Lista de obras - Jennifer L Fish - Dominio Público Uruguay

Aspm specifically maintains symmetric proliferative divisions of neuroepithelial cells

artículo científico publicado en 2006

Assessing species-specific contributions to craniofacial development using quail-duck chimeras

artículo científico publicado en 2014

Bone health and SATB2-associated syndrome.

artículo científico publicado en 2017

Craniofacial modularity, character analysis, and the evolution of the premaxilla in early African hominins.

artículo científico publicado en 2014

Developmental mechanisms underlying variation in craniofacial disease and evolution.

artículo científico

Developmental nonlinearity drives phenotypic robustness.

artículo científico publicado en 2017

Developmental processes regulate craniofacial variation in disease and evolution

artículo científico publicado en 2018

Dietary constraints on encephalization in primates

artículo científico publicado en 2003

Discovery of a major D-loop replication origin reveals two modes of human mtDNA synthesis

artículo científico publicado en 2004

Evolution of the Alx homeobox gene family: parallel retention and independent loss of the vertebrate Alx3 gene.

artículo científico

Fgf8 dosage determines midfacial integration and polarity within the nasal and optic capsules

artículo científico publicado en 2012

Further supporting evidence for theSATB2-associated syndrome found through whole exome sequencing

scientific article published on 01 May 2015

Genotype and phenotype in 12 additional individuals with SATB2-associated syndrome

artículo científico publicado en 2017

Left-right asymmetry of the gnathostome skull: its evolutionary, developmental, and functional aspects

artículo científico publicado en 2014

Making bigger brains-the evolution of neural-progenitor-cell division.

artículo científico publicado en 2008

Multiple developmental mechanisms regulate species-specific jaw size.

scientific article published on February 2014

Mutation update for the SATB2 gene

article

Mutations in mouse Aspm (abnormal spindle-like microcephaly associated) cause not only microcephaly but also major defects in the germline

scientific journal article

OSVZ progenitors of human and ferret neocortex are epithelial-like and expand by integrin signaling

artículo científico publicado en 2010

Pattern and polarity in the development and evolution of the gnathostome jaw: both conservation and heterotopy in the branchial arches of the shark, Scyliorhinus canicula.

artículo científico publicado en 2013

Pax6 regulates craniofacial form through its control of an essential cephalic ectodermal patterning center.

artículo científico publicado en 2011

SATB2-Associated Syndrome

artículo científico publicado en 2017

SATB2-associated syndrome: Mechanisms, phenotype, and practical recommendations.

artículo científico publicado en 2016

Satb2 regulates proliferation and nuclear integrity of pre-osteoblasts

scientific article published on 17 July 2019

Satb2, modularity, and the evolvability of the vertebrate jaw.

artículo científico publicado en 2011

Strikingly higher frequency in centenarians and twins of mtDNA mutation causing remodeling of replication origin in leukocytes

artículo científico publicado en 2003

Tfap2a-dependent changes in mouse facial morphology result in clefting that can be ameliorated by a reduction in Fgf8 gene dosage.

artículo científico publicado en 2014

The society for craniofacial genetics and developmental biology 39th annual meeting.

artículo científico publicado en 2017

miR-302 Is Required for Timing of Neural Differentiation, Neural Tube Closure, and Embryonic Viability

artículo científico publicado en 2015

Lista de obras de Jennifer L Fish

Aspm specifically maintains symmetric proliferative divisions of neuroepithelial cells

Assessing species-specific contributions to craniofacial development using quail-duck chimeras

Bone health and SATB2-associated syndrome.

Craniofacial modularity, character analysis, and the evolution of the premaxilla in early African hominins.

Developmental mechanisms underlying variation in craniofacial disease and evolution.

Developmental nonlinearity drives phenotypic robustness.

Developmental processes regulate craniofacial variation in disease and evolution

Dietary constraints on encephalization in primates

Discovery of a major D-loop replication origin reveals two modes of human mtDNA synthesis

Evolution of the Alx homeobox gene family: parallel retention and independent loss of the vertebrate Alx3 gene.

Fgf8 dosage determines midfacial integration and polarity within the nasal and optic capsules

Further supporting evidence for theSATB2-associated syndrome found through whole exome sequencing

Genotype and phenotype in 12 additional individuals with SATB2-associated syndrome

Left-right asymmetry of the gnathostome skull: its evolutionary, developmental, and functional aspects

Making bigger brains-the evolution of neural-progenitor-cell division.

Multiple developmental mechanisms regulate species-specific jaw size.

Mutation update for the SATB2 gene

Mutations in mouse Aspm (abnormal spindle-like microcephaly associated) cause not only microcephaly but also major defects in the germline

OSVZ progenitors of human and ferret neocortex are epithelial-like and expand by integrin signaling

Pattern and polarity in the development and evolution of the gnathostome jaw: both conservation and heterotopy in the branchial arches of the shark, Scyliorhinus canicula.

Pax6 regulates craniofacial form through its control of an essential cephalic ectodermal patterning center.

SATB2-Associated Syndrome

SATB2-associated syndrome: Mechanisms, phenotype, and practical recommendations.

Satb2 regulates proliferation and nuclear integrity of pre-osteoblasts

Satb2, modularity, and the evolvability of the vertebrate jaw.

Strikingly higher frequency in centenarians and twins of mtDNA mutation causing remodeling of replication origin in leukocytes

Tfap2a-dependent changes in mouse facial morphology result in clefting that can be ameliorated by a reduction in Fgf8 gene dosage.

The society for craniofacial genetics and developmental biology 39th annual meeting.

miR-302 Is Required for Timing of Neural Differentiation, Neural Tube Closure, and Embryonic Viability