听力与言语-语言病理学

行为科学

医学伦理学

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  • Expression analysis, genomic structure, and mapping to 7q31 of the human sperm adhesion molecule gene SPAM1.

    abstract::During the course of systematic sequence tag analysis of clones isolated from an adult testis cDNA library, clones 296 and 576 were found to detect 71-74% sequence identity to the guinea pig sperm surface protein PH-20. This surface protein is involved in sperm-egg adhesion in the guinea pig. Nucleotide sequence for 1...

    journal_title:Genomics

    pub_type: 杂志文章

    doi:10.1006/geno.1995.9931

    authors: Jones MH,Davey PM,Aplin H,Affara NA

    更新日期:1995-10-10 00:00:00

  • Cloning and chromosomal mapping of three novel genes, GPR9, GPR10, and GPR14, encoding receptors related to interleukin 8, neuropeptide Y, and somatostatin receptors.

    abstract::We employed the polymerase chain reaction and genomic DNA library screening to clone novel human genes, GPR9 and GPR10, and a rat gene, GPR14. GPR9, GPR10, and GPR14 each encode G protein-coupled receptors. GPR10 and GPR14 are intronless within their coding regions, while GPR9 contains at least one intron. The recepto...

    journal_title:Genomics

    pub_type: 杂志文章

    doi:10.1006/geno.1995.9996

    authors: Marchese A,Heiber M,Nguyen T,Heng HH,Saldivia VR,Cheng R,Murphy PM,Tsui LC,Shi X,Gregor P

    更新日期:1995-09-20 00:00:00

  • Construction and characterization of a bovine bacterial artificial chromosome library.

    abstract::A bacterial artificial chromosome (BAC) library has been constructed for use in bovine genome mapping using constructed for use in bovine genome mapping using the pBeloBAC11 vector. Currently, the library consists of 23,040 clones, which achieves a 70% probability (P=0.70) of the library containing a specific unique D...

    journal_title:Genomics

    pub_type: 杂志文章

    doi:10.1006/geno.1995.9986

    authors: Cai L,Taylor JF,Wing RA,Gallagher DS,Woo SS,Davis SK

    更新日期:1995-09-20 00:00:00

  • Construction of two YAC contigs in human Xp11.23-p11.22, one encompassing the loci OATL1, GATA, TFE3, and SYP, the other linking DXS255 to DXS146.

    abstract::We have constructed two YAC contigs in the Xp11.23-p11.22 interval of the human X chromosome, a region that was previously poorly characterized. One contig, of at least 1.4 Mb, links the pseudogene OATL1 to the genes GATA1, TFE3, and SYP and also contains loci implicated in Wiskott-Aldrich syndrome and synovial sarcom...

    journal_title:Genomics

    pub_type: 杂志文章

    doi:10.1006/geno.1995.9976

    authors: Fisher SE,Hatchwell E,Chand A,Ockenden N,Monaco AP,Craig IW

    更新日期:1995-09-20 00:00:00

  • Molecular cloning and characterization of the mouse carboxyl ester lipase gene and evidence for expression in the lactating mammary gland.

    abstract::DNA hybridization was used to isolate a 2.04-kb cDNA encoding carboxyl ester lipase (CEL) from a mouse lactating mammary gland, lambda gt10 cDNA library. The cDNA sequence translated into a protein of 599 amino acids, including 20 amino acids of a putative signal peptide. Comparison of the deduced amino acid sequence ...

    journal_title:Genomics

    pub_type: 杂志文章

    doi:10.1006/geno.1995.1221

    authors: Lidmer AS,Kannius M,Lundberg L,Bjursell G,Nilsson J

    更新日期:1995-09-01 00:00:00

  • Fructose-1,6-bisphosphatase: genetic and physical mapping to human chromosome 9q22.3 and evaluation in non-insulin-dependent diabetes mellitus.

    abstract::PCR primers specific to the human liver fructose-1,6-bisphosphatase (FBP) gene were designed and used to isolate a cosmid clone. Physical mapping of the FBP cosmid by FISH, and genetic mapping of an associated GA repeat polymorphism (PIC = 0.35), located the liver FBP gene to chromosome 9q22.3 with no recombination be...

    journal_title:Genomics

    pub_type: 杂志文章

    doi:10.1006/geno.1995.1230

    authors: Rothschild CB,Freedman BI,Hodge R,Rao PN,Pettenati MJ,Anderson RA,Akots G,Qadri A,Roh B,Fajans SS

    更新日期:1995-09-01 00:00:00

  • Structure of the gene encoding the murine protein kinase CK2 beta subunit.

    abstract::The mouse protein kinase CK2 beta subunit gene (Csnk2b) is composed of seven exons contained within 7874 bp. The exon and intron lengths extend from 76 to 321 and 111 to 1272 bp, respectively. The lengths of the murine coding exons correspond exactly to the lengths of the exons in the human CK2 beta gene. Both genes c...

    journal_title:Genomics

    pub_type: 杂志文章

    doi:10.1006/geno.1995.1239

    authors: Boldyreff B,Issinger OG

    更新日期:1995-09-01 00:00:00

  • Identification of an alternative transcript from the human iduronate-2-sulfatase (IDS) gene.

    abstract::Iduronate-2-sulfatase (IDS) is involved in the degradation of heparan sulfate and dermatan sulfate in the lysosomes, and a deficiency in this enzyme results in Hunter syndrome. A 2.3-kb cDNA clone that contains the entire coding sequence of IDS has previously been reported. Here we describe the identification of a 1.4...

    journal_title:Genomics

    pub_type: 杂志文章

    doi:10.1006/geno.1995.1249

    authors: Malmgren H,Carlberg BM,Pettersson U,Bondeson ML

    更新日期:1995-09-01 00:00:00

  • Isolation and regional assignment of human chromosome 12p cDNAs.

    abstract::We have characterized 117 cDNAs isolated by direct cDNA selection using pools of human chromosome 12p cosmids. Sequencing revealed that 41 clones did overlap with other cDNAs. Of the remaining 76 cDNA sequences, 11 matched previously identified human chromosome 12p genes and 3 matched previously determined cDNA sequen...

    journal_title:Genomics

    pub_type: 杂志文章

    doi:10.1006/geno.1995.1213

    authors: Baens M,Aerssens J,van Zand K,Van den Berghe H,Marynen P

    更新日期:1995-09-01 00:00:00

  • A comparative transcriptional map of a region of 250 kb on the human and mouse X chromosome between the G6PD and the FLN1 genes.

    abstract::The transcriptional organization of the region of the mouse X chromosome between the G6pd and the Fln1 genes was studied in detail, and it was compared with the syntenic region of the human chromosome. A cosmid contig of 250 kb was constructed by screening mouse cosmid libraries with probes for human genes and with wh...

    journal_title:Genomics

    pub_type: 杂志文章

    doi:10.1006/geno.1995.1164

    authors: Rivella S,Tamanini F,Bione S,Mancini M,Herman G,Chatterjee A,Maestrini E,Toniolo D

    更新日期:1995-08-10 00:00:00

  • Mammalian mitochondrial intermediate peptidase: structure/function analysis of a new homologue from Schizophyllum commune and relationship to thimet oligopeptidases.

    abstract::Mitochondrial intermediate peptidase (MIP) is a component of the mitochondrial protein import machinery required for maturation of nuclear-encoded precursor proteins targeted to the mitochondrial matrix or inner membrane. We previously characterized this enzyme in rat (RMIP) and Saccharomyces cerevisiae (YMIP) and sho...

    journal_title:Genomics

    pub_type: 杂志文章

    doi:10.1006/geno.1995.1174

    authors: Isaya G,Sakati WR,Rollins RA,Shen GP,Hanson LC,Ullrich RC,Novotny CP

    更新日期:1995-08-10 00:00:00

  • Developmental expression of p107 mRNA and evidence for alternative splicing of the p107 (RBL1) gene product.

    abstract::Expression of p107, a protein with homology to the retinoblastoma tumor suppressor (pRB), was monitored during murine development. Northern blot tissue surveys identified two transcripts of 4.9 and 2.4 kb that hybridized to a p107 cDNA clone. Expression of both transcripts was detected in fetal tissues, with particula...

    journal_title:Genomics

    pub_type: 杂志文章

    doi:10.1006/geno.1995.1184

    authors: Kim KK,Soonpaa MH,Wang H,Field LJ

    更新日期:1995-08-10 00:00:00

  • Molecular cloning and chromosomal mapping of the mouse cyclin-dependent kinase 5 gene.

    abstract::Cyclin-dependent kinase 5 (Cdk5) is predominantly expressed in neurons. In vitro, Cdk5 purified from the nervous tissue phosphorylates both high-molecular-weight neurofilament and microtubule-associated tau. The mouse gene encoding Cdk5 (Cdk5) was found to be 5 kb in length and divided into 12 exons. All of the exon-i...

    journal_title:Genomics

    pub_type: 杂志文章

    doi:10.1006/geno.1995.1194

    authors: Ohshima T,Nagle JW,Pant HC,Joshi JB,Kozak CA,Brady RO,Kulkarni AB

    更新日期:1995-08-10 00:00:00

  • Construction of 110 cosmid markers and a 4.5-Mb YAC contig on human chromosome 8p12-q11.

    abstract::Microcell hybrids containing various regions of human chromosome 8 were formed by microcell-mediated transfer of neo-tagged chromosome 8 into the cells derived from severe combined immunodeficiency (SCID) mouse. Thus, 110 cosmid markers were isolated from SV40-transformed SCID fibroblast cell line (SCVA) containing a ...

    journal_title:Genomics

    pub_type: 杂志文章

    doi:10.1006/geno.1995.1125

    authors: Kurimasa A,Suzuki N,Kumano S,Li H,Wells D,Wagner MJ,Chen F,Chen DJ,Oshimura M

    更新日期:1995-07-20 00:00:00

  • Complex genetic organization of junB: multiple blocks of flanking evolutionarily conserved sequence at the murine and human junB loci.

    abstract::A comparison of the murine and human junB loci reveals nine regions of distal 5'- and 3'-flanking DNA that exhibit greater than 72% sequence identity. A large fraction (over 50%) of the junB locus is contained in these flanking evolutionarily conserved sequences (FECS), which may be required for effecting the proper t...

    journal_title:Genomics

    pub_type: 杂志文章

    doi:10.1006/geno.1995.1135

    authors: Phinney DG,Tseng SW,Ryder K

    更新日期:1995-07-20 00:00:00

  • Identification of a novel conserved human gene, TEGT.

    abstract::A novel gene, TEGT (testis enhanced gene transcript), has been identified in humans. It does not belong to any known gene family of vertebrates. The deduced amino acid sequence of the gene and a bacterial protein of unknown function show low but significant homology and very similar hydrophobicity profiles. Two differ...

    journal_title:Genomics

    pub_type: 杂志文章

    doi:10.1006/geno.1995.1145

    authors: Walter L,Marynen P,Szpirer J,Levan G,Günther E

    更新日期:1995-07-20 00:00:00

  • Assignment of the 49-kDa (PRIM1) and 58-kDa (PRIM2A and PRIM2B) subunit genes of the human DNA primase to chromosome bands 1q44 and 6p11.1-p12.

    abstract::DNA primase is an essential replication protein that catalyzes the synthesis of oligoribonucleotide primers. DNA primase, consisting of two subunits (p49 and p58), plays a key role in both the initiation of DNA replication and the synthesis of Okazaki fragments for lagging strand synthesis. We mapped the locations of ...

    journal_title:Genomics

    pub_type: 杂志文章

    doi:10.1006/geno.1995.1155

    authors: Shiratori A,Okumura K,Nogami M,Taguchi H,Onozaki T,Inoue T,Ando T,Shibata T,Izumi M,Miyazawa H

    更新日期:1995-07-20 00:00:00

  • Structure, chromosomal location, and expression pattern of three mouse genes homologous to the human MAGE genes.

    abstract::The human MAGE1 gene directs the expression of an antigen recognized on a melanoma by autologous cytolytic T lymphocytes. MAGE1 belongs to a family of genes that are expressed in a number of tumors of various histological types but not in normal tissues except testis. The MAGE genes are arranged in two groups that are...

    journal_title:Genomics

    pub_type: 杂志文章

    doi:10.1006/geno.1995.1108

    authors: De Backer O,Verheyden AM,Martin B,Godelaine D,De Plaen E,Brasseur R,Avner P,Boon T

    更新日期:1995-07-01 00:00:00

  • Genomic cloning of mouse MIF (macrophage inhibitory factor) and genetic mapping of the human and mouse expressed gene and nine mouse pseudogenes.

    abstract::The single functional mouse gene for MIF (macrophage migration inhibitory factor) has been cloned from a P1 library, and its exon/intron structure determined and shown to resemble that of the human gene. The gene was mapped to chromosome 10 using two multilocus crosses between laboratory strains and either Mus musculu...

    journal_title:Genomics

    pub_type: 杂志文章

    doi:10.1006/geno.1995.1070

    authors: Kozak CA,Adamson MC,Buckler CE,Segovia L,Paralkar V,Wistow G

    更新日期:1995-06-10 00:00:00

  • Primary structure of human lumican (keratan sulfate proteoglycan) and localization of the gene (LUM) to chromosome 12q21.3-q22.

    abstract::A human corneal fibroblast cDNA library was screened with a bovine lumican cDNA probe to obtain three clones. Sequencing of the longest clone (1.75 kb) yielded an open reading frame of 1014 bp coding for a 338-amino-acid core protein. Amino acid sequencing of a tryptic peptide resulted in a 9-amino-acid match with the...

    journal_title:Genomics

    pub_type: 杂志文章

    doi:10.1006/geno.1995.1080

    authors: Chakravarti S,Stallings RL,SundarRaj N,Cornuet PK,Hassell JR

    更新日期:1995-06-10 00:00:00

  • The frequency and position of Alu repeats in cDNAs, as determined by database searching.

    abstract::The Alu repeat sequence is estimated to account for 5% of human genomic DNA. The precise relationship of Alu sequences to human fully spliced cDNA has yet to be determined, although many new protocols for cloning cDNAs either depend on the presence of Alus or--more usually--rely on their absence in a population of mes...

    journal_title:Genomics

    pub_type: 杂志文章

    doi:10.1006/geno.1995.1090

    authors: Yulug IG,Yulug A,Fisher EM

    更新日期:1995-06-10 00:00:00

  • Isolation and fine mapping of 16 novel human zinc finger-encoding cDNAs identify putative candidate genes for developmental and malignant disorders.

    abstract::We have isolated and chromosomally fine-mapped 16 novel genes belonging to the human zinc finger Krüppel family (ZNF131-140, 142, 143, 148, 151, 154, and 155), including 1 of the GLI type (ZNF143) and 3 containing a KRAB (Krüppel-associated box) segment (ZNF133, 136, and 140). Based on their map position, several of t...

    journal_title:Genomics

    pub_type: 杂志文章

    doi:10.1006/geno.1995.1040

    authors: Tommerup N,Vissing H

    更新日期:1995-05-20 00:00:00

  • Structure and organization of the human thrombospondin 3 gene (THBS3).

    abstract::The promoter/5' flank sequence, cDNA sequence, and exon/intron structures of the human thrombospondin 3 (THBS3) gene have been determined. THBS3 cDNA clones were obtained by PCR amplification of human fetal lung cDNA using THBS3-specific primers. Analysis of cDNA and genomic sequences showed the THBS3 gene to be compo...

    journal_title:Genomics

    pub_type: 杂志文章

    doi:10.1006/geno.1995.1050

    authors: Adolph KW,Long GL,Winfield S,Ginns EI,Bornstein P

    更新日期:1995-05-20 00:00:00

  • A human homologue of the Drosophila polarity gene frizzled has been identified and mapped to 17q21.1.

    abstract::The frizzled (fz) locus in Drosophila is required for the transmission of polarity signals across the plasma membrane in epidermal cells, as well as to their neighboring cells in the developing wing. The identification of a tissue polarity gene from the fz locus in Drosophila melanogaster has been reported. The fz gen...

    journal_title:Genomics

    pub_type: 杂志文章

    doi:10.1006/geno.1995.1060

    authors: Zhao Z,Lee CC,Baldini A,Caskey CT

    更新日期:1995-05-20 00:00:00

  • Characterization of a human and murine gene (CLCN3) sharing similarities to voltage-gated chloride channels and to a yeast integral membrane protein.

    abstract::We describe the isolation and characterization of a human gene (CLCN3) and its murine homologue (Clcn3) sharing significant sequence and structural similarities with all previously identified members of the voltage-gated chloride channel (ClC) family. This gene is expressed primarily in tissues derived from neuroectod...

    journal_title:Genomics

    pub_type: 杂志文章

    doi:10.1006/geno.1995.1015

    authors: Borsani G,Rugarli EI,Taglialatela M,Wong C,Ballabio A

    更新日期:1995-05-01 00:00:00

  • The gene for the serpin thrombin inhibitor (PI7), protease nexin I, is located on human chromosome 2q33-q35 and on syntenic regions in the mouse and sheep genomes.

    abstract::Protease nexin I (PNI) is the most important physiologic regulator of alpha-thrombin in tissues. PNI is highly expressed and developmentally regulated in the nervous system where it is concentrated at neuromuscular junctions and also central synapses in the hippocampus and striatum. Approximately 10% of identified pro...

    journal_title:Genomics

    pub_type: 杂志文章

    doi:10.1006/geno.1995.1025

    authors: Carter RE,Cerosaletti KM,Burkin DJ,Fournier RE,Jones C,Greenberg BD,Citron BA,Festoff BW

    更新日期:1995-05-01 00:00:00

  • Genetic basis of neural tube defects: the mouse gene loop-tail maps to a region of chromosome 1 syntenic with human 1q21-q23.

    abstract::A genetic basis for neural tube defects (NTD) is rarely doubted, but the genes involved have not yet been identified. This is partly due to a lack of suitable families on which to perform linkage analysis. An alternative approach is to use the many mouse genes that cause NTD as a means of isolating their human homolog...

    journal_title:Genomics

    pub_type: 杂志文章

    doi:10.1016/0888-7543(95)80165-i

    authors: Stanier P,Henson JN,Eddleston J,Moore GE,Copp AJ

    更新日期:1995-04-10 00:00:00

  • Uroporphyrinogen-III synthase: molecular cloning, nucleotide sequence, expression of a mouse full-length cDNA, and its localization on mouse chromosome 7.

    abstract::Uroporphyrinogen-III synthase (URO-S; EC 4.2.1.75), the fourth enzyme in the heme biosynthetic pathway, is responsible for the conversion of hydroxymethylbilane to the cyclic tetrapyrrole, uroporphyrinogen III. The deficient activity of URO-S is the enzymatic defect in congenital erythropoietic porphyria (CEP), an aut...

    journal_title:Genomics

    pub_type: 杂志文章

    doi:10.1016/0888-7543(95)80175-l

    authors: Xu W,Kozak CA,Desnick RJ

    更新日期:1995-04-10 00:00:00

  • Identification of a new murine runt domain-containing gene, Cbfa3, and localization of the human homolog, CBFA3, to chromosome 1p35-pter.

    abstract::Core binding factor (CBF) is a heterodimeric transcription factor composed of two distinct subunits. The monomeric beta subunit is ubiquitously expressed, whereas expression of the three alpha subunits isolated previously seems to be restricted mainly to hematopoietic tissues. To isolate additional alpha genes, degene...

    journal_title:Genomics

    pub_type: 杂志文章

    doi:10.1016/0888-7543(95)80185-o

    authors: Wijmenga C,Speck NA,Dracopoli NC,Hofker MH,Liu P,Collins FS

    更新日期:1995-04-10 00:00:00

  • Insertional mutation of the motor endplate disease (med) locus on mouse chromosome 15.

    abstract::Homozygous transgenic mice from line A4 have an early-onset progressive neuromuscular disorder characterized by paralysis of the rear limbs, muscle atrophy, and lethality by 4 weeks of age. The transgene insertion site was mapped to distal chromosome 15 close to the locus motor endplate disease (med). The sequence of ...

    journal_title:Genomics

    pub_type: 杂志文章

    doi:10.1016/0888-7543(95)80198-u

    authors: Kohrman DC,Plummer NW,Schuster T,Jones JM,Jang W,Burgess DL,Galt J,Spear BT,Meisler MH

    更新日期:1995-03-20 00:00:00

  • The NACP/synuclein gene: chromosomal assignment and screening for alterations in Alzheimer disease.

    abstract::The major component of the vascular and plaque amyloid deposits in Alzheimer disease is the amyloid beta peptide (A beta). A second intrinsic component of amyloid, the NAC (non-A beta component of amyloid) peptide, has recently been identified, and its precursor protein was named NACP. A computer homology search allow...

    journal_title:Genomics

    pub_type: 杂志文章

    doi:10.1016/0888-7543(95)80208-4

    authors: Campion D,Martin C,Heilig R,Charbonnier F,Moreau V,Flaman JM,Petit JL,Hannequin D,Brice A,Frebourg T

    更新日期:1995-03-20 00:00:00

  • EMR1, an unusual member in the family of hormone receptors with seven transmembrane segments.

    abstract::Proteins with seven transmembrane segments (7TM) define a superfamily of receptors (7TM receptors) sharing the same topology: an extracellular N-terminus, three extramembranous loops on either side of the plasma membrane, and a cytoplasmic C-terminal tail. Upon ligand binding, cytoplasmic portions of the activated rec...

    journal_title:Genomics

    pub_type: 杂志文章

    doi:10.1016/0888-7543(95)80218-b

    authors: Baud V,Chissoe SL,Viegas-Péquignot E,Diriong S,N'Guyen VC,Roe BA,Lipinski M

    更新日期:1995-03-20 00:00:00

  • Cloning and mapping of the mouse alpha 7-neuronal nicotinic acetylcholine receptor.

    abstract::We report the isolation of cDNA clones for the mouse alpha 7 neuronal nicotinic acetylcholine receptor subunit (gene symbol Acra7), the only nicotinic receptor subunit known to bind alpha-bungarotoxin in mammalian brain. This gene may have relevance to nicotine sensitivity and to some electrophysiologic findings in sc...

    journal_title:Genomics

    pub_type: 杂志文章

    doi:10.1016/0888-7543(95)80228-e

    authors: Orr-Urtreger A,Seldin MF,Baldini A,Beaudet AL

    更新日期:1995-03-20 00:00:00

  • Chromosomal assignment of the genes for proprotein convertases PC4, PC5, and PACE 4 in mouse and human.

    abstract::The genes for three subtilisin/kexin-like proprotein convertases, PC4, PC5, and PACE4, were mapped in the mouse by RFLP analysis of a DNA panel from a (C57BL/6JEi x SPRET/Ei)F1 x SPRET/Ei backcross. The chromosomal locations of the human homologs were determined by Southern blot analysis of a DNA panel from human-rode...

    journal_title:Genomics

    pub_type: 杂志文章

    doi:10.1016/0888-7543(95)80090-9

    authors: Mbikay M,Seidah NG,Chrétien M,Simpson EM

    更新日期:1995-03-01 00:00:00

  • Genomic mapping by end-characterized random clones: a mathematical analysis.

    abstract::Physical maps can be constructed by "fingerprinting" a large number of random clones and inferring overlap between clones when the fingerprints are sufficiently similar. E. Lander and M. Waterman (Genomics 2: 231-239, 1988) gave a mathematical analysis of such mapping strategies. The analysis is useful for comparing v...

    journal_title:Genomics

    pub_type: 杂志文章

    doi:10.1016/0888-7543(95)80086-2

    authors: Port E,Sun F,Martin D,Waterman MS

    更新日期:1995-03-01 00:00:00

  • Identification and characterization of a human cDNA homologous to yeast SKI2.

    abstract::A monoclonal antibody, 170A1, which recognizes a nucleolar peptide of molecular weight 90,000, was raised. The protein was conserved among various vertebrates. To characterize the antigen, we screened a human fetal liver expression library using the monoclonal antibody as a probe. Molecular analyses of immunopositive ...

    journal_title:Genomics

    pub_type: 杂志文章

    doi:10.1016/0888-7543(95)80008-a

    authors: Lee SG,Lee I,Park SH,Kang C,Song K

    更新日期:1995-02-10 00:00:00

  • Chromosomal localization of the gastric and brain receptors for cholecystokinin (CCKAR and CCKBR) in human and mouse.

    abstract::Receptors for cholcystokinin (CCK) can be pharmacologically classified into at least two distinct subtypes, CCKAR and CCKBR. In an effort to determine whether the CCKA and CCKB receptors may be associated with certain CNS or gastrointestinal diseases, we have localized and compared the human and mouse chromosomal loci...

    journal_title:Genomics

    pub_type: 杂志文章

    doi:10.1016/0888-7543(95)80018-h

    authors: Huppi K,Siwarski D,Pisegna JR,Wank S

    更新日期:1995-02-10 00:00:00

  • The L19 ribosomal protein gene (RPL19): gene organization, chromosomal mapping, and novel promoter region.

    abstract::The intron-containing genes encoding rat and human ribosomal protein L19 (RPL19) have been cloned. The DNA sequences of the entire rat RPL19 gene and the 5' end of the human RPL19 gene have been determined. Sequence comparison of corresponding regions of the two genes reveals a striking interspecies homology in the 5'...

    journal_title:Genomics

    pub_type: 杂志文章

    doi:10.1016/0888-7543(95)80036-l

    authors: Davies B,Fried M

    更新日期:1995-01-20 00:00:00

  • Molecular cloning and chromosomal localization of a pseudogene related to the human acyl-CoA binding protein/diazepam binding inhibitor.

    abstract::The acyl-CoA binding protein (ACBP) and the diazepam binding inhibitor (DBI) or endozepine are independent isolates of a single 86-amino-acid, 10-kDa protein. ACBP/DBI is highly conserved between species and has been identified in several diverse organisms, including human, cow, rat, frog, duck, insects, plants, and y...

    journal_title:Genomics

    pub_type: 杂志文章

    doi:10.1016/0888-7543(95)80047-p

    authors: Gersuk VH,Rose TM,Todaro GJ

    更新日期:1995-01-20 00:00:00

  • CLONEPLACER: a software tool for simulating contig formation for ordered shotgun sequencing.

    abstract::This communication describes a software tool that enables one to simulate large-scale regional mapping using an ordered shotgun sequencing approach. The analysis routines that are provided yield an estimate of the depth of coverage of the physical map, the largest contig formed, and the number of gaps remaining at any...

    journal_title:Genomics

    pub_type: 杂志文章

    doi:10.1016/0888-7543(95)80057-s

    authors: Singh GB,Krawetz SA

    更新日期:1995-01-20 00:00:00

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