Published in PLoS One on April 28, 2011
Selkirk Rex: morphological and genetic characterization of a new cat breed. J Hered (2012) 1.01
To the Root of the Curl: A Signature of a Recent Selective Sweep Identifies a Mutation That Defines the Cornish Rex Cat Breed. PLoS One (2013) 0.88
Identification of the causative gene for Simmental arachnomelia syndrome using a network-based disease gene prioritization approach. PLoS One (2013) 0.77
LIPH expression in skin and hair follicles of normal coat and Rex rabbits. PLoS One (2012) 0.75
Primer3 on the WWW for general users and for biologist programmers. Methods Mol Biol (2000) 128.08
CAP3: A DNA sequence assembly program. Genome Res (1999) 50.04
Tandem repeats finder: a program to analyze DNA sequences. Nucleic Acids Res (1999) 49.21
Multiple sequence alignment with hierarchical clustering. Nucleic Acids Res (1988) 32.89
novoSNP, a novel computational tool for sequence variation discovery. Genome Res (2005) 7.42
A rapid method for the purification of DNA from blood. Nucleic Acids Res (1987) 5.96
HaploPainter: a tool for drawing pedigrees with complex haplotypes. Bioinformatics (2004) 4.00
Multipoint estimation of identity-by-descent probabilities at arbitrary positions among marker loci on general pedigrees. Hum Hered (2001) 3.32
G protein-coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth. Nat Genet (2008) 3.00
Two pathways for lysophosphatidic acid production. Biochim Biophys Acta (2008) 2.20
Desmoglein 4 in hair follicle differentiation and epidermal adhesion: evidence from inherited hypotrichosis and acquired pemphigus vulgaris. Cell (2003) 2.06
Mutations in the lipase H gene underlie autosomal recessive woolly hair/hypotrichosis. J Invest Dermatol (2008) 1.96
Human hair growth deficiency is linked to a genetic defect in the phospholipase gene LIPH. Science (2006) 1.71
Genomewide scan for linkage reveals evidence of several susceptibility loci for alopecia areata. Am J Hum Genet (2007) 1.55
A novel phosphatidic acid-selective phospholipase A1 that produces lysophosphatidic acid. J Biol Chem (2002) 1.49
A mutation in the lipase H (LIPH) gene underlie autosomal recessive hypotrichosis. Hum Genet (2007) 1.16
Founder mutations in the lipase h gene in families with autosomal recessive woolly hair/hypotrichosis. J Invest Dermatol (2009) 1.13
The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71. Mamm Genome (2010) 1.09
The effect of inbreeding on the distribution of compound heterozygotes: a lesson from Lipase H mutations in autosomal recessive woolly hair/hypotrichosis. Hum Hered (2009) 1.09
Structure and function of extracellular phospholipase A1 belonging to the pancreatic lipase gene family. Biochimie (2006) 1.02
In vitro analysis of LIPH mutations causing hypotrichosis simplex: evidence confirming the role of lipase H and lysophosphatidic acid in hair growth. J Invest Dermatol (2009) 1.00
Structural basis for the substrate selectivity of pancreatic lipases and some related proteins. Biochim Biophys Acta (1998) 0.96
Mutations in the LIPH gene in three Japanese families with autosomal recessive woolly hair/hypotrichosis. J Dermatol Sci (2009) 0.95
A novel deletion mutation in LIPH gene causes autosomal recessive hypotrichosis (LAH2). Clin Genet (2008) 0.95
Prevalent LIPH founder mutations lead to loss of P2Y5 activation ability of PA-PLA1alpha in autosomal recessive hypotrichosis. Hum Mutat (2010) 0.91
Biochemical and molecular characterization of two phosphatidic acid-selective phospholipase A1s, mPA-PLA1alpha and mPA-PLA1beta. J Biol Chem (2003) 0.91
Involvement of the Arg-Asp-His catalytic triad in enzymatic cleavage of the phosphodiester bond. Biochemistry (2001) 0.91
A first-generation microsatellite-based integrated genetic and cytogenetic map for the European rabbit (Oryctolagus cuniculus) and localization of angora and albino. Anim Genet (2006) 0.87
Construction of a rabbit bacterial artificial chromosome (BAC) library: application to the mapping of the major histocompatibility complex to position 12q.1.1. Mamm Genome (2001) 0.87
Novel missense mutations in lipase H (LIPH) gene causing autosomal recessive hypotrichosis (LAH2). J Dermatol Sci (2009) 0.87
Identification of the rat Rex mutation as a 7-bp deletion at splicing acceptor site of the Krt71 gene. J Vet Med Sci (2010) 0.86
German rex: a rexoid coat mutant in the cat. Genetica (1968) 0.85
Lipase H, a new member of the triglyceride lipase family synthesized by the intestine. Genomics (2002) 0.85
Expanded comparative mapping between man and rabbit and detection of a new conserved segment between HSA22 and OCU4. Cytogenet Genome Res (2005) 0.84
A large duplication in LIPH underlies autosomal recessive hypotrichosis simplex in four Middle Eastern families. Arch Dermatol Res (2008) 0.84
Rex mutant in the Norway rat. J Hered (1981) 0.83
Characterization of lpd (lipid defect): a novel mutation on mouse chromosome 16 associated with a defect in triglyceride metabolism. Hum Mol Genet (1998) 0.81
A novel deletion mutation in the phospholipase H (LIPH) gene in a consanguineous Pakistani family with autosomal recessive hypotrichosis (LAH2). Br J Dermatol (2008) 0.80
mRNA encoding a new lipolytic enzyme expressed in rabbit lacrimal glands. Invest Ophthalmol Vis Sci (2002) 0.77
Characteristics of Angora rabbit fiber using optical fiber diameter analyzer. J Anim Sci (2007) 0.76
A high density SNP array for the domestic horse and extant Perissodactyla: utility for association mapping, genetic diversity, and phylogeny studies. PLoS Genet (2012) 1.66
A mutation in the MATP gene causes the cream coat colour in the horse. Genet Sel Evol (2003) 1.39
Evolutionary movement of centromeres in horse, donkey, and zebra. Genomics (2006) 1.34
Genome-wide analysis reveals selection for important traits in domestic horse breeds. PLoS Genet (2013) 1.26
Genetic diversity in the modern horse illustrated from genome-wide SNP data. PLoS One (2013) 1.18
Novel insights into the bovine polled phenotype and horn ontogenesis in Bovidae. PLoS One (2013) 1.15
The first-generation whole-genome radiation hybrid map in the horse identifies conserved segments in human and mouse genomes. Genome Res (2003) 1.15
Activin signaling pathways in ovine pituitary and LbetaT2 gonadotrope cells. Biol Reprod (2002) 1.07
Overexpression of miR-30b in the developing mouse mammary gland causes a lactation defect and delays involution. PLoS One (2012) 0.99
A 3.7 Mb deletion encompassing ZEB2 causes a novel polled and multisystemic syndrome in the progeny of a somatic mosaic bull. PLoS One (2012) 0.98
Construction of a 5000(rad) whole-genome radiation hybrid panel in the horse and generation of a comprehensive and comparative map for ECA11. Mamm Genome (2002) 0.96
Population structure of the fish pathogen Flavobacterium psychrophilum at whole-country and model river levels in Japan. Vet Res (2013) 0.90
A mutation in the LAMC2 gene causes the Herlitz junctional epidermolysis bullosa (H-JEB) in two French draft horse breeds. Genet Sel Evol (2003) 0.89
Clinical and histopathological characterization of cutaneous melanomas in the melanoblastoma-bearing Libechov minipig model. Pigment Cell Res (2004) 0.88
Prion protein and Shadoo are involved in overlapping embryonic pathways and trophoblastic development. PLoS One (2012) 0.87
Characterization of the rabbit agouti signaling protein (ASIP) gene: transcripts and phylogenetic analyses and identification of the causative mutation of the nonagouti black coat colour. Genomics (2009) 0.87
Exploration of the functional hierarchy of the basal layer of human epidermis at the single-cell level using parallel clonal microcultures of keratinocytes. Exp Dermatol (2010) 0.87
Chromosomal distribution of endogenous Jaagsiekte sheep retrovirus proviral sequences in the sheep genome. J Virol (2003) 0.86
Cytogenetic localization of 136 genes in the horse: comparative mapping with the human genome. Mamm Genome (2002) 0.85
Gene expression profiling in equine polysaccharide storage myopathy revealed inflammation, glycogenesis inhibition, hypoxia and mitochondrial dysfunctions. BMC Vet Res (2009) 0.84
Linkage disequilibrium interval mapping of quantitative trait loci. BMC Genomics (2006) 0.83
Characterization of the equine glycogen debranching enzyme gene (AGL): Genomic and cDNA structure, localization, polymorphism and expression. Gene (2007) 0.83
Next-generation sequencing identifies equine cartilage and subchondral bone miRNAs and suggests their involvement in osteochondrosis physiopathology. BMC Genomics (2014) 0.83
Identification of five chromosomal regions involved in predisposition to melanoma by genome-wide scan in the MeLiM swine model. Int J Cancer (2004) 0.81
Relationship between MT1 melatonin receptor gene polymorphism and seasonal physiological responses in Ile-de-France ewes. Reprod Nutr Dev (2005) 0.81
Modulation of peripheral-type benzodiazepine receptor during ischemia reperfusion injury in a pig kidney model: a new partner of leukemia inhibitory factor in tubular regeneration. J Am Coll Surg (2006) 0.81
A composite six bp in-frame deletion in the melanocortin 1 receptor (MC1R) gene is associated with the Japanese brindling coat colour in rabbits (Oryctolagus cuniculus). BMC Genet (2010) 0.80
Quantitative trait loci linked to PRNP gene controlling health and production traits in INRA 401 sheep. Genet Sel Evol (2007) 0.80
[Therapeutic effect of human mesenchymal stem cells in skin after radiation damage]. J Soc Biol (2005) 0.79
Characterization of the beta2-microglobulin gene of the horse. Immunogenetics (2002) 0.79
Molecular characterization of the equine AEG1 locus. Gene (2002) 0.78
Chromosomal assignment of six genes (EIF4G3, HSP90, RBBP6, IL8, TERT, and TERC) in four species of the genus Equus. Anim Biotechnol (2011) 0.78
A specific pattern of splicing for the horse alphaS1-Casein mRNA and partial genomic characterization of the relevant locus. Genet Sel Evol (2002) 0.78
Expression of the prion-like protein Shadoo in the developing mouse embryo. Biochem Biophys Res Commun (2011) 0.78
Detection of QTL controlling digestive efficiency and anatomy of the digestive tract in chicken fed a wheat-based diet. Genet Sel Evol (2014) 0.78
Mapping of quantitative trait loci affecting classical scrapie incubation time in a population comprising several generations of scrapie-infected sheep. J Gen Virol (2009) 0.77
Genetic mapping of the (G)-locus, responsible for the coat color phenotype "progressive greying with age" in horses (Equus caballus). Mamm Genome (2002) 0.76
A method for proteomic analysis of equine subchondral bone and epiphyseal cartilage. Proteomics (2012) 0.76
LIPH expression in skin and hair follicles of normal coat and Rex rabbits. PLoS One (2012) 0.75
Omics technologies provide new insights into the molecular physiopathology of equine osteochondrosis. BMC Genomics (2014) 0.75
Divergent selection on 63-day body weight in the rabbit: response on growth, carcass and muscle traits. Genet Sel Evol (2004) 0.75
cDNA sequence of the horse (Equus caballus) LAMA3 gene and characterization of two intronic SNP markers. DNA Seq (2005) 0.75
Drawing together the knowledge of forestry and pastoralism experts in the construction of a technical support tool for silvopastoralism. J Environ Manage (2013) 0.75