Isolation and regional mapping of random X sequences from distal human X chromosome

1985 ◽  
Vol 11 (5) ◽  
pp. 433-444 ◽  
Author(s):  
Patricia D. Murphy ◽  
Frank H. Ruddle
Keyword(s):  
X Chromosome ◽  
Regional Mapping

Regional mapping of the human No. 1 and X chromosome in interspecific cell hybrids using an X/1 translocation

1975 ◽  
Vol 15 (3) ◽  
pp. 129-137 ◽  
Author(s):  
J. De Wit ◽  
D. Bootsma ◽  
P.L. Pearson ◽  
A. Westerveld
Keyword(s):  
X Chromosome ◽  
Regional Mapping ◽  
Cell Hybrids ◽  
Interspecific Cell Hybrids

scholarly journals Characterization of a panel of somatic cell hybrids for regional mapping of the mouse X chromosome.

1987 ◽  
Vol 84 (15) ◽  
pp. 5330-5334 ◽  
Author(s):  
P. Avner ◽  
D. Arnaud ◽  
L. Amar ◽  
J. Cambrou ◽  
H. Winking ◽  
...  
Keyword(s):  
Somatic Cell ◽  
X Chromosome ◽  
Regional Mapping ◽  
Somatic Cell Hybrids ◽  
Cell Hybrids

A Transcript Map of a 2-Mb BAC Contig in the Proximal Portion of the Mouse X Chromosome and Regional Mapping of the scurfy Mutation

Genomics ◽  
2000 ◽  
Vol 65 (3) ◽  
pp. 213-223 ◽  
Author(s):  
Gary D. Means ◽  
Dean Y. Toy ◽  
Peter R. Baum ◽  
Jonathan M.J. Derry
Keyword(s):  
X Chromosome ◽  
Proximal Portion ◽  
Regional Mapping ◽  
Bac Contig ◽  
Transcript Map

Characterization of a set of X-linked sequences and of a panel of somatic cell hybrids useful for the regional mapping of the human X chromosome

1986 ◽  
Vol 72 (1) ◽  
pp. 43-49 ◽  
Author(s):  
I. Oberlé ◽  
G. Camerino ◽  
C. Kloepfer ◽  
J. P. Moisan ◽  
K. H. Grzeschik ◽  
...  
Keyword(s):  
Somatic Cell ◽  
X Chromosome ◽  
Regional Mapping ◽  
Somatic Cell Hybrids ◽  
Cell Hybrids

X-linked CNV and skewed X-chromosome inactivation

2020 ◽  
pp. 19-21
Author(s):  
Е.А. Фонова ◽  
Е.Н. Толмачева ◽  
А.А. Кашеварова ◽  
М.Е. Лопаткина ◽  
К.А. Павлова ◽  
...  
Keyword(s):  
Cell Proliferation ◽  
Intellectual Disability ◽  
X Chromosome ◽  
Copy Number ◽  
Copy Number Variations ◽  
X Chromosome Inactivation ◽  
Chromosome Inactivation ◽  
Chromosome X ◽  
Skewed X Chromosome Inactivation

Смещение инактивации Х-хромосомы может быть следствием и маркером нарушения клеточной пролиферации при вариациях числа копий ДНК на Х-хромосоме. Х-сцепленные CNV выявляются как у женщин с невынашиванием беременности и смещением инактивации Х-хромосомы (с частотой 33,3%), так и у пациентов с умственной отсталостью и смещением инактивацией у их матерей (с частотой 40%). A skewed X-chromosome inactivation can be a consequence and a marker of impaired cell proliferation in the presence of copy number variations (CNV) on the X chromosome. X-linked CNVs are detected in women with miscarriages and a skewed X-chromosome inactivation (with a frequency of 33.3%), as well as in patients with intellectual disability and skewed X-chromosome inactivation in their mothers (with a frequency of 40%).

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