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Recovery from arterial growth delay reduces penetrance of cardiovascular defects in mice deleted for the DiGeorge syndrome region
HUMAN MOLECULAR GENETICS
Mice deleted for the DiGeorge/velocardiofacial syndrome region show abnormal sensorimotor gating and learning and memory impairments
HUMAN MOLECULAR GENETICS
Patella resurfacing in total knee replacement: functional evaluation and complications
KNEE SURGERY SPORTS TRAUMATOLOGY ARTHROSCOPY
Matter effects in upward-going muons and sterile neutrino oscillations
PHYSICS LETTERS B
Cloning and chromosome mapping of human and chicken Iroquois (IRX) genes
CYTOGENETICS AND CELL GENETICS
Tbx1 haploinsufficiency in the DiGeorge syndrome region causes aortic archdefects in mice
NATURE
Neutrino astronomy with the MACRO detector
ASTROPHYSICAL JOURNAL
Nuclearite search with the MACRO detector at Gran Sasso
EUROPEAN PHYSICAL JOURNAL C
DiGeorge syndrome: complex pathogenesis? Maybe, maybe not
MOLECULAR MEDICINE TODAY
Search for lightly ionizing particles with the MACRO detector - art. no. 052003
PHYSICAL REVIEW D
Determination of neutrino incoming direction in the CHOOZ experiment and its application to supernova explosion location by scintillator detectors - art. no. 012001
PHYSICAL REVIEW D
Low energy atmospheric muon neutrinos in MACRO
PHYSICS LETTERS B
Limits on neutrino oscillations from the CHOOZ experiment (vol 466, pg 415, 1999)
PHYSICS LETTERS B
Effect of tourniquet use on activation of coagulation in total knee replacement
CLINICAL ORTHOPAEDICS AND RELATED RESEARCH
Resting metabolic rate, fat-free mass and catecholamine excretion during weight loss in female obese patients
BRITISH JOURNAL OF NUTRITION
Disease severity and health-related quality of life across different chronic conditions
JOURNAL OF THE AMERICAN GERIATRICS SOCIETY
A 12-Mb complete coverage BAC contig map in human chromosome 16p13.1-p11.2
GENOME RESEARCH
Structure and chromosomal locations of mouse steroid receptor coactivator gene family
IN VITRO CELLULAR & DEVELOPMENTAL BIOLOGY-ANIMAL
Short-term persistent depression following hip fracture: A risk factor andtarget to increase resilience in elderly people
SOCIAL WORK RESEARCH
Is the genetic basis of DiGeorge syndrome in HAND?
NATURE GENETICS
Measurement of the energy spectrum of underground muons at Gran Sasso witha transition radiation detector
ASTROPARTICLE PHYSICS
Relevance of the hadronic interaction model in the interpretation of multiple muon data as detected with the MACRO experiment
NUCLEAR PHYSICS B-PROCEEDINGS SUPPLEMENTS
Identification of a putative regulatory subunit of a calcium-activated potassium channel in the dup(3q) syndrome region and a related sequence on 22q11.2
GENOMICS
Limits on dark matter WIMPs using upward-going muons in the MACRO detector- art. no. 082002.
PHYSICAL REVIEW D
High statistics measurement of the underground muon pair separation at Gran Sasso - art. no. 032001
PHYSICAL REVIEW D
Observation of the shadowing of cosmic rays by the Moon using a deep underground detector - art. no. 012003
PHYSICAL REVIEW D
Limits on neutrino oscillations from the CHOOZ experiment
PHYSICS LETTERS B
Procedure-dependence and tissue factor-independence of hypercoagulability during orthopaedic surgery
THROMBOSIS AND HAEMOSTASIS
Identification of a gene that reverses the immortal phenotype of a subset of cells and is a member of a novel family of transcription factor-like genes
MOLECULAR AND CELLULAR BIOLOGY
Congenital heart disease in mice deficient for the DiGeorge syndrome region
NATURE
CONGENITAL HEART-DEFECTS AND 22Q11 DELETIONS - WHICH GENES COUNT
Molecular medicine today
MUTATIONS IN LMX1B CAUSE ABNORMAL SKELETAL PATTERNING AND RENAL DYSPLASIA IN NAIL-PATELLA SYNDROME
Nature genetics
ISOLATION AND CHARACTERIZATION OF A HUMAN LIM-HOMEODOMAIN GENE AND MUTATION ANALYSIS IN PATIENTS WITH NAIL-PATELLA SYNDROME
European journal of human genetics
ES2, A GENE DELETED IN DIGEORGE-SYNDROME, ENCODES A NUCLEAR-PROTEIN AND IS EXPRESSED DURING EARLY MOUSE DEVELOPMENT, WHERE IT SHARES AN EXPRESSION DOMAIN WITH A GOOSECOID-LIKE GENE
Human molecular genetics
FUNCTIONAL-ANALYSIS OF GSCL IN THE PATHOGENESIS OF THE DIGEORGE AND VELOCARDIOFACIAL SYNDROMES
Human molecular genetics (Print)
DOC-2, A CANDIDATE TUMOR-SUPPRESSOR GENE IN HUMAN EPITHELIAL OVARIAN-CANCER
Oncogene
COMPARATIVE MAPPING OF THE DIGEORGE-SYNDROME REGION IN MOUSE SHOWS INCONSISTENT GENE ORDER AND DIFFERENTIAL DEGREE OF GENE CONSTRUCTION (VOL 8, PG 890, 1997)
Mammalian genome
THE OBSERVATION OF UP-GOING CHARGED-PARTICLES PRODUCED BY HIGH-ENERGYMUONS IN UNDERGROUND DETECTORS
Astroparticle physics
REAL-TIME SUPERNOVA NEUTRINO BURST DETECTION WITH MACRO
Astroparticle physics
STATUS OF THE CHOOZ EXPERIMENT
Nuclear physics. B, Proceedings supplement
CHARACTERIZATION AND PHYSICAL MAPPING IN HUMAN AND MOUSE OF A NOVEL RING FINGER GENE IN XP22
Genomics (San Diego, Calif.)
MEASUREMENT OF THE ATMOSPHERIC NEUTRINO-INDUCED UPGOING MUON FLUX USING MACRO
Physics letters. Section B
INITIAL RESULTS FROM THE CHOOZ LONG-BASE-LINE REACTOR NEUTRINO OSCILLATION EXPERIMENT
Physics letters. Section B
FUNCTIONAL-EVALUATION OF ALZHEIMER PATIENTS DURING CLINICAL-TRIALS - A REVIEW
Archives of gerontology and geriatrics
STRUCTURE AND EXPRESSION OF THE HUMAN UBIQUITIN FUSION DEGRADATION GENE (UFD1L)
Biochimica et biophysica acta, N. Gene structure and expression
ACTIVATION OF COAGULATION DURING PRIMARY TOTAL HIP-ARTHROPLASTY IS HIGHER IN THE LATERAL THAN POSTERIOR LATERAL APPROACH AND IT IS NOT ASSOCIATED WITH HIGH TISSUE FACTOR PLASMA-LEVELS
Thrombosis research
ACTIVATION OF COAGULATION DURING PRIMARY TOTAL KNEE REPLACEMENT WITH AND WITHOUT TOURNIQUET
Thrombosis research
ALTERNATIVE INTERPRETATION OF REPORTED PARACENTRIC INVERSION - REPLY TO GALLEN
American journal of human genetics
CORONARY-ARTERY CONSTRICTION IN RATS - NECROTIC AND APOPTOTIC MYOCYTEDEATH
The American journal of cardiology
MISSENSE MUTATIONS ABOLISHING DNA-BINDING OF THE OSTEOBLAST-SPECIFIC TRANSCRIPTION FACTOR OSF2 CBFA1 IN CLEIDOCRANIAL DYSPLASIA/
Nature genetics
DEVELOPMENT OF BI-2223 AG TAPES AND COILS
IEEE transactions on applied superconductivity
INTERCHROMOSOMAL DUPLICATIONS OF THE ADRENOLEUKODYSTROPHY LOCUS - A PHENOMENON OF PERICENTROMERIC PLASTICITY
Human molecular genetics
COMPARATIVE MAPPING OF THE DIGEORGE-SYNDROME REGION IN MOUSE SHOWS INCONSISTENT GENE ORDER AND DIFFERENTIAL DEGREE OF GENE CONSERVATION
Mammalian genome
SEASONAL-VARIATIONS IN THE UNDERGROUND MUON INTENSITY AS SEEN BY MACRO
Astroparticle physics
THE PERFORMANCE OF MACRO LIQUID SCINTILLATOR IN THE SEARCH FOR MAGNETIC MONOPOLES WITH 10(-3)LESS-THAN-BETA-LESS-THAN-1
Astroparticle physics
LOCALIZATION OF BRRN1, THE HUMAN HOMOLOG OF DROSOPHILA BARR, TO 2Q11.2
Genomics
THE HUMAN TRANSALDOLASE GENE (TALDO1) IS LOCATED ON CHROMOSOME-11 AT P15.4-P15.5
Genomics
MUTATIONS IN THE DNA-BINDING DOMAIN OF THE OSTEOBLAST-SPECIFIC TRANSCRIPTION FACTOR OSF2 CBFA1 RESULT IN CLEIDOCRANIAL DYSPLASIA/
Journal of bone and mineral research
HIGH-ENERGY COSMIC-RAY PHYSICS WITH UNDERGROUND MUONS IN MACRO .1. ANALYSIS-METHODS AND EXPERIMENTAL RESULTS
Physical review. D. Particles and fields
HIGH-ENERGY COSMIC-RAY PHYSICS WITH UNDERGROUND MUONS IN MACRO .2. PRIMARY SPECTRA AND COMPOSITION
Physical review. D. Particles and fields
SEARCH FOR NEUTRINO BURSTS FROM STELLAR GRAVITATIONAL COLLAPSES WITH MACRO
Nuclear physics. B
HIGH-ENERGY COSMIC-RAY PHYSICS WITH THE MACRO EXPERIMENT AT GRAN SASSO
Nuclear physics. B
BSCCO-2223 AG-SHEATHED TAPES PRODUCTION
Nuovo cimento della Societa italiana di fisica. D, Condensed matter,atomic, molecular and chemical physics, biophysics
STACKED DOUBLE-PANCAKE COILS USING BI-2223 AG TAPES/
Nuovo cimento della Societa italiana di fisica. D, Condensed matter,atomic, molecular and chemical physics, biophysics
MAGNETIC MONOPOLE SEARCH WITH THE MACRO DETECTOR AT GRAN-SASSO
Physics letters. Section B
A MOUSE GENE (DGCR6) RELATED TO THE DROSOPHILA GONADAL GENE IS EXPRESSED IN EARLY EMBRYOGENESIS AND IS THE HOMOLOG OF A HUMAN GENE DELETED IN DIGEORGE-SYNDROME
Cytogenetics and cell genetics
ASSIGNMENT OF THE GENE FOR A UBIQUITIN FUSION DEGRADATION PROTEIN (UFD1L) MOUSE-CHROMOSOME 16B1-B4, SYNTENIC WITH THE TUPLE-1 GENE
Cytogenetics and cell genetics
THE NEURAL-NETWORK-BASED 2ND-LEVEL TRIGGER DEVELOPED FOR THE CHOOZ EXPERIMENT
Nuclear instruments & methods in physics research. Section A, Accelerators, spectrometers, detectors and associated equipment
DIGEORGE-ANOMALY AND CHROMOSOME 10P DELETIONS - ONE OR 2 LOCI
American journal of medical genetics
DELETION OF CHROMOSOME 22Q11 AND PSEUDOHYPOPARATHYROIDISM
American journal of medical genetics
DELINEATION OF A DUPLICATION MAP OF CHROMOSOME 3Q - A NEW CASE CONFIRMS THE EXCLUSION OF 3Q25-Q26.2 FROM THE DUPLICATION 3Q SYNDROME CRITICAL REGION
American journal of medical genetics
GOOSECOID AND GOOSECOID-RELATED GENES IN MOUSE EMBRYOGENESIS
Cold Spring Harbor Symposia on Quantitative Biology
MAGNETIC MEASUREMENTS OF CRITICAL CURRENTS IN AG-BPSCCO TAPES - A COMPARISON
Physica status solidi. a, Applied research
Le ragioni di un incontro scientifico
Il Pensiero politico
Albergati contro Bodin: dall'Antibodino ai Discorsi politici
Il Pensiero politico
HUMAN ACETYL-COA CARBOXYLASE-2 - MOLECULAR-CLONING, CHARACTERIZATION,CHROMOSOMAL MAPPING, AND EVIDENCE FOR 2 ISOFORMS
The Journal of biological chemistry
CHARACTERIZATION OF A TRANSCRIPTIONALLY COMPLEX LOCUS CONTAINING A MOUSE SEPTIN GENE AND THE PLATELET GLYCOPROTEIN IB-BETA GENE
Blood
GOOSECOID-LIKE SEQUENCES AND THE SMALLEST REGION OF DELETION OVERLAP IN DIGEORGE AND VELOCARDIOFACIAL SYNDROMES
American journal of human genetics
A MEMBER OF THE SEPTIN GENE FAMILY IS DELETED IN DIGEORGE-SYNDROME AND ITS MOUSE HOMOLOG IS HIGHLY EXPRESSED DURING EMBRYOGENESIS IN THE NERVOUS-SYSTEM AND SKELETAL PRIMORDIA
American journal of human genetics
COMPARATIVE MAPPING OF THE DIGEORGE-SYNDROME REGION IN MOUSE SHOWS INCONSISTENT GENE ORDER AND DIFFERENTIAL DEGREE OF GENE CONSERVATION
American journal of human genetics
4 GENES FROM THE DGS VCFS CRITICAL REGION ARE EXPRESSED DURING EARLY MOUSE DEVELOPMENT IN A TISSUE-SPECIFIC MANNER/
American journal of human genetics
GENE STRUCTURE AND MUTATIONS IN THE OSTEOBLAST-SPECIFIC TRANSCRIPTIONFACTOR CBFA1 OSF2 IN CLEIDOCRANIAL DYSPLASIA/
American journal of human genetics
MOLECULAR ANALYSIS OF DELETION (17)(P11.2P11.2) IN A FAMILY SEGREGATING A 17P PARACENTRIC INVERSION - IMPLICATIONS FOR CARRIERS OF PARACENTRIC INVERSIONS
American journal of human genetics
A GENETIC ETIOLOGY FOR INTERRUPTION OF THE AORTIC-ARCH TYPE-B
The American journal of cardiology
Girolamo Frachetta: vicissitudini e percorsi culturali di un pensatore politico nell'Italia della Controriforma
Annali di storia moderna e contemporanea
22Q11 DELETIONS AND CARDIAC DISEASE
Progress in pediatric cardiology
DUPLICATION OF A GENE-RICH CLUSTER BETWEEN 16P11.1 AND XQ28 - A NOVELPERICENTROMERIC-DIRECTED MECHANISM FOR PARALOGOUS GENOME EVOLUTION
Human molecular genetics
CLONING AND COMPARATIVE MAPPING OF A GENE FROM THE COMMONLY DELETED REGION OF DIGEORGE AND VELOCARDIOFACIAL SYNDROMES CONSERVED IN C-ELEGANS
Mammalian genome
GENETIC AND PHYSICAL MAPPING OF A VOLTAGE-DEPENDENT CHLORIDE CHANNEL GENE TO HUMAN 4Q32 AND TO MOUSE-8
Genomics
A TRANSCRIPTION MAP IN THE CATCH22 CRITICAL REGION - IDENTIFICATION, MAPPING, AND ORDERING OF 4 NOVEL TRANSCRIPTS EXPRESSED IN HEART
Genomics
SEARCH FOR NEUTRINOS FROM THE SUN AND THE EARTH WITH THE MACRO DETECTOR
Nuclear physics. B
STUDY OF PRIMARY INTERACTIONS WITH MULTIPLE MUONS IN MACRO
Nuclear physics. B
L'office automation nella pubblica amministrazione
Studi economici e sociali
QUANTIFICATION BY FLOW-CYTOMETRY OF CHROMOSOME-17 DELETIONS IN SMITH-MAGENIS SYNDROME PATIENTS
Human genetics
THE PHOTOMULTIPLIER TEST FACILITY FOR THE REACTOR NEUTRINO OSCILLATION EXPERIMENT CHOOZ AND THE MEASUREMENTS OF 250 8-IN EMI9356KA B53 PHOTOMULTIPLIERS
Nuclear instruments & methods in physics research. Section A, Accelerators, spectrometers, detectors and associated equipment
MOSAICISM FOR DEL(17)(P11.2P11.2) UNDERLYING THE SMITH-MAGENIS SYNDROME
American journal of medical genetics
A GENETIC ETIOLOGY FOR INTERRUPTED AORTIC-ARCH TYPE-B
Circulation
IDENTIFICATION OF A NOVEL TRANSCRIPT DISRUPTED BY A BALANCED TRANSLOCATION ASSOCIATED WITH DIGEORGE-SYNDROME
American journal of human genetics
MOLECULAR ANALYSES OF 17P11.2 DELETIONS IN 62 SMITH-MAGENIS SYNDROME PATIENTS
American journal of human genetics
ORDERED MAPPING OF 3 ALPHA-SATELLITE DNA SUBSETS ON HUMAN-CHROMOSOME-22
Chromosome research