Published in Hereditas on January 01, 2003
Molecular organization and evolution of 5S rDNA in the genus Merluccius and their phylogenetic implications. J Mol Evol (2009) 1.03
Organization and variation analysis of 5S rDNA in different ploidy-level hybrids of red crucian carp × topmouth culter. PLoS One (2012) 0.98
Molecular organization of 5S rDNA in bitterlings (Cyprinidae). Genetica (2008) 0.90
The 5S rDNA high dynamism in Diplodus sargus is a transposon-mediated mechanism. Comparison with other multigene families and Sparidae species. J Mol Evol (2013) 0.87
Evidence for 5S rDNA horizontal transfer in the toadfish Halobatrachus didactylus (Schneider, 1801) based on the analysis of three multigene families. BMC Evol Biol (2012) 0.85
Molecular organization of 5S rDNAs in Rajidae (Chondrichthyes): Structural features and evolution of piscine 5S rRNA genes and nontranscribed intergenic spacers. J Mol Evol (2006) 0.83
The formation of diploid and triploid hybrids of female grass carp × male blunt snout bream and their 5S rDNA analysis. BMC Genet (2013) 0.83
Fanconi anemia in brothers initially diagnosed with VACTERL association with hydrocephalus, and subsequently with Baller-Gerold syndrome. Am J Med Genet (1996) 2.76
Expression of two Xenopus laevis ribosomal protein genes in injected frog oocytes. A specific splicing block interferes with the L1 RNA maturation. J Mol Biol (1984) 2.03
The parkin gene is not involved in late-onset Parkinson's disease. Neurology (2001) 1.51
A new locus for autosomal dominant nocturnal frontal lobe epilepsy maps to chromosome 1. Neurology (2000) 1.45
Classical and molecular cytogenetics of the zebrafish, Danio rerio (Cyprinidae, Cypriniformes): an overview. Genetica (2001) 1.34
Splicing of Xenopus laevis ribosomal protein RNAs is inhibited in vivo by antisera to ribonucleoproteins containing U1 small nuclear RNA. J Mol Biol (1984) 1.23
Cytogenetics of bisexual/unisexual species of Poecilia. II. Analysis of heterochromatin and nucleolar organizer regions in Poecilia mexicana mexicana by C-banding and DAPI, quinacrine, chromomycin A3, and silver staining. Cytogenet Cell Genet (1992) 1.12
Investigating factors associated with adherence behaviour in patients with chronic myeloid leukemia: an observational patient-centered outcome study. Br J Cancer (2012) 1.11
The fragile X premutation presenting as postprandial hypotension. Neurology (2004) 0.95
Vitamin E deficiency due to chylomicron retention disease in Marinesco-Sjögren syndrome. Ann Neurol (2000) 0.95
Molecular systematics and evolutionary biogeography of the genus Talpa (Soricomorpha: Talpidae). Mol Phylogenet Evol (2010) 0.89
Sequence of the gene coding for ribosomal protein S8 of Xenopus laevis. Gene (1993) 0.88
Spinal muscular atrophy due to an isolated deletion of exon 8 of the telomeric survival motor neuron gene. Ann Neurol (1998) 0.88
Observation of time-domain modulation of free-electron-laser pulses by multipeaked electron-energy spectrum. Phys Rev Lett (2013) 0.87
DJ-1 is a Parkinson's disease susceptibility gene in southern Italy. Clin Genet (2009) 0.87
SIL1 and SARA2 mutations in Marinesco-Sjögren and chylomicron retention diseases. Clin Genet (2007) 0.84
Association of tau gene polymorphism with Parkinson's disease. Neurol Sci (2003) 0.83
Structure of Xenopus laevis ribosomal protein L32 and its expression during development. Nucleic Acids Res (1990) 0.82
Extended Hückel calculations on polypeptide chains. II. The phi-psi energy surface for a tetrapeptide of glycine. J Phys Chem (1970) 0.82
Cytogenetic analysis of a self-fertilizing fish, Rivulus marmoratus: remarkable chromosomal constancy over a vast geographic range. Genome (1997) 0.82
Zebrafish 5S rRNA genes map to the long arms of chromosome 3. Chromosome Res (2000) 0.82
Cytogenetic analysis of Liza ramada (Pisces, Perciformes) by different staining techniques and fluorescent in situ hybridization. Heredity (Edinb) (1997) 0.81
NACP-REP1 polymorphism is not involved in Parkinson's disease: a case-control study in a population sample from southern Italy. Neurosci Lett (2003) 0.81
The dopamine D2 receptor gene is a susceptibility locus for Parkinson's disease. Mov Disord (2000) 0.81
Human ribosomal protein L4: cloning and sequencing of the cDNA and primary structure of the protein. Biochim Biophys Acta (1993) 0.81
The parkin gene is not a major susceptibility locus for typical late-onset Parkinson's disease. Neurol Sci (2001) 0.80
Self-amplified spontaneous emission free-electron laser with an energy-chirped electron beam and undulator tapering. Phys Rev Lett (2011) 0.80
Alpha-synuclein promoter haplotypes and dementia in Parkinson's disease. Am J Med Genet B Neuropsychiatr Genet (2008) 0.80
Chromosomal evolution in Mugilidae (Pisces, Mugiliformes): FISH mapping of the (TTAGGG) telomeric repeat in the six Mediterranean mullets. Hereditas (2004) 0.79
LRRK2 G6055A mutation in Italian patients with familial or sporadic Parkinson's disease. Clin Genet (2007) 0.78
Experimental demonstration of emittance compensation with velocity bunching. Phys Rev Lett (2010) 0.78
Contact zones between chromosomal races of Mus musculus domesticus. 3. Molecular and chromosomal evidence of restricted gene flow between the CD race (2n = 22) and the ACR race (2n = 24). Heredity (Edinb) (2002) 0.78
The selection of patients for breast reduction: should health commissions have a say? Br J Plast Surg (1999) 0.78
Comparative molecular cytogenetic analysis of two congeneric species, Mugil curema and M. liza (Pisces, Mugiliformes), characterized by significant karyotype diversity. Genetica (2005) 0.78
Novel human pathological mutations. Gene symbol: PARK2. Disease: Parkinson's disease. Hum Genet (2007) 0.77
Novel human pathological mutations. Gene symbol: SCN1A. Disease: Myoclonic epilepsy of infancy. Hum Genet (2010) 0.76
Interleukins 2 and 12 activate natural killer cytolytic responses of peripheral blood mononuclear cells from patients with head and neck squamous cell carcinoma. Arch Otolaryngol Head Neck Surg (1996) 0.76
Cytogenetics of bisexual/unisexual species of Poecilia. V. Unisexual poeciliids with anomalous karyotypes from northeastern Mexico. Cytogenet Cell Genet (1993) 0.75
Chromosomal localization of zebrafish AluI repeats by primed in situ (PRINS) labeling. Cytogenet Cell Genet (1999) 0.75
Novel human pathological mutations. Gene symbol: PARK2. Disease: Parkinson's disease. Hum Genet (2007) 0.75
Association of the 5-HT6 receptor gene polymorphism C267T with Parkinson's disease. Neurology (2002) 0.75
Novel human pathological mutations. Gene symbol: PARK2. Disease: Parkinson's disease. Hum Genet (2007) 0.75
[Oral and maxillofacial aspects of von Recklinghausen's neurofibromatosis]. Arch Stomatol (Napoli) (1988) 0.75
Additions and Corrections: Synthesis of Two Bis-m-quinomethanes. An Experimental Study of Connectivity Effects on the Equal-Parity Criterion for Low-Spin Ground States in Alternant Non-Kekule Molecules. J Am Chem Soc (1986) 0.75
Novel human pathological mutations. Gene symbol: PINK1. Disease: Parkinson disease. Hum Genet (2010) 0.75
Direct measurement of the double emittance minimum in the beam dynamics of the sparc high-brightness photoinjector. Phys Rev Lett (2007) 0.75
Novel human pathological mutations. Gene symbol: SCN1A. Disease: severe myoclonic epilepsy of infancy. Hum Genet (2009) 0.75
[Effects of aflatoxins B1 on glucose-6-phosphatase activity in kidney and liver of rats (Rattus rattus norvegicus)]. Rev Farm Bioquim Univ Sao Paulo (1977) 0.75
Cytogenetics of bisexual/unisexual species of Poecilia. III. The karyotype of Poecilia formosa, a gynogenetic species of hybrid origin. Cytogenet Cell Genet (1992) 0.75
A procedure for cloning genomic DNA fragments with increasing thermoresistance. Gene (1998) 0.75
[Aminoaciduria screening in newborn infants using, comparatively, chromatographic and colorimetric methods]. Rev Farm Bioquim Univ Sao Paulo (1977) 0.75
Gene dosage influences the age at onset of SCA2 in a family from southern Italy. Clin Genet (2007) 0.75
Analysis methodology of movable emittance-meter measurements for low energy electron beams. Rev Sci Instrum (2008) 0.75
Novel human pathological mutations. Gene symbol: PARK7. Disease: Parkinson disease. Hum Genet (2010) 0.75
Extended Hückel calculations on polypeptide chains. IV. The phy-psi energy surface for a tetrapeptide of poly-L-alanine. J Phys Chem (1972) 0.75