Results 61 to 70 of about 2,265 (159)

Pulmonary alveolar microlithiasis: A report of two unique cases

Respiratory Medicine Case Reports, 2020
Pulmonary alveolar microlithiasis (PAM) is an inherited autosomal recessive disease. PAM is classically characterized by calcium phosphate deposition within alveolar airspaces due to SLC34A2 (solute carrier family 34 member 2) gene mutation located on ...
Haneen Al-Maghrabi, Ghadeer Mokhtar, Jaudah Al-Maghrabi, Abdelrazak Meliti   +3 more
doaj   +1 more source

Pulmonary Alveolar Microlithiasis: A Unique Case of Familial PAM Complicated by Transplant Rejection

Case Reports in Pathology, 2021
Background. Pulmonary alveolar microlithiasis (PAM) is a rare lung disease characterized by the deposition of calcium phosphate microliths or calcospherites, within the alveolar airspace.
Austin Helmink, Samir Atiya, Ernesto Martinez Duarte   +2 more
doaj   +1 more source

Fine Mapping QTLs Affecting Milk Production Traits on BTA6 in Chinese Holstein with SNP Markers

Journal of Integrative Agriculture, 2013
Our previous studies demonstrated that the region around markers BMS470 and BMS1242 on BTA6 showed a linkage to 305-d milk yield and composition traits in the Chinese Holstein population.
Rui LIU, Dong-xiao SUN, Ya-chun WANG, Ying YU, Yi ZHANG, Hui-yong CHEN, Qin ZHANG, Sheng-li ZHANG, Yuan ZHANG   +8 more
doaj   +1 more source

A Catalog of 5’ Fusion Partners in ROS1-Positive NSCLC Circa 2020

JTO Clinical and Research Reports, 2020
ROS1 fusion–positive (ROS1+) NSCLC was discovered in 2007, the same year as the discovery of ALK-positive (ALK+) NSCLC but has trailed ALK+ NSCLC in terms of development.
Sai-Hong Ignatius Ou, MD PhD, Misako Nagasaka, MD   +1 more
doaj   +1 more source

Molecular Genetic Characterization of Individual Cancer Cells Isolated via Single-Cell Printing. [PDF]

PLoS ONE, 2016
Intratumoral genetic heterogeneity may impact disease outcome. Gold standard for dissecting clonal heterogeneity are single-cell analyses. Here, we present an efficient workflow based on an advanced Single-Cell Printer (SCP) device for the study of gene ...
Julian Riba, Nathalie Renz, Christoph Niemöller, Sabine Bleul, Dietmar Pfeifer, Juliane M Stosch, Klaus H Metzeler, Björn Hackanson, Michael Lübbert, Justus Duyster, Peter Koltay, Roland Zengerle, Rainer Claus, Stefan Zimmermann, Heiko Becker   +14 more
doaj   +1 more source

Toward a Topology-Based Therapeutic Design of Membrane Proteins: Validation of NaPi2b Topology in Live Ovarian Cancer Cells

Frontiers in Molecular Biosciences, 2022
NaPi2b is a sodium-dependent phosphate transporter that belongs to the SLC34 family of transporters which is mainly responsible for phosphate homeostasis in humans.
Leisan Bulatova, Daria Savenkova, Alsina Nurgalieva, Daria Reshetnikova, Arina Timonina, Vera Skripova, Mikhail Bogdanov, Mikhail Bogdanov, Ramziya Kiyamova   +8 more
doaj   +1 more source

Pulmonary alveolar microlithiasis: Lungs of stone!

Journal of Advanced Lung Health, 2022
Pulmonary alveolar microlithiasis (PAM) is a rare autosomal recessive disorder characterized by diffuse bilateral deposition of calcispherites in lung alveoli due to mutations in the SLC34A2 gene.
N Neenu, Ketaki Utpat, Unnati Desai, Gautam Sarawade   +3 more
doaj   +1 more source

Molecular and clinicopathological characteristics of ROS1‐rearranged non‐small‐cell lung cancers identified by next‐generation sequencing

Molecular Oncology, 2020
ROS1 gene rearrangements have been reported in diverse cancer types including non‐small‐cell lung cancer (NSCLC), and with a notably higher prevalence in lung adenocarcinoma.
Meiying Cui, Yuchen Han, Pan Li, Jianying Zhang, Qiuxiang Ou, Xiaoling Tong, Ruiying Zhao, Nan Dong, Xue Wu, Wencai Li, Guozhong Jiang   +10 more
doaj   +1 more source

Pulmonary Alveolar Microlithiasis: A Case Report

Oman Medical Journal, 2020
Pulmonary alveolar microlithiasis (PAM) is a rare disease caused by a mutation in the SLC34A2 gene encoding the type IIb sodium phosphate cotransporter in alveolar type II cells.
Rashid Al Umairi, Fatma Al Lawati, Mahmood Al-Riyami, Faiza Al Kindi, Atheel Kamona, Fadhila Al Busaidi, Nabil Al Lawati, Adil Al Lawati, Zulfikar Habibulla   +8 more
doaj   +1 more source

A case report of pulmonary alveolar microlithiasis with pulmonary tuberculosis

Lung India, 2023
Pulmonary alveolar microlithiasis (PAM) is a rare autosomal recessive disease characterised by the deposition of calcium phosphate microliths in the alveoli. PAM has been reported in all continents and there is often a familial history. There is clinical-
Malay Sarkar, Sudarshan K Sharma, Anupam Jhobta, Anchana Gulati   +3 more
doaj   +1 more source