Published in Mamm Genome on May 01, 1994
Genome-wide linkage analysis of inguinal hernia in pigs using affected sib pairs. BMC Genet (2006) 1.13
The cytogenetic map of the domestic pig. Mamm Genome (1997) 0.94
Genetic variation in the porcine myogenin gene locus. Mamm Genome (1997) 0.75
A deletion in the bovine myostatin gene causes the double-muscled phenotype in cattle. Nat Genet (1997) 7.15
Human Y chromosome azoospermia factors (AZF) mapped to different subregions in Yq11. Hum Mol Genet (1996) 3.78
A genetic linkage map for cattle. Genetics (1994) 3.64
The dynamics of chromosome evolution in birds and mammals. Nature (1999) 2.95
Cloning of a gene highly overexpressed in cancer coding for a novel KH-domain containing protein. Oncogene (1997) 2.58
Abnormal myotonic dystrophy protein kinase levels produce only mild myopathy in mice. Nat Genet (1996) 2.47
Mutations in the SALL1 putative transcription factor gene cause Townes-Brocks syndrome. Nat Genet (1998) 2.39
Targeted disruption of the Insl3 gene causes bilateral cryptorchidism. Mol Endocrinol (1999) 1.99
Pharmacological profile of BIBN4096BS, the first selective small molecule CGRP antagonist. Br J Pharmacol (2000) 1.95
Visualization of the conservation of synteny between humans and pigs by heterologous chromosomal painting. Genomics (1995) 1.94
Comparative genome map of human and cattle. Genomics (1995) 1.93
Dysferlin deletion in SJL mice (SJL-Dysf) defines a natural model for limb girdle muscular dystrophy 2B. Nat Genet (1999) 1.93
First report on chicken genes and chromosomes 2000. Cytogenet Cell Genet (2000) 1.92
Isolation, characterization, and organ-specific expression of two novel human zinc finger genes related to the Drosophila gene spalt. Genomics (1996) 1.89
300 million years of conserved synteny between chicken Z and human chromosome 9. Nat Genet (1999) 1.78
Molecular cloning and characterization of the human protein kinase D2. A novel member of the protein kinase D family of serine threonine kinases. J Biol Chem (2000) 1.76
SALL3, a new member of the human spalt-like gene family, maps to 18q23. Genomics (1999) 1.70
Rett syndrome: analysis of MECP2 and clinical characterization of 31 patients. Hum Mol Genet (2000) 1.65
Expression of the highly conserved RNA binding protein KOC in embryogenesis. Mech Dev (1999) 1.64
Nucleotide sequence of a bovine protamine cDNA. Biol Chem Hoppe Seyler (1987) 1.61
The nucleotide sequence of a human protamine 1 cDNA. Nucleic Acids Res (1987) 1.61
Evaluation of canine lymphocyte proliferation: comparison of three different colorimetric methods with the 3H-thymidine incorporation assay. Vet Immunol Immunopathol (1999) 1.60
Expression and differential regulation of connective tissue growth factor in pancreatic cancer cells. Oncogene (1999) 1.60
Mitral-valve repair without annuloplasty rings: results after repair of anterior leaflet versus posterior-leaflet defects using polytetrafluoroethylene sutures for chordal replacement. Eur J Cardiothorac Surg (2000) 1.56
Heating and humidifying of carbon dioxide during pneumoperitoneum is not indicated: a prospective randomized trial. Surg Endosc (2005) 1.55
Male mice deficient for germ-cell cyritestin are infertile. Biol Reprod (1999) 1.54
Expression of p53 during mouse embryogenesis. Development (1991) 1.50
Nucleotide sequence of the gene for human transition protein 1 and its chromosomal localization on chromosome 2. Genomics (1990) 1.49
An integrated cytogenetic and meiotic map of the bovine genome. Anim Genet (1995) 1.49
Presumed trisomy for the short arm of chromosome No. 9 not due to inherited translocation. Humangenetik (1971) 1.48
A high density of X-linked genes for general cognitive ability: a run-away process shaping human evolution? Trends Genet (2001) 1.46
MECP2 mutations in sporadic cases of Rett syndrome are almost exclusively of paternal origin. Am J Hum Genet (2001) 1.45
The first highly potent and selective non-peptide neuropeptide Y Y1 receptor antagonist: BIBP3226. Eur J Pharmacol (1994) 1.43
Assessment of heart rate variability by using different commercially available systems. Am J Cardiol (1996) 1.42
Translational control in spermatogenesis. Dev Biol (1995) 1.39
Decreasing fibrogenesis: an immunohistochemical study of paired liver biopsies following lamivudine therapy for chronic hepatitis B. J Hepatol (2001) 1.38
Mutation analysis of the spastin gene (SPG4) in patients in Germany with autosomal dominant hereditary spastic paraplegia. Hum Mutat (2002) 1.38
BIIE0246: a selective and high affinity neuropeptide Y Y(2) receptor antagonist. Eur J Pharmacol (1999) 1.38
Effects of DGAT1 variants on milk production traits in German cattle breeds. J Anim Sci (2003) 1.34
Expression, phosphorylation and nuclear localization of the human P1 protein, a homologue of the yeast Mcm 3 replication protein. J Cell Sci (1995) 1.34
The expression pattern of the Hmgic gene during development. Genes Chromosomes Cancer (1998) 1.33
Haploid expression of a protamine gene during bovine spermatogenesis. Biol Chem Hoppe Seyler (1987) 1.28
Subtype selectivity of the novel nonpeptide neuropeptide Y Y1 receptor antagonist BIBO 3304 and its effect on feeding in rodents. Br J Pharmacol (1998) 1.28
In situ hybridization studies on variant t(2;8) translocations in Burkitt lymphoma lines. Hum Genet (1986) 1.25
Dynamic expression pattern of the myc protooncogene in midgestation mouse embryos. Science (1989) 1.24
Assignment of the gene for human glucose dehydrogenase (E.C. 1.1.1.47) to chromosome 1 using somatic cell hybrids. Cytogenet Cell Genet (1978) 1.22
Partial monosomy 22pter leads to q11 in a newborn with the clinical features of trisomy 13 syndrome. Ann Genet (1980) 1.20
Disruption of an inner arm dynein heavy chain gene results in asthenozoospermia and reduced ciliary beat frequency. Hum Mol Genet (2001) 1.19
International system for cytogenetic nomenclature of domestic animals. The Second International Conference on Standardization of Domestic Animal Karyotypes, INRA, Jouy-en Josas, France, 22nd-26th May, 1989. Cytogenet Cell Genet (1990) 1.19
Breakpoint analysis of the pericentric inversion between chimpanzee chromosome 10 and the homologous chromosome 12 in humans. Cytogenet Genome Res (2005) 1.18
Teratozoospermia in mice lacking the transition protein 2 (Tnp2). Mol Hum Reprod (2001) 1.18
Novel mutations in the Atlastin gene (SPG3A) in families with autosomal dominant hereditary spastic paraplegia and evidence for late onset forms of HSP linked to the SPG3A locus. Hum Mutat (2004) 1.18
An X-chromosome linked locus contributes to abnormal placental development in mouse interspecific hybrid. Nat Genet (1996) 1.18
Localization of the active type I DNA topoisomerase gene on human chromosome 20q11.2-13.1, and two pseudogenes on chromosomes 1q23-24 and 22q11.2-13.1. Hum Genet (1989) 1.17
Localization of the human bona fide calmodulin genes CALM1, CALM2, and CALM3 to chromosomes 14q24-q31, 2p21.1-p21.3, and 19q13.2-q13.3. Genomics (1993) 1.17
Influence of mutation type and location on phenotype in 123 patients with Rett syndrome. Neuropediatrics (2002) 1.17
Expansion of the (CAG)n repeat causing Huntington's disease in 352 patients of German origin. Hum Mol Genet (1993) 1.16
Reevaluation of the incidence of thromboembolic complications in congenital factor XII deficiency--a study on 73 subjects from 14 Swiss families. Thromb Haemost (1999) 1.16
Standardization of cattle karyotype nomenclature: report of the committee for the standardization of the cattle karyotype. Cytogenet Cell Genet (1996) 1.15
Mice deficient for spermatid perinuclear RNA-binding protein show neurologic, spermatogenic, and sperm morphological abnormalities. Dev Biol (2001) 1.14
Detection and characterization of SNPs useful for identity control and parentage testing in major European dairy breeds. Anim Genet (2004) 1.14
Isolation and mapping of polymorphic microsatellites in cattle. Anim Genet (1993) 1.13
c-myc and immunoglobulin kappa light chain constant genes are on the 8q+ chromosome of three Burkitt lymphoma lines with t(2;8) translocations. EMBO J (1984) 1.12
Genetic polymorphism of lactate dehydrogenase isoenzymes in the carp (Cyprinus carpio) apparently due to a "null allele". Biochem Genet (1973) 1.12
Biochemical and genetic investigation of round-headed spermatozoa in infertile men including two brothers and their father. Andrologia (1984) 1.11
Rat transition nuclear protein 2 regulatory region directs haploid expression of reporter gene in male germ cells of transgenic mice. Mol Reprod Dev (2001) 1.11
Differences in gene density on chicken macrochromosomes and microchromosomes. Anim Genet (2000) 1.11
Structural organization and developmental expression pattern of the mouse WD-repeat gene DMR-N9 immediately upstream of the myotonic dystrophy locus. Hum Mol Genet (1995) 1.09
Cloning of a cDNA for a novel insulin-like peptide of the testicular Leydig cells. J Biol Chem (1993) 1.09
Involvement of insulin-like factor 3 (Insl3) in diethylstilbestrol-induced cryptorchidism. Endocrinology (2000) 1.09
Demonstration of a heritable fragile site in human chromosome 16 with distamycin A. Cytogenet Cell Genet (1980) 1.09
Coeliac disease: in vivo toxicity of the putative immunodominant epitope. Gut (2003) 1.08
[Autoradiographic studies on X-autosomal translocation in man: 45,X.15-,tan(15qZq+)+]. Cytogenetics (1971) 1.08
A comparative analysis of N-myc and c-myc expression and cellular proliferation in mouse organogenesis. Mech Dev (1991) 1.08
Molecular analysis of SALL1 mutations in Townes-Brocks syndrome. Am J Hum Genet (1999) 1.07
Clinical performance of interns after being on call. South Med J (1987) 1.06
Delineation of the 6p22 amplification unit in urinary bladder carcinoma cell lines. Cancer Res (2000) 1.05
Allelic association of the cystic fibrosis locus and two DNA markers, XV2c and KM19, in 55 German families. Hum Genet (1988) 1.05
DGAT1, a new positional and functional candidate gene for intramuscular fat deposition in cattle. Anim Genet (2003) 1.05
Isochores and replication time zones: a perfect match. Cytogenet Genome Res (2007) 1.05
Mapping of the oncogenes Myc, Sis, and int-1 to the distal part of mouse chromosome 15. Cytogenet Cell Genet (1987) 1.05
Genomic cloning, chromosomal mapping, and expression analysis of msal-2. Mamm Genome (2000) 1.04
T cell expressed PKCtheta demonstrates cell-type selective function. Eur J Immunol (2000) 1.04
Interactions between mouse ZP2 glycoprotein and proacrosin; a mechanism for secondary binding of sperm to the zona pellucida during fertilization. J Cell Sci (2001) 1.04
[The mechanism of diploidization in vertebrate evolution: coexistence of tetrasomic and disomic gene loci for the isocitrate dehydrogenases in trout (salmo irideus)]. Humangenetik (1970) 1.03
Studies on the function of H-Y antigen: dissociation and reorganization experiments on rat gonadal tissue. Cytogenet Cell Genet (1978) 1.02
A direct demonstration of somatically paired heterochromatin of human chromosomes. Cytogenet Cell Genet (1983) 1.02
Acrosin and the acrosome in human spermatogenesis. Hum Genet (1983) 1.02
Mapping chromosomal breakpoints of Burkitt's t(8;14) translocations far upstream of c-myc. Cancer Res (1992) 1.02
Spermatozoa lacking acrosin protein show delayed fertilization. Mol Reprod Dev (1997) 1.01
Paternal transmission of X-linked placental dysplasia in mouse interspecific hybrids. Genetics (1997) 1.01
A comparison of the expression pattern of five genes of the family of small leucine-rich proteoglycans during mouse development. J Bone Miner Res (2000) 1.01