Partial transcriptome of the developing pituitary gland

Genomics

Volumn 70, Issue 3, 2000, Pages 335-346

  Douglas, Kristin R ^a   Camper, Sally A ^a  

^a UNIVERSITY OF MICHIGAN MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

HORMONE; TRANSCRIPTION FACTOR;

ADENOHYPOPHYSIS; ANIMAL CELL; ANIMAL TISSUE; ARTICLE; CELL DIFFERENTIATION; CELL PROLIFERATION; CELL SPECIFICITY; CONTROLLED STUDY; EMBRYO; GENETIC TRANSCRIPTION; MOUSE; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; TISSUE DISTRIBUTION; TRANSCRIPTION REGULATION;

EID: 0034671096     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.2000.6400     Document Type: Article

References (56)

1. An α-subunit-secreting cell line derived from a mouse thyrotrope tumor
2. Gapped BLAST and PSI-BLAST: A new generation of protein database search programs
3. Structure of the murine rab3A gene: Correlation of genomic organization with antibody epitopes
4. Normalization and subtraction: Two approaches to facilitate gene discovery
5. Chromosomal localization of murine and human oligodendrocyte-specific protein genes
6. Involvement of OSP/claudin-11 in oligodendrocyte membrane interactions: Role in biology and disease
7. Genealogy of the anterior pituitary gland: Tracing a family tree
8. The Pit-1 transcription factor gene is a candidate for the Snell dwarf mutation
9. The PROP1 2-base pair deletion is a common cause of combined pituitary hormone deficiency
10. Synaptotagrain V: A novel synaptotagmin isoform expressed in rat brain
11. Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse
12. The molecular basis for developmental disorders of the pituitary gland in man
13. Human Prop-1: Cloning, mapping, genomic structure
14. Phenotypic variability in familial combined pituitary hormone deficiency caused by a PROP1 gene mutation resulting in the substitution of Arg → Cys at codon 120 (R120C)*
15. The Ames dwarf gene, df, is required early in pituitary ontogeny for the extinction of Rpx transcription and initiation of lineage specific cell proliferation
16. Dosage requirement of Pitx2 for development of multiple organs
17. Two distinct intracellular pathways transport secretory and membrane glycoproteins to the surface of pituitary tumor cells
18. Differential expression of putative transbilayer amphipath transporters
19. Rpx: A novel anterior-restricted homeobox gene progressively activated in the prechordal plate, anterior neural plate, and Rathke's pouch of the mouse embryo
20. Developmental changes in proliferative activity of cells of the murine Rathke's pouch
21. Amphiphysin (Amph) maps to the proximal region of mouse chromosome 13
22. A molecular genetic linkage map of mouse chromosome 18 reveals extensive linkage conservation with human chromosomes 5 and 18
23. Identification of a set of genes with developmentally down-regulated expression in the mouse brain
24. Isolation and sequence of a cDNA clone that maps at the mouse c-albino locus
25. Murine CASK is disrupted in a sex-linked cleft palate mouse mutant
26. GHF-1 promotertargeted immortalization of a somatotropic progenitor cell results in dwarfism in transgenic mice
27. Dwarf locus mutants lacking three pituitary cell types result from mutations in the POU-domain gene Pit-1
28. Distribution and cloning of eukaryotic mRNAs by means of differential display: Refinements and optimization
29. Analysis of altered gene expression by differential display
30. Differential display of eukaryotic messenger RNA by means of the polymerase chain reaction
31. An encyclopedia of mouse genes
32. A first-generation whole genome-radiation hybrid map spanning the mouse genome
33. Chromosomal mapping of the potassium channel genes Kcnq2 and Kcnq3 in mouse
34. Longitudinal hormonal and pituitary imaging changes in two females with combined pituitary hormone deficiency due to deletion of A301,G302 in the PROP1 gene
35. Improvements to the differential display method for gene analysis
36. KQT2, a new putative potasslum channel family produced by alternative splicing. Isolation, genomic structure, and alternative splicing of the putative potassium channels
37. Mutations in LHX3 result in a new syndrome revealed by combined pituitary hormone deficiency
38. Glucose induced genes in bovine aortic smooth muscle cells identified by mRNA differential display
39. Impaired adrenocorticotropin-adrenal axis in combined pituitary hormone deficiency caused by a two-base pair deletion (301-302delAG) in the prophet of Pit-1 gene
40. Pit-1: Clinical aspects
41. Clinical and biochemical phenotype of familial anterior hypopituitarism from mutation of the PROP1 gene
42. The mouse homeoprotein mLIM-3 is expressed early in cells derived from the neuroepithelium and persists in adult pituitary
43. Specification of pituitary cell lineages by the LIM homeobox gene Lhx3
44. Pituitary lineage determination by the Prophet of Pit-1 homeodomain factor defective in Ames dwarfism
45. Molecular cloning of five messenger RNAs differentially expressed in preneoplastic or neoplastic JB6 mouse epidermal cells: One is homologous to human tissue inhibitor of metalloproteinases-3
46. A ribonucleotide reductase gene involved in a p53-dependent cell-cycle checkpoint for DNA damage
47. Clonal strains of hormone-producing pituitary cells
48. Establishment of clonal strains of rat pituitary tumor cells that secrete growth hormone
49. Radiation hybrid map of the mouse genome
50. Identification, characterization, and mapping of a mouse homolog of the gene mutated in Nijmegen breakage syndrome
51. How many homeobox genes does it take to make a pituitary gland?
52. The amphiphysin family of proteins and their role in endocytosis at the synapse
53. Mouse chromosome 7
54. Cell lines of the pituitary gonadotrope lineage derived by targeted oncogenesis in transgenic mice
55. Mutations in PROP1 cause familial combined pituitary hormone deficiency
56. The gene encoding PRBP, the mouse homolog of human TRBP, maps to distal chromosome 15