Results 191 to 200 of about 5,548 (213)

Mapping of a new RFLP marker RN1 (DXS369) close to the fragile site FRAXA on Xq27–q28

American Journal of Medical Genetics, 1991
AbstractA new polymorphic DNA marker RN1, defining locus DXS369, was recently isolated. Using different somatic cell hybrids, RN1 was mapped between markers 4D‐8 and U6.2. We have narrowed the localization of RN1 to the region between 4D‐8 and FRAXA by genetic mapping in fragile X [fra(X)] families.
B A, Oostra, D F, Majoor-Krakauer, J O, van Hemel, E, Bakker, D F, Callen, M, Schmidt, B A, van Oost   +6 more
openaire   +2 more sources

[Localization of PTH gene on pig chromosome 14q25-q28 by in situ hybridization].

Yi chuan xue bao = Acta genetica Sinica, 1997
The human parathyroid hormone (PTH) genic DNA, as a probe, was labelled with tritium(3H) using nick translation and random oligonucleotide primers methods. Metaphase chromosomal G-bands were prepared from cultured blood lymphocytes of domestic pig. After in situ hybridization and autoradiographly, the number of silver grains on every chromosome was ...
Q, Ji, X, Zhang, Y, Chen
openaire   +1 more source

Evi-1 expression in leukemic patients with rearrangements of the 3q25-q28 chromosomal region.

Leukemia, 1992
The Evi-1 zinc-finger protein gene is normally not expressed in hematopoietic cells. However, high Evi-1 mRNA expression has been reported in mouse myeloblastic leukemias, due to transcriptional activation by proviral integration in either the Fim-3 or Evi-1 loci. The human Evi-1 gene is located on chromosome 3q24-q28.
S, Fichelson, F, Dreyfus, R, Berger, J, Melle, C, Bastard, J M, Miclea, S, Gisselbrecht   +6 more
openaire   +1 more source

Characterization of a deletion at Xq27-q28 associated with unbalanced inactivation of the nonmutant X chromosome.

American journal of human genetics, 1992
We report the results of studies on the characterization of the mutation associated with marked unbalanced expression of the mutant X chromosome in a karyotypically normal girl with Hunter disease (mucopolysaccharidosis type II). Southern analysis of DNA extracted from somatic cell hybrids containing only the mutant X chromosome showed deletion of the ...
J T, Clarke, P J, Wilson, C P, Morris, J J, Hopwood, R I, Richards, G R, Sutherland, P N, Ray   +6 more
openaire   +1 more source

MPEC 2024-Q28 : DAILY ORBIT UPDATE (2024 August 21)

The Minor Planet Electronic Circulars contain information on unusual minor planets, routine data on comets and natural satellites, and occasional editorial announcements. They are published on behalf of Division F of the International Astronomical Union by the Minor Planet Center, Smithsonian Astrophysical Observatory, Cambridge, MA 02138, U.S.A.
openaire   +1 more source

Dinucleotide repeat polymorphism close to IDS gene in Xq27.3–q28 (DXS1113)

Human Molecular Genetics, 1993
C, Weber, C, Oudet, S, Johnson, G, Pilia, D, Schlessinger, A, Hanauer   +5 more
openaire   +2 more sources

An exotic presentation of Q28

Algebraic and Geometric Topology, 2021
Tomasz Popiel
exaly  

A familial analysis of two brothers with azoospermia caused by maternal 46,Y, t(X; 1) (q28; q21) chromosomal abnormality

Andrologia, 2021
Yuanzhi Xie
exaly  

Phenotypic expression of the C282Y/Q283P compound heterozygosity in HFE and molecular modeling of the Q283P mutation effect

Blood Cells, Molecules, and Diseases, 2003
Claude Férec, Gerald le Gac, Jacques Rochette   +2 more
exaly   +2 more sources

T-Cell Prolymphocytic Leukemia With t(X;14)(q28;q11.2): A Clinicopathologic Study of 15 Cases

American Journal of Clinical Pathology, 2023
Deniz Peker, Adan Rios
exaly