Did nucleotides or amino acids drive evolutionary conservation of the WT1 ± KTS alternative splice?

By Davies Rachel C.   Bratt Eva   Hastie Nicholas D.  

Human Molecular Genetics, Vol. 9, Iss. 8, 2000-05 ,pp. : 1177-1183

Oxford University Press

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Biochemical and functional interaction between ZNF224 and ZNF255, two members of the Krppel-like zinc-finger protein family and WT1 protein isoforms

By Florio Francesca   Cesaro Elena   Montano Giorgia   Izzo Paola   Miles Colin   Costanzo Paola  

Human Molecular Genetics, Vol. 19, Iss. 18, 2010-09 ,pp. : 3544-3556

Oxford University Press

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Alternative Splicing of Exon 14 Determines Nuclear or Cytoplasmic Localisation of FMR1 Protein Isoforms

By Sittler Annie   Devys Didier   Weber Chantal   Mandel Jean-Louis  

Human Molecular Genetics, Vol. 5, Iss. 1, 1996-01 ,pp. : 95-102

Oxford University Press

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A murine model of DenysDrash syndrome reveals novel transcriptional targets of WT1 in podocytes

By Ratelade Julien   Arrondel Christelle   Hamard Ghislaine   Garbay Serge   Harvey Scott   Biebuyck Nathalie   Schulz Herbert   Hastie Nick   Pontoglio Marco   Gubler Marie-Claire   Antignac Corinne   Heidet Laurence  

Human Molecular Genetics, Vol. 19, Iss. 1, 2010-01 ,pp. : 1-15

Oxford University Press

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WT1 Haploinsufficiency Supports Milder Renal Manifestation in Two Patients with Denys-Drash Syndrome

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Sexual Development, Vol. 11, Iss. 1, 2017-01 ,pp. : 34-39

Karger

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