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Hunter Genetics

As seen in: Frontiers
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Articles by Hunter Genetics

Epigenetic Equilibrium in Chromatinopathies: Network Instability in Neurodevelopment

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By Hunter Genetics
| Frontiers
Abstract Background: Chromatin-modifying systems regulate transcriptional programs essential for human neurodevelopment through dynamic modification of histones, DNA, and higher-order chromatin architecture.
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A mainstreaming oncogenomics model: improving the identification of Lynch syndrome

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By Hunter Genetics, Alanna Kulchak, Gad Rennert, Mujeeb Z. Banday
| Frontiers
Rosie O’Shea1*, Ashley Crook2†, Chris Jacobs2†, Maira Kentwell3,4†, Margaret Gleeson5†, Katherine M. Tucker6†, Heather Hampel7†, Alanna Kulchak Rahm8†, Natalie Taylor1,9†, Sarah Lewis1† and Nicole M.
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PRDM1 DNA-binding zinc finger domain is required for normal limb development and is disrupted in split hand/foot malformation

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By Hunter Genetics, Brittany Truong, Lomeli Shull, Ezra Lencer
| The Company of Biologists
Keywords: Pectoral fin, Limb, PRDM1, Split hand/foot malformation, Zebrafish Vertebrate limb development is controlled by a complex gene regulatory network (GRN) governed by signaling pathways, transcription factors and epigenetic modifiers. Limb growth begins at the lateral plate mesoderm, where mesenchyme precursors form a small bud surrounded by an ectodermal layer.
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Hemiscrotal agenesis with complete testicular descent in Van der Woude syndrome: a new phenotypic feature

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By Paediatric Orthopaedic Surgery, Dilharan D Eliezer, Himanshu Goel, Hunter Genetics
| bmj.com
Hemiscrotal agenesis with complete testicular descent in Van der Woude syndrome: a new phenotypic feature Dilharan D Eliezer1,2, Himanshu Goel2,3, Virginia M Turner4 and Aniruddh Deshpande1,2,5 1 Paediatric Surgery, John Hunter Children’s Hospital, New Lambton Heights, New South Wales, Australia 2 Medicine and Public Health, University of Newcastle, Callaghan, New South Wales, Australia 3 Hunter Genetics, Waratah, Australia 4 Paediatric Medicine, John Hunter Children’s Hospital, New Lambton...
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