Pages that link to "Q71068742"
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The following pages link to Loss of human genetic markers in man--Chinese hamster somatic cell hybrids (Q71068742):
Displaying 50 items.
- A gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motif (Q24301723) (← links)
- Comparison of human ZFY and ZFX transcripts (Q24558774) (← links)
- Assignment of ecto-5'-nucleotidase to human chromosome 6 (Q28281615) (← links)
- Assignment of human ferritin genes to chromosomes 11 and 19q13.3----19qter (Q28305793) (← links)
- Assignment of the genes for thymidine kinase and galactokinase toMus musculus chromosome 11 and the preferential segregation of this chromosome in Chinese hamster/mouse somatic cell hybrids (Q28504629) (← links)
- Somatic cell hybrids, sequence-tagged sites, simple repeat polymorphisms, and yeast artificial chromosomes for physical and genetic mapping of proximal 17p (Q33230917) (← links)
- The human PGM-2 and its chromosomal localization in man-mouse hybrids (Q34401513) (← links)
- Reexpression of the rat hypoxanthine phosphoribosyltransferase gene in rat-human hybrids (Q34733360) (← links)
- Assignment of the T-antigen gene of simian virus 40 to human chromosome C-7 (Q34749469) (← links)
- Cytological mapping of human X-linked genes by use of somatic cell hybrids involving an X-autosome translocation (mouse-hamster-human X-linked markers). (Q34766259) (← links)
- Assignment of the human gene for hexose-1-phosphate uridylyltransferase to chromosome 3. (Q35112332) (← links)
- Microdeletions of chromosome 17p13 as a cause of isolated lissencephaly (Q35195332) (← links)
- Adult and infantile glycogenosis type II in one family, explained by allelic diversity (Q35197662) (← links)
- Mapping DNA sequences in a human X-chromosome deletion which extends across the region of the Duchenne muscular dystrophy mutation (Q35200300) (← links)
- Characterization of beta-D-N-acetylhexosaminidase isoenzymes in man-Chinese hamster somatic cell hybrids (Q35201969) (← links)
- Assignment of the AK1:Np:ABO linkage group to human chromosome 9 (Q35988188) (← links)
- Inducible operation of the erythropoietin 3' enhancer in multiple cell lines: evidence for a widespread oxygen-sensing mechanism (Q36174439) (← links)
- Restoration of the conversion of desmosterol to cholesterol in L-cells after hybridization with human fibroblasts (Q37428406) (← links)
- Human antigen and enzyme markers in man-Chinese hamster somatic cell hybrids: evidence for synteny between the HL-A, PGM3, ME1, and IPO-B loci (Q37435864) (← links)
- Complete structure of the alpha B-crystallin gene: conservation of the exon-intron distribution in the two nonlinked alpha-crystallin genes (Q37530622) (← links)
- Expression of human myeloid-associated surface antigens in human-mouse myeloid cell hybrids (Q37615249) (← links)
- The c-myc oncogene is translocated to the involved chromosome 12 in mouse plasmacytoma (Q37692254) (← links)
- Schizophrenia-associated chromosome 11q21 translocation: identification of flanking markers and development of chromosome 11q fragment hybrids as cloning and mapping resources. (Q38512882) (← links)
- Characterization of whole genome radiation hybrid mapping resources for non-mammalian vertebrates (Q38550997) (← links)
- A first-generation whole genome-radiation hybrid map spanning the mouse genome (Q38554333) (← links)
- A new immunochemical method for the quantitative measurement of specific gene products in man-rodent somatic cell hybrids (Q39523958) (← links)
- Assignment of structural β-galactosidase loci to human chromosomes 3 and 22 (Q39699568) (← links)
- Human lysosomal genes: Arylsulfatase A and ?-Galactosidase (Q39713928) (← links)
- Identification of the myelin protein plasmolipin as the cell entry receptor for Mus caroli endogenous retrovirus. (Q39764047) (← links)
- Reduced glycosylation of human cell lines increases susceptibility to CD4-independent infection by human immunodeficiency virus type 2 (LAV-2/B) (Q39870236) (← links)
- Utilization of somatic cell hybrids for genetic studies in man. (Q39898562) (← links)
- Chromosomally depleted interspecific hybrid cell clones selected with cytotoxic antisera: Utilization in the study of control of murine leukemia virus host-range (Q39980920) (← links)
- Transfer of the human genes coding for thymidine kinase and galactokinase to Chinese hamster cells and human-Chinese hamster cell hybrids (Q40132162) (← links)
- Reexpression of HPRT activity following cell fusion with polyethylene glycol (Q40164061) (← links)
- Localization of a gene for human α-galactosidase B (=N-Acetyl-α-D-Galactosaminidase) on chromosome 22 (Q40197930) (← links)
- Irradiation and fusion gene transfer. (Q40451196) (← links)
- Segregation of rat chromosomes in somatic cell hybrids between rat cells and HT 1080 human fibrosarcoma cells (Q40636853) (← links)
- A hypotetraploid human T lymphoid cell line established by cell fusion (Q40664419) (← links)
- Translocation of oncogene c-sis from chromosome 22 to chromosome 11 in a Ewing sarcoma-derived cell line (Q40665788) (← links)
- Analysis of cis-acting sequences required for operation of the erythropoietin 3' enhancer in different cell lines. (Q40753416) (← links)
- A radiation hybrid map of the rat genome containing 5,255 markers (Q40814016) (← links)
- Characterization of ?-galactosidase isoenzymes in normal and fabry human-Chinese hamster somatic cell hybrids (Q41249708) (← links)
- Characterization of residual hexosaminidase activity in Sandhoff's disease using man-Chinese hamster cell hybrids (Q41354658) (← links)
- Regional localization of aβ-galactosidase locus on human chromosome 22 (Q41360520) (← links)
- A method for constructing radiation hybrid maps of whole genomes (Q41470289) (← links)
- Characterisation of functional domains within the mouse erythropoietin 3' enhancer conveying oxygen-regulated responses in different cell lines (Q41474828) (← links)
- Isolation of DNA markers from a region between incontinentia pigmenti 1 (IP1) X-chromosomal translocation breakpoints by a comparative PCR analysis of a radiation hybrid subclone mapping panel (Q41595610) (← links)
- Chromosome localization and gene synteny of the major histocompatibility complex in the owl monkey, Aotus (Q41611445) (← links)
- Characterization of the central region containing the X-inactivation center and terminal region of the mouse X chromosome using irradiation and fusion gene transfer hybrids (Q41646646) (← links)
- Fabry's disease: the search for a regulator gene mutation in man (Q42040290) (← links)