distinctive presentation of frontonasal dysplasia caused by recessive mutations in the ALX3 homeobox gene. , 2009, American journal of human genetics.

[18]  N. Pedersen,et al.  The ascent of cat breeds: genetic evaluations of breeds and worldwide random-bred populations. , 2008, Genomics.

[19]  A. Slavotinek,et al.  Subtypes of frontonasal dysplasia are useful in determining clinical prognosis , 2007, American journal of medical genetics. Part A.

[20]  Manuel A. R. Ferreira,et al.  PLINK: a tool set for whole-genome association and population-based linkage analyses. , 2007, American journal of human genetics.

[21]  N. Pedersen,et al.  An international parentage and identification panel for the domestic cat (Felis catus) , 2007, Animal genetics.

[22]  L. Lyons,et al.  Tyrosinase mutations associated with Siamese and Burmese patterns in the domestic cat (Felis catus). , 2005, Animal genetics.

[23]  Mark Daly,et al.  Haploview: analysis and visualization of LD and haplotype maps , 2005, Bioinform..

[24]  Martin R. Clutterbuck Siamese cats : legends and reality , 2004 .

[25]  R. Agarwala,et al.  Radiation hybrid mapping of 304 novel microsatellites in the domestic cat genome , 2004, Cytogenetic and Genome Research.

[26]  P. Oliveri,et al.  Alx1, a member of the Cart1/Alx3/Alx4 subfamily of Paired-class homeodomain proteins, is an essential component of the gene network controlling skeletogenic fate specification in the sea urchin embryo , 2003, Development.

[27]  F. Meijlink,et al.  The OAR/aristaless domain of the homeodomain protein Cart1 has an attenuating role in vivo , 2003, Mechanisms of Development.

[28]  R J Toonen,et al.  Increased throughput for fragment analysis on an ABI PRISM 377 automated sequencer using a membrane comb and STRand software. , 2001, BioTechniques.

[29]  M. Breen,et al.  Canine TCOF1; cloning, chromosome assignment and genetic analysis in dogs with different head types , 2001, Mammalian Genome.

[30]  R. Gorlin,et al.  Frontonasal dysplasia. , 2020, The Journal of pediatrics.

[31]  A A Schäffer,et al.  A genetic linkage map of microsatellites in the domestic cat (Felis catus). , 1999, Genomics.

[32]  S. O’Brien,et al.  Development of a feline whole genome radiation hybrid panel and comparative mapping of human chromosome 12 and 22 loci. , 1999, Genomics.

[33]  A. Leonard,et al.  Frontonasal dysostosis in two successive generations. , 1999, American journal of medical genetics.

[34]  S. O’Brien,et al.  Comparative genomics: lessons from cats. , 1997, Trends in genetics : TIG.

[35]  J. Spencer,et al.  Comparative gene mapping in the domestic cat (Felis catus). , 1997, The Journal of heredity.

[36]  J. Rand,et al.  Over representation of Burmese cats with diabetes mellitus. , 1997, Australian veterinary journal.

[37]  R. Behringer,et al.  Prenatal folic acid treatment suppresses acrania and meroanencephaly in mice mutant for the Cart1 homeobox gene , 1996, Nature Genetics.

[38]  M. Seldin,et al.  The gene for the homeodomain-containing protein Cart-1 is expressed in cells that have a chondrogenic potential during embryonic development , 1994, Mechanisms of Development.

[39]  B. de Crombrugghe,et al.  Cartilage homeoprotein 1, a homeoprotein selectively expressed in chondrocytes. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[40]  J. Persing,et al.  Frontonasal dysplasia in two successive generations. , 1993, American journal of medical genetics.

[41]  Y. Lignereux,et al.  Détermination Radiologique et Statistique des Types Morphologiques Crâniens chez le Chien: Dolichocéphalic, Mésocéphalie et Brachycéphalie , 1991 .

[42]  T. Gruffydd-Jones,et al.  Hypokalemia in the cat. , 1990, The Cornell veterinarian.

[43]  R. Gorlin,et al.  Frontonasal malformation as a field defect and in syndromic associations. , 1988, Oral surgery, oral medicine, and oral pathology.

[44]  G. Lathrop,et al.  Efficient computations in multilocus linkage analysis. , 1988, American journal of human genetics.

[45]  Shirley A. Miller,et al.  A simple salting out procedure for extracting DNA from human nucleated cells. , 1988, Nucleic acids research.

[46]  P. Wotton,et al.  Periodic muscle weakness in Burmese kittens , 1986, Veterinary Record.

[47]  Noden Dm,et al.  Inherited homeotic midfacial malformations in Burmese cats. , 1986 .

[48]  D. Sponenberg,et al.  Hereditary meningoencephalocele in Burmese cats. , 1986, The Journal of heredity.

[49]  H. Evans,et al.  Inherited homeotic midfacial malformations in Burmese cats. , 1986, Journal of craniofacial genetics and developmental biology. Supplement.

[50]  J. Opitz,et al.  Familial occurrence of a developmental defect of the medial nasal processes. , 1985, American journal of medical genetics.

[51]  J. Ott,et al.  Strategies for multilocus linkage analysis in humans. , 1984, Proceedings of the National Academy of Sciences of the United States of America.

[52]  G. Lathrop,et al.  Easy calculations of lod scores and genetic risks on small computers. , 1984, American journal of human genetics.

[53]  H. M. Moreno Fuenmayor The spectrum of frontonasal dysplasia in an inbred pedigree. , 1980, Clinical genetics.

[54]  P. Lüps,et al.  [Biometric and mechanism of development of the symptoms of brachycephaly in the dog]. , 1968, Archiv der Julius Klaus-Stiftung fur Vererbungsforschung, Sozialanthropologie und Rassenhygiene.