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Familial pericentric inversion of chromosome 12

Human Genetics, 1986
A pericentric inversion in one of the chromosomes 12, found in two families living in the same region, is described. This inversion was detected during routine chromosomal analysis in two separate laboratories. The breakpoints were at 12p112 and 12q13. The inverted segment represented approximately 20% of the length of chromosome 12.
I, Voiculescu   +5 more
openaire   +2 more sources

Sequence of Plasmodium falciparum chromosome 12

Nature, 2002
The human malaria parasite Plasmodium falciparum is responsible for the death of more than a million people every year. To stimulate basic research on the disease, and to promote the development of effective drugs and vaccines against the parasite, the complete genome of P.
Richard W, Hyman   +10 more
openaire   +2 more sources

Chimpanzee chromosome 12 is homologous to human chromosome arm 2q

Cytogenetic and Genome Research, 1978
Most of the 46 human chromosomes find their counterparts in the 48 chimpanzee chromosomes except for chromosome 2 which has been hypothesized to have been derived from a centric fusion of two chimpanzee acrocentric chromosomes. These two chromosomes correspond to the human chromosomes 2p and 2g.
N C, Sun, C R, Sun, T, Ho
openaire   +2 more sources

Involvement of Chromosome 12 in Uterine Leiomyoma

1994
Leiomyomas are the most common benign mesenchymal tumors of the uterus. They occur mostly in women older than 30 years, less frequently after menopause, and very rarely below the age of 18. Their pathogenesis is not clearly understood, but a role for sex steroid hormones is likely since they increase in size during pregnancy or after administration of ...
VANNI, ROBERTA, Dal Cin P.
openaire   +2 more sources

Nucleotide sequence comparison of a chromosome rearrangement on human chromosome 12 and the corresponding ape chromosomes

Cytogenetic and Genome Research, 2004
Chromosome rearrangement has been considered to be important in the evolutionary process. Here, we demonstrate the evolutionary relationship of the rearranged human chromosome 12 and the corresponding chromosome XII in apes (chimpanzee, bonobo, gorilla, orangutan, and gibbon) by examining PCR products derived from the breakpoints of inversions and by ...
M K, Shimada   +5 more
openaire   +2 more sources

Chromosome-centric Human Proteome Project (C-HPP): Chromosome 12

Journal of Proteome Research, 2014
Following an official announcement of the Chromosome-centric Human Proteome Project (C-HPP), the Chromosome 12 (Ch12) Consortium has been established by five representative teams from five Asian countries including Thailand (Siriraj Hospital, Mahidol University), Singapore (National University of Singapore), Taiwan (Academia Sinica), Hong Kong (The ...
Chaiyarit, Sakdithep   +15 more
openaire   +3 more sources

A BrdU-requiring fragile site on chromosome 12

Human Genetics, 1988
A BrdU-requiring fragile site, fra(12)(q24.2), on human chromosome 12 of some individuals is reported. This fragile site is inherited in a Mendelian codominant fashion and does not seem to be associated with any physical or mental abnormality in carriers.
I, Voiculescu   +3 more
openaire   +2 more sources

Molecular cytogenetic resources specific for chromosome 12

American Journal of Medical Genetics, 1999
We have generated a panel of 20 somatic cell hybrids retaining fragments of human chromosome 12. Each hybrid was characterized cytogenetically by reverse fluorescence in situ hybridization (FISH) and molecularly by 24 sequence tagged sites (STSs) spaced evenly along the chromosome.
VIGGIANO, Luigi   +9 more
openaire   +2 more sources

Trisomy of chromosome 12 in a case of thecoma of the ovary

Gynecologic Oncology, 1990
Cytogenetic analysis was performed after short-term tissue culture of a thecoma of the ovary. Trisomy of chromosome 12 was revealed as the sole chromosome abnormality. This is the first report of a chromosomal aberration in thecoma of the ovary.
K, Mrózek   +6 more
openaire   +2 more sources

Pericentric inversions of chromosome 12 in two families

Human Genetics, 1981
Two cases of pericentric inversion of chromosome 12 are presented, one 46,XX,inv(12)(p13;q11) and the other was also a heterozygotic carrier of the inversion. These inversions were detected among 4035 cytogenetic analyses carried out in patients with psychosomatic retardation and/or malformations (357 with a Down phenotype) and in patients with ...
F, Prieto   +4 more
openaire   +2 more sources

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