Pages that link to "Q68166997"
Jump to navigation
Jump to search
The following pages link to A molecular genetic linkage map of mouse chromosome 7 (Q68166997):
Displayed 50 items.
- The mouse alpha 1(XII) and human alpha 1(XII)-like collagen genes are localized on mouse chromosome 9 and human chromosome 6 (Q24294442) (← links)
- Identification of a putative gamma-aminobutyric acid (GABA) receptor subunit rho2 cDNA and colocalization of the genes encoding rho2 (GABRR2) and rho1 (GABRR1) to human chromosome 6q14-q21 and mouse chromosome 4 (Q24336310) (← links)
- Linking yeast genetics to mammalian genomes: identification and mapping of the human homolog of CDC27 via the expressed sequence tag (EST) data base (Q24564533) (← links)
- The human homolog of a mouse-imprinted gene, Peg3, maps to a zinc finger gene-rich region of human chromosome 19q13.4 (Q24628692) (← links)
- A linkage map of mouse chromosome 19: definition of comparative mapping relationships with human chromosomes 10 and 11 including the MEN1 locus (Q28183783) (← links)
- Chromosomal mapping of the human (MACS) and mouse (Macs) genes encoding the MARCKS protein (Q30997753) (← links)
- Characterization of the human kallikrein locus (Q31172280) (← links)
- Identification of a novel transforming growth factor-beta (TGF-beta6) gene in fish: regulation in skeletal muscle by nutritional state (Q33575668) (← links)
- Molecular analysis of radiation-induced albino (c)-locus mutations that cause death at preimplantation stages of development (Q33962014) (← links)
- Epistatic control of non-Mendelian inheritance in mouse interspecific crosses (Q33968160) (← links)
- Glycogen synthase: a putative locus for diet-induced hyperglycemia. (Q34235447) (← links)
- Localization of insulin-2 (Ins-2) and the obesity mutant tubby (tub) to distinct regions of mouse chromosome 7. (Q34244874) (← links)
- Chromosomal localization of the gene encoding the human DNA helicase RECQL and its mouse homologue (Q34299699) (← links)
- Mapping of the calcium-sensing receptor gene (CASR) to human chromosome 3q13.3-21 by fluorescence in situ hybridization, and localization to rat chromosome 11 and mouse chromosome 16. (Q34374794) (← links)
- Location of the DBP transcription factor gene in human and mouse (Q34406144) (← links)
- Comparative map for mice and humans (Q35364327) (← links)
- Mouse chromosome 7. (Q35675706) (← links)
- Mouse chromosome 17. (Q35675786) (← links)
- The role of nitric oxide in the pathogenesis of spontaneous murine autoimmune disease: increased nitric oxide production and nitric oxide synthase expression in MRL-lpr/lpr mice, and reduction of spontaneous glomerulonephritis and arthritis by orall (Q36362801) (← links)
- Cloning, structural analysis and mapping of the mouse selenocysteine tRNA([Ser]Sec) gene (Trsp). (Q36682358) (← links)
- Cloning and chromosomal mapping of the mouse Mgat3 gene encoding N-acetylglucosaminyltransferase III (Q36685113) (← links)
- Zinc finger protein genes in the mouse genome (Q36986691) (← links)
- Mouse map of paralogous genes (Q36999136) (← links)
- Antisense transcription of the myotonic dystrophy locus yields low-abundant RNAs with and without (CAG)n repeat. (Q39012706) (← links)
- The Genetic Basis of Autoimmune Disease in MRL-lpr/lpr Mice (Q40393393) (← links)
- Anchored reference loci for comparative genome mapping in mammals. (Q40910230) (← links)
- Allele-specific replication timing of imprinted gene regions (Q41541045) (← links)
- Mouse chromosome 17. (Q44324711) (← links)
- A proximal mouse chromosome 9 linkage map that further defines linkage groups homologous with segments of human chromosomes 11, 15, and 19 (Q44586822) (← links)
- Organization and chromosomal locations of Rap1a/Krev sequences in the mouse. (Q45911280) (← links)
- Genomic organisation of rainbow trout, Oncorhynchus mykiss TGF-beta (Q47967676) (← links)
- Murine serotonin transporter: sequence and localization to chromosome 11. (Q48137908) (← links)
- Characterization of murine carcinoembryonic antigen gene family members (Q48191059) (← links)
- Physical analysis of murine albino deletions that disrupt liver-specific gene regulation or mesoderm development (Q52233987) (← links)
- Mapping of recombinant retrovirus integration sites that cause expression of the viral genome in murine embryonal carcinoma cells (Q54279099) (← links)
- Genetic mapping of the ?-arrestin 1 and 2 genes on mouse Chromosomes 7 and 11 respectively (Q57186323) (← links)
- Chromosomal mapping of the high affinity Fc gamma receptor gene (Q62394150) (← links)
- Genomic mapping within the albino-deletion complex using individual early postimplantation mouse embryos (Q63951741) (← links)
- Mapping of the mouse Rxr loci encoding nuclear retinoid X receptors RXR alpha, RXR beta, and RXR gamma (Q67522993) (← links)
- Genetic mapping of the integrin alpha 1 gene (Vla1) to mouse chromosome 13 (Q67577186) (← links)
- Linkage analysis demonstrates that the Timp-2 locus is on mouse chromosome 11 (Q67577242) (← links)
- Comparative map for mice and humans (Q67871559) (← links)
- Mouse chromosome 7 (Q67871563) (← links)
- A linkage map of mouse chromosome 8: Further definition of homologous linkage relationships between mouse chromosome 8 and human chromosomes 8, 16, and 19 (Q68302487) (← links)
- Molecular genetic linkage maps of mouse chromosomes 4 and 6 (Q68329378) (← links)
- Mapping genes encoding drug-metabolizing enzymes in recombinant inbred mice (Q68329754) (← links)
- The functional genes for protein synthesis initiation factor 4AI and 4AII map to mouse chromosomes 11 and 16 (Q70576513) (← links)
- An anchored molecular map of mouse chromosome 6 with an analysis of interference (Q70903951) (← links)
- Mapping of the genes for four members of the transmembrane 4 superfamily: mouse Cd9, Cd63, Cd81, and Cd82 (Q71819466) (← links)
- The gene encoding the mouse serum amyloid A protein, apo-SAA5, maps to proximal chromosome 7 (Q71867342) (← links)