Longo-Guess Chantal相关文献与解析，生知库

A spontaneous mouse deletion in Mctp1 uncovers a long-range cis-regulatory region crucial for NR2F1 function during inner ear development

Mctp1基因的自发性小鼠缺失揭示了一个对NR2F1在内耳发育过程中的功能至关重要的长程顺式调控区域

期刊:Developmental Biology

影响因子:2.1

doi:10.1016/j.ydbio.2018.09.011

Tarchini, Basile; Longo-Guess, Chantal; Tian, Cong; Tadenev, Abigail L D; Devanney, Nicholas; Johnson, Kenneth R

Hearing loss without overt metabolic acidosis in ATP6V1B1 deficient MRL mice, a new genetic model for non-syndromic deafness with enlarged vestibular aqueducts

ATP6V1B1缺陷型MRL小鼠出现无明显代谢性酸中毒的听力损失，这是一种新的非综合征性耳聋伴前庭导水管扩大的遗传模型

期刊:Human Molecular Genetics

影响因子:3.2

doi:10.1093/hmg/ddx257

Tian, Cong; Gagnon, Leona H; Longo-Guess, Chantal; Korstanje, Ron; Sheehan, Susan M; Ohlemiller, Kevin K; Schrader, Angela D; Lett, Jaclynn M; Johnson, Kenneth R

代谢

发表日期：2017

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N-acetyl-cysteine prevents age-related hearing loss and the progressive loss of inner hair cells in Î³-glutamyl transferase 1 deficient mice.

N-乙酰半胱氨酸可预防年龄相关性听力损失和α³-谷氨酰转移酶1缺乏小鼠的内毛细胞进行性丧失

期刊:Aging-Us

影响因子:3.9

doi:10.18632/aging.100927

Ding Dalian, Jiang Haiyan, Chen Guang-Di, Longo-Guess Chantal, Muthaiah Vijaya Prakash Krishnan, Tian Cong, Sheppard Adam, Salvi Richard, Johnson Kenneth R

细胞生物学

发表日期：2016

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A QTL on Chr 5 modifies hearing loss associated with the fascin-2 variant of DBA/2J mice

位于 5 号染色体上的一个数量性状基因座 (QTL) 会影响 DBA/2J 小鼠 fascin-2 变体相关的听力损失。

期刊:Mammalian Genome

影响因子:2.7

doi:10.1007/s00335-015-9574-y

Johnson, Kenneth R; Longo-Guess, Chantal M; Gagnon, Leona H

发表日期：2015

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Association of a citrate synthase missense mutation with age-related hearing loss in A/J mice

柠檬酸合酶错义突变与A/J小鼠年龄相关性听力损失的关联

期刊:Neurobiology of Aging

影响因子:3.5

doi:10.1016/j.neurobiolaging.2011.05.009

Johnson, Kenneth R; Gagnon, Leona H; Longo-Guess, Chantal; Kane, Kelly L

发表日期：2012

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Mutations of the mouse ELMO domain containing 1 gene (Elmod1) link small GTPase signaling to actin cytoskeleton dynamics in hair cell stereocilia

小鼠 ELMO 结构域包含基因 1 (Elmod1) 的突变将小 GTP 酶信号传导与毛细胞立体纤毛中的肌动蛋白细胞骨架动力学联系起来

期刊:PLoS One

影响因子:2.6

doi:10.1371/journal.pone.0036074

Johnson, Kenneth R; Longo-Guess, Chantal M; Gagnon, Leona H

Genetic background effects on age-related hearing loss associated with Cdh23 variants in mice

小鼠Cdh23变异体相关的年龄相关性听力损失的遗传背景效应

期刊:Hearing Research

影响因子:2.5

doi:10.1016/j.heares.2011.11.007

Kane, Kelly L; Longo-Guess, Chantal M; Gagnon, Leona H; Ding, Dalian; Salvi, Richard J; Johnson, Kenneth R

发表日期：2012

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NPHP4 is necessary for normal photoreceptor ribbon synapse maintenance and outer segment formation, and for sperm development

NPHP4对于维持正常的感光细胞带状突触和外节形成以及精子发育是必需的。

期刊:Human Molecular Genetics

影响因子:3.2

doi:10.1093/hmg/ddq494

Won, Jungyeon; Marín de Evsikova, Caralina; Smith, Richard S; Hicks, Wanda L; Edwards, Malia M; Longo-Guess, Chantal; Li, Tiansen; Naggert, Jürgen K; Nishina, Patsy M

Mutation of the Cyba gene encoding p22phox causes vestibular and immune defects in mice

编码 p22phox 的 Cyba 基因突变会导致小鼠出现前庭和免疫缺陷。

期刊:Journal of Clinical Investigation

影响因子:13.6

doi:10.1172/JCI33835

Nakano, Yoko; Longo-Guess, Chantal M; Bergstrom, David E; Nauseef, William M; Jones, Sherri M; Bánfi, Botond

免疫/内分泌

发表日期：2008

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Deletion of a Long-Range Dlx5 Enhancer Disrupts Inner Ear Development in Mice

删除长程Dlx5增强子会破坏小鼠内耳发育

A spontaneous mouse deletion in Mctp1 uncovers a long-range cis-regulatory region crucial for NR2F1 function during inner ear development

Mctp1基因的自发性小鼠缺失揭示了一个对NR2F1在内耳发育过程中的功能至关重要的长程顺式调控区域

Hearing loss without overt metabolic acidosis in ATP6V1B1 deficient MRL mice, a new genetic model for non-syndromic deafness with enlarged vestibular aqueducts

ATP6V1B1缺陷型MRL小鼠出现无明显代谢性酸中毒的听力损失，这是一种新的非综合征性耳聋伴前庭导水管扩大的遗传模型

N-acetyl-cysteine prevents age-related hearing loss and the progressive loss of inner hair cells in Î³-glutamyl transferase 1 deficient mice.

N-乙酰半胱氨酸可预防年龄相关性听力损失和α³-谷氨酰转移酶1缺乏小鼠的内毛细胞进行性丧失

A QTL on Chr 5 modifies hearing loss associated with the fascin-2 variant of DBA/2J mice

位于 5 号染色体上的一个数量性状基因座 (QTL) 会影响 DBA/2J 小鼠 fascin-2 变体相关的听力损失。

Association of a citrate synthase missense mutation with age-related hearing loss in A/J mice

柠檬酸合酶错义突变与A/J小鼠年龄相关性听力损失的关联

Mutations of the mouse ELMO domain containing 1 gene (Elmod1) link small GTPase signaling to actin cytoskeleton dynamics in hair cell stereocilia

小鼠 ELMO 结构域包含基因 1 (Elmod1) 的突变将小 GTP 酶信号传导与毛细胞立体纤毛中的肌动蛋白细胞骨架动力学联系起来

Genetic background effects on age-related hearing loss associated with Cdh23 variants in mice

小鼠Cdh23变异体相关的年龄相关性听力损失的遗传背景效应

NPHP4 is necessary for normal photoreceptor ribbon synapse maintenance and outer segment formation, and for sperm development

NPHP4对于维持正常的感光细胞带状突触和外节形成以及精子发育是必需的。

Mutation of the Cyba gene encoding p22phox causes vestibular and immune defects in mice

编码 p22phox 的 Cyba 基因突变会导致小鼠出现前庭和免疫缺陷。