Pages that link to "Q45134122"
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The following pages link to Cytogenetics and Cell Genetics (Q45134122):
Displaying 50 items.
- Cytogenetics and Genome Research (Q1524623) (← links)
- Characterisation and mapping of the human SOX14 gene (Q22008737) (← links)
- VPREB3: cDNA characterization and expression in human and chromosome mapping in human and mouse (Q22253282) (← links)
- HMG20A and HMG20B map to human chromosomes 15q24 and 19p13.3 and constitute a distinct class of HMG-box genes with ubiquitous expression (Q22253936) (← links)
- Human secretin (SCT): gene structure, chromosome location, and distribution of mRNA (Q24290473) (← links)
- Human prostate-specific antigen (APS) is a member of the glandular kallikrein gene family at 19q13 (Q24294222) (← links)
- Assignment of C0X6A1 to 6p21 and a pseudogene (C0X6A1P) to 1p31.1 by in situ hybridization and somatic cell hybrids (Q24309125) (← links)
- cDNA cloning, expression and chromosome mapping of the human STAT4 gene: both STAT4 and STAT1 genes are mapped to 2q32.2→q32.3 (Q24309161) (← links)
- Chromosomal assignment of the heparin-binding cytokine genes MDK and PTN in mouse and man (Q24311346) (← links)
- Assignment of the human alpha-tropomyosin gene TPM4 to band 19p13.1 by fluorescence in situ hybridization (Q24313577) (← links)
- Cloning, expression, and mapping of UBE2I, a novel gene encoding a human homologue of yeast ubiquitin-conjugating enzymes which are critical for regulating the cell cycle (Q24317480) (← links)
- Isolation and mapping of a human gene (PDCD2) that is highly homologous to Rp8, a rat gene associated with programmed cell death (Q24318299) (← links)
- Assignment of the human beta tropomyosin gene (TPM2) to band 9p13 by fluorescence in situ hybridisation (Q24318347) (← links)
- Genomic organization and chromosomal localization of the interphotoreceptor matrix proteoglycan-1 (IMPG1) gene: a candidate for 6q-linked retinopathies (Q24321098) (← links)
- A mammalian homologue of Drosophila heterochromatin protein 1 (HP1) is a component of constitutive heterochromatin (Q24328832) (← links)
- Isolation, characterization and chromosomal assignment of human colligin-2 gene (CBP2) (Q24336324) (← links)
- cDNA cloning, characterization, and chromosome mapping of UBE2E2 encoding a human ubiquitin-conjugating E2 enzyme (Q24336811) (← links)
- Cytogenetics (Q27710588) (← links)
- Cloning and chromosome assignment to 1q32 of a human cDNA (RAB7L1) encoding a small GTP-binding protein, a member of the RAS superfamily (Q28116201) (← links)
- Molecular cloning, expression, and chromosomal localization of a ubiquitously expressed human 6-phosphofructo-2-kinase/ fructose-2, 6-bisphosphatase gene (PFKFB3) (Q28138539) (← links)
- Characterization of the human laminin beta2 chain locus (LAMB2): linkage to a gene containing a nonprocessed, transcribed LAMB2-like pseudogene (LAMB2L) and to the gene encoding glutaminyl tRNA synthetase (QARS) (Q28138721) (← links)
- Comparative cytogenetic mapping of COL14A1, the gene for human and mouse collagen XIV (Q28138742) (← links)
- Assignment1 of the PTP-SL/PTPBR7 gene (Ptprr/PTPRR) to mouse chromosome region 8A2 by in situ hybridization (Q28138772) (← links)
- Refined physical mapping and genomic structure of the EXTL1 gene (Q28138787) (← links)
- Assignment of the 160-kDa subunit of cleavage and polyadenylation specificity factor (CPSF1) to human chromosome 8q24.23 by radiation hybrid mapping (Q28140764) (← links)
- The small GTPase RAC3 gene is located within chromosome band 17q25.3 outside and telomeric of a region commonly deleted in breast and ovarian tumours (Q28140798) (← links)
- Assignment of a novel bifurcated SET domain gene, SETDB1, to human chromosome band 1q21 by in situ hybridization and radiation hybrids (Q28144658) (← links)
- Assignment of the L11 ribosomal protein gene (RPL11) to human chromosome 1p36.1-->p35 by in situ hybridization (Q28144675) (← links)
- Assignment of the calcium-binding mitochondrial carrier Aralar1 gene (SLC25A12) to human chromosome band 2q31 by in situ hybridization (Q28144911) (← links)
- Assignment of the human zinc finger gene, ZNF288, to chromosome 3 band q13.2 by radiation hybrid mapping and fluorescence in situ hybridisation (Q28144915) (← links)
- Assignment of CDK5R2 coding for the cyclin-dependent kinase 5, regulatory subunit 2 (NCK5AI protein) to human chromosome band 2q35 by fluorescent in situ hybridization (Q28144924) (← links)
- Assignment of the GPR14 gene coding for the G-protein-coupled receptor 14 to human chromosome 17q25.3 by fluorescent in situ hybridization (Q28145285) (← links)
- Assignment of the SLC25A12 gene coding for the human calcium-binding mitochondrial solute carrier protein aralar to human chromosome 2q24 (Q28145838) (← links)
- Mapping of the CCXCR1, CX3CR1, CCBP2 and CCR9 genes to the CCR cluster within the 3p21.3 region of the human genome (Q28145869) (← links)
- Assignment of the human cyclin D3 gene (CCND3) to chromosome 6p----q13 (Q28189049) (← links)
- Elevated DNA sequence diversity in the genomic region of the phosphatase PPP2R3L gene in the human pseudoautosomal region (Q28199972) (← links)
- Assignment of panopsin (OPN3) to human chromosome band 1q43 by in situ hybridization and somatic cell hybrids (Q28204458) (← links)
- Comparative genomic sequencing reveals a strikingly similar architecture of a conserved syntenic region on human chromosome 11p15.3 (including gene ST5) and mouse chromosome 7 (Q28214741) (← links)
- The assignment of PRKCI to bovine chromosome 1q34-->q36 by FISH suggests a new assignment to human chromosome 3 (Q28215973) (← links)
- The human chromosome 19 linkage group FUT1 (H), FUT2 (SE), LE, LU, PEPD, C3, APOC2, D19S7 and D19S9 (Q28237023) (← links)
- Assignment of the gene for human tetranectin (TNA) to chromosome 3p22-->p21.3 by somatic cell hybrid mapping (Q28238470) (← links)
- Assignment of the human TAFII30 gene (TAF2H) to human chromosome band 11p15.3 using somatic cell hybrids (Q28238481) (← links)
- Comparative mapping of the imprinted U2afbpL gene on mouse chromosome 11 and human chromosome 5 (Q28240346) (← links)
- Regional mapping of the gene for autosomal dominant spinocerebellar ataxia (SCA1) by localizing the closely linked D6S89 locus to 6p24.2----p23.05 (Q28244473) (← links)
- Localization of a putative human brain sodium channel gene (SCN1A) to chromosome band 2q24 (Q28246771) (← links)
- Cloning and mapping of a human and mouse gene with homology to ecto-ATPase genes (Q28247322) (← links)
- Assignment of the mouse heme oxygenase genes: heme oxygenase-1 (Hmox1)to chromosome 10 band C1 and heme oxygenase-2 (Hmox2)to chromosome 16 band B1 (Q28247941) (← links)
- Minibrain (MNBH) is a single copy gene mapping to human chromosome 21q22.2 (Q28247952) (← links)
- Assignment of SATB1 to human chromosome band 3p23 by in situ hybridization (Q28247965) (← links)
- Assignment of Death Associated Protein 3 (DAP3) to human chromosome 1q21 by in situ hybridization (Q28247974) (← links)