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Chromosome Microdissection

Current Protocols in Human Genetics, 1997
AbstractThis unit describes chromosome microdissection methodologies that are useful in both clinical and research laboratories. In combination with FISH, region‐specific probes can be made to determine the origin of marker chromosomes. Another application of the microdissection technology is in the generation of regionspecific cDNA libraries, known as
P, Meltzer, M, Bittner
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Chromosome kissing

Current Opinion in Genetics & Development, 2007
Eukariotic chromosomes occupy distinct territories in the cell nucleus. These territories intermingle little with other chromosomes. Nevertheless, several contacts between different chromosomal loci have been documented, a phenomenon called chromosome kissing.
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[Chromosomes and chromosome disorders].

Nordisk medicin, 1990
The risk of bearing a child with chromosomal defects increases once the mother reaches the age of 35; the principal indication for chromosomal examination of the fetus is that the pregnant woman is "older". Chromosomal examination of new-born babies is indicated if it is suspected that dysmorphic features may depend on cytogenetic deviation.
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Chromosome Recognition

2016
Chromosomal analysis of human cells serves to characterize aberrations of chromosome number and structure. Individual chromosome can be identified precisely by recognition of its morphological characteristics and staining patterns according to specific landmarks, regions, and bands as described in the ideogram.
Thomas S K, Wan   +2 more
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Chromosome evolution

Current Opinion in Plant Biology, 2007
The idea of evolution as a principle for the origin of biodiversity fits all phenomena of life, including the carriers of nuclear inheritance, the chromosomes. Insights into the evolutionary mechanisms that contribute to the shape, size, composition, number and redundancy of chromosomes elucidate the high plasticity of nuclear genomes at the ...
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Capturing Chromosome Conformation

Science, 2002
J. Dekker   +3 more
semanticscholar   +1 more source

Identification of a candidate tumour suppressor gene, MMAC1, at chromosome 10q23.3 that is mutated in multiple advanced cancers

Nature Genetics, 1997
P. Steck   +14 more
semanticscholar   +1 more source

Chromosome preparations of leukocytes cultured from human peripheral blood.

Experimental Cell Research, 1960
P. Moorhead   +4 more
semanticscholar   +1 more source

Candidate gene for the chromosome 1 familial Alzheimer's disease locus

Science, 1995
E. Levy-Lahad   +18 more
semanticscholar   +1 more source

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