Chromosomal banding patterns in human large bowel adenomas

1985 ◽  
Vol 70 (1) ◽  
pp. 28-31 ◽  
Author(s):  
Amelia Reichmann ◽  
Paulette Martin ◽  
B. Levin
1981 ◽  
Vol 28 (4) ◽  
pp. 431-440 ◽  
Author(s):  
Amelia Reichmann ◽  
Paulette Martin ◽  
Bernard Levin

Hereditas ◽  
2004 ◽  
Vol 127 (3) ◽  
pp. 255-262 ◽  
Author(s):  
Katia Cristina Machado Pellegrino ◽  
Sanae Kasahara ◽  
Miguel Trefaut Rodrigues ◽  
Yatiyo Yonenaga-Yassuda

1986 ◽  
Vol 67 (1) ◽  
pp. 69-80 ◽  
Author(s):  
A. D. Vitullo ◽  
M. S. Merani ◽  
O. A. Reig ◽  
A. E. Kajon ◽  
O. Scaglia ◽  
...  

1973 ◽  
Vol 51 (4) ◽  
pp. 1197-1203 ◽  
Author(s):  
Mitsuo Oshimura ◽  
Motomichi Sasaki ◽  
Sajiro Makino

1996 ◽  
Vol 74 (3) ◽  
pp. 203-210 ◽  
Author(s):  
Y. Yonenaga-Yassuda ◽  
L. Mori ◽  
T.H. Chu ◽  
M.T. Rodrigues

Blood ◽  
1976 ◽  
Vol 47 (5) ◽  
pp. 705-721 ◽  
Author(s):  
JD Rowley ◽  
D Potter

Bone marrow chromosomes obtained from 50 of 55 consecutive adult patients with acute nonlymphocytic leukemia were analyzed with quinacrine fluorescence. Twenty-five patients showed a normal karyotype and 25 an abnormal karyotype on the initial samples available for analysis. Among the 25 patients with abnormalities, the marrow cells contained 48 chromosomes in one case, 47 in two, 46 in ten, 45 in nine, 43 in two, and 42 chromosomes in one case. Seven of the ten patients with 46 chromosomes had abnormalities, primarily balanced translocations, that were not detected with the standard Giemsa stains. The analysis of all of the data available revealed the presence of nonrandom chromosome changes such as the addition of No. 8, the loss of No. 7, and a gain or loss of one No. 21. the most frequent structural rearrangement was the translocation between the long arm of No. 8 and No. 21, which may also be associated with the loss of a sex chromosome. Chromosomal abnormalities decreased or disappeared during remission; the same abnormality recurred in relapse. Chemotherapy did not appear to produce a stable clone of aberrant cells. Evolution of the karyotype occurred in eight patients, in five of whom an additional No. 8 was observed. This pattern of chromosomal evolution in patients with acute leukemia was very similar to that observed in patients with chronic myelogenous leukemia in the blast phase.


1987 ◽  
pp. 67-96 ◽  
Author(s):  
Robert J. Baker ◽  
Mazin B. Qumsiyeh ◽  
Craig S. Hood

1985 ◽  
Vol 77 (1) ◽  
pp. 167-183 ◽  
Author(s):  
D.C. Bennett ◽  
K. Bridges ◽  
I.A. McKay

Strains of pigmented melanocytes can be derived reproducibly from normal human skin. Published procedures have been modified here to yield a strain, ‘Nohm-1’, comprising many unpigmented cells as well as cells with various degrees of pigmentation observable by light microscopy. The unpigmented cells contain early melanosomes (pigment organelles) and the specific enzyme tyrosinase. They are on average smaller and less dendritic than the pigmented cells. Nohm-1 cells show normal chromosomal banding patterns and normal proliferative behaviour, including senescence. They form no tumours in immunodeficient (nude) mice. Nohm-1 cells have been cloned and yield two distinct types of colony, depending on the progenitor cell. Well-pigmented melanocytes engender pure colonies of pigmented cells, but cells with little or no pigment can produce both unpigmented and pigmented progeny. Thus there is a separate cell type, or premelanocyte, which can differentiate spontaneously and stably in culture; this cell type includes both unpigmented and faintly pigmented cells. Usefully, most premelanocytes are viable after frozen storage, unlike well-pigmented melanocytes. Some components of the culture medium affect the proportion of pigmented cells in Nohm-1 cultures, and hence probably the ratio of mature melanocytes to premelanocytes. Rapid pigmentation can be induced artificially and simply, by using a medium with increased extracellular pH and tyrosine concentration.


Sign in / Sign up

Export Citation Format

Share Document