1995
The CEPH Consortium Linkage Map of Human Chromosome 11
Litt M, Kramer P, Kort E, Fain P, Cox S, Root D, White R, Weissenbach J, Donis-Keller H, Gatti R, Weber J, Nakamura Y, Julier C, Hayashi K, Spurr N, Dean M, Mandel J, Kidd K, Kruse T, Retief A, Bale A, Meo T, Vergnaud G, Warren S, Willard H. The CEPH Consortium Linkage Map of Human Chromosome 11. Genomics 1995, 27: 101-112. PMID: 7665156, DOI: 10.1006/geno.1995.1011.Peer-Reviewed Original Research
1994
Mapping the gene for hereditary hyperparathyroidism and prolactinoma (MEN1Burin) to chromosome 11q: evidence for a founder effect in patients from Newfoundland.
Petty E, Green J, Marx S, Taggart R, Farid N, Bale A. Mapping the gene for hereditary hyperparathyroidism and prolactinoma (MEN1Burin) to chromosome 11q: evidence for a founder effect in patients from Newfoundland. American Journal Of Human Genetics 1994, 54: 1060-6. PMID: 7911003, PMCID: PMC1918205.Peer-Reviewed Original ResearchMeSH KeywordsBase SequenceCarcinoid TumorChildChromosome MappingChromosomes, Human, Pair 11FemaleGenetic LinkageGenetic MarkersHaplotypesHumansHyperparathyroidismMaleMolecular Sequence DataMultiple Endocrine NeoplasiaNewfoundland and LabradorNorthwestern United StatesParentsPedigreePituitary NeoplasmsProlactinomaSyndrome
1993
A Pulsed-Field Gel Electrophoresis (PFGE) Map of Twelve Loci on Chromosome 11q11-q13
Petty E, Arnold A, Marx S, Bale A. A Pulsed-Field Gel Electrophoresis (PFGE) Map of Twelve Loci on Chromosome 11q11-q13. Genomics 1993, 15: 423-425. PMID: 8449512, DOI: 10.1006/geno.1993.1080.Peer-Reviewed Original ResearchAutoradiographyCells, CulturedChromosome MappingChromosomes, Human, Pair 11DNA ProbesElectrophoresis, Gel, Two-DimensionalHumansProgression of uremic hyperparathyroidism involves allelic loss on chromosome 11.
Falchetti A, Bale A, Amorosi A, Bordi C, Cicchi P, Bandini S, Marx S, Brandi M. Progression of uremic hyperparathyroidism involves allelic loss on chromosome 11. The Journal Of Clinical Endocrinology & Metabolism 1993, 76: 139-144. PMID: 8421078, DOI: 10.1210/jcem.76.1.8421078.Peer-Reviewed Original Research
1992
Allelic loss from chromosome 11 in parathyroid tumors.
Friedman E, De Marco L, Gejman P, Norton J, Bale A, Aurbach G, Spiegel A, Marx S. Allelic loss from chromosome 11 in parathyroid tumors. Cancer Research 1992, 52: 6804-9. PMID: 1360870.Peer-Reviewed Original ResearchAdenomaAllelesChromosome DeletionChromosomes, Human, Pair 11HumansMultiple Endocrine NeoplasiaParathyroid GlandsParathyroid NeoplasmsPRAD1 (cyclin D1): a parathyroid neoplasia gene on 11q13.
Arnold A, Motokura T, Bloom T, Rosenberg C, Bale A, Kronenberg H, Ruderman J, Brown M, Kim H. PRAD1 (cyclin D1): a parathyroid neoplasia gene on 11q13. Henry Ford Hospital Medical Journal 1992, 40: 177-80. PMID: 1483873.Peer-Reviewed Original ResearchMeSH KeywordsAmino Acid SequenceChromosomes, Human, Pair 11CyclinsHumansMolecular Sequence DataOncogenesParathyroid NeoplasmsConceptsPossible primaryMultiple endocrine neoplasia type 1Sporadic parathyroid adenomasParathyroid diseaseParathyroid adenomaMEN-1Pathogenetic featuresType 1Familial formsCandidate oncogeneBcl-2PTH locusC-MycField gel electrophoresisPRAD1Cell cycleOncogeneImmunoglobulin genesHyperparathyroidismCyclin proteinsAdenomasNeoplasiaPathogenesisTumorsDisease
1991
PRAD1, a candidate BCL1 oncogene: mapping and expression in centrocytic lymphoma.
Rosenberg C, Wong E, Petty E, Bale A, Tsujimoto Y, Harris N, Arnold A. PRAD1, a candidate BCL1 oncogene: mapping and expression in centrocytic lymphoma. Proceedings Of The National Academy Of Sciences Of The United States Of America 1991, 88: 9638-9642. PMID: 1682919, PMCID: PMC52773, DOI: 10.1073/pnas.88.21.9638.Peer-Reviewed Original ResearchAllelic loss on chromosome 11 in hereditary and sporadic tumors related to familial multiple endocrine neoplasia type 1.
Bale A, Norton J, Wong E, Fryburg J, Maton P, Oldfield E, Streeten E, Aurbach G, Brandi M, Friedman E. Allelic loss on chromosome 11 in hereditary and sporadic tumors related to familial multiple endocrine neoplasia type 1. Cancer Research 1991, 51: 1154-7. PMID: 1671755.Peer-Reviewed Original ResearchConceptsFamilial multiple endocrine neoplasia type 1Multiple endocrine neoplasia type 1Anterior pituitary tumorsPancreatic islet tumorsIslet tumorsPituitary tumorsAllelic lossType 1Autosomal dominant disorderMalignant gastrinomaBronchial carcinoidParathyroid glandsParathyroid tumorsAnterior pituitaryLoss of heterozygosityTumorsPancreatic isletsSporadic tumorsDominant disorderMEN1 genePatientsRestriction fragment length polymorphismFragment length polymorphismHomozygous inactivationInformative restriction fragment length polymorphisms
1990
Genetic Abnormalities in Sporadic Parathyroid Adenomas
Friedman E, Bale A, Marx S, Norton J, Arnold A, Tu T, Aurbach G, Spiegel A. Genetic Abnormalities in Sporadic Parathyroid Adenomas. The Journal Of Clinical Endocrinology & Metabolism 1990, 71: 293-297. PMID: 2199477, DOI: 10.1210/jcem-71-2-293.Peer-Reviewed Original ResearchMeSH KeywordsAdenomaBlotting, SouthernChromosomes, Human, Pair 11CodonDNAGene RearrangementGenes, rasHumansHyperparathyroidismMutationParathyroid HormoneParathyroid Neoplasms
1989
Clonality of Parathyroid Tumors in Familial Multiple Endocrine Neoplasia Type 1
Friedman E, Sakaguchi K, Bale A, Falchetti A, Streeten E, Zimering M, Weinstein L, McBride W, Nakamura Y, Brandi M, Norton J, Aurbach G, Spiegel A, Marx S. Clonality of Parathyroid Tumors in Familial Multiple Endocrine Neoplasia Type 1. New England Journal Of Medicine 1989, 321: 213-218. PMID: 2568586, DOI: 10.1056/nejm198907273210402.Peer-Reviewed Original ResearchMeSH KeywordsAdenomaAllelesChromosome DeletionChromosomes, Human, Pair 11Clone CellsHumansHyperplasiaMultiple Endocrine NeoplasiaParathyroid NeoplasmsLinkage analysis of multiple endocrine neoplasia type 1 with INT2 and other markers on chromosome 11
Bale S, Bale A, Stewart K, Dachowski L, McBride O, Glaser T, Green J, Mulvihill J, Brandi M, Sakaguchi K, Aurbach G, Marx S. Linkage analysis of multiple endocrine neoplasia type 1 with INT2 and other markers on chromosome 11. Genomics 1989, 4: 320-322. PMID: 2565877, DOI: 10.1016/0888-7543(89)90336-4.Peer-Reviewed Original ResearchMeSH KeywordsChromosomes, Human, Pair 11FemaleGenetic MarkersHumansLod ScoreMaleMultiple Endocrine NeoplasiaPedigreePhosphorylasesPolymorphism, Restriction Fragment LengthConceptsChromosome 11Skeletal muscle glycogen phosphorylasePolymorphic DNA (RAPD) markersMuscle glycogen phosphorylaseSingle large pedigreeDNA markersGene locusFibroblast growth factorBasic fibroblast growth factorMultiple endocrine neoplasia type 1Glycogen phosphorylaseLarge pedigreeGenesLociRecent findingsMultipoint analysisGrowth factorMEN1 geneMarkersINT2PedigreeMEN1 patientsPhosphorylaseType 1
1986
Linkage relationships among four 11p markers in the Utah dataset
Bale S, Harris E, Bale A. Linkage relationships among four 11p markers in the Utah dataset. Genetic Epidemiology. Supplement 1986, 3: 117-121. PMID: 3471653, DOI: 10.1002/gepi.1370030718.Peer-Reviewed Original ResearchChromosome MappingChromosomes, Human, Pair 11FemaleGenetic LinkageGenetic MarkersHumansMaleRecombination, GeneticSex FactorsUtah