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The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association
|
November 16, 2006
The craniofacial phenotype of the Crouzon mouse: analysis of a model for syndromic craniosynostosis using three-dimensional MicroCT
Chad A Perlyn, Valerie B DeLeon, Christian Babbs, et al.
Genome Biology
|
April 3, 2016
Predicting the three-dimensional folding of cis-regulatory regions in mammalian genomes using bioinformatic data and polymer models
Chris A Brackley, Jill M Brown, Dominic Waithe, et al.
Human Genetics
|
June 15, 2007
A new locus for split hand/foot malformation with long bone deficiency (SHFLD) at 2q14.2 identified from a chromosome translocation
Christian Babbs, Raoul Heller, David B Everman, et al.
Rheumatology (Oxford, England)
|
August 5, 2019
Majeed syndrome: description of a novel mutation and therapeutic response to bisphosphonates and IL-1 blockade with anakinra
Noémi B A Roy, Ahmad I Zaal, Georgina Hall, et al.
Human Mutation
|
May 5, 2011
Duplication of the EFNB1 gene in familial hypertelorism: imbalance in ephrin-B1 expression and abnormal phenotypes in humans and mice
Christian Babbs, Helen S Stewart, Louise J Williams, et al.
Journal of Clinical Medicine
|
January 28, 2026
Using Patient Feedback to Improve Treatment Outcomes for Patients with Congenital Dyserythropoietic Anaemia Type I Receiving Interferon Therapy
Karl Frey, Sanja Brolih, Caroline Scott, et al.
Cell
|
December 15, 2023
Super-enhancers include classical enhancers and facilitators to fully activate gene expression
Joseph W Blayney, Helena Francis, Alexandra Rampasekova, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists
|
December 17, 2008
Skeletal analysis of the Fgfr3(P244R) mouse, a genetic model for the Muenke craniosynostosis syndrome
Stephen R F Twigg, Chris Healy, Christian Babbs, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 29, 2004
Mutations of ephrin-B1 (EFNB1), a marker of tissue boundary formation, cause craniofrontonasal syndrome
Stephen R F Twigg, Rui Kan, Christian Babbs, et al.
Plos One
|
January 7, 2022
Scalable in vitro production of defined mouse erythroblasts
Helena S Francis, Caroline L Harold, Robert A Beagrie, et al.
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of 5
Search research articles
Search
Showing results (11-20 of 47) with videos related to
Sort By:
Page
of 5
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association
|
November 16, 2006
The craniofacial phenotype of the Crouzon mouse: analysis of a model for syndromic craniosynostosis using three-dimensional MicroCT
Chad A Perlyn, Valerie B DeLeon, Christian Babbs, et al.
Genome Biology
|
April 3, 2016
Predicting the three-dimensional folding of cis-regulatory regions in mammalian genomes using bioinformatic data and polymer models
Chris A Brackley, Jill M Brown, Dominic Waithe, et al.
Human Genetics
|
June 15, 2007
A new locus for split hand/foot malformation with long bone deficiency (SHFLD) at 2q14.2 identified from a chromosome translocation
Christian Babbs, Raoul Heller, David B Everman, et al.
Rheumatology (Oxford, England)
|
August 5, 2019
Majeed syndrome: description of a novel mutation and therapeutic response to bisphosphonates and IL-1 blockade with anakinra
Noémi B A Roy, Ahmad I Zaal, Georgina Hall, et al.
Human Mutation
|
May 5, 2011
Duplication of the EFNB1 gene in familial hypertelorism: imbalance in ephrin-B1 expression and abnormal phenotypes in humans and mice
Christian Babbs, Helen S Stewart, Louise J Williams, et al.
Journal of Clinical Medicine
|
January 28, 2026
Using Patient Feedback to Improve Treatment Outcomes for Patients with Congenital Dyserythropoietic Anaemia Type I Receiving Interferon Therapy
Karl Frey, Sanja Brolih, Caroline Scott, et al.
Cell
|
December 15, 2023
Super-enhancers include classical enhancers and facilitators to fully activate gene expression
Joseph W Blayney, Helena Francis, Alexandra Rampasekova, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists
|
December 17, 2008
Skeletal analysis of the Fgfr3(P244R) mouse, a genetic model for the Muenke craniosynostosis syndrome
Stephen R F Twigg, Chris Healy, Christian Babbs, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 29, 2004
Mutations of ephrin-B1 (EFNB1), a marker of tissue boundary formation, cause craniofrontonasal syndrome
Stephen R F Twigg, Rui Kan, Christian Babbs, et al.
Plos One
|
January 7, 2022
Scalable in vitro production of defined mouse erythroblasts
Helena S Francis, Caroline L Harold, Robert A Beagrie, et al.
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of 5