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The role of X-chromosome inactivation in female predisposition to autoimmunity (vol 2, pg 399, 2000)
ARTHRITIS RESEARCH
Linkage studies of SOX13, the ICA12 autoantigen gene, in families with type 1 diabetes
MOLECULAR GENETICS AND METABOLISM
Diaper dermatitis: A therapeutic dilemma. Results of a double-blind placebo controlled trial of miconazole nitrate 0.25%
PEDIATRIC DERMATOLOGY
Seasonal changes in serum leptin, food intake, and body weight in photoentrained woodchucks
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY
Distinct functional domains of nibrin mediate Mre11 binding, focus formation, and nuclear localization
MOLECULAR AND CELLULAR BIOLOGY
Chk2 activation dependence on Nbs1 after DNA damage
MOLECULAR AND CELLULAR BIOLOGY
Increased frequency of ATM mutations in breast carcinoma patients with early onset disease and positive family history
CANCER
Seven regions of the genome show evidence of linkage to type 1 diabetes ina consensus analysis of 767 multiplex families
AMERICAN JOURNAL OF HUMAN GENETICS
The role of X-chromosome inactivation in female predisposition to autoimmunity
ARTHRITIS RESEARCH
Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus
NATURE GENETICS
ATM-dependent phosphorylation of nibrin in response to radiation exposure
NATURE GENETICS
Intussusception presenting as profound lethargy
JOURNAL OF PAEDIATRICS AND CHILD HEALTH
Expression pattern of the Nijmegen breakage syndrome gene, Nbs1, during murine development
HUMAN MOLECULAR GENETICS
Retroviral expression of the NBS1 gene in cultured Nijmegen breakage syndrome cells restores normal radiation sensitivity and nuclear focus formation
MUTAGENESIS
V(D)J rearrangement in Nijmegen breakage syndrome
MOLECULAR IMMUNOLOGY
Somatic versus germline origin of ATM mutations in T-PLL - Response
BLOOD
Nijmegen breakage syndrome
ARCHIVES OF DISEASE IN CHILDHOOD
Cancer risk in ATM heterozygotes: A model of phenotypic and mechanistic differences between missense and truncating mutations
MOLECULAR GENETICS AND METABOLISM
Loci on chromosomes 2 (NIDDM1) and 15 interact to increase susceptibility to diabetes in Mexican Americans
NATURE GENETICS
Identification, characterization, and mapping of a mouse homolog of the gene mutated in Nijmegen breakage syndrome
CYTOGENETICS AND CELL GENETICS
Physical map of the region surrounding the Ataxia-Telangiectasia gene on human chromosome 11q22-23
NEUROPEDIATRICS
Systematic mutagenesis of TCR complementarity-determining region 3 residues: A single conservative substitution dramatically improves response to both multiple HLA-DR alleles and peptide variants
JOURNAL OF IMMUNOLOGY
Regulated genomic instability and neoplasia in the lymphoid lineage
BLOOD
Splicing defects in the ataxia-telangiectasia gene, ATM: Underlying mutations and consequences
AMERICAN JOURNAL OF HUMAN GENETICS
MAGE XP-2 - A MEMBER OF THE MAGE GENE FAMILY ISOLATED FROM AN EXPRESSION LIBRARY USING SYSTEMIC LUPUS-ERYTHEMATOSUS SERA
MOLECULAR GENETICS AND METABOLISM
A 2ND-GENERATION SCREEN OF THE HUMAN GENOME FOR SUSCEPTIBILITY TO INSULIN-DEPENDENT DIABETES-MELLITUS
Nature genetics
FAMILIAL SPINOCEREBELLAR ATAXIA WITH CEREBELLAR ATROPHY, PERIPHERAL NEUROPATHY, AND ELEVATED LEVEL OF SERUM CREATINE-KINASE, GAMMA-GLOBULIN, AND ALPHA-FETOPROTEIN
Annals of neurology
NIBRIN, A NOVEL DNA DOUBLE-STRAND BREAK REPAIR PROTEIN, IS MUTATED INNIJMEGEN BREAKAGE SYNDROME
Cell
PROTEIN-KINASE MUTANTS OF HUMAN ATR INCREASE SENSITIVITY TO UV AND IONIZING-RADIATION AND ABROGATE CELL-CYCLE CHECKPOINT CONTROL
Proceedings of the National Academy of Sciences of the United Statesof America
FINE LOCALIZATION OF THE NIJMEGEN BREAKAGE SYNDROME GENE TO 8Q21 - EVIDENCE FOR A COMMON FOUNDER HAPLOTYPE
American journal of human genetics
ATAXIA-TELANGIECTASIA - IDENTIFICATION AND DETECTION OF FOUNDER-EFFECT MUTATIONS IN THE ATM GENE IN ETHNIC POPULATIONS
American journal of human genetics
TEACHERS QUESTIONNAIRE FOR VISION PROBLEMS - IS IT A HELP OR A HINDRANCE FOR SCHOOL-HEALTH SCREENING
Australian and New Zealand journal of public health
GENETICS OF NIDDM IN THE MEXICAN-AMERICANS OF STARR COUNTY, TEXAS - AN UPDATE
Diabetes reviews
DIVERSITY OF ATM GENE-MUTATIONS DETECTED IN PATIENTS WITH ATAXIA-TELANGIECTASIA
Human mutation
CAND3 - A UBIQUITOUSLY EXPRESSED GENE IMMEDIATELY ADJACENT AND IN OPPOSITE TRANSCRIPTIONAL ORIENTATION TO THE ATM GENE AT 11Q23.1
Mammalian genome
ORGANIZATION, POLYMORPHISM, AND EXPRESSION OF THE HUMAN T-CELL RECEPTOR AV1 SUBFAMILY
Immunogenetics
ATAXIA-TELANGIECTASIA - DETECTION OF ATM MUTATIONS IN ETHNIC POPULATIONS
Journal of allergy and clinical immunology
ESTRUS, FERTILITY, EARLY EMBRYO DEVELOPMENT, AND AUTOLOGOUS EMBRYO-TRANSFER IN LABORATORY WOODCHUCKS (MARMOTA-MONAX)
Laboratory animal science
TERMINATION OF OBLIGATE ANESTRUS AND INDUCTION OF FERTILE OVARIAN CYCLES IN DOGS BY ADMINISTRATION OF PURIFIED PIG LH
Journal of Reproduction and Fertility
REPRODUCTION IN DOGS, CATS AND EXOTIC CARNIVORES - PROCEEDINGS OF THE3RD INTERNATIONAL-SYMPOSIUM ON CANINE AND FELINE REPRODUCTION - VELDHOVEN, THE NETHERLANDS HOSTED BY THE UNIVERSITY-OF-UTRECHT, SEPTEMBER 1996 - FOREWORD
Journal of Reproduction and Fertility
LH-RELEASE, INDUCTION OF ESTRUS AND FERTILE OVULATIONS IN RESPONSE TOPULSATILE ADMINISTRATION OF GNRH TO ANESTROUS DOGS
Journal of Reproduction and Fertility
INCIDENCE OF SPONTANEOUS OVULATION IN YOUNG, GROUP-HOUSED CATS BASED ON SERUM AND FECAL CONCENTRATIONS OF PROGESTERONE
Journal of Reproduction and Fertility
CLINICAL USE OF DEXAMETHASONE FOR TERMINATION OF UNWANTED PREGNANCY IN DOGS
Journal of Reproduction and Fertility
PRESENTATION OF ABUNDANT ENDOGENOUS CLASS-II DR-RESTRICTED ANTIGENS BY DM-NEGATIVE B-CELL LINES
European Journal of Immunology
LONG-TERM ENTRAINMENT OF CIRCANNUAL REPRODUCTIVE AND METABOLIC CYCLESBY NORTHERN AND SOUTHERN-HEMISPHERE PHOTOPERIODS IN WOODCHUCKS (MARMOTA-MONAX)
Biology of reproduction
LONG-TERM ENTRAINMENT OF WOODCHUCK CIRCANNUAL REPRODUCTIVE AND METABOLIC CYCLES TO NORTHERN AND SOUTHERN-HEMISPHERE PHOTOPERIODS
Biology of reproduction
MAPPING NIJMEGEN-BREAKAGE-SYNDROME TO 8Q21 AND CONSTRUCTION OF A RADIATION HYBRID MAP OF THE D8S1757-D8S506 REGION
American journal of human genetics
SCREENING FOR ATAXIA-TELANGIECTASIS MUTATIONS IN A POPULATION-BASED SAMPLE OF WOMEN WITH EARLY-ONSET BREAST-CANCER
American journal of human genetics
SUSCEPTIBILITY TO IDDM - A 2ND-GENERATION SCREEN OF THE GENOME
American journal of human genetics
CHARACTERIZATION AND DETECTION OF MUTATIONS IN THE ATM GENE
American journal of human genetics
A GENOME-WIDE SEARCH FOR HUMAN NON-INSULIN-DEPENDENT (TYPE-2) DIABETES GENES REVEALS A MAJOR SUSCEPTIBILITY LOCUS ON CHROMOSOME-2
Nature genetics
REPERTOIRE AND ORGANIZATION OF HUMAN T-CELL RECEPTOR-ALPHA REGION VARIABLE GENES
Genomics
TCR EXPRESSION AND CLONALITY ANALYSIS IN PULMONARY SARCOIDOSIS
Human immunology
COLLECTION OF SEASONALLY SPERMATOZOA-RICH SEMEN BY ELECTROEJACULATIONOF LABORATORY WOODCHUCKS (MARMOTA-MONAX), WITH AND WITHOUT REMOVAL OFBULBOURETHRAL GLANDS
Laboratory animal science
MODULATION OF PROMISCUOUS T-CELL RECEPTOR RECOGNITION BY MUTAGENESIS OF CDR2 RESIDUES
The Journal of experimental medicine
AN APPROACH FOR IDENTIFYING SIMPLE SEQUENCE REPEAT DNA POLYMORPHISMS NEAR CLONED CDNAS AND GENES - LINKAGE STUDIES OF THE ISLET AMYLOID POLYPEPTIDE AMYLIN AND LIVER-GLYCOGEN SYNTHASE GENES AND NIDDM
Diabetes
CIRCANNUAL CHANGES IN BASAL AND GNRH-STIMULATED SERUM LH IN MALE WOODCHUCKS (MARMOTA-MONAX) MAINTAINED IN NORTHERN-HEMISPHERE VS SOUTHERN-HEMISPHERE PHOTOPERIODS
Biology of reproduction
SUPPRESSION OF SPONTANEOUS OVULATION AND ALTERATION OF ESTRUS BEHAVIOR BY CHRONIC GNRH-AGONIST IN CATS
Biology of reproduction
HIGH-FREQUENCY OF DISTINCT ATM GENE-MUTATIONS IN ATAXIA-TELANGIECTASIA
American journal of human genetics
ATAXIA-TELANGIECTASIA - MUTATIONS IN ATM CDNA DETECTED BY PROTEIN-TRUNCATION SCREENING
American journal of human genetics
LINKAGE AND ASSOCIATION BETWEEN INSULIN-DEPENDENT DIABETES-MELLITUS (IDDM) SUSCEPTIBILITY AND MARKERS NEAR THE GLUCOKINASE GENE ON CHROMOSOME-7
Nature genetics
LINKAGE AND ASSOCIATION STUDIES IN INSULIN-DEPENDENT DIABETES WITH A NEW DINUCLEOTIDE REPEAT POLYMORPHISM AT THE GAD(65) LOCUS
Autoimmunity
FREQUENCY AND POLYMORPHISM OF SIMPLE SEQUENCE REPEATS IN A CONTIGUOUS685-KB DNA-SEQUENCE CONTAINING THE HUMAN T-CELL RECEPTOR BETA-CHAIN GENE-COMPLEX
Genomics
RELATIVE SIZE AND EVOLUTION OF THE GERMLINE REPERTOIRE OF T-CELL RECEPTOR BETA-CHAIN GENE SEGMENTS IN NONHUMAN-PRIMATES
Genomics
STRUCTURAL COMPONENTS OF HUMAN TCRS WHICH RECOGNIZE INFLUENZA HEMAGGLUTININ-307-319 IN THE CONTEXT OF HLA-DR4 OR HLA-DR7
Journal of cellular biochemistry
PCR-BASED GENOTYPING AND HAPLOTYPE ANALYSIS OF HUMAN TCRBV GENE SEGMENT POLYMORPHISMS
Immunogenetics
TERMINATION OF PREGNANCY IN DOGS BY ORAL-ADMINISTRATION OF DEXAMETHASONE
Theriogenology
LINKAGE STUDIES IN NIDDM WITH MARKERS NEAR THE SULFONYLUREA RECEPTOR GENE
Diabetologia
IDENTIFICATION OF MICROSATELLITE MARKERS NEAR THE HUMAN OB GENE AND LINKAGE STUDIES IN NIDDM-AFFECTED SIB PAIRS
Diabetes
ISOLATION OF A CDNA CLONE ENCODING A K-ATP CHANNEL-LIKE PROTEIN EXPRESSED IN INSULIN-SECRETING CELLS, LOCALIZATION OF THE HUMAN GENE TO CHROMOSOME BAND 21Q22.1. AND LINKAGE STUDIES WITH NIDDM
Diabetes
ELECTROEJACULATION OF COAGULUM-FREE, URETHRAL PLUG-FREE, SEASONALLY SPERM-RICH SEMEN FOLLOWING REMOVAL OF BULBOURETHRAL GLANDS IN LABORATORY WOODCHUCKS (MARMOTA-MONAX)
Biology of reproduction
PATTERNS OF CIRCULATING PROLACTIN, LH AND FSH DURING DOPAMINE-AGONISTINDUCED TERMINATION OF ANESTRUS IN BEAGLE DOGS
Biology of reproduction
POSTIMPLANTATION ELEVATION IN PLASMA-FIBRINOGEN AS A PREGNANCY TEST IN DOGS
Biology of reproduction
SUBLOCALIZATION OF AN ATAXIAL-TELANGIECTASIA GENE DISTAL TO D115384 BY ANCESTRAL HAPLOTYPING IN COSTA-RICAN FAMILIES
American journal of human genetics
LOCATION OF AN ATAXIA-TELANGIECTASIA GENE TO AN SIMILAR-TO-500-KB INTERVAL ON CHROMOSOME 11Q23.1 - LINKAGE ANALYSIS OF 176 FAMILIES BY AN INTERNATIONAL CONSORTIUM
American journal of human genetics
HUMAN T-CELL RECEPTOR V-BETA GENE POLYMORPHISM AND MULTIPLE-SCLEROSIS
American journal of human genetics
DINUCLEOTIDE REPEAT POLYMORPHISM AT THE NCAM LOCUS
Human molecular genetics
GENETIC HAPLOTYPING OF ATAXIA-TELANGIECTASIA FAMILIES LOCALIZES THE MAJOR GENE TO AN SIMILAR-TO-850 KB REGION ON CHROMOSOME 11Q23.1
International journal of radiation biology
T-CELL RECEPTOR POLYMORPHISMS IN TLINGIT INDIANS WITH RHEUMATOID-ARTHRITIS
Autoimmunity
A PULSED-FIELD GEL-ELECTROPHORESIS MAP IN THE ATAXIA-TELANGIECTASIA REGION OF CHROMOSOME-11Q22-3
Genomics
TRANSFECTED HUMAN T-CELL RECEPTOR GENES RECONSTITUTE HLA RESTRICTED ANTIGEN RECOGNITION IN A RECEPTOR-NEGATIVE HUMAN T-CELL LINE
Journal of cellular biochemistry
DINUCLEOTIDE REPEAT POLYMORPHISM AT 11Q23
Human genetics
IDENTIFICATION OF A NOVEL HUMAN T-CELL RECEPTOR V-BETA SUBFAMILY BY GENOMIC CLONING
Human immunology
THE EXTENT OF THE HUMAN GERMLINE T-CELL RECEPTOR-V-BETA GENE SEGMENT REPERTOIRE
Immunogenetics
SCHOOL SCREENING FOR SCOLIOSIS - A TIME TO RETHINK
Medical journal of Australia
INFLUENCE OF CODING REGION POLYMORPHISM ON THE PERIPHERAL EXPRESSION OF A HUMAN TCR V-BETA-GENE
The Journal of immunology
LEVEL OF HUMAN TCRBV3S1 (V-BETA-3) EXPRESSION CORRELATES WITH ALLELICPOLYMORPHISM IN THE SPACER REGION OF THE RECOMBINATION SIGNAL SEQUENCE
The Journal of experimental medicine
HLA AND T-CELL RECEPTOR BETA-CHAIN DNA POLYMORPHISMS IDENTIFY A DISTINCT SUBSET OF PATIENTS WITH PAUCIARTICULAR-ONSET JUVENILE RHEUMATOID-ARTHRITIS
Arthritis and rheumatism
POLYMORPHISMS IN THE TCRB-V2 GENE SEGMENTS LOCALIZE THE TCRB ORPHON GENES TO HUMAN-CHROMOSOME 9P21
Immunogenetics
POLYMORPHISM AND PHYLOGENY OF DINUCLEOTIDE REPEATS IN HUMAN T-CELL RECEPTOR VB6 GENES
Immunogenetics
THE INHIBITION OF DIFFERENT T-CELL LINES SPECIFIC FOR THE SAME ANTIGEN WITH TCR ANTAGONIST PEPTIDES
The Journal of immunology
T-CELL RECEPTOR ANTAGONISM MEDIATED BY INTERACTION BETWEEN T-CELL RECEPTOR JUNCTIONAL RESIDUES AND PEPTIDE ANTIGEN ANALOGS
The Journal of immunology
ALTERATION OF GROWTH, ADVANCEMENT OF PUBERTY, AND SEASON-APPROPRIATE CIRCANNUAL BREEDING DURING 28 MONTHS OF PHOTOPERIOD REVERSAL IN WOODCHUCKS (MARMOTA-MONAX)
Biology of reproduction
LOCALIZATION OF POLYMORPHIC PROBES IN THE REGION OF ATAXIA-TELANGLECTASIA AT CHROMOSOME-11Q22
American journal of human genetics
A PFGE MAP OF THE ATAXIA-TELANGIECTASIA REGION AT 11Q22.3
American journal of human genetics