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

Sod1 trisomy causes ENS developmental defects and susceptibility to Hirschsprung disease via neuronal Ret suppression and glial remodeling

Sod1三体性通过抑制神经元Ret信号通路和神经胶质细胞重塑,导致肠神经系统发育缺陷和易患先天性巨结肠症。

Grullon, Gabriel; Rollins, Jarod; Wilkes, Lauren; Zuberi, Aamir; Chakravarti, Aravinda; Chatterjee, Sumantra

Whole Genome Sequencing Reveals a RET Enhancer Risk Haplotype Associated with Hirschsprung Disease in Mowat Wilson Syndrome

全基因组测序揭示了与莫瓦特-威尔逊综合征中的先天性巨结肠相关的RET增强子风险单倍型

Collins, Sydney; Bah, Ibrahim; Pysar, Ryan; Mowat, David; Turner, Tychele N; Chatterjee, Sumantra

Variability in proliferative and migratory defects in Hirschsprung disease-associated RET pathogenic variants.

与先天性巨结肠症相关的RET致病变异导致增殖和迁移缺陷的变异性

Fries Lauren E, Dharma Sree, Chakravarti Aravinda, Chatterjee Sumantra

Synergistic effects of Ret coding and enhancer loss-of-function alleles cause progressive loss of inhibitory motor neurons in the enteric nervous system

Ret编码基因和增强子功能丧失等位基因的协同作用导致肠神经系统中抑制性运动神经元的进行性丧失。

Fries, Lauren E; Grullon, Gabriel; Wilkes, Lauren; Berk-Rauch, Hanna E; Chakravarti, Aravinda; Chatterjee, Sumantra

RET enhancer haplotype-dependent remodeling of the human fetal gut development program

RET增强子单倍型依赖的人类胎儿肠道发育程序重塑

Chatterjee, Sumantra; Fries, Lauren E; Yaacov, Or; Hu, Nan; Berk-Rauch, Hanna E; Chakravarti, Aravinda

Cumulative temporal vegetation indices from unoccupied aerial systems allow maize (Zea mays L.) hybrid yield to be estimated across environments with fewer flights

利用无人值守航航系统的累积时间植被指数,可以减少飞行次数,从而估算不同环境下玉米(Zea mays L.)杂交品种的产量。

Chatterjee, Sumantra; Adak, Alper; Wilde, Scott; Nakasagga, Shakirah; Murray, Seth C

A multi-enhancer RET regulatory code is disrupted in Hirschsprung disease

先天性巨结肠症中多增强子RET调控密码遭到破坏

Chatterjee, Sumantra; Karasaki, Kameko M; Fries, Lauren E; Kapoor, Ashish; Chakravarti, Aravinda

Coding and noncoding variants in EBF3 are involved in HADDS and simplex autism

EBF3基因的编码和非编码变异与HADDS和单纯型自闭症有关。

Padhi, Evin M; Hayeck, Tristan J; Cheng, Zhang; Chatterjee, Sumantra; Mannion, Brandon J; Byrska-Bishop, Marta; Willems, Marjolaine; Pinson, Lucile; Redon, Sylvia; Benech, Caroline; Uguen, Kevin; Audebert-Bellanger, Séverine; Le Marechal, Cédric; Férec, Claude; Efthymiou, Stephanie; Rahman, Fatima; Maqbool, Shazia; Maroofian, Reza; Houlden, Henry; Musunuri, Rajeeva; Narzisi, Giuseppe; Abhyankar, Avinash; Hunter, Riana D; Akiyama, Jennifer; Fries, Lauren E; Ng, Jeffrey K; Mehinovic, Elvisa; Stong, Nick; Allen, Andrew S; Dickel, Diane E; Bernier, Raphael A; Gorkin, David U; Pennacchio, Len A; Zody, Michael C; Turner, Tychele N

Genome-wide association study of Hirschsprung disease detects a novel low-frequency variant at the RET locus

全基因组关联研究发现先天性巨结肠症RET基因位点存在一种新的低频变异

Fadista, João; Lund, Marie; Skotte, Line; Geller, Frank; Nandakumar, Priyanka; Chatterjee, Sumantra; Matsson, Hans; Granström, Anna Löf; Wester, Tomas; Salo, Perttu; Virtanen, Valtter; Carstensen, Lisbeth; Bybjerg-Grauholm, Jonas; Hougaard, David Michael; Pakarinen, Mikko; Perola, Markus; Nordenskjöld, Agneta; Chakravarti, Aravinda; Melbye, Mads; Feenstra, Bjarke

Population variation in total genetic risk of Hirschsprung disease from common RET, SEMA3 and NRG1 susceptibility polymorphisms

常见RET、SEMA3和NRG1易感基因多态性导致的先天性巨结肠总遗传风险的群体变异

Kapoor, Ashish; Jiang, Qian; Chatterjee, Sumantra; Chakraborty, Prakash; Sosa, Maria X; Berrios, Courtney; Chakravarti, Aravinda