| P2093 | author name string | Read AP | |
| P2860 | cites work | Crystal structure of a paired domain-DNA complex at 2.5 A resolution reveals structural basis for Pax developmental mutations | Q27730378 |
| | Pax-5 encodes the transcription factor BSAP and is expressed in B lymphocytes, the developing CNS, and adult testis | Q28263987 |
| | Pax-8, a paired domain-containing protein, binds to a sequence overlapping the recognition site of a homeodomain and activates transcription from two thyroid-specific promoters | Q28570171 |
| | Mutation of the PAX2 gene in a family with optic nerve colobomas, renal anomalies and vesicoureteral reflux. | Q34314263 |
| | Fusion of a fork head domain gene to PAX3 in the solid tumour alveolar rhabdomyosarcoma | Q34347334 |
| | Molecular basis of splotch and Waardenburg Pax-3 mutations | Q35191281 |
| | The molecular basis of the undulated/Pax-1 mutation | Q38333435 |
| | Mammalian Pax genes | Q40613979 |
| | PAX genes | Q40628053 |
| | Roles of Pax-genes in developing and adult brain as suggested by expression patterns. | Q48163580 |
| | DNA sequence recognition by Pax proteins: bipartite structure of the paired domain and its binding site. | Q52222420 |
| | Deregulation of Pax-2 expression in transgenic mice generates severe kidney abnormalities. | Q52226238 |
| | Human haploinsufficiency — one for sorrow, two for joy | Q57813416 |
| | Complete block of early B cell differentiation and altered patterning of the posterior midbrain in mice lacking Pax5/BSAP | Q58326934 |
| | PAX genes in human developmental anomalies | Q59662102 |
| | Kidney and retinal defects (Krd), a transgene-induced mutation with a deletion of mouse chromosome 19 that includes the Pax2 locus | Q72462617 |
| P433 | issue | 4 | |
| P304 | page(s) | 333-334 | |
| P577 | publication date | 1995-04-01 | |
| P1433 | published in | Nature Genetics | Q976454 |
| P1476 | title | Pax genes--paired feet in three camps | |
| P478 | volume | 9 | |