Search Results - "Soukup, Shirley W."
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1
Association of chromosome 4 abnormalities with ethylnitrosourea-induced neuro-oncogenesis in the rat
Published in Cancer research (Chicago, Ill.) (01-02-1984)“…Cytogenetic studies of rat neurogenic tumor lines induced by ethylnitrosourea (ENU) have shown specific involvement of chromosome 4. The study reported here…”
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2
Continuous human glioma-derived cell lines UC-11MG and UC-302MG. Morphologic, immunocytochemical and chromosomal characterization
Published in Journal of neuro-oncology (1986)“…Two continuous human glioma-derived cell lines, UC-11MG and UC-302MG were established in our laboratory. Both cell lines persistently showed cytologic features…”
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3
Chromosome analysis of a human neuroblastoma
Published in Cancer research (Chicago, Ill.) (01-08-1981)“…Samplings of tumor cells from a patient with Stage IV neuroblastoma were analyzed for chromosome constitution. Chromosome preparations of the tumor cells from…”
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4
Cat eye syndrome. Partial trisomy 22 due to translocation in the mother
Published in American journal of diseases of children (1960) (01-08-1977)“…We describe a case of cat eye syndrome with 47,XX, +22q--. A balanced translocation, 46,XX,t(11;22), was found by banding studies in the mother. The clinical…”
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5
CHROMOSOME CHANGES IN RAT EMBRYOS FOLLOWING X-IRRADIATION
Published in Cytogenetics (01-01-1965)Get more information
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6
A presumptive Y-autosome translocation in a boy with congenital malformations
Published in American journal of diseases of children (1960) (01-08-1968)Get more information
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7
Trisomy 2 and 20 in two hepatoblastomas
Published in Genes chromosomes & cancer (01-05-1991)“…Cytogenetic analysis of two pediatric hepatoblastomas is presented, comparing results in primary tumor samples, nude mouse xenographs, and lung metastases in…”
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8
The effect of ethylnitrosourea on chromosome aberrations in vitro and in vivo
Published in Human genetics (01-12-1975)Get full text
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9
Clonal sublines of rat neurotumor RT4 and cell differentiation
Published in Developmental biology (01-07-1984)Get full text
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10
Mutation, Cancer, and Malformation
Published in American Scientist (01-01-1986)Get full text
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Clonal sublines of rat neurotumor RT4 and cell differentiation: VI. Chromosome analysis
Published in Developmental biology (1984)“…The RT4 neurotumor cell system consists of clonally derived cell lines where a stem cell type segregates in vitro into three biochemically and morphologically…”
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12
A chromosomal abnormality in a girl with some features of Down's syndrome (mongolism)
Published in The Journal of pediatrics (01-06-1963)Get more information
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13
CHROMOSOME ANALYSES IN A CHILDREN'S HOSPITAL
Published in Pediatrics (Evanston) (01-03-1964)“…Chromosome analyses were performed in 227 persons, most of them pediatric patients. The majority of these were selected because of mongolism, other forms of…”
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14
CHROMOSOME ANALYSES IN A CHILDREN'S HOSPITAL
Published in Pediatrics (Evanston) (01-02-1964)“…SINCE 1956 the chromosome number of man has been 2 and it has become possible to classify human chromosomes according to size and position of the centromere…”
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15
Congenital leukemia associated with mosaic trisomy 9
Published in The Journal of pediatrics (01-04-1976)Get more information
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16
Chromosome features of two retinoblastomas
Published in Cancer genetics and cytogenetics (01-08-1984)“…Giemsa-banded chromosomal analysis of two unilateral retinoblastoma tumors from unrelated patients with normal constitutional chromosomes revealed near-diploid…”
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17
Type II glycogenosis in adults
Published in The New England journal of medicine (25-01-1973)Get more information
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18
Biologic characteristics of four Ewing's sarcomas
Published in Cancer genetics and cytogenetics (15-02-1985)“…Four Ewing's sarcomas were examined for chromosomal characteristics, growth in cell culture, tumorigenicity in nude mice, and presence of beta-adrenergic…”
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19
A familial MCA/MR syndrome due to translocation t(10;16) (q26;p13.1): report of six cases
Published in American journal of medical genetics (01-01-1991)“…A minute familial translocation t(10;16) (q26;p13.1) was detected in a family with 6 affected children in 2 generations and 9 carriers in 3 generations. This…”
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