Results for &quot;&quot;Paired Box Transcription Factors&quot;&quot;[mesh_terms]

Transforming Growth Factor Beta and Alveolar Rhabdomyosarcoma: A Challenge of Tumor Differentiation and Chemotherapy Response.

Simone C da Silva Rosa, Joseph W Gordon, Saeid Ghavami, Bhavya Bhushan, Rosa Iranpour, Amirmohammad Eshtiaghi, Benjamin W Lindsey

International journal of molecular sciences 2024;25(5):

Pigmentation PAX-ways: the role of Pax3 in melanogenesis, melanocyte stem cell maintenance, and disease.

Jennifer D Kubic, Kacey P Young, Rebecca S Plummer, Anton E Ludvik, Deborah Lang

Pigment cell & melanoma research 2009;21(6):627-45

Plasma Membrane Domain Patterning and Self-Reinforcing Polarity in Arabidopsis.

Petra Marhava, Ana Cecilia Aliaga Fandino, Samuel W H Koh, Adriana Jelínková, Martina Kolb, Dorina P Janacek, Alice S Breda, Pietro Cattaneo, Ulrich Z Hammes, Jan Petrášek, Christian S Hardtke

Developmental cell 2020;52(2):223-235.e5

Molecular Modelling of Islet β-Cell Adaptation to Inflammation in Pregnancy and Gestational Diabetes Mellitus.

Petra I Lorenzo, Alejandro Martín-Montalvo, Nadia Cobo Vuilleumier, Benoit R Gauthier

International journal of molecular sciences 2020;20(24):6171

Paired box genes, PAX-2 and PAX-8, are not frequently mutated in Wilms tumor.

Yahya Tamimi, Kevin Dietrich, Kathryn Stone, Paul Grundy

Mutation research 2007;601(1-2):46-50

Structural basis for DNA recognition by the human PAX3 homeodomain.

John A A Ladias, Aditi Soni, Gabriel Birrane

Biochemistry 2009;48(6):1148-55

Using protein design algorithms to understand the molecular basis of disease caused by protein-DNA interactions: the Pax6 example.

Andreu Alibés, Alejandro D Nadra, Federico De Masi, Martha L Bulyk, Luis Serrano, François Stricher

Nucleic acids research 2011;38(21):7422-31

Darier disease, multiple bone cysts, and aniridia due to double de novo heterozygous mutations in ATP2A2 and PAX6.

Marco Castori, Luana Barboni, Philippa J Duncan, Mauro Paradisi, Luigi Laino, Carmelilia De Bernardo, David O Robinson, Paola Grammatico

American journal of medical genetics. Part A 2009;149A(8):1768-72

Cervical dysplasia: assessing methylation status (Methylight) of CCNA1, DAPK1, HS3ST2, PAX1 and TFPI2 to improve diagnostic accuracy.

Elaine H Lim, Shi Len Ng, Jia Liang Li, Alexander R Chang, Joseph Ng, A Ilancheran, Jeffrey Low, Swee Chong Quek, Eng Hseon Tay

Gynecologic oncology 2010;119(2):225-31

NeuroD1 A45T and PAX4 R121W polymorphisms are associated with plasma glucose level of repaglinide monotherapy in Chinese patients with type 2 diabetes.

Zhi-Cheng Gong, Qiong Huang, Xing-Ping Dai, Guang-Hua Lei, Hong-Bin Lu, Ji-Ye Yin, Xiao-Jing Xu, Jian Qu, Qi Pei, Min Dong, Bo-Ting Zhou, Jie Shen, Gan Zhou, Hong-Hao Zhou, Zhao-Qian Liu

British journal of clinical pharmacology 2013;74(3):501-9

Lack of effective T-lymphocyte response to the PAX3/FKHR translocation area in alveolar rhabdomyosarcoma.

David A Rodeberg, Rebecca A Nuss, Carrie J Heppelmann, Esteban Celis

Cancer immunology, immunotherapy : CII 2005;54(6):526-34

Regulation of insulin synthesis and secretion and pancreatic Beta-cell dysfunction in diabetes.

Zhuo Fu, Elizabeth R Gilbert, Dongmin Liu

Current diabetes reviews 2013;9(1):25-53

A spatiotemporal study of gliosis in relation to depth electrode tracks in drug-resistant epilepsy.

Sanjay M Sisodiya, Maria Thom, Joan Y W Liu, Joanna Goc

The European journal of neuroscience 2015;39(12):2151-62

A common variant upstream of the PAX6 gene influences islet function in man.

E Ahlqvist, F Turrini, S T Lang, J Taneera, Y Zhou, P Almgren, O Hansson, B Isomaa, T Tuomi, K Eriksson, J G Eriksson, V Lyssenko, L Groop

Diabetologia 2012;55(1):94-104