Results 201 to 210 of about 53,668 (220)

Intravenous leiomyomatosis is characterized by a der(14)t(12;14)(q15;q24)

Genes, Chromosomes and Cancer, 2002
AbstractIntravenous leiomyomatosis (IVL) is a rare smooth‐muscle proliferation that is of special interest because of its quasi‐malignant behavior. Our finding of a specific chromosomal aberration, a der(14)t(12;14)(q15;q24), in a second case of IVL suggests that it may be characteristic of IVL.
Dal Cin, Paola, Quade, Bradley J, Neskey, David M, Kleinman, Michael S, Weremowicz, Stanislawa, Morton, Cynthia C   +5 more
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F4E-OFC-280-02Quarterly Activity Progress Report Q15 [PDF]

, 2020
In the quarters covered with the report,very intensive activities werecarried out toextensively test theSafety Instrumented Functions(SIF)of the SPIDER Central Safety System(CSS). This activity has takena very long time due to the high number of tests required, slow and accurate test proceduresand the fact that most tests were possible only outside the
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Translocation (10;12)(q24;q15) in a T-Cell Lymphoblastic Lymphoma with Myeloid Hyperplasia

Cancer Genetics and Cytogenetics, 1998
We present a case of childhood T-cell lymphoblastic lymphoma (T-LBL) with a translocation (10;12)(q24;q15) as a main clonal abnormality, which to our knowledge is the first reported karyotype of this malignancy. The patient's peripheral blood and bone marrow showed marked leukocytosis mostly myeloid lineage cells, at diagnosis.
K, Sano, J, Goji, Y, Kosaka, H, Nakamura, F, Nakamura, E, Tatsumi   +5 more
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Trophoblast glycoprotein recognised by monoclonal antibody 5T4 maps to human chromosome 6q14?q15

Human Genetics, 1990
Human X rodent hybrids were stained by indirect immunofluorescence with 5T4, a murine monoclonal antibody that recognises a 72 kdalton glycoprotein expressed by human trophoblasts and a very restricted range of adult tissues; they were analysed by flow cytometry.
J M, Boyle, K H, Grzeschik, P R, Heath, J E, Morten, P L, Stern   +4 more
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MPEC 2025-Q15 : 2025 PR2

The Minor Planet Electronic Circulars contain information on unusual minor planets, routine data on comets and natural satellites, and occasional editorial announcements. They are published on behalf of Division F of the International Astronomical Union by the Minor Planet Center, Smithsonian Astrophysical Observatory, Cambridge, MA 02138, U.S.A.
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MPEC 2024-Q15 : 2024 QB

The Minor Planet Electronic Circulars contain information on unusual minor planets, routine data on comets and natural satellites, and occasional editorial announcements. They are published on behalf of Division F of the International Astronomical Union by the Minor Planet Center, Smithsonian Astrophysical Observatory, Cambridge, MA 02138, U.S.A.
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Molecular analysis of a familial case of renal cell cancer and a t(3;6)(q12;q15)

Genes, Chromosomes and Cancer, 2001
AbstractWe identified a novel familial case of clear‐cell renal cancer and a t(3;6)(q12;q15). Subsequent cytogenetic and molecular analyses showed the presence of several abnormalities within tumour samples obtained from different patients. Loss of the der(3) chromosome was noted in some, but not all, of the samples. A concomitant VHL gene mutation was
Eleveld, M. J., Bodmer, D., Merkx, G., Siepman, A., Sprenger, S. H., Weterman, M. A., Ligtenberg, M. J., Kamp, J., Stapper, W., Jeuken, J. W., Smeets, D., Smits, A., Geurts van Kessel, A.   +12 more
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Novel t(15;19)(q15;p13) chromosome abnormality in a thymic carcinoma.

Cancer research, 1991
A 22-year-old female with a thymic carcinoma is reported. The tumor was refractory to both chemotherapy and irradiation. The patient died with an aggressive clinical course. Cytogenetic study showed that the tumor cells had a chromosome translocation, t(15;19)(q15;p13), which was not identified previously in human cancer.
I, Kubonishi, N, Takehara, J, Iwata, H, Sonobe, Y, Ohtsuki, T, Abe, I, Miyoshi   +6 more
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Partial monosomy 15q due to de novo t(15;22)(q15;p11).

Annales de genetique, 1988
We report a 2-years-old infant who presented psychomotor delay and facial dysmorphic features. He has a partial monosomy of 15q resulting from de novo t(15;22)(q15;p11). Up to now three other cases with a similar 15q monosomy have been reported, but the present case is the first one with a "pure" monosomy 15q.
M A, Mori, L, Rodriguez, I, Pinel, J M, Casas, A, Diaz de Bustamante, M L, Martinez-Frias   +5 more
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Sotos syndrome with a balanced reciprocal translocation t(2;12)(q33.3;q15).

Annales de genetique, 1990
A balanced reciprocal translocation, 46,XY, t(2;12), was detected in a male infant who had the characteristic features of Sotos syndrome. His father's karyotype was normal, but his mother and an older brother had the same chromosomal abnormality without a history or clinical features of Sotos syndrome.
K, Tamaki, K, Horie, T, Go, T, Okuno, H, Mikawa, Z Y, Hua, T, Abe   +6 more
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