日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Atlas of multilineage stem cell differentiation reveals TMEM88 as a developmental regulator of blood pressure

多系干细胞分化图谱揭示TMEM88是血压发育的调节因子

Sophie Shen ,Tessa Werner ,Samuel W Lukowski ,Stacey Andersen ,Yuliangzi Sun ,Woo Jun Shim ,Dalia Mizikovsky ,Sakurako Kobayashi ,Jennifer Outhwaite ,Han Sheng Chiu ,Xiaoli Chen ,Gavin Chapman ,Ella M M A Martin ,Di Xia ,Duy Pham ,Zezhuo Su ,Daniel Kim ,Pengyi Yang ,Men Chee Tan ,Enakshi Sinniah ,Qiongyi Zhao ,Sumedha Negi ,Meredith A Redd ,Joseph E Powell ,Sally L Dunwoodie ,Patrick P L Tam ,Mikael Bodén ,Joshua W K Ho ,Quan Nguyen ,Nathan J Palpant

Myhre syndrome is caused by dominant-negative dysregulation of SMAD4 and other co-factors

Myhre 综合征是由 SMAD4 和其他辅助因子的显性负性失调引起的

Dimuthu Alankarage, Annabelle Enriquez, Robert D Steiner, Cathy Raggio, Megan Higgins, Di Milnes, David T Humphreys, Emma L Duncan, Duncan B Sparrow, Philip F Giampietro, Gavin Chapman, Sally L Dunwoodie

Quantitative 3D analysis and visualization of cardiac fibrosis by microcomputed tomography

通过微型计算机断层扫描对心脏纤维化进行定量 3D 分析和可视化

Vaibhao Janbandhu, Ella M M A Martin, Gavin Chapman, Sally L Dunwoodie, Richard P Harvey

Functional genomics and gene-environment interaction highlight the complexity of congenital heart disease caused by Notch pathway variants

功能基因组学和基因-环境相互作用凸显了 Notch 通路变异引起的先天性心脏病的复杂性

Gavin Chapman, Julie L M Moreau, Eddie I P, Justin O Szot, Kavitha R Iyer, Hongjun Shi, Michelle X Yam, Victoria C O'Reilly, Annabelle Enriquez, Joelene A Greasby, Dimuthu Alankarage, Ella M M A Martin, Bernadette C Hanna, Matthew Edwards, Steven Monger, Gillian M Blue, David S Winlaw, Helen E Ritch

Functional characterization of a novel PBX1 de novo missense variant identified in a patient with syndromic congenital heart disease

在患有先天性心脏病的患者中发现的新型 PBX1 从头错义变异的功能表征

Dimuthu Alankarage, Justin O Szot, Nick Pachter, Anne Slavotinek, Licia Selleri, Joseph T Shieh, David Winlaw, Eleni Giannoulatou, Gavin Chapman, Sally L Dunwoodie

De novo, deleterious sequence variants that alter the transcriptional activity of the homeoprotein PBX1 are associated with intellectual disability and pleiotropic developmental defects

改变同源蛋白 PBX1 转录活性的新生有害序列变异与智力障碍和多效性发育缺陷有关

Anne Slavotinek, Maurizio Risolino, Marta Losa, Megan T Cho, Kristin G Monaghan, Dina Schneidman-Duhovny, Sarah Parisotto, Johanna C Herkert, Alexander P A Stegmann, Kathryn Miller, Natasha Shur, Jacqueline Chui, Eric Muller, Suzanne DeBrosse, Justin O Szot, Gavin Chapman, Nicholas S Pachter, David

NKX2-5 mutations causative for congenital heart disease retain functionality and are directed to hundreds of targets

导致先天性心脏病的 NKX2-5 突变保留了功能,并针对数百个目标

Romaric Bouveret, Ashley J Waardenberg, Nicole Schonrock, Mirana Ramialison, Tram Doan, Danielle de Jong, Antoine Bondue, Gurpreet Kaur, Stephanie Mohamed, Hananeh Fonoudi, Chiann-Mun Chen, Merridee A Wouters, Shoumo Bhattacharya, Nicolas Plachta, Sally L Dunwoodie, Gavin Chapman, Cédric Blanpain, R

Gene-environment interaction demonstrates the vulnerability of the embryonic heart

基因-环境相互作用表明胚胎心脏的脆弱性

Victoria C O'Reilly, Kylie Lopes Floro, Hongjun Shi, Bogdan E Chapman, Jost I Preis, Alexander C James, Gavin Chapman, Richard P Harvey, Randall S Johnson, Stuart M Grieve, Duncan B Sparrow, Sally L Dunwoodie2

Divergent functions and distinct localization of the Notch ligands DLL1 and DLL3 in vivo

Notch 配体 DLL1 和 DLL3 在体内的不同功能和不同定位

Insa Geffers, Katrin Serth, Gavin Chapman, Robert Jaekel, Karin Schuster-Gossler, Ralf Cordes, Duncan B Sparrow, Elisabeth Kremmer, Sally L Dunwoodie, Thomas Klein, Achim Gossler

High levels of Notch signaling down-regulate Numb and Numblike

高水平的 Notch 信号下调 Numb 和 Numblike

Gavin Chapman, Lining Liu, Cecilia Sahlgren, Camilla Dahlqvist, Urban Lendahl