Sister-chromatid exchanges: a report of the GENE-TOX program
SA Latt, J Allen, SE Bloom, A Carrano, E Falke… - … Research/Reviews in …, 1981 - Elsevier
Slster-chromatid exchanges (SCEs) represent the interchange of DNA replication products
at apparently homologous loci. The exchange process presumably involves DNA breakage …
at apparently homologous loci. The exchange process presumably involves DNA breakage …
Cytogenetic screening of livestock populations in Europe: an overview
A Ducos, T Revay, A Kovacs, A Hidas… - … and genome research, 2008 - karger.com
Clinical animal cytogenetics development began in the 1960's, almost at the same time as
human cytogenetics. However, the development of the two disciplines has been very …
human cytogenetics. However, the development of the two disciplines has been very …
Preferential inactivation of the paternally derived X chromosome in the extraembryonic membranes of the mouse
N Takagi, M Sasaki - Nature, 1975 - nature.com
RANDOM X inactivation makes the female mammal a natural mosaic for clones of cells
having either the maternally derived X (Xm) or paternally derived one (Xp) which is …
having either the maternally derived X (Xm) or paternally derived one (Xp) which is …
Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and …
U Francke, HD Ochs, B de Martinville… - American journal of …, 1985 - ncbi.nlm.nih.gov
We are reporting a male patient who suffered from chronic granulomatous disease
associated with cytochrome b− 245 deficiency and McLeod red cell phenotype, Duchenne …
associated with cytochrome b− 245 deficiency and McLeod red cell phenotype, Duchenne …
Mechanism of origin of complete hydatidiform moles
PA Jacobs, CM Wilson, JA Sprenkle, NB Rosenshein… - Nature, 1980 - nature.com
Complete or 'true'hydatidiform mole, an abnormality of human gestation, is characterized by
hydropic degeneration of all placental villi, marked hypertrophy of the trophoblast, absence …
hydropic degeneration of all placental villi, marked hypertrophy of the trophoblast, absence …
Epigenotype switching of imprintable loci in embryonic germ cells
T Tada, M Tada, K Hilton, SC Barton, T Sado… - Development genes and …, 1998 - Springer
Expression of imprinted genes is dependent on their parental origin. This is reflected in the
heritable differential methylation of parental alleles. The gametic imprints are however …
heritable differential methylation of parental alleles. The gametic imprints are however …
Regional and temporal changes in the pattern of X-chromosome replication during the early post-implantation development of the female mouse
N Takagi, O Sugawara, M Sasaki - Chromosoma, 1982 - Springer
We have made a detailed study of the X-chromosome replication pattern during the period
when X-inactivation is occurring in the mouse embryo. Our observations show unequivocal …
when X-inactivation is occurring in the mouse embryo. Our observations show unequivocal …
Bromodeoxyuridine: a diagnostic tool in biology and medicine, Part I: Historical perspectives, histochemical methods and cell kinetics
F Dolbeare - The Histochemical Journal, 1995 - Springer
Bromodeoxyuridine (BrdUrd), a thymidine analogue incorporated into DNA, can be
quantified by fluorescent or chromophoric quenching of dyes bound to DNA or with …
quantified by fluorescent or chromophoric quenching of dyes bound to DNA or with …
Pericentric inversions: problems and significance for clinical genetics
P Kaiser - Human genetics, 1984 - Springer
A review is given of the incidence, cytogenetics, and biologic relevance of pericentric
inversions (pii). In 251 cases in the literature and our patients, 96 different inversion forms …
inversions (pii). In 251 cases in the literature and our patients, 96 different inversion forms …
Chromosome 15 abnormalities and the Prader-Willi syndrome: a follow-up report of 40 cases.
DH Ledbetter, JT Mascarello, VM Riccardi… - American Journal of …, 1982 - ncbi.nlm.nih.gov
High-resolution chromosome analysis and multiple banding techniques were performed on
blood samples from 40 patients with Prader-Willi syndrome (PWS) as a follow-up to our …
blood samples from 40 patients with Prader-Willi syndrome (PWS) as a follow-up to our …