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Effect of triplet repeat expansion on chromatin structure and expression of DMPK and neighboring genes, SIX5 and DMWD, in myotonic dystrophy
MOLECULAR GENETICS AND METABOLISM
Egg to adult identification of 13 freshwater fishes from Italy: a biochemical-genetic key
AQUATIC SCIENCES
Gene assignment in Ateles paniscus chamek (Platyrrhini, Primates). Allocation of 18 markers of human syntenic groups 1, 2, 7, 14, 15, 17 and 22
CHROMOSOME RESEARCH
From xeroderma pigmentosum to the biological clock contributions of Dirk Bootsma to human genetics
MUTATION RESEARCH-DNA REPAIR
CDNA cloning and physical mapping of porcine 3 beta-hydroxysteroid dehydrogenase/Delta 5-Delta 4 isomerase
ANIMAL GENETICS
Isolation of expressed sequence tags of skeletal muscle of neonatal healthy and splay leg piglets and mapping by somatic cell hybrid analysis
ANIMAL GENETICS
Human acrocentric chromosomes with transcriptionally silent nucleolar organizer regions associate with nucleoli
EMBO JOURNAL
Molecular analysis of HPRT1(+) somatic cell hybrids derived from a carrierof an HPRT1 mutation responsible for Lesch-Nyhan syndrome
AMERICAN JOURNAL OF MEDICAL GENETICS
Differential sensitivity of human papillomavirus type 16(+) and type 18(+)cervical carcinoma cells to CD95-mediated apoptosis
INTERNATIONAL JOURNAL OF CANCER
Early phase karyotype analysis of chromosome segregation after formation of mouse-mouse hybridomas with chromosome painting probes
CHROMOSOME RESEARCH
Differential transcriptional regulation of the monocyte-chemoattractant protein-1 (MCP-1) gene in tumorigenic and non-tumorigenic HPV 18 positive cells: The role of the chromatin structure and AP-1 composition
ONCOGENE
Structure and mutation analysis of the gene encoding DNA fragmentation factor 40 (caspase-activated nuclease), a candidate neuroblastoma tumour suppressor gene
HUMAN GENETICS
Nucleolar dominance: uniparental gene silencing on a multi-megabase scale in genetic hybrids
PLANT MOLECULAR BIOLOGY
A high-resolution physical map of human chromosome 21p using yeast artificial chromosomes
GENOME RESEARCH
Reprogramming a somatic nucleus by trans-modification activity in germ cells
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY
Studies of gene expression and activity of hexokinase, phosphofructokinaseand glycogen synthase in human skeletal muscle in states of altered insulin-stimulated glucose metabolism
DANISH MEDICAL BULLETIN
Regional mapping panels for chromosomes 6, 9, and 16
GENOMICS
Evolutionary disruptions of human syntenic groups 3, 12, 14, and 15 in Ateles paniscus chamek (Platyrrhini, Primates)
CYTOGENETICS AND CELL GENETICS
Neonatal metabolic myopathies
SEMINARS IN PERINATOLOGY
XISTential wanderings: The role of XIST RNA in X-chromosome inactivation
CURRENT SCIENCE
An upstream repressor element that contributes to hepatocyte-specific expression of the rat serum amyloid A1 gene
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
ESTIMATION OF DISTANCES AND MAP CONSTRUCTION USING RADIATION HYBRIDS
PCR methods and applications
PHYSICAL MAPPING OF THE MOUSE GENOME
Methods
CHROMOSOME REGION 8P11-P21 - REFINED MAPPING AND MOLECULAR ALTERATIONS IN BREAST-CANCER
Genes, chromosomes & cancer
NB4S, A MEMBER OF THE TBC1 DOMAIN FAMILY OF GENES, IS TRUNCATED AS A RESULT OF A CONSTITUTIONAL T(1-10)(P22-Q21) CHROMOSOME-TRANSLOCATION IN A PATIENT WITH STAGE 4S NEUROBLASTOMA
Human molecular genetics (Print)
ASYMMETRIC SOMATIC-CELL HYBRIDS BETWEEN ALFALFA AND BIRDSFOOT-TREFOIL
Ikushugaku Zasshi
CHARACTERIZATION OF WHOLE GENOME RADIATION HYBRID MAPPING RESOURCES FOR NONMAMMALIAN VERTEBRATES
Nucleic acids research
COMPARATIVE-ANALYSIS OF GLUCOSEPHOSPHATE ISOMERASE, LACTATE-DEHYDROGENASE AND MALATE-DEHYDROGENASE ISOZYMES IN 9 CYPRINID SPECIES FROM ITALY
Zoological science
REGIONAL LOCALIZATIONS OF VIM, HSD3B, ACTA1 AND PGM1 IN PIGS
Animal genetics
A model system to study genomic imprinting of human genes
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
RESTRICTED EXPRESSION OF EPSTEIN-BARR-VIRUS (EBV)-ENCODED, GROWTH TRANSFORMATION-ASSOCIATED ANTIGENS IN AN EBV-HERPESVIRUS AND HUMAN-HERPESVIRUS TYPE 8-CARRYING BODY CAVITY LYMPHOMA LINE
Journal of General Virology
Expression and localization of hepatocyte domain-specific plasma membrane proteins in hepatoma x fibroblast hybrids and in hepatoma dedifferentiated variants
JOURNAL OF CELL SCIENCE
QUANTITATIVE TRAIT LOCI AFFECTING 4-NITROQUINOLINE 1-OXIDE-INDUCED TONGUE CARCINOGENESIS IN THE RAT
Cancer research
ALTERED BRAIN GLUCOSE-METABOLISM IN TRANSGENIC-PFKL MICE WITH ELEVATED L-PHOSPHOFRUCTOKINASE - IN-VIVO NMR-STUDIES
Brain research
GENETIC-MAPPING REFINES DFNB3 TO 17P11.2, SUGGESTS MULTIPLE ALLELES OF DFNB3, AND SUPPORTS HOMOLOGY TO THE MOUSE MODEL SHAKER-2
American journal of human genetics
COMPARISON OF ISOZYMIC AND MUSCLE PROTEIN IN 3 TAXA OF LEUCISCUS FROMNORTHERN ITALY
Italian journal of zoology
HOMOLOGOUS RECOMBINATION OF A FLANKING REPEAT GENE-CLUSTER IS A MECHANISM FOR A COMMON CONTIGUOUS GENE DELETION SYNDROME
Nature genetics
APPLICATION OF INTERSPERSED REPETITIVE SEQUENCE POLYMERASE CHAIN-REACTION FOR CONSTRUCTION OF YEAST ARTIFICIAL CHROMOSOME CONTIGS
Methods
EVIDENCE OF A DOMINANT TRANSCRIPTIONAL PATHWAY WHICH REGULATES AN UNDIFFERENTIATED AND COMPLETE METASTATIC PHENOTYPE
Oncogene
ISOLATION OF MONOCHROMOSOMAL HYBRIDS FOR MOUSE CHROMOSOME-3, CHROMOSOME-6, CHROMOSOME-10, CHROMOSOME-12, CHROMOSOME-14, AND CHROMOSOME-18
Mammalian genome
EPIGENETIC SILENCING OF RNA-POLYMERASE-I TRANSCRIPTION - A ROLE FOR DNA METHYLATION AND HISTONE MODIFICATION IN NUCLEOLAR DOMINANCE
Genes & development
REGIONAL MAPPING PANELS FOR CHROMOSOME-3, CHROMOSOME-4, CHROMOSOME-5,CHROMOSOME-11, CHROMOSOME-15, CHROMOSOME-17, CHROMOSOME-18, AND CHROMOSOME-X
Genomics
MOLECULAR CHARACTERIZATION OF A GENETICALLY UNSTABLE REGION CONTAINING THE SMS CRITICAL AREA AND A BREAKPOINT CLUSTER FOR HUMAN PNETS
Genomics
LOCALIZATION OF HUMAN LIVER 6-PHOSPHOFRUCTO-2-KINASE FRUCTOSE-2,6-BISPHOSPHATASE (PFKFB1) WITHIN A YAC CONTIG IN XP11.21/
Genomics
CONTRIBUTION OF ZEBRAFISH-MOUSE CELL HYBRIDS TO THE MAPPING OF THE ZEBRAFISH GENOME
Biochemistry and cell biology
SELECTIVE LOSS OF THE HEPATIC PHENOTYPE DUE TO THE ABSENCE OF A TRANSCRIPTIONAL ACTIVATION PATHWAY
Somatic cell and molecular genetics
REASSESSMENT OF IMMORTALIZATION COMPLEMENTATION GROUP-D
Experimental gerontology
REPORT OF THE 6TH INTERNATIONAL WORKSHOP ON HUMAN-CHROMOSOME-21 MAPPING 1996
Cytogenetics and cell genetics
A PANEL OF TRANSFERABLE FRAGMENTS OF HUMAN-CHROMOSOME 11Q
Cytogenetics and cell genetics
ASSIGNMENT OF TCF1, TGM1, CALM1, CKB, THBS1, B2M, AND FES IN ATELES PANISCUS CHAMEK (PLATYRRHINI, PRIMATES)
Cytogenetics and cell genetics
CONCOMITANT DOWN-REGULATION OF IGH 3' ENHANCER ACTIVITY AND C-MYC EXPRESSION IN A PLASMACYTOMA X FIBROBLAST ENVIRONMENT - IMPLICATIONS FOR DYSREGULATION OF TRANSLOCATED C-MYC
Molecular immunology
MITOCHONDRIAL-DNA MAINTENANCE IN VERTEBRATES
Annual review of biochemistry
ALLOZYMIC CHARACTERIZATION OF SCOTTISH AND AEGEAN POPULATIONS OF NEPHROPS-NORVEGICUS
Journal of the Marine Biological Association of the United Kingdom
DIFFERENTIAL ACTIVITY OF PROGESTERONE AND GLUCOCORTICOID RECEPTORS ONMOUSE MAMMARY-TUMOR VIRUS TEMPLATES DIFFERING IN CHROMATIN STRUCTURE
The Journal of biological chemistry
ASSIGNMENT OF THE CELLULAR RETINOL-BINDING PROTEIN-1 (RBP1) AND HEPATIC LIPASE (LIPC) GENES TO RAT CHROMOSOME-8
Folia biologica
NEGATIVE REGULATION OF THE ALPHA-FETOPROTEIN GENE IN FIBROBLASTS - IDENTIFICATION AND CHARACTERIZATION OF CIS AND TRANS ELEMENTS
Folia biologica
THE HEMORPHINS - A NEW CLASS OF OPIOID-PEPTIDES DERIVED FROM THE BLOOD PROTEIN HEMOGLOBIN
Biopolymers
LOCALIZATION OF THE FAST SKELETAL-MUSCLE TROPONIN-I GENE (TNNI2) TO 11PL5.5 - GENES FOR TROPONIN-I AND TROPONIN-T ARE ORGANIZED IN PAIRS
Annals of Human Genetics
ECTOPIC G-CSF EXPRESSION IN HUMAN-MELANOMA LINES MARKS A TRANSDOMINANT PATHWAY OF TUMOR PROGRESSION
The American journal of pathology
HYBRID SELECTION AS A METHOD OF INCREASING MAPPING POWER FOR RADIATION HYBRIDS
PCR methods and applications
TRANSCRIPTIONAL ANALYSIS OF THE CANDIDATE REGION FOR INCONTINENTIA PIGMENTI (IP2) IN XQ28
PCR methods and applications
EVIDENCE FOR 2 SENESCENCE LOCI ON HUMAN-CHROMOSOME-I
Genes, chromosomes & cancer
GENOMIC STRUCTURE AND CHROMOSOMAL LOCALIZATION OF THE HUMAN INTERLEUKIN-15 GENE (IL-15)
Cytokine
RESISTANCE TO TUMOR NECROSIS FACTOR-INDUCED APOPTOSIS IN MOUSE FIBROBLASTS IS A GENETICALLY DOMINANT PHENOTYPE
International journal of oncology
MAPPING OF 22 NOTI LINKING CLONES ON HUMAN-CHROMOSOME-3 BY POLYMERASECHAIN-REACTION AND SOMATIC-CELL HYBRID PANELS
Chromosome research
THE CHROMOSOMAL DISTRIBUTION AND ORGANIZATION OF SHEEP SATELLITE-I AND SATELLITE-II CENTROMERIC DNA USING CHARACTERIZED SHEEP-HAMSTER SOMATIC-CELL HYBRIDS
Chromosome research
A UBIQUITIN C-TERMINAL HYDROLASE GENE ON THE PROXIMAL SHORT ARM OF THE X-CHROMOSOME - IMPLICATIONS FOR X-LINKED RETINAL DISORDERS
Human molecular genetics
ONTOGENY OF PITUITARY TRANSCRIPTION FACTOR-I (PIT-1), GROWTH-HORMONE (GH) AND PROLACTIN (PRL) MESSENGER-RNA LEVELS IN MALE AND FEMALE RATS AND THE DIFFERENTIAL EXPRESSION OF PIT-1 IN LACTOTROPHS AND SOMATOTROPHS
Journal of neuroendocrinology
COMPARATIVE MAPPING ON THE MOUSE X-CHROMOSOME DEFINES A MYOTUBULAR MYOPATHY EQUIVALENT REGION
Mammalian genome
PHYSICAL AND GENETIC-MAPPING OF THE MUSCLE PHOSPHOFRUCTOKINASE GENE (PFKM) - REASSIGNMENT TO HUMAN-CHROMOSOME 12Q
Genomics
A HIGH-RESOLUTION WHOLE GENOME RADIATION HYBRID MAP OF HUMAN-CHROMOSOME 17Q22-Q25.3 ACROSS THE GENES FOR GH AND TK
Genomics
EXTINCTION OF ALBUMIN GENE-EXPRESSION IN A PANEL OF HUMAN-CHROMOSOME-2 MICROCELL HYBRIDS
Genomics
EAGI AND NOTI LINKING CLONES FROM HUMAN-CHROMOSOME-11 AND HUMAN-CHROMOSOME-XP
Human genetics
GENERATION OF SEQUENCE-TAGGED SITES FROM XP22.3 BY ISOLATING COMMON ALU-PCR PRODUCTS OF RADIATION HYBRIDS RETAINING OVERLAPPING HUMAN X-CHROMOSOME FRAGMENTS
Human genetics
CHARACTERIZATION OF A SHORT INTERSPERSED REPEAT (MERMAID) THAT HAS FAMILY MEMBERS ON HUMAN-CHROMOSOME-21 AND ELSEWHERE IN THE HUMAN GENOME
Human genetics
PREDOMINANCE OF THE METASTATIC PHENOTYPE IN HYBRIDS FORMED BY FUSION OF MOUSE AND HUMAN-MELANOMA CLONES
Clinical & experimental metastasis
MUSCLE PHOSPHOFRUCTOKINASE DEFICIENCY IN 2 GENERATIONS
Journal of the neurological sciences
MAPPING THE CHICKEN GENOME - PROBLEMS AND PROSPECTIVES
Genetika
GENOMIC ALTERATIONS IN CERVICAL-CARCINOMA - LOSSES OF CHROMOSOME HETEROZYGOSITY AND HUMAN PAPILLOMA-VIRUS TUMOR STATUS
Cancer research
REPRODUCTION AND GENETIC-VARIATION IN CLAM SHRIMPS (CRUSTACEA, BRANCHIOPODA, CONCHOSTRACA)
Canadian journal of zoology
PAIRWISE ANALYSIS OF RADIATION HYBRID MAPPING DATA
Annals of Human Genetics
MAPPING OF HUMAN NONMUSCLE TYPE COFILIN (CFL1) TO CHROMOSOME-11Q13 AND MUSCLE-TYPE COFILIN (CFL2) TO CHROMOSOME-14
Annals of Human Genetics
MUTATIONS IN MUSCLE PHOSPHOFRUCTOKINASE GENE
Human mutation
AN EXPRESSION-INDEPENDENT CATALOG OF GENES FROM HUMAN-CHROMOSOME 22
PCR methods and applications
TRANSCRIPTION FACTOR PIT-1 AND ITS CLINICAL IMPLICATIONS - FROM BENCHTO BEDSIDE
The Endocrinologist
THE FRAGILE-X SYNDROMES
Seminars in cell biology
PLACEMENT AND REFINED MAPPING OF ESTABLISHED AND NEW MARKERS ON HUMAN-CHROMOSOME 11Q USING A SMALL PANEL OF SOMATIC-CELL HYBRIDS
European journal of human genetics
THE AMINO-TERMINAL PHOSPHORYLATION SITES OF C-MYC ARE FREQUENTLY MUTATED IN BURKITTS-LYMPHOMA LINES BUT NOT IN MOUSE PLASMACYTOMAS AND RAT IMMUNOCYTOMAS
European journal of cancer
GENETIC-MAPPING OF THE MULTIPLE ENDOCRINE NEOPLASIA TYPE-1 LOCUS AT 11Q13
Journal of internal medicine
THE MICROSATELLITE MUTATOR PHENOTYPE OF COLON-CANCER CELLS IS OFTEN RECESSIVE
Oncogene
CONSTITUTIONAL TRANSLOCATION T(1-17)(P36.31-P36.13-Q11.2Q12.1) IN A NEUROBLASTOMA PATIENT. ESTABLISHMENT OF SOMATIC-CELL HYBRIDS AND IDENTIFICATION OF PND A12M2 ON CHROMOSOME-1 AND NF1/SCYA7 ON CHROMOSOME-17 AS BREAKPOINT FLANKING SINGLE-COPY MARKERS/
Oncogene
TRANSCRIPTIONAL REGULATION OF MHC CLASS-II GENES
International journal of clinical & laboratory research
REFINED MAPPING OF CALTRACTIN IN HUMAN XQ28 AND IN THE HOMOLOGOUS REGION OF THE MOUSE X-CHROMOSOME PLACES THE GENE WITHIN THE BARE PATCHES (BPA) AND STRIATED (STR) CRITICAL REGIONS
Mammalian genome
REGIONAL CHROMOSOMAL ASSIGNMENTS FOR 4 MEMBERS OF THE MADS DOMAIN TRANSCRIPTION ENHANCER FACTOR-2 (MEF2) GENE FAMILY TO HUMAN-CHROMOSOMES 15Q26, 19P12, 5Q14 AND 1Q12-Q23
Genomics
THE MELANOMA ANTIGEN GENE (MAGE) FAMILY IS CLUSTERED IN THE CHROMOSOMAL BAND XQ28
Genomics
A 4-MEGABASE YAC CONTIG THAT SPANS THE LANGER-GIEDION SYNDROME REGIONON HUMAN-CHROMOSOME 8Q24.1 - USE IN REFINING THE LOCATION OF THE TRICHORHINOPHALANGEAL SYNDROME AND MULTIPLE EXOSTOSES GENES (TRPS1 AND EXT1)
Genomics
STRUCTURE, CHROMOSOMAL LOCATION, AND EXPRESSION PATTERN OF 3 MOUSE GENES HOMOLOGOUS TO THE HUMAN MAGE GENES
Genomics
GENOMIC ORGANIZATION AND CHROMOSOMAL LOCALIZATION OF THE DUSP2 GENE, ENCODING A MAP KINASE PHOSPHATASE, TO HUMAN 2P11.2-Q11
Genomics
HUMAN SP4 TRANSCRIPTION FACTOR CONE (SP4) MAPS TO CHROMOSOME 7P15
Genomics
COSMID ASSEMBLY AND ANCHORING TO HUMAN-CHROMOSOME-21
Genomics