Sökresultat - "TRAPPC9"

Overexpression of ZFP69B promotes hepatocellular carcinoma growth by upregulating the expression of TLX1 and TRAPPC9

Xie, Wei, Bao, Zhongming, Yao, Dan, Yang, Yong^{Aff4, IDs1300802400131z_cor4}

Case Report: Whole exome sequencing identifies compound heterozygous variants in the TRAPPC9 gene in a child with developmental delay

Bingxuan Yu, Jing Chen, Shuo Yang, He Wang, Yuanyuan Xiao, Shanling Liu

electronic resource

Visa; Visa

DNA methylation patterns in the peripheral blood of Xinjiang brown cattle with variable somatic cell counts

Dan Wang, Shengchao Ma, Mengjie Yan, Mingming Dong, Menghua Zhang, Tao Zhang, Xiaoxue Zhang, Lei Xu, Xixia Huang

electronic resource

Visa; Visa

Microcephaly with a disproportionate hippocampal reduction, stem cell loss and neuronal lipid droplet symptoms in Trappc9 KO mice

Sultan Aljuraysi, Mark Platt, Michela Pulix, Harish Poptani, Antonius Plagge

electronic resource

Visa; Visa

A novel homozygous mutation in TRAPPC9 gene causing autosomal recessive non-syndromic intellectual disability

Mutaz Amin, Cedric Vignal, Esraa Eltaraifee, Inaam N. Mohammed, Ahlam A. A. Hamed, Maha A. Elseed, Arwa Babai, Iman Elbadi, Doua Mustafa, Rayan Abubaker, Mohamed Mustafa, Severine Drunat, Liena E. O. Elsayed, Ammar E. Ahmed, Odile Boespflug-Tanguy, Imen Dorboz

electronic resource

Visa

Genetic polymorphisms of TRAPPC9 and CD4 genes and their association with milk production and mastitis resistance phenotypic traits in Chinese Holstein

Muhammad Zahoor Khan, Gerile Dari, Adnan Khan, Ying Yu

electronic resource

Visa; Visa

Identification of TRAPPC9 and BAIAP2 Gene Polymorphisms and Their Association With Fat Deposition-Related Traits in Hu Sheep

Panpan Cui, Weimin Wang, Deyin Zhang, Chong Li, Yongliang Huang, Zongwu Ma, Xiaojuan Wang, Liming Zhao, Yukun Zhang, Xiaobin Yang, Dan Xu, Jiangbo Cheng, Xiaolong Li, Xiwen Zeng, Yuan Zhao, Wenxin Li, Jianghui Wang, Changchun Lin, Bubo Zhou, Jia Liu, Rui Zhai, Xiaoxue Zhang

electronic resource

Visa; Visa

Denna resultat visas inte till gäster.
Logga in för full Login for full tillgång.

Identification of two novel homozygous nonsense mutations in TRAPPC9 in two unrelated consanguineous families with intellectual Disability from Iran

Farideh Yousefipour, Hossein Mozhdehipanah, Frouzandeh Mahjoubi

electronic resource

Visa

Two Novel Compound Heterozygous Mutations in the TRAPPC9 Gene Reveal a Connection of Non-syndromic Intellectual Disability and Autism Spectrum Disorder

Johannes Krämer, Meinrad Beer, Harald Bode, Benedikt Winter

electronic resource

Visa; Visa

Profound intellectual disability caused by homozygous TRAPPC9 pathogenic variant in a man from Malta

Katelynn M. Wilton, Lauren B. Gunderson, Linda Hasadsri, Christopher P. Wood, Lisa A. Schimmenti

electronic resource

Visa

Novel Compound Heterozygous Mutations in the TRAPPC9 Gene in Two Siblings With Autism and Intellectual Disability

Areerat Hnoonual, Potchanapond Graidist, Supika Kritsaneepaiboon, Pornprot Limprasert

electronic resource

Visa; Visa

COPI–TRAPPII activates Rab18 and regulates its lipid droplet association

Li, Chunman^{Aff1, Aff2}, Luo, Xiaomin, Zhao, Shan, Siu, Gavin KY, Liang, Yongheng, Chan, Hsiao Chang^{Aff2, Aff4}, Satoh, Ayano, Yu, Sidney SB^{Aff2, Aff4, IDEMBJ201694866_cor8}

Denna resultat visas inte till gäster.
Logga in för full Login for full tillgång.

Denna resultat visas inte till gäster.
Logga in för full Login for full tillgång.

Denna resultat visas inte till gäster.
Logga in för full Login for full tillgång.

Identification of novel determinants of resistance to lapatinib in ERBB2-amplified cancers

Wetterskog, D, Shiu, K-K, Chong, I^{Aff1, Aff2}, Meijer, T, Mackay, A, Lambros, M, Cunningham, D, Reis-Filho, J S^{Aff1, IDonc201341_cor8}, Lord, C J^{Aff1, IDonc201341_cor9}, Ashworth, A^{Aff1, IDonc201341_cor10}

Denna resultat visas inte till gäster.
Logga in för full Login for full tillgång.

Denna resultat visas inte till gäster.
Logga in för full Login for full tillgång.

Denna resultat visas inte till gäster.
Logga in för full Login for full tillgång.