نتایج جستجو برای: hypomineralization

تعداد نتایج: 275  

Journal: :Development 1999
M J Depew J K Liu J E Long R Presley J J Meneses R A Pedersen J L Rubenstein

We report the generation and analysis of mice homozygous for a targeted deletion of the Dlx5 homeobox gene. Dlx5 mutant mice have multiple defects in craniofacial structures, including their ears, noses, mandibles and calvaria, and die shortly after birth. A subset (28%) exhibit exencephaly. Ectodermal expression of Dlx5 is required for the development of olfactory and otic placode-derived epit...

Journal: :Endocrinology 2001
D Miao X Bai D Panda M McKee A Karaplis D Goltzman

To explore how the loss of Phex function contributes to the pathogenesis of osteomalacia, we examined the abnormalities of mineralization, Phex, and bone matrix protein expression occurring in Hyp mice in vivo and in ex vivo bone marrow cell cultures. The results in vivo show that mineralization was decreased significantly in Hyp mouse bone. Phex protein was identifiable in osteoblasts and oste...

2016
Aki Nakamura-Takahashi Koichi Miyake Atsushi Watanabe Yukihiko Hirai Osamu Iijima Noriko Miyake Kumi Adachi Yuko Nitahara-Kasahara Hideaki Kinoshita Taku Noguchi Shinichi Abe Sonoko Narisawa Jose Luis Millán Takashi Shimada Takashi Okada

Hypophosphatasia (HPP) is an inherited disease caused by genetic mutations in the gene encoding tissue-nonspecific alkaline phosphatase (TNALP). This results in defects in bone and tooth mineralization. We recently demonstrated that TNALP-deficient (Akp2 (-/-) ) mice, which mimic the phenotype of the severe infantile form of HPP, can be treated by intravenous injection of a recombinant adeno-as...

2012
Ola B. Al-Batayneh

Tricho-dento-osseous (TDO) syndrome is a rare, autosomal dominant disorder principally characterised by curly hair at infancy, severe enamel hypomineralization and hypoplasia and taurodontism of teeth, sclerotic bone, and other defects. Diagnostic criteria are based on the generalized enamel defects, severe taurodontism especially of the mandibular first permanent molars, an autosomal dominant ...

Banijamali, Seyede Niloofar, Moazami, Fatemeh, Salem, Katayoun,

Talon cusp is an odontogenic anomaly in anterior teeth, caused by hyperactivity of enamel in morphodifferentiation stage. Talon cusp is an additional cusp with several types based on its extension and shape. It has enamel, dentin, and sometimes pulp tissue.  Moreover, it can cause clinical problems such as poor aesthetic, dental caries, attrition, occlusal interferences, and periodontal di...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید