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Showing 1 to 12 of 589 entries
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Chronic granulocytic leukemia occurring in blast crisis.

Archives of pathology & laboratory medicine

Kapadia SB, Krause JR, Pan SF, Cotelingam J, Nitiyanant P.
PMID: 287416
Arch Pathol Lab Med. 1979 Jun;103(6):291-2.

Cytogenetic studies of marrow using chromosomal banding techniques revealed the presence of the Philadelphia (PH1) chromosome in two patients with clinical and hematologic findings of acute myelogenous leukemia (AML). A review of the literature since the use of chromosomal...

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Kapadia SB, Krause JR, Pan SF, et al. Chronic granulocytic leukemia occurring in blast crisis. Arch Pathol Lab Med. 1979;103(6):291-2
Kapadia, S. B., Krause, J. R., Pan, S. F., Cotelingam, J., & Nitiyanant, P. (1979). Chronic granulocytic leukemia occurring in blast crisis. Archives of pathology & laboratory medicine, 103(6), 291-2.
Kapadia, S B, et al. "Chronic granulocytic leukemia occurring in blast crisis." Archives of pathology & laboratory medicine vol. 103,6 (1979): 291-2.
Kapadia SB, Krause JR, Pan SF, Cotelingam J, Nitiyanant P. Chronic granulocytic leukemia occurring in blast crisis. Arch Pathol Lab Med. 1979 Jun;103(6):291-2. PMID: 287416.
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c-src is consistently conserved in the chromosomal deletion (20q) observed in myeloid disorders.

Proceedings of the National Academy of Sciences of the United States of America

Le Beau MM, Westbrook CA, Diaz MO, Rowley JD.
PMID: 2413444
Proc Natl Acad Sci U S A. 1985 Oct;82(19):6692-6. doi: 10.1073/pnas.82.19.6692.
Free PMC Article

The proto-oncogene c-src has been mapped to two bands in human chromosomes, 1p36 and 20q13, both of which are involved in rearrangements in human tumors. In particular, deletions (loss of part of a chromosome) of the long arm of...

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Le Beau MM, Westbrook CA, Diaz MO, et al. c-src is consistently conserved in the chromosomal deletion (20q) observed in myeloid disorders. Proc Natl Acad Sci U S A. 1985;82(19):6692-6doi: 10.1073/pnas.82.19.6692.
Le Beau, M. M., Westbrook, C. A., Diaz, M. O., & Rowley, J. D. (1985). c-src is consistently conserved in the chromosomal deletion (20q) observed in myeloid disorders. Proceedings of the National Academy of Sciences of the United States of America, 82(19), 6692-6. https://doi.org/10.1073/pnas.82.19.6692
Le Beau, M M, et al. "c-src is consistently conserved in the chromosomal deletion (20q) observed in myeloid disorders." Proceedings of the National Academy of Sciences of the United States of America vol. 82,19 (1985): 6692-6. doi: https://doi.org/10.1073/pnas.82.19.6692
Le Beau MM, Westbrook CA, Diaz MO, Rowley JD. c-src is consistently conserved in the chromosomal deletion (20q) observed in myeloid disorders. Proc Natl Acad Sci U S A. 1985 Oct;82(19):6692-6. doi: 10.1073/pnas.82.19.6692. PMID: 2413444; PMCID: PMC391276.
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Chromosomes and causation of human cancer and leukemia. X. Banding patterns in cancerous effusions.

Cancer

Kakati S, Hayata I, Oshimura M, Sandberg AA.
PMID: 1192362
Cancer. 1975 Nov;36(5):1729-38. doi: 10.1002/1097-0142(197511)36:5<1729::aid-cncr2820360528>3.0.co;2-#.

Cells from five cancer effusions (two ovarian carcinomas, two lung cancers, and one carcinoma of the breast) were analyzed by G-, C-, and Q-banding techniques. The following observations were made: 1) The origin of some marker chromosomes could be...

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Kakati S, Hayata I, Oshimura M, et al. Chromosomes and causation of human cancer and leukemia. X. Banding patterns in cancerous effusions. Cancer. 1975;36(5):1729-38doi: 10.1002/1097-0142(197511)36:5<1729::aid-cncr2820360528>3.0.co;2-#.
Kakati, S., Hayata, I., Oshimura, M., & Sandberg, A. A. (1975). Chromosomes and causation of human cancer and leukemia. X. Banding patterns in cancerous effusions. Cancer, 36(5), 1729-38. https://doi.org/10.1002/1097-0142(197511)36:5<1729::aid-cncr2820360528>3.0.co;2-#
Kakati, S, et al. "Chromosomes and causation of human cancer and leukemia. X. Banding patterns in cancerous effusions." Cancer vol. 36,5 (1975): 1729-38. doi: https://doi.org/10.1002/1097-0142(197511)36:5<1729::aid-cncr2820360528>3.0.co;2-#
Kakati S, Hayata I, Oshimura M, Sandberg AA. Chromosomes and causation of human cancer and leukemia. X. Banding patterns in cancerous effusions. Cancer. 1975 Nov;36(5):1729-38. doi: 10.1002/1097-0142(197511)36:5<1729::aid-cncr2820360528>3.0.co;2-#. PMID: 1192362.
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Follow-up of infants with amniotic fluid trisomy 20 mosaicism.

American journal of medical genetics

Abuelo DN, Barsel-Bowers G, Zartler AS.
PMID: 3728566
Am J Med Genet. 1986 Jul;24(3):475-81. doi: 10.1002/ajmg.1320240310.

The finding of trisomy 20 mosaicism in amniotic fluid is a cause of considerable anxiety for both physicians and parents. Although the significance of this finding is still not clear, some reassurance can be given to prospective parents, since...

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Abuelo DN, Barsel-Bowers G, Zartler AS. Follow-up of infants with amniotic fluid trisomy 20 mosaicism. Am J Med Genet. 1986;24(3):475-81doi: 10.1002/ajmg.1320240310.
Abuelo, D. N., Barsel-Bowers, G., & Zartler, A. S. (1986). Follow-up of infants with amniotic fluid trisomy 20 mosaicism. American journal of medical genetics, 24(3), 475-81. https://doi.org/10.1002/ajmg.1320240310
Abuelo, D N, et al. "Follow-up of infants with amniotic fluid trisomy 20 mosaicism." American journal of medical genetics vol. 24,3 (1986): 475-81. doi: https://doi.org/10.1002/ajmg.1320240310
Abuelo DN, Barsel-Bowers G, Zartler AS. Follow-up of infants with amniotic fluid trisomy 20 mosaicism. Am J Med Genet. 1986 Jul;24(3):475-81. doi: 10.1002/ajmg.1320240310. PMID: 3728566.
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Identification and characterization of heterochromatic regions in the human metaphase and interphase nucleus.

Humangenetik

Kim MA.
PMID: 4837300
Humangenetik. 1974 Mar 28;21(4):331-40. doi: 10.1007/BF00273371.

No abstract available.

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Kim MA. Identification and characterization of heterochromatic regions in the human metaphase and interphase nucleus. Humangenetik. 1974;21(4):331-40doi: 10.1007/BF00273371.
Kim, M. A. (1974). Identification and characterization of heterochromatic regions in the human metaphase and interphase nucleus. Humangenetik, 21(4), 331-40. https://doi.org/10.1007/BF00273371
Kim, M A. "Identification and characterization of heterochromatic regions in the human metaphase and interphase nucleus." Humangenetik vol. 21,4 (1974): 331-40. doi: https://doi.org/10.1007/BF00273371
Kim MA. Identification and characterization of heterochromatic regions in the human metaphase and interphase nucleus. Humangenetik. 1974 Mar 28;21(4):331-40. doi: 10.1007/BF00273371. PMID: 4837300.
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Isolation of duplicated human c-src genes located on chromosomes 1 and 20.

Molecular and cellular biology

Parker RC, Mardon G, Lebo RV, Varmus HE, Bishop JM.
PMID: 2581127
Mol Cell Biol. 1985 Apr;5(4):831-8. doi: 10.1128/mcb.5.4.831-838.1985.
Free PMC Article

The oncogene (v-src) of Rous sarcoma virus apparently arose by transduction of the chicken gene known as c-src(chicken). We isolated DNA fragments representative of two src-related loci from recombinant DNA bacteriophage libraries of the human genome. One of these...

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Parker RC, Mardon G, Lebo RV, et al. Isolation of duplicated human c-src genes located on chromosomes 1 and 20. Mol Cell Biol. 1985;5(4):831-8doi: 10.1128/mcb.5.4.831-838.1985.
Parker, R. C., Mardon, G., Lebo, R. V., Varmus, H. E., & Bishop, J. M. (1985). Isolation of duplicated human c-src genes located on chromosomes 1 and 20. Molecular and cellular biology, 5(4), 831-8. https://doi.org/10.1128/mcb.5.4.831-838.1985
Parker, R C, et al. "Isolation of duplicated human c-src genes located on chromosomes 1 and 20." Molecular and cellular biology vol. 5,4 (1985): 831-8. doi: https://doi.org/10.1128/mcb.5.4.831-838.1985
Parker RC, Mardon G, Lebo RV, Varmus HE, Bishop JM. Isolation of duplicated human c-src genes located on chromosomes 1 and 20. Mol Cell Biol. 1985 Apr;5(4):831-8. doi: 10.1128/mcb.5.4.831-838.1985. PMID: 2581127; PMCID: PMC366788.
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Chromosome studies in untreated polycythaemia vera.

Scandinavian journal of haematology

Westin J, Wahlström J, Swolin B.
PMID: 968448
Scand J Haematol. 1976 Sep;17(3):183-96. doi: 10.1111/j.1600-0609.1976.tb01174.x.

Bone marrow chromosomes were studied in a series of 50 consecutive, unselected cases of untreated polycythaemia vera (PV). A pathological cell line was present in 7 patients (= 14%). 3 patients each had 1 extra chromosome no. 8 and...

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Westin J, Wahlström J, Swolin B. Chromosome studies in untreated polycythaemia vera. Scand J Haematol. 1976;17(3):183-96doi: 10.1111/j.1600-0609.1976.tb01174.x.
Westin, J., Wahlström, J., & Swolin, B. (1976). Chromosome studies in untreated polycythaemia vera. Scandinavian journal of haematology, 17(3), 183-96. https://doi.org/10.1111/j.1600-0609.1976.tb01174.x
Westin, J, et al. "Chromosome studies in untreated polycythaemia vera." Scandinavian journal of haematology vol. 17,3 (1976): 183-96. doi: https://doi.org/10.1111/j.1600-0609.1976.tb01174.x
Westin J, Wahlström J, Swolin B. Chromosome studies in untreated polycythaemia vera. Scand J Haematol. 1976 Sep;17(3):183-96. doi: 10.1111/j.1600-0609.1976.tb01174.x. PMID: 968448.
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Trisomy of the short arm of chromosome 10.

Journal of medical genetics

Nakagome Y, Kobayashi H.
PMID: 1219122
J Med Genet. 1975 Dec;12(4):412-4. doi: 10.1136/jmg.12.4.412.
Free PMC Article

A case of a fetus with multiple malformations is described. The mother showed a 46,XX,rcp(10;22) (p11;p11) karyotype. Amniocentesis at the 16th week of gestation revealed that the male fetus had a der(22) chromosome--that is, he was trisomic for a...

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Nakagome Y, Kobayashi H. Trisomy of the short arm of chromosome 10. J Med Genet. 1975;12(4):412-4doi: 10.1136/jmg.12.4.412.
Nakagome, Y., & Kobayashi, H. (1975). Trisomy of the short arm of chromosome 10. Journal of medical genetics, 12(4), 412-4. https://doi.org/10.1136/jmg.12.4.412
Nakagome, Y, and Kobayashi, H. "Trisomy of the short arm of chromosome 10." Journal of medical genetics vol. 12,4 (1975): 412-4. doi: https://doi.org/10.1136/jmg.12.4.412
Nakagome Y, Kobayashi H. Trisomy of the short arm of chromosome 10. J Med Genet. 1975 Dec;12(4):412-4. doi: 10.1136/jmg.12.4.412. PMID: 1219122; PMCID: PMC1013323.
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Trisomy 14q-.

Birth defects original article series

Fawcett WA, McCord WK, Francke U.
PMID: 1218218
Birth Defects Orig Artic Ser. 1975;11(5):223-8.

Trisomy 14q- syndrome is relatively new and needs further delineation. In comparing our case with other reported cases (Table 1), some similarities are seen. Although the comparison of our case of partial trisomy 14 with the other cases reported...

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Fawcett WA, McCord WK, Francke U. Trisomy 14q-. Birth Defects Orig Artic Ser. 1975;11(5):223-8
Fawcett, W. A., McCord, W. K., & Francke, U. (1975). Trisomy 14q-. Birth defects original article series, 11(5), 223-8.
Fawcett, W A, et al. "Trisomy 14q-." Birth defects original article series vol. 11,5 (1975): 223-8.
Fawcett WA, McCord WK, Francke U. Trisomy 14q-. Birth Defects Orig Artic Ser. 1975;11(5):223-8. PMID: 1218218.
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Report of the Committee on the Genetic Constitution of Chromosomes 17, 18 and 19.

Cytogenetics and cell genetics

Naylor S, Lalouel JM, Shaw DJ.
PMID: 3864596
Cytogenet Cell Genet. 1985;40(1):242-67. doi: 10.1159/000132176.

No abstract available.

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Naylor S, Lalouel JM, Shaw DJ. Report of the Committee on the Genetic Constitution of Chromosomes 17, 18 and 19. Cytogenet Cell Genet. 1985;40(1):242-67doi: 10.1159/000132176.
Naylor, S., Lalouel, J. M., & Shaw, D. J. (1985). Report of the Committee on the Genetic Constitution of Chromosomes 17, 18 and 19. Cytogenetics and cell genetics, 40(1), 242-67. https://doi.org/10.1159/000132176
Naylor, S, et al. "Report of the Committee on the Genetic Constitution of Chromosomes 17, 18 and 19." Cytogenetics and cell genetics vol. 40,1 (1985): 242-67. doi: https://doi.org/10.1159/000132176
Naylor S, Lalouel JM, Shaw DJ. Report of the Committee on the Genetic Constitution of Chromosomes 17, 18 and 19. Cytogenet Cell Genet. 1985;40(1):242-67. doi: 10.1159/000132176. PMID: 3864596.
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[A small supernumerary metacentric chromosome: interprétation test (author's transl)].

Journal de genetique humaine

Ayraud N, Noel B, Llyod M, Letourneau J, Martinon J.
PMID: 965953
J Genet Hum. 1976 Jun;24(2):81-93.

The report relates to a new case of small supernumerary metacentric chromosome. The phenotypical variability of previously published cases suggests that this chromosomal anomaly may arise from multiple origins. Our study shows the difficulties of a cytogenetic interpretation and...

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Ayraud N, Noel B, Llyod M, et al. Petit chromosome métacentrique surnuméraire: essai d'interpretation [A small supernumerary metacentric chromosome: interprétation test (author's transl)]. J Genet Hum. 1976;24(2):81-93
Ayraud, N., Noel, B., Llyod, M., Letourneau, J., & Martinon, J. (1976). Petit chromosome métacentrique surnuméraire: essai d'interpretation [A small supernumerary metacentric chromosome: interprétation test (author's transl)]. Journal de genetique humaine, 24(2), 81-93.
Ayraud, N, et al. "Petit chromosome métacentrique surnuméraire: essai d'interpretation" [A small supernumerary metacentric chromosome: interprétation test (author's transl)]. Journal de genetique humaine vol. 24,2 (1976): 81-93.
Ayraud N, Noel B, Llyod M, Letourneau J, Martinon J. Petit chromosome métacentrique surnuméraire: essai d'interpretation [A small supernumerary metacentric chromosome: interprétation test (author's transl)]. J Genet Hum. 1976 Jun;24(2):81-93. French. PMID: 965953.
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Mapping of human autosomal phosphoglycerate kinase sequence to chromosome 19.

Somatic cell and molecular genetics

Gartler SM, Riley DE, Lebo RV, Cheung MC, Eddy RL, Shows TB.
PMID: 3016919
Somat Cell Mol Genet. 1986 Jul;12(4):395-401. doi: 10.1007/BF01570734.

In order to map human PGK sequences, DNA was prepared from 55 human-mouse somatic cell lines. The DNA was digested to completion with HindIII and Southern filters prepared. These filters were hybridized at high stringency conditions to a human...

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Gartler SM, Riley DE, Lebo RV, et al. Mapping of human autosomal phosphoglycerate kinase sequence to chromosome 19. Somat Cell Mol Genet. 1986;12(4):395-401doi: 10.1007/BF01570734.
Gartler, S. M., Riley, D. E., Lebo, R. V., Cheung, M. C., Eddy, R. L., & Shows, T. B. (1986). Mapping of human autosomal phosphoglycerate kinase sequence to chromosome 19. Somatic cell and molecular genetics, 12(4), 395-401. https://doi.org/10.1007/BF01570734
Gartler, S M, et al. "Mapping of human autosomal phosphoglycerate kinase sequence to chromosome 19." Somatic cell and molecular genetics vol. 12,4 (1986): 395-401. doi: https://doi.org/10.1007/BF01570734
Gartler SM, Riley DE, Lebo RV, Cheung MC, Eddy RL, Shows TB. Mapping of human autosomal phosphoglycerate kinase sequence to chromosome 19. Somat Cell Mol Genet. 1986 Jul;12(4):395-401. doi: 10.1007/BF01570734. PMID: 3016919.
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Showing 1 to 12 of 589 entries