Pages that link to "Q35364327"
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The following pages link to Comparative map for mice and humans (Q35364327):
Displaying 50 items.
- Identification of polymorphisms and sequence variants in the human homologue of the mouse natural resistance-associated macrophage protein gene (Q24314240) (← links)
- Isolation of the human genomic brain-2/N-Oct 3 gene (POUF3) and assignment to chromosome 6q16 (Q24317240) (← links)
- The new kallikrein-like gene, KLK-L2. Molecular characterization, mapping, tissue expression, and hormonal regulation (Q28118219) (← links)
- Mapping of the ACTH, MSH, and neural (MC3 and MC4) melanocortin receptors in the mouse and human (Q28239929) (← links)
- Chromosomal localization of seven PAX genes and cloning of a novel family member, PAX-9 (Q28242005) (← links)
- Evolutionary study of multigenic families mapping close to the human MHC class I region (Q28249974) (← links)
- Point mutation of glycine receptor alpha 1 subunit in the spasmodic mouse affects agonist responses (Q28505212) (← links)
- Chromosomal localization of the genes encoding rat CD4, CD8alpha, and CD8beta (Q28507744) (← links)
- Mouse model for Usher syndrome: linkage mapping suggests homology to Usher type I reported at human chromosome 11p15. (Q33756436) (← links)
- Identification of hepatocarcinogen-resistance genes in DBA/2 mice (Q33964289) (← links)
- Murine c-mpl: a member of the hematopoietic growth factor receptor superfamily that transduces a proliferative signal (Q34054413) (← links)
- An animal model for the study of the genetic bases of behaviour in men: the multiple marker strains (MMS). (Q34288895) (← links)
- Ileal lipid-binding protein (Illbp) gene maps to mouse chromosome 11. (Q34321177) (← links)
- The HOX complex neighbored by the EVX gene, as well as two other homeobox-containing genes, the GBX-class and the EN-class, are located on the same chromosomes 2 and 7 in humans (Q34321799) (← links)
- Genetic map of seven polymorphic markers comprising a single linkage group on rat chromosome 5. (Q34321851) (← links)
- Genetic basis of anxiety-like behaviour: a critical review (Q34517497) (← links)
- Genetic susceptibility to chronic periodontal disease (Q34935264) (← links)
- Structural analysis of chromosomal rearrangements associated with the developmental mutations Ph, W19H, and Rw on mouse chromosome 5. (Q35623624) (← links)
- Accelerated tumor development in interferon-treated B6.C-Hyal-1 a mice. (Q36371647) (← links)
- Maps from two interspecific backcross DNA panels available as a community genetic mapping resource (Q36738873) (← links)
- Expression of a novel human homeobox-containing gene that maps to chromosome 7q36.1 in hematopoietic cells (Q36741301) (← links)
- Mouse genes encoding DNA topoisomerase I. (Q36742567) (← links)
- Comparative analysis of the cattle and human genomes: detection of ZOO-FISH and gene mapping-based chromosomal homologies (Q36802708) (← links)
- Two-hit model for sporadic congenital anomalies in mice with the disorganization mutation (Q40529537) (← links)
- Mutagenesis and human genetic disease: an introduction (Q40549882) (← links)
- Anchored reference loci for comparative genome mapping in mammals. (Q40910230) (← links)
- Linkage homology for bronchial hyperresponsiveness between DNA markers on human chromosome 5q31-q33 and mouse chromosome 13. (Q40963150) (← links)
- MMTV-induced mutations in mouse mammary tumors: their potential relevance to human breast cancer (Q41062162) (← links)
- Mouse models for the study of human hair loss (Q41545375) (← links)
- Comparative linkage maps for the mosquitoes, Aedes albopictus and Ae. aegypti, based on common RFLP loci (Q43039906) (← links)
- A Rosetta stone of mammalian genetics (Q47632291) (← links)
- Utility of a C-jun microsatellite marker in determining gene dosage for fatty (fa). (Q47958911) (← links)
- A region of mouse chromosome 16 is syntenic to the DiGeorge, velocardiofacial syndrome minimal critical region (Q48056033) (← links)
- Structure and localization of the IGFBP-1 gene and its expression during liver regeneration (Q48084826) (← links)
- Drawing genetic linkage maps via email (Q48639777) (← links)
- Urogenital syndrome (us): a developmental mutation on chromosome 2 of the mouse. (Q52223399) (← links)
- Homologs of genes and anonymous loci on human chromosome 13 map to mouse chromosomes 8 and 14. (Q55064125) (← links)
- Absence of linkage between the retinoblastoma gene and hts gene in the LEC rat: a model of human Wilson's disease. (Q55378865) (← links)
- Human and rodent genomes: Discrepant patterns of DNA sequence similarity (Q58179555) (← links)
- Striking sequence similarity over almost 100 kilobases of human and mouse T–cell receptor DNA (Q58515580) (← links)
- The genetics of tasting in mice. VII. Glycine revisited, and the chromosomal location of Sac and Soa (Q59765753) (← links)
- Localization of the corticotropin-releasing hormone receptor gene on mouse Chromosome 11 (Q60719548) (← links)
- Corticotropin-releasing hormone (Crh) maps to mouse Chromosome 3 (Q60719566) (← links)
- Lysyl oxidase (Lox) maps between Grl-1 and Adrb-2 on mouse Chromosome 18 (Q60719576) (← links)
- Mapping the midkine family of developmentally regulated signaling molecules (Q63869188) (← links)
- The IL-2 receptor beta chain gene (Il-2rb) is closely linked to the Pdgfb locus on mouse chromosome 15 (Q70681389) (← links)
- Assignment of the rat genes coding for dopa decarboxylase (DDC) and glutamic acid decarboxylases (GAD1 and GAD2) (Q70731822) (← links)
- A putative vulnerability locus to multiple sclerosis maps to 5p14-p12 in a region syntenic to the murine locus Eae2 (Q71230115) (← links)
- Toward a unified genetic map of higher plants, transcending the monocot-dicot divergence (Q71835115) (← links)
- A genetic linkage map of rat chromosome 5 reveals extensive linkage conservation with mouse chromosome 4 (Q72016792) (← links)