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Linkage analysis of melanoma alone and chromosome 1p markers PND, D1S47, and LMYC.

Cytogenetics and cell genetics

Goldstein AM, Bale SJ, Tucker MA.
PMID: 1737501
Cytogenet Cell Genet. 1992;59(2):203-5. doi: 10.1159/000133246.

No abstract available.

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Goldstein AM, Bale SJ, Tucker MA. Linkage analysis of melanoma alone and chromosome 1p markers PND, D1S47, and LMYC. Cytogenet Cell Genet. 1992;59(2):203-5doi: 10.1159/000133246.
Goldstein, A. M., Bale, S. J., & Tucker, M. A. (1992). Linkage analysis of melanoma alone and chromosome 1p markers PND, D1S47, and LMYC. Cytogenetics and cell genetics, 59(2), 203-5. https://doi.org/10.1159/000133246
Goldstein, A M, et al. "Linkage analysis of melanoma alone and chromosome 1p markers PND, D1S47, and LMYC." Cytogenetics and cell genetics vol. 59,2 (1992): 203-5. doi: https://doi.org/10.1159/000133246
Goldstein AM, Bale SJ, Tucker MA. Linkage analysis of melanoma alone and chromosome 1p markers PND, D1S47, and LMYC. Cytogenet Cell Genet. 1992;59(2):203-5. doi: 10.1159/000133246. PMID: 1737501.
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Chromosome studies of solid tumours.

Journal of clinical pathology

Bown NP.
PMID: 1517454
J Clin Pathol. 1992 Jul;45(7):556-60. doi: 10.1136/jcp.45.7.556.
Free PMC Article

No abstract available.

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Bown NP. Chromosome studies of solid tumours. J Clin Pathol. 1992;45(7):556-60doi: 10.1136/jcp.45.7.556.
Bown, N. P. (1992). Chromosome studies of solid tumours. Journal of clinical pathology, 45(7), 556-60. https://doi.org/10.1136/jcp.45.7.556
Bown, N P. "Chromosome studies of solid tumours." Journal of clinical pathology vol. 45,7 (1992): 556-60. doi: https://doi.org/10.1136/jcp.45.7.556
Bown NP. Chromosome studies of solid tumours. J Clin Pathol. 1992 Jul;45(7):556-60. doi: 10.1136/jcp.45.7.556. PMID: 1517454; PMCID: PMC495176.
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Mapping of a human fibrillar collagen gene, pro alpha 1 (XI) (COL11A1), to the p21 region of chromosome 1.

Genomics

Henry I, Bernheim A, Bernard M, van der Rest M, Kimura T, Jeanpierre C, Barichard F, Berger R, Olsen BR, Ramirez F.
PMID: 3220479
Genomics. 1988 Jul;3(1):87-90. doi: 10.1016/0888-7543(88)90165-6.

Type XI collagen is a minor and poorly characterized structural component of cartilage. Recently, cDNA and genomic clones coding for the pro alpha 1 chain of human Type XI collagen, formerly 1 alpha collagen, have been isolated and fully...

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Henry I, Bernheim A, Bernard M, et al. Mapping of a human fibrillar collagen gene, pro alpha 1 (XI) (COL11A1), to the p21 region of chromosome 1. Genomics. 1988;3(1):87-90doi: 10.1016/0888-7543(88)90165-6.
Henry, I., Bernheim, A., Bernard, M., van der Rest, M., Kimura, T., Jeanpierre, C., Barichard, F., Berger, R., Olsen, B. R., & Ramirez, F. (1988). Mapping of a human fibrillar collagen gene, pro alpha 1 (XI) (COL11A1), to the p21 region of chromosome 1. Genomics, 3(1), 87-90. https://doi.org/10.1016/0888-7543(88)90165-6
Henry, I, et al. "Mapping of a human fibrillar collagen gene, pro alpha 1 (XI) (COL11A1), to the p21 region of chromosome 1." Genomics vol. 3,1 (1988): 87-90. doi: https://doi.org/10.1016/0888-7543(88)90165-6
Henry I, Bernheim A, Bernard M, van der Rest M, Kimura T, Jeanpierre C, Barichard F, Berger R, Olsen BR, Ramirez F. Mapping of a human fibrillar collagen gene, pro alpha 1 (XI) (COL11A1), to the p21 region of chromosome 1. Genomics. 1988 Jul;3(1):87-90. doi: 10.1016/0888-7543(88)90165-6. PMID: 3220479.
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Complex intrachromosomal rearrangement in the process of amplification of the L-myc gene in small-cell lung cancer.

Molecular and cellular biology

Sekido Y, Takahashi T, Mäkelä TP, Obata Y, Ueda R, Hida T, Hibi K, Shimokata K, Alitalo K, Takahashi T.
PMID: 1312669
Mol Cell Biol. 1992 Apr;12(4):1747-54. doi: 10.1128/mcb.12.4.1747-1754.1992.
Free PMC Article

The L-myc gene was first isolated from a human small-cell lung cancer (SCLC) cell line on the basis of its amplification and sequence similarity to c-myc and N-myc. A new mechanism of L-myc activation which results from the production...

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Sekido Y, Takahashi T, Mäkelä TP, et al. Complex intrachromosomal rearrangement in the process of amplification of the L-myc gene in small-cell lung cancer. Mol Cell Biol. 1992;12(4):1747-54doi: 10.1128/mcb.12.4.1747-1754.1992.
Sekido, Y., Takahashi, T., Mäkelä, T. P., Obata, Y., Ueda, R., Hida, T., Hibi, K., Shimokata, K., Alitalo, K., & Takahashi, T. (1992). Complex intrachromosomal rearrangement in the process of amplification of the L-myc gene in small-cell lung cancer. Molecular and cellular biology, 12(4), 1747-54. https://doi.org/10.1128/mcb.12.4.1747-1754.1992
Sekido, Y, et al. "Complex intrachromosomal rearrangement in the process of amplification of the L-myc gene in small-cell lung cancer." Molecular and cellular biology vol. 12,4 (1992): 1747-54. doi: https://doi.org/10.1128/mcb.12.4.1747-1754.1992
Sekido Y, Takahashi T, Mäkelä TP, Obata Y, Ueda R, Hida T, Hibi K, Shimokata K, Alitalo K, Takahashi T. Complex intrachromosomal rearrangement in the process of amplification of the L-myc gene in small-cell lung cancer. Mol Cell Biol. 1992 Apr;12(4):1747-54. doi: 10.1128/mcb.12.4.1747-1754.1992. PMID: 1312669; PMCID: PMC369618.
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Molecular cloning of cDNAs for the human granulocyte colony-stimulating factor receptor from HL-60 and mapping of the gene to chromosome region 1p32-34.

Blood

Tweardy DJ, Anderson K, Cannizzaro LA, Steinman RA, Croce CM, Huebner K.
PMID: 1371413
Blood. 1992 Mar 01;79(5):1148-54.

Early studies examining the effects of purified or recombinant granulocyte colony-stimulating factor (G-CSF) on human leukemia cell lines demonstrated that some cell lines, such as HL-60, could be induced to differentiate in response to G-CSF. In two recent studies...

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Tweardy DJ, Anderson K, Cannizzaro LA, et al. Molecular cloning of cDNAs for the human granulocyte colony-stimulating factor receptor from HL-60 and mapping of the gene to chromosome region 1p32-34. Blood. 1992;79(5):1148-54
Tweardy, D. J., Anderson, K., Cannizzaro, L. A., Steinman, R. A., Croce, C. M., & Huebner, K. (1992). Molecular cloning of cDNAs for the human granulocyte colony-stimulating factor receptor from HL-60 and mapping of the gene to chromosome region 1p32-34. Blood, 79(5), 1148-54.
Tweardy, D J, et al. "Molecular cloning of cDNAs for the human granulocyte colony-stimulating factor receptor from HL-60 and mapping of the gene to chromosome region 1p32-34." Blood vol. 79,5 (1992): 1148-54.
Tweardy DJ, Anderson K, Cannizzaro LA, Steinman RA, Croce CM, Huebner K. Molecular cloning of cDNAs for the human granulocyte colony-stimulating factor receptor from HL-60 and mapping of the gene to chromosome region 1p32-34. Blood. 1992 Mar 01;79(5):1148-54. PMID: 1371413.
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Chromosomal mapping and nucleotide sequence of a human DNA autonomously replicating sequence.

Genomics

Aguinaga M, Sharan C, Singh DN, Kegler D, Siddiqui KA, Valenzuela MS.
PMID: 2613242
Genomics. 1989 Oct;5(3):605-11. doi: 10.1016/0888-7543(89)90029-3.

A 1.1-kb human DNA fragment (ARSH1) capable of functioning as a putative origin of replication in yeast cells has been characterized both by in situ hybridization to human metaphase chromosomes and by DNA sequencing. Our hybridization studies show a...

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Aguinaga M, Sharan C, Singh DN, et al. Chromosomal mapping and nucleotide sequence of a human DNA autonomously replicating sequence. Genomics. 1989;5(3):605-11doi: 10.1016/0888-7543(89)90029-3.
Aguinaga, M., Sharan, C., Singh, D. N., Kegler, D., Siddiqui, K. A., & Valenzuela, M. S. (1989). Chromosomal mapping and nucleotide sequence of a human DNA autonomously replicating sequence. Genomics, 5(3), 605-11. https://doi.org/10.1016/0888-7543(89)90029-3
Aguinaga, M, et al. "Chromosomal mapping and nucleotide sequence of a human DNA autonomously replicating sequence." Genomics vol. 5,3 (1989): 605-11. doi: https://doi.org/10.1016/0888-7543(89)90029-3
Aguinaga M, Sharan C, Singh DN, Kegler D, Siddiqui KA, Valenzuela MS. Chromosomal mapping and nucleotide sequence of a human DNA autonomously replicating sequence. Genomics. 1989 Oct;5(3):605-11. doi: 10.1016/0888-7543(89)90029-3. PMID: 2613242.
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Isolation and use of chromosome 1 probes for linkage studies on Charcot-Marie-Tooth disease.

Annals of human genetics

Griffiths LR, Zwi MB, Mesterovic N, Ross DA, Board PG, Callen DF, Mohandas T, Buckland R, Fletcher JM, Driesel AJ.
PMID: 2321912
Ann Hum Genet. 1990 Jan;54(1):31-7. doi: 10.1111/j.1469-1809.1990.tb00358.x.

Nine probes were isolated from a human chromosome 1 enriched library and mapped to regions of chromosome 1 using somatic cell hybrid lines. One clone, LR67, which mapped to 1q12----q23 detected a BglI RFLP. This probe, as well as...

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Griffiths LR, Zwi MB, Mesterovic N, et al. Isolation and use of chromosome 1 probes for linkage studies on Charcot-Marie-Tooth disease. Ann Hum Genet. 1990;54(1):31-7doi: 10.1111/j.1469-1809.1990.tb00358.x.
Griffiths, L. R., Zwi, M. B., Mesterovic, N., Ross, D. A., Board, P. G., Callen, D. F., Mohandas, T., Buckland, R., Fletcher, J. M., & Driesel, A. J. (1990). Isolation and use of chromosome 1 probes for linkage studies on Charcot-Marie-Tooth disease. Annals of human genetics, 54(1), 31-7. https://doi.org/10.1111/j.1469-1809.1990.tb00358.x
Griffiths, L R, et al. "Isolation and use of chromosome 1 probes for linkage studies on Charcot-Marie-Tooth disease." Annals of human genetics vol. 54,1 (1990): 31-7. doi: https://doi.org/10.1111/j.1469-1809.1990.tb00358.x
Griffiths LR, Zwi MB, Mesterovic N, Ross DA, Board PG, Callen DF, Mohandas T, Buckland R, Fletcher JM, Driesel AJ. Isolation and use of chromosome 1 probes for linkage studies on Charcot-Marie-Tooth disease. Ann Hum Genet. 1990 Jan;54(1):31-7. doi: 10.1111/j.1469-1809.1990.tb00358.x. PMID: 2321912.
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Non-synonymous polymorphism in the coding sequence of human 3-beta hydroxysteroid dehydrogenase (HSD3B).

Nucleic acids research

Russell AJ, Gaffney D, Edwards CR, Sutcliffe RG.
PMID: 1754419
Nucleic Acids Res. 1991 Dec 11;19(23):6667. doi: 10.1093/nar/19.23.6667.
Free PMC Article

No abstract available.

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Russell AJ, Gaffney D, Edwards CR, et al. Non-synonymous polymorphism in the coding sequence of human 3-beta hydroxysteroid dehydrogenase (HSD3B). Nucleic Acids Res. 1991;19(23):6667doi: 10.1093/nar/19.23.6667.
Russell, A. J., Gaffney, D., Edwards, C. R., & Sutcliffe, R. G. (1991). Non-synonymous polymorphism in the coding sequence of human 3-beta hydroxysteroid dehydrogenase (HSD3B). Nucleic acids research, 19(23), 6667. https://doi.org/10.1093/nar/19.23.6667
Russell, A J, et al. "Non-synonymous polymorphism in the coding sequence of human 3-beta hydroxysteroid dehydrogenase (HSD3B)." Nucleic acids research vol. 19,23 (1991): 6667. doi: https://doi.org/10.1093/nar/19.23.6667
Russell AJ, Gaffney D, Edwards CR, Sutcliffe RG. Non-synonymous polymorphism in the coding sequence of human 3-beta hydroxysteroid dehydrogenase (HSD3B). Nucleic Acids Res. 1991 Dec 11;19(23):6667. doi: 10.1093/nar/19.23.6667. PMID: 1754419; PMCID: PMC329279.
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Partial trisomy 1q in idiopathic myelofibrosis.

Leukemia research

Donti E, Tabilio A, Bocchini F, Falzetti F, Martelli MF, Grignani F, Donti GV.
PMID: 2280601
Leuk Res. 1990;14(11):1035-40. doi: 10.1016/0145-2126(90)90117-r.

Three cases of idiopathic myelofibrosis with partial trisomy of the long arm of chromosome 1 are described. Partial trisomy 1q was the only karyotypic change detectable in unstimulated peripheral blood cell cultures of one and bone-marrow cultures of two...

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Donti E, Tabilio A, Bocchini F, et al. Partial trisomy 1q in idiopathic myelofibrosis. Leuk Res. 1990;14(11):1035-40doi: 10.1016/0145-2126(90)90117-r.
Donti, E., Tabilio, A., Bocchini, F., Falzetti, F., Martelli, M. F., Grignani, F., & Donti, G. V. (1990). Partial trisomy 1q in idiopathic myelofibrosis. Leukemia research, 14(11), 1035-40. https://doi.org/10.1016/0145-2126(90)90117-r
Donti, E, et al. "Partial trisomy 1q in idiopathic myelofibrosis." Leukemia research vol. 14,11 (1990): 1035-40. doi: https://doi.org/10.1016/0145-2126(90)90117-r
Donti E, Tabilio A, Bocchini F, Falzetti F, Martelli MF, Grignani F, Donti GV. Partial trisomy 1q in idiopathic myelofibrosis. Leuk Res. 1990;14(11):1035-40. doi: 10.1016/0145-2126(90)90117-r. PMID: 2280601.
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Neuroblastoma and other childhood neural tumors: a review.

Pediatric pathology

Triche TJ.
PMID: 1690416
Pediatr Pathol. 1990;10(1):175-93. doi: 10.3109/15513819009067106.

Neuroblastoma is the most common nonhematopoietic solid tumor of childhood and has been intensively studied for at least 4 decades. Despite this, few predictive histopathologic clues to its behavior exist. Age, anatomic sites of occurrence, and clinical stage have...

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Triche TJ. Neuroblastoma and other childhood neural tumors: a review. Pediatr Pathol. 1990;10(1):175-93doi: 10.3109/15513819009067106.
Triche, T. J. (1990). Neuroblastoma and other childhood neural tumors: a review. Pediatric pathology, 10(1), 175-93. https://doi.org/10.3109/15513819009067106
Triche, T J. "Neuroblastoma and other childhood neural tumors: a review." Pediatric pathology vol. 10,1 (1990): 175-93. doi: https://doi.org/10.3109/15513819009067106
Triche TJ. Neuroblastoma and other childhood neural tumors: a review. Pediatr Pathol. 1990;10(1):175-93. doi: 10.3109/15513819009067106. PMID: 1690416.
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Feasibility of in situ hybridisation with chromosome specific DNA probes on paraffin wax embedded tissue.

Journal of clinical pathology

Arnoldus EP, Dreef EJ, Noordermeer IA, Verheggen MM, Thierry RF, Peters AC, Cornelisse CJ, Van der Ploeg M, Raap AK.
PMID: 1752979
J Clin Pathol. 1991 Nov;44(11):900-4. doi: 10.1136/jcp.44.11.900.
Free PMC Article

The feasibility was studied of in situ hybridisation using chromosome specific DNA probes on paraffin wax embedded normal and malignant tissues from different organs. Both isolated nuclei and 5 microns sections were used in in situ hybridisation experiments with...

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Arnoldus EP, Dreef EJ, Noordermeer IA, et al. Feasibility of in situ hybridisation with chromosome specific DNA probes on paraffin wax embedded tissue. J Clin Pathol. 1991;44(11):900-4doi: 10.1136/jcp.44.11.900.
Arnoldus, E. P., Dreef, E. J., Noordermeer, I. A., Verheggen, M. M., Thierry, R. F., Peters, A. C., Cornelisse, C. J., Van der Ploeg, M., & Raap, A. K. (1991). Feasibility of in situ hybridisation with chromosome specific DNA probes on paraffin wax embedded tissue. Journal of clinical pathology, 44(11), 900-4. https://doi.org/10.1136/jcp.44.11.900
Arnoldus, E P, et al. "Feasibility of in situ hybridisation with chromosome specific DNA probes on paraffin wax embedded tissue." Journal of clinical pathology vol. 44,11 (1991): 900-4. doi: https://doi.org/10.1136/jcp.44.11.900
Arnoldus EP, Dreef EJ, Noordermeer IA, Verheggen MM, Thierry RF, Peters AC, Cornelisse CJ, Van der Ploeg M, Raap AK. Feasibility of in situ hybridisation with chromosome specific DNA probes on paraffin wax embedded tissue. J Clin Pathol. 1991 Nov;44(11):900-4. doi: 10.1136/jcp.44.11.900. PMID: 1752979; PMCID: PMC496626.
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Fragile site 1p13.1 in neuroblastoma patients.

Cancer genetics and cytogenetics

Vernole P, Tedeschi B, Caporossi D, Nicoletti B.
PMID: 2758396
Cancer Genet Cytogenet. 1989 Jul 01;40(1):135-6. doi: 10.1016/0165-4608(89)90155-6.

No abstract available.

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Vernole P, Tedeschi B, Caporossi D, et al. Fragile site 1p13.1 in neuroblastoma patients. Cancer Genet Cytogenet. 1989;40(1):135-6doi: 10.1016/0165-4608(89)90155-6.
Vernole, P., Tedeschi, B., Caporossi, D., & Nicoletti, B. (1989). Fragile site 1p13.1 in neuroblastoma patients. Cancer genetics and cytogenetics, 40(1), 135-6. https://doi.org/10.1016/0165-4608(89)90155-6
Vernole, P, et al. "Fragile site 1p13.1 in neuroblastoma patients." Cancer genetics and cytogenetics vol. 40,1 (1989): 135-6. doi: https://doi.org/10.1016/0165-4608(89)90155-6
Vernole P, Tedeschi B, Caporossi D, Nicoletti B. Fragile site 1p13.1 in neuroblastoma patients. Cancer Genet Cytogenet. 1989 Jul 01;40(1):135-6. doi: 10.1016/0165-4608(89)90155-6. PMID: 2758396.
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Showing 13 to 24 of 7659 entries