Results 91 to 100 of about 212 (100)
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Contribution of PGAP3 Co-Amplified and Co-Overexpressed With ERBB2 at 17q12 Involved Poor Prognosis in Gastric Cancer

Journal of Cellular and Molecular Medicine, 2023
Jingcui Yu, Xiangning Meng, Xiaobo Cui
exaly  

PGAP3 Associated With Hyperphosphatasia With Mental Retardation Plays a Novel Role in Brain Morphogenesis and Neuronal Wiring at Early Development

Cells, 2020
Waleed Aamer   +2 more
exaly  

Excluding Digenic Inheritance of PGAP2 and PGAP3 Variants in Mabry Syndrome (OMIM 239300) Patient: Phenotypic Spectrum Associated With PGAP2 Gene Variants in Hyperphosphatasia With Mental Retardation Syndrome-3 (HPMRS3)

Genes, 2023
Taroh Kinoshita   +2 more
exaly  

PGAP3-Related Hyperphosphatasia With Mental Retardation Syndrome: Report of 10 New Patients and a Homozygous Founder Mutation

Clinical Genetics, 2018
Maha Zaki   +2 more
exaly  

Rare Noncoding Mutations Extend the Mutational Spectrum in the PGAP3 Subtype of Hyperphosphatasia With Mental Retardation Syndrome

Human Mutation, 2016
Taroh Kinoshita   +2 more
exaly  

A novel PGAP3 mutation in two siblings with hyperphosphatasia with mental retardation syndrome

2020
YILMAZ, ÜNSAL   +3 more
openaire   +1 more source

PGAP3 is differentially expressed in HER2+ breast cancer.

openaire   +1 more source

The Novel Circular RNA Circ-PGAP3 Promotes the Proliferation and Invasion of Triple Negative Breast Cancer by Regulating the miR-330-3p/Myc Axis

OncoTargets and Therapy, 2020
exaly  

Compound Heterozygosity in PGAP3 Causing Mabry Syndrome in a South African Patient

American Journal of Medical Genetics, Part A
Shahida Moosa
exaly  

PGAP3 geninde yeni tanımlanmış mutasyona bağlı hiperfosfatazya mental retardasyon sendromu

2017
ALİKAŞİFOĞLU, MEHMET   +7 more
openaire   +1 more source
humans
carboxylic ester hydrolases
3. good health
receptors, cell surface
intellectual disability
female
genetics
abnormalities, multiple
male
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