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Structure and chromosomal localization of the human prochymosin pseudogene.

Advances in experimental medicine and biology

Ord T, Kolmer M, Jänne J, Villems R, Saarma M.
PMID: 1812698
Adv Exp Med Biol. 1991;306:121-6. doi: 10.1007/978-1-4684-6012-4_15.

No abstract available.

Cite
Ord T, Kolmer M, Jänne J, et al. Structure and chromosomal localization of the human prochymosin pseudogene. Adv Exp Med Biol. 1991;306:121-6doi: 10.1007/978-1-4684-6012-4_15.
Ord, T., Kolmer, M., Jänne, J., Villems, R., & Saarma, M. (1991). Structure and chromosomal localization of the human prochymosin pseudogene. Advances in experimental medicine and biology, 306121-6. https://doi.org/10.1007/978-1-4684-6012-4_15
Ord, T, et al. "Structure and chromosomal localization of the human prochymosin pseudogene." Advances in experimental medicine and biology vol. 306 (1991): 121-6. doi: https://doi.org/10.1007/978-1-4684-6012-4_15
Ord T, Kolmer M, Jänne J, Villems R, Saarma M. Structure and chromosomal localization of the human prochymosin pseudogene. Adv Exp Med Biol. 1991;306:121-6. doi: 10.1007/978-1-4684-6012-4_15. PMID: 1812698.
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BsmI polymorphism in N-ras intron I (RASN).

Nucleic acids research

Heighway J.
PMID: 1672756
Nucleic Acids Res. 1991 Feb 11;19(3):682. doi: 10.1093/nar/19.3.682.
Free PMC Article

No abstract available.

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Heighway J. BsmI polymorphism in N-ras intron I (RASN). Nucleic Acids Res. 1991;19(3):682doi: 10.1093/nar/19.3.682.
Heighway, J. (1991). BsmI polymorphism in N-ras intron I (RASN). Nucleic acids research, 19(3), 682. https://doi.org/10.1093/nar/19.3.682
Heighway, J. "BsmI polymorphism in N-ras intron I (RASN)." Nucleic acids research vol. 19,3 (1991): 682. doi: https://doi.org/10.1093/nar/19.3.682
Heighway J. BsmI polymorphism in N-ras intron I (RASN). Nucleic Acids Res. 1991 Feb 11;19(3):682. doi: 10.1093/nar/19.3.682. PMID: 1672756; PMCID: PMC333673.
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Three RFLPs are detected by an alpha spectrin genomic clone.

Nucleic acids research

Hoffman N, Stanislovitis P, Watkins PC, Klinger KW, Linnenbach AJ, Forget BG.
PMID: 2884629
Nucleic Acids Res. 1987 Jun 11;15(11):4696. doi: 10.1093/nar/15.11.4696.
Free PMC Article

No abstract available.

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Hoffman N, Stanislovitis P, Watkins PC, et al. Three RFLPs are detected by an alpha spectrin genomic clone. Nucleic Acids Res. 1987;15(11):4696doi: 10.1093/nar/15.11.4696.
Hoffman, N., Stanislovitis, P., Watkins, P. C., Klinger, K. W., Linnenbach, A. J., & Forget, B. G. (1987). Three RFLPs are detected by an alpha spectrin genomic clone. Nucleic acids research, 15(11), 4696. https://doi.org/10.1093/nar/15.11.4696
Hoffman, N, et al. "Three RFLPs are detected by an alpha spectrin genomic clone." Nucleic acids research vol. 15,11 (1987): 4696. doi: https://doi.org/10.1093/nar/15.11.4696
Hoffman N, Stanislovitis P, Watkins PC, Klinger KW, Linnenbach AJ, Forget BG. Three RFLPs are detected by an alpha spectrin genomic clone. Nucleic Acids Res. 1987 Jun 11;15(11):4696. doi: 10.1093/nar/15.11.4696. PMID: 2884629; PMCID: PMC340898.
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Is there a neuroblastoma anti-oncogene?.

Progress in clinical and biological research

Schwab M.
PMID: 2068129
Prog Clin Biol Res. 1991;366:1-9.

No abstract available.

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Schwab M. Is there a neuroblastoma anti-oncogene?. Prog Clin Biol Res. 1991;366:1-9
Schwab, M. (1991). Is there a neuroblastoma anti-oncogene?. Progress in clinical and biological research, 3661-9.
Schwab, M. "Is there a neuroblastoma anti-oncogene?." Progress in clinical and biological research vol. 366 (1991): 1-9.
Schwab M. Is there a neuroblastoma anti-oncogene?. Prog Clin Biol Res. 1991;366:1-9. PMID: 2068129.
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Infantile form of neuronal ceroid lipofuscinosis (CLN1) maps to the short arm of chromosome 1.

Genomics

Järvelä I, Schleutker J, Haataja L, Santavuori P, Puhakka L, Manninen T, Palotie A, Sandkuijl LA, Renlund M, White R.
PMID: 1672288
Genomics. 1991 Jan;9(1):170-3. doi: 10.1016/0888-7543(91)90235-7.

The neuronal ceroid lipofuscinoses (CLNs) are one of the most common progressive encephalopathies of childhood in Western countries. They are divided into three main types: infantile, late infantile, and juvenile. The inheritance of all forms is autosomal recessive, and...

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Järvelä I, Schleutker J, Haataja L, et al. Infantile form of neuronal ceroid lipofuscinosis (CLN1) maps to the short arm of chromosome 1. Genomics. 1991;9(1):170-3doi: 10.1016/0888-7543(91)90235-7.
Järvelä, I., Schleutker, J., Haataja, L., Santavuori, P., Puhakka, L., Manninen, T., Palotie, A., Sandkuijl, L. A., Renlund, M., & White, R. (1991). Infantile form of neuronal ceroid lipofuscinosis (CLN1) maps to the short arm of chromosome 1. Genomics, 9(1), 170-3. https://doi.org/10.1016/0888-7543(91)90235-7
Järvelä, I, et al. "Infantile form of neuronal ceroid lipofuscinosis (CLN1) maps to the short arm of chromosome 1." Genomics vol. 9,1 (1991): 170-3. doi: https://doi.org/10.1016/0888-7543(91)90235-7
Järvelä I, Schleutker J, Haataja L, Santavuori P, Puhakka L, Manninen T, Palotie A, Sandkuijl LA, Renlund M, White R. Infantile form of neuronal ceroid lipofuscinosis (CLN1) maps to the short arm of chromosome 1. Genomics. 1991 Jan;9(1):170-3. doi: 10.1016/0888-7543(91)90235-7. PMID: 1672288.
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[Heteromorphism of chromosome 1, 9 and 16 homologs in persons living in regions differing in the level of longevity].

TSitologiia i genetika

Kuznetsova SM, Zaritskaia MIu, Berdyshev GD.
PMID: 2973673
Tsitol Genet. 1988 Jul-Aug;22(4):27-32.

Regional and age-related peculiarities of chromosomal polymorphism are established as a result of studies in C-band heteromorphism of chromosomes 1, 9 and 16 in the long-lived subjects, their relatives and population groups of the Abkhaz and Ukrainian Republics. Heteromorphism...

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Kuznetsova SM, Zaritskaia MIu, Berdyshev GD. Geteromorfizm gomologov khromosom 1, 9, 16 u lits, prozhivaiushchikh v regionakh s razlichnym urovnem dolgoletiia. [Heteromorphism of chromosome 1, 9 and 16 homologs in persons living in regions differing in the level of longevity]. Tsitol Genet. 1988;22(4):27-32
Kuznetsova, S. M., Zaritskaia, M. I. u., & Berdyshev, G. D. (1988). Geteromorfizm gomologov khromosom 1, 9, 16 u lits, prozhivaiushchikh v regionakh s razlichnym urovnem dolgoletiia. [Heteromorphism of chromosome 1, 9 and 16 homologs in persons living in regions differing in the level of longevity]. TSitologiia i genetika, 22(4), 27-32.
Kuznetsova, S M, et al. "Geteromorfizm gomologov khromosom 1, 9, 16 u lits, prozhivaiushchikh v regionakh s razlichnym urovnem dolgoletiia." [Heteromorphism of chromosome 1, 9 and 16 homologs in persons living in regions differing in the level of longevity]. TSitologiia i genetika vol. 22,4 (1988): 27-32.
Kuznetsova SM, Zaritskaia MIu, Berdyshev GD. Geteromorfizm gomologov khromosom 1, 9, 16 u lits, prozhivaiushchikh v regionakh s razlichnym urovnem dolgoletiia. [Heteromorphism of chromosome 1, 9 and 16 homologs in persons living in regions differing in the level of longevity]. Tsitol Genet. 1988 Jul-Aug;22(4):27-32. Russian. PMID: 2973673.
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Complex familial translocation.

Clinical genetics

Cruz-Coke R.
PMID: 2311267
Clin Genet. 1990 Feb;37(2):158-9. doi: 10.1111/j.1399-0004.1990.tb03494.x.

No abstract available.

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Cruz-Coke R. Complex familial translocation. Clin Genet. 1990;37(2):158-9doi: 10.1111/j.1399-0004.1990.tb03494.x.
Cruz-Coke, R. (1990). Complex familial translocation. Clinical genetics, 37(2), 158-9. https://doi.org/10.1111/j.1399-0004.1990.tb03494.x
Cruz-Coke, R. "Complex familial translocation." Clinical genetics vol. 37,2 (1990): 158-9. doi: https://doi.org/10.1111/j.1399-0004.1990.tb03494.x
Cruz-Coke R. Complex familial translocation. Clin Genet. 1990 Feb;37(2):158-9. doi: 10.1111/j.1399-0004.1990.tb03494.x. PMID: 2311267.
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Chromosome 1 localization of the gene for CD34, a surface antigen of human stem cells.

Cytogenetics and cell genetics

Tenen DG, Satterthwaite AB, Borson R, Simmons D, Eddy RL, Shows TB.
PMID: 1691071
Cytogenet Cell Genet. 1990;53(1):55-7. doi: 10.1159/000132894.

CD34 is a surface antigen expressed on normal human hematopoietic stem cells, as well as on the blast cells of many patients with both lymphocytic and myelocytic leukemias. By Southern blot analysis of DNA from a panel of human...

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Tenen DG, Satterthwaite AB, Borson R, et al. Chromosome 1 localization of the gene for CD34, a surface antigen of human stem cells. Cytogenet Cell Genet. 1990;53(1):55-7doi: 10.1159/000132894.
Tenen, D. G., Satterthwaite, A. B., Borson, R., Simmons, D., Eddy, R. L., & Shows, T. B. (1990). Chromosome 1 localization of the gene for CD34, a surface antigen of human stem cells. Cytogenetics and cell genetics, 53(1), 55-7. https://doi.org/10.1159/000132894
Tenen, D G, et al. "Chromosome 1 localization of the gene for CD34, a surface antigen of human stem cells." Cytogenetics and cell genetics vol. 53,1 (1990): 55-7. doi: https://doi.org/10.1159/000132894
Tenen DG, Satterthwaite AB, Borson R, Simmons D, Eddy RL, Shows TB. Chromosome 1 localization of the gene for CD34, a surface antigen of human stem cells. Cytogenet Cell Genet. 1990;53(1):55-7. doi: 10.1159/000132894. PMID: 1691071.
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Abnormal chromosomes including small metacentrics in 14 ovarian cancers.

Cancer genetics and cytogenetics

Atkin NB, Baker MC.
PMID: 3032405
Cancer Genet Cytogenet. 1987 Jun;26(2):355-61. doi: 10.1016/0165-4608(87)90070-7.

In direct preparations of 14 ovarian cancers including 11 primary tumors, chromosomes #1 (12 tumors), #3 (12 tumors, including 3q- chromosomes in five), #6 [eight tumors, including six with a 6q- and two with an i(6p)], #11 (11p +...

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Atkin NB, Baker MC. Abnormal chromosomes including small metacentrics in 14 ovarian cancers. Cancer Genet Cytogenet. 1987;26(2):355-61doi: 10.1016/0165-4608(87)90070-7.
Atkin, N. B., & Baker, M. C. (1987). Abnormal chromosomes including small metacentrics in 14 ovarian cancers. Cancer genetics and cytogenetics, 26(2), 355-61. https://doi.org/10.1016/0165-4608(87)90070-7
Atkin, N B, and Baker, M C. "Abnormal chromosomes including small metacentrics in 14 ovarian cancers." Cancer genetics and cytogenetics vol. 26,2 (1987): 355-61. doi: https://doi.org/10.1016/0165-4608(87)90070-7
Atkin NB, Baker MC. Abnormal chromosomes including small metacentrics in 14 ovarian cancers. Cancer Genet Cytogenet. 1987 Jun;26(2):355-61. doi: 10.1016/0165-4608(87)90070-7. PMID: 3032405.
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Structure and chromosomal location of the gene for endothelial-leukocyte adhesion molecule 1.

The Journal of biological chemistry

Collins T, Williams A, Johnston GI, Kim J, Eddy R, Shows T, Gimbrone MA, Bevilacqua MP.
PMID: 1703529
J Biol Chem. 1991 Feb 05;266(4):2466-73.
Free Article

Endothelial-leukocyte adhesion molecule 1 is a cell surface glycoprotein expressed by cytokine-activated endothelium that mediates the adhesion of blood neutrophils. Endothelial-leukocyte adhesion molecule 1 is a member of the selectin family of cell adhesion molecules each of which contain...

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Collins T, Williams A, Johnston GI, et al. Structure and chromosomal location of the gene for endothelial-leukocyte adhesion molecule 1. J Biol Chem. 1991;266(4):2466-73
Collins, T., Williams, A., Johnston, G. I., Kim, J., Eddy, R., Shows, T., Gimbrone, M. A., & Bevilacqua, M. P. (1991). Structure and chromosomal location of the gene for endothelial-leukocyte adhesion molecule 1. The Journal of biological chemistry, 266(4), 2466-73.
Collins, T, et al. "Structure and chromosomal location of the gene for endothelial-leukocyte adhesion molecule 1." The Journal of biological chemistry vol. 266,4 (1991): 2466-73.
Collins T, Williams A, Johnston GI, Kim J, Eddy R, Shows T, Gimbrone MA, Bevilacqua MP. Structure and chromosomal location of the gene for endothelial-leukocyte adhesion molecule 1. J Biol Chem. 1991 Feb 05;266(4):2466-73. PMID: 1703529.
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De novo dir dup (1)(q3200----4200) in an adult. Further delineation of the pure 1q trisomy syndrome.

Annales de genetique

Barros-Núñez P, Sánchez-Corona J, Rolón A, Medina C, García-Ochoa C, García-Cruz MO, Nazará Z, García-Cruz D.
PMID: 2667459
Ann Genet. 1989;32(2):97-101.

An adult male patient with a "de novo" pure trisomy 1q32---q42 was studied. Literature review of 33 cases with 1q trisomy allowed singling out a distinctive phenotype by eliminating clinical features of concomitant aneusomies. It is concluded, however, that...

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Barros-Núñez P, Sánchez-Corona J, Rolón A, et al. De novo dir dup (1)(q3200----4200) in an adult. Further delineation of the pure 1q trisomy syndrome. Ann Genet. 1989;32(2):97-101
Barros-Núñez, P., Sánchez-Corona, J., Rolón, A., Medina, C., García-Ochoa, C., García-Cruz, M. O., Nazará, Z., & García-Cruz, D. (1989). De novo dir dup (1)(q3200----4200) in an adult. Further delineation of the pure 1q trisomy syndrome. Annales de genetique, 32(2), 97-101.
Barros-Núñez, P, et al. "De novo dir dup (1)(q3200----4200) in an adult. Further delineation of the pure 1q trisomy syndrome." Annales de genetique vol. 32,2 (1989): 97-101.
Barros-Núñez P, Sánchez-Corona J, Rolón A, Medina C, García-Ochoa C, García-Cruz MO, Nazará Z, García-Cruz D. De novo dir dup (1)(q3200----4200) in an adult. Further delineation of the pure 1q trisomy syndrome. Ann Genet. 1989;32(2):97-101. PMID: 2667459.
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Nonrandom t(1;22)(p12-p13;q13) in acute megakaryocytic malignant proliferation.

Cancer genetics and cytogenetics

Baruchel A, Daniel MT, Schaison G, Berger R.
PMID: 1884357
Cancer Genet Cytogenet. 1991 Jul 15;54(2):239-43. doi: 10.1016/0165-4608(91)90213-e.

A case of acute megakaryocytic leukemia (M7) and one of acute myeloid hemopathy affecting megakaryocytic and erythrocytic cell lineages in infants are reported. Both patients had t(1;22)(p12-p13;q13). This translocation was previously observed in a congenital M7 leukemia. These studies...

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Baruchel A, Daniel MT, Schaison G, et al. Nonrandom t(1;22)(p12-p13;q13) in acute megakaryocytic malignant proliferation. Cancer Genet Cytogenet. 1991;54(2):239-43doi: 10.1016/0165-4608(91)90213-e.
Baruchel, A., Daniel, M. T., Schaison, G., & Berger, R. (1991). Nonrandom t(1;22)(p12-p13;q13) in acute megakaryocytic malignant proliferation. Cancer genetics and cytogenetics, 54(2), 239-43. https://doi.org/10.1016/0165-4608(91)90213-e
Baruchel, A, et al. "Nonrandom t(1;22)(p12-p13;q13) in acute megakaryocytic malignant proliferation." Cancer genetics and cytogenetics vol. 54,2 (1991): 239-43. doi: https://doi.org/10.1016/0165-4608(91)90213-e
Baruchel A, Daniel MT, Schaison G, Berger R. Nonrandom t(1;22)(p12-p13;q13) in acute megakaryocytic malignant proliferation. Cancer Genet Cytogenet. 1991 Jul 15;54(2):239-43. doi: 10.1016/0165-4608(91)90213-e. PMID: 1884357.
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Showing 25 to 36 of 7659 entries