Human Developmental Biology Resource (HDBR)

News & Publications

NEW PUBLICATION: 5-hydroxymethylcytosine is highly dynamic across human fetal brain development

5-hydroxymethylcytosine is highly dynamic across human fetal brain development - Read more

October 11, 2017

NEW PUBLICATION: A genomic atlas of human adrenal and gonad development.

A genomic atlas of human adrenal and gonad development. - Read more

October 11, 2017

NEW PUBLICATION: Neurexins 1-3 Each Have a Distinct Pattern of Expression in the Early Developing Human Cerebral Cortex.

Neurexins 1-3 Each Have a Distinct Pattern of Expression in the Early Developing Human Cerebral Cortex. - Read more

October 11, 2017

New variant and expression studies provide further insight into the genotype-phenotype correlation in YAP1-related developmental eye disorders

New variant and expression studies provide further insight into the genotype-phenotype correlation in YAP1-related developmental eye disorders - Read more

August 11, 2017

Left-Right Asymmetry of Maturation Rates in Human Embryonic Neural Development.

Left-Right Asymmetry of Maturation Rates in Human Embryonic Neural Development. - Read more

July 25, 2017

Fgf8 Expression and Degradation of Retinoic Acid Are Required for Patterning a High-Acuity Area in the Retina

Fgf8 Expression and Degradation of Retinoic Acid Are Required for Patterning a High-Acuity Area in the Retina - Read more

July 10, 2017

Neurodevelopmental protein Musashi-1 interacts with the Zika genome and promotes viral replication

Neurodevelopmental protein Musashi-1 interacts with the Zika genome and promotes viral replication - Read more

July 7, 2017

Kisspeptin is a novel regulator of human fetal adrenocortical development and function a finding with important implications for the human feto-placental unit

Kisspeptin is a novel regulator of human fetal adrenocortical development and function – a finding with important implications for the human feto-placental unit
  - Read more

June 21, 2017

Integrated genome and transcriptome sequencing identifies a noncoding mutation in the genome replication factor DONSON as the cause of microcephaly-micromelia syndrome.

Integrated genome and transcriptome sequencing identifies a noncoding mutation in the genome replication factor DONSON as the cause of microcephaly-micromelia syndrome. - Read more

June 19, 2017

Distinct cortical and sub-cortical neurogenic domains for GABAergic interneuron precursor transcription factors NKX2.1, OLIG2

Distinct cortical and sub-cortical neurogenic domainsfor GABAergic interneuron precursor transcription factorsNKX2.1, OLIG2 - Read more

March 16, 2017

← back   1 2 3   next →