Search Results | Development | The Company of Biologists

1-20 of 27

Sort by

Sort Order Select

Journal Articles

Diseases of development: leveraging developmental biology to understand human disease

Sally L. Dunwoodie, John B. Wallingford

Development (2020) 147 (21): dev197863.

DOI: https://doi.org/10.1242/dev.197863

Published: 12 November 2020

View article

Journal Articles

Control of skeletal morphogenesis by the Hippo-YAP/TAZ pathway

Hannah K. Vanyai, Fabrice Prin, Oriane Guillermin, Bishara Marzook, Stefan Boeing, Alexander Howson, Rebecca E. Saunders, Thomas Snoeks, Michael Howell, Timothy J. Mohun, Barry Thompson

Development (2020) 147 (21): dev187187.

DOI: https://doi.org/10.1242/dev.187187

Published: 12 November 2020

View article

Includes: Supplementary data

Journal Articles

Challenges and opportunities at the interface of birth defects, human genetics and developmental biology

In collection:

Human development

Mustafa K. Khokha, Karen J. Liu, John B. Wallingford

Development (2020) 147 (21): dev197871.

DOI: https://doi.org/10.1242/dev.197871

Published: 9 November 2020

View article

Journal Articles

RET overactivation leads to concurrent Hirschsprung disease and intestinal ganglioneuromas

Nandor Nagy, Richard A. Guyer, Ryo Hotta, Dongcheng Zhang, Donald F. Newgreen, Viktoria Halasy, Tamas Kovacs, Allan M. Goldstein

Development (2020) 147 (21): dev190900.

DOI: https://doi.org/10.1242/dev.190900

Published: 5 November 2020

View article

Includes: Supplementary data

Journal Articles

Mitchell-Riley syndrome iPSCs exhibit reduced pancreatic endoderm differentiation due to a mutation in RFX6

In collection:

Human development

Development (2020) 147 (21): dev194878.

DOI: https://doi.org/10.1242/dev.194878

Published: 5 November 2020

View article

Includes: Supplementary data

Journal Articles

Downregulation of the GHRH/GH/IGF1 axis in a mouse model of Börjeson-Forssman-Lehman syndrome

Helen M. McRae, Samantha Eccles, Lachlan Whitehead, Warren S. Alexander, Jozef Gécz, Tim Thomas, Anne K. Voss

Development (2020) 147 (21): dev187021.

DOI: https://doi.org/10.1242/dev.187021

Published: 23 October 2020

View article

Includes: Supplementary data

Journal Articles

The developing heart: from The Wizard of Oz to congenital heart disease

In collection:

Advocacy , Cardiovascular development and regeneration , Stem cells & regeneration

Benoit G. Bruneau

Development (2020) 147 (21): dev194233.

DOI: https://doi.org/10.1242/dev.194233

Published: 21 October 2020

View article

Journal Articles

The Fgf8 subfamily (Fgf8, Fgf17 and Fgf18) is required for closure of the embryonic ventral body wall

Michael Boylan, Matthew J. Anderson, David M. Ornitz, Mark Lewandoski

Development (2020) 147 (21): dev189506.

DOI: https://doi.org/10.1242/dev.189506

Published: 19 October 2020

View article

Includes: Supplementary data

Journal Articles

Development of a straight vertebrate body axis

Michel Bagnat, Ryan S. Gray

Development (2020) 147 (21): dev175794.

DOI: https://doi.org/10.1242/dev.175794

Published: 6 October 2020

View article

Journal Articles

Using Drosophila to drive the diagnosis and understand the mechanisms of rare human diseases

Nichole Link, Hugo J. Bellen

Development (2020) 147 (21): dev191411.

DOI: https://doi.org/10.1242/dev.191411

Published: 28 September 2020

View article

Journal Articles

Deficiency and overexpression of Rtl1 in the mouse cause distinct muscle abnormalities related to Temple and Kagami-Ogata syndromes

In collection:

Human development

Moe Kitazawa, Shinichiro Hayashi, Michihiro Imamura, Shin'ichi Takeda, Yumiko Oishi, Tomoko Kaneko-Ishino, Fumitoshi Ishino

Development (2020) 147 (21): dev185918.

DOI: https://doi.org/10.1242/dev.185918

Published: 2 September 2020

View article

Includes: Supplementary data

Journal Articles

Temporal-specific roles of fragile X mental retardation protein in the development of the hindbrain auditory circuit

Xiaoyu Wang, Ayelet Kohl, Xiaoyan Yu, Diego A. R. Zorio, Avihu Klar, Dalit Sela-Donenfeld, Yuan Wang

Development (2020) 147 (21): dev188797.

DOI: https://doi.org/10.1242/dev.188797

Published: 25 August 2020

View article

Includes: Supplementary data

Journal Articles

Loss of U11 small nuclear RNA in the developing mouse limb results in micromelia

Kyle D. Drake, Christopher Lemoine, Gabriela S. Aquino, Anna M. Vaeth, Rahul N. Kanadia

Development (2020) 147 (21): dev190967.

DOI: https://doi.org/10.1242/dev.190967

Published: 14 August 2020

View article

Includes: Supplementary data

Journal Articles

NPC1 deficiency impairs cerebellar postnatal development of microglia and climbing fiber refinement in a mouse model of Niemann–Pick disease type C

Bridget R. Boyle, Sierra E. Melli, Ruth S. Altreche, Zachary M. Padron, Fawad A. K. Yousufzai, Sarah Kim, Mariella D. Vasquez, Dawn M. Carone, Benjamin R. Carone, Ileana Soto

Development (2020) 147 (21): dev189019.

DOI: https://doi.org/10.1242/dev.189019

Published: 3 August 2020

View article

Includes: Supplementary data

Journal Articles

Stromal β-catenin activation impacts nephron progenitor differentiation in the developing kidney and may contribute to Wilms tumor

In collection:

Human development

Keri A. Drake, Christopher P. Chaney, Amrita Das, Priti Roy, Callie S. Kwartler, Dinesh Rakheja, Thomas J. Carroll

Development (2020) 147 (21): dev189597.

DOI: https://doi.org/10.1242/dev.189597

Published: 31 July 2020

View article

Includes: Supplementary data

Journal Articles

The KMT2D Kabuki syndrome histone methylase controls neural crest cell differentiation and facial morphology

Karl B. Shpargel, Cassidy L. Mangini, Guojia Xie, Kai Ge, Terry Magnuson

Development (2020) 147 (21): dev187997.

DOI: https://doi.org/10.1242/dev.187997

Published: 17 July 2020

View article

Includes: Supplementary data

Journal Articles

Gene-environment interactions: aligning birth defects research with complex etiology

Tyler G. Beames, Robert J. Lipinski

Development (2020) 147 (21): dev191064.

DOI: https://doi.org/10.1242/dev.191064

Published: 17 July 2020

View article

Journal Articles

Mitf-family transcription factor function is required within cranial neural crest cells to promote choroid fissure closure

Katie L. Sinagoga, Alessandra M. Larimer-Picciani, Stephanie M. George, Samantha A. Spencer, James A. Lister, Jeffrey M. Gross

Development (2020) 147 (21): dev187047.

DOI: https://doi.org/10.1242/dev.187047

Published: 13 July 2020

View article

Includes: Supplementary data

Journal Articles

Disruption of the nectin-afadin complex recapitulates features of the human cleft lip/palate syndrome CLPED1

In collection:

Human development

Kendall J. Lough, Danielle C. Spitzer, Abby J. Bergman, Jessica J. Wu, Kevin M. Byrd, Scott E. Williams

Development (2020) 147 (21): dev189241.

DOI: https://doi.org/10.1242/dev.189241

Published: 13 July 2020

View article

Includes: Supplementary data

Journal Articles

Embracing human genetics: a primer for developmental biologists

Elizabeth J. Leslie

Development (2020) 147 (21): dev191114.

DOI: https://doi.org/10.1242/dev.191114

Published: 2 July 2020

View article

NARROW

Diseases of development: leveraging developmental biology to understand human disease

Control of skeletal morphogenesis by the Hippo-YAP/TAZ pathway

Challenges and opportunities at the interface of birth defects, human genetics and developmental biology

RET overactivation leads to concurrent Hirschsprung disease and intestinal ganglioneuromas

Mitchell-Riley syndrome iPSCs exhibit reduced pancreatic endoderm differentiation due to a mutation in RFX6

Downregulation of the GHRH/GH/IGF1 axis in a mouse model of Börjeson-Forssman-Lehman syndrome

The developing heart: from The Wizard of Oz to congenital heart disease

The Fgf8 subfamily (Fgf8, Fgf17 and Fgf18) is required for closure of the embryonic ventral body wall

Development of a straight vertebrate body axis

Using Drosophila to drive the diagnosis and understand the mechanisms of rare human diseases

Deficiency and overexpression of Rtl1 in the mouse cause distinct muscle abnormalities related to Temple and Kagami-Ogata syndromes

Temporal-specific roles of fragile X mental retardation protein in the development of the hindbrain auditory circuit

Loss of U11 small nuclear RNA in the developing mouse limb results in micromelia

NPC1 deficiency impairs cerebellar postnatal development of microglia and climbing fiber refinement in a mouse model of Niemann–Pick disease type C

Stromal β-catenin activation impacts nephron progenitor differentiation in the developing kidney and may contribute to Wilms tumor

The KMT2D Kabuki syndrome histone methylase controls neural crest cell differentiation and facial morphology

Gene-environment interactions: aligning birth defects research with complex etiology

Mitf-family transcription factor function is required within cranial neural crest cells to promote choroid fissure closure

Disruption of the nectin-afadin complex recapitulates features of the human cleft lip/palate syndrome CLPED1

Embracing human genetics: a primer for developmental biologists

Email alerts

Email alerts

This Feature Is Available To Subscribers Only