Results 191 to 200 of about 10,834 (202)

ALPL gene mutation in a family

Bone Abstracts, 2019
Silvia Vai, Francesca Broggi, Bianchi Maria Luisa, Emanuela Ponti, Alessandra Mihalich, Di Blasio Anna Maria   +5 more
openaire   +1 more source

Different Dental Manifestations in Sisters with the Same ALPL Gene Mutation: A Report of Two Cases

Children, 2022
Rena Okawa, Kazuhiko Nakano
exaly  

Gene Therapy Using Adeno-Associated Virus Serotype 8 Encoding TNAP-D10 Improves the Skeletal and Dentoalveolar Phenotypes in Alpl−/− Mice

Journal of Bone and Mineral Research, 2021
Yuka Kinoshita, Fatma Faiez A Mohamed, Flávia Amadeu de Oliveira   +2 more
exaly  

Novel human pathological mutations. Gene symbol: ALPL. Disease: hypophosphatasia.

Human genetics, 2009
Bertola, F, Arosio, C, Casati, G, PIPERNO, ALBERTO, Crosti, F, Colombo, C.   +5 more
openaire   +2 more sources

Alpl prevents bone ageing sensitivity by specifically regulating senescence and differentiation in mesenchymal stem cells

Bone Research, 2018
Wenjia Liu, Liqiang Zhang, Kun Xuan
exaly  

ALPL regulates the aggressive potential of high grade serous ovarian cancer cells via a non-canonical WNT pathway

Biochemical and Biophysical Research Communications, 2019
Lin Zhou
exaly  

Presence of two novel mutations of the ALPL gene in a Chinese patient with hypophosphatasia

Bone, 2010
Haijuan Liu, Mei Li, Xiaoping Xing, Weibo Xia, Wei Yu, Min Nie, Ou Wang, Yan Jiang, Xunwu Meng, Xueying Zhou, Yingying Hu, Huaicheng Liu   +11 more
openaire   +1 more source

A case of perinatal hypophosphatasia with a novel mutation in the <i>ALPL</i> gene: clinical course and review of the literature

Clinical Pediatric Endocrinology, 2018
Tomoyuki Akiyama
exaly  

A Rare ALPL Gene Mutation in Adult-Onset Hypophosphatasia

Endocrine Practice
openaire   +1 more source

Compound heterozygosity of two functional null mutations in the ALPL gene associated with deleterious neurological outcome in an infant with hypophosphatasia

Bone, 2013
exaly