Results 51 to 60 of about 30,215 (266)

Integrated high‐resolution copy number and histomolecular analysis of diffuse hemispheric glioma, H3 G34‐mutant reveals universal TP53 abnormalities

Brain Pathology, EarlyView.
This integrated high‐resolution copy number and histomolecular analysis of diffuse hemispheric glioma, H3 G34‐mutant expands the spectrum of associated genetic changes and underscores the presence of universal TP53 abnormalities at copy number, sequence, and protein expression level, with frequent yet largely unrecognized TP53 copy‐neutral loss of ...
Jorge A. Trejo‐Lopez, Cinthya Zepeda Mendoza, Thomas M. Kollmeyer, Kristen L. Drucker, Vanessa M. Pazdernik, Paul A. Decker, Corinne E. Praska, Jayson Hardcastle, Stephanie Smoley, Matthew Isaacson, Mallika Gandham, Surendra Dasari, Aditya Raghunathan, Caterina Giannini, Gang Zheng, Aaron Wagner, M. Beatriz Lopes, Kar‐Ming A. Fung, JoElle G. Peterson, Andreana L. Rivera, Christopher Rossi, Meggen A. Walsh, Zied Abdullaev, Kenneth Aldape, Martha Quezado, Drew Pratt, Patrick Joseph Cimino, Robert B. Jenkins, Cristiane M. Ida   +28 more
wiley   +1 more source

Target cells of human adenovirus type 12 in subtentorial brain tissue of newborn mice. I. Cyto-histomorphologic and immunofluorescent microscopic studies In vivo [PDF]

, 1976
Human adenovirus type 12 (Ad 12) was inoculated through subtentorial route into inbred newborn mice (C3H/BifB/Ki), and sequential changes of the brain and tumor induction were examined by histological and immunofluorescent methods.
Athanasiou, T, Barrett, H, Camelliti, P, Pinto, K, Prodromakis, T, Rao, C, Terracciano, CM, Toumazou, C, Trantidou, T, Yacoub, MH   +9 more
core   +1 more source

A Population‐Based Assessment of Cancer Risk in Children With VACTERL

American Journal of Medical Genetics Part A, Volume 200, Issue 5, Page 1004-1011, May 2026.
ABSTRACT Cancer risk in children with VACTERL, a nonrandom co‐occurrence of ≥ 3 defects (vertebral, anal, cardiac, tracheoesophogeal fistula, renal, and limb), remains unclear. We evaluated this association in a population‐based study. We analyzed data from the Genetic Overlap Between Anomalies and Cancer in Kids (GOBACK) Study, a US registry linkage ...
Ji Yun Tark, Alexander Renwick, Giorgio Tettamanti, Rachel D. Harris, Tania A. Desrosiers, Andrew F. Olshan, Amanda E. Janitz, Michael E. Scheurer, Charles J. Shumate, Angela E. Scheuerle, Sharon E. Plon, Chad D. Huff, Ann Nordgren, Barbara Luke, Philip J. Lupo, Jeremy M. Schraw   +15 more
wiley   +1 more source

A Systematic Review of Evidence on the Clinical Effectiveness of Surveillance Imaging in Children With Medulloblastoma and Ependymoma

Pediatric Blood &Cancer, Volume 73, Issue 4, April 2026.
ABSTRACT Surveillance imaging aims to detect tumour relapse before symptoms develop, but it's unclear whether earlier detection of relapse leads to better outcomes in children and young people (CYP) with medulloblastoma and ependymoma. This systematic review aims to identify relevant literature to determine the efficacy of surveillance magnetic ...
Lucy Shepherd, Melissa Taylor, Helen Fulbright, Bob Phillips   +3 more
wiley   +1 more source

Pluripotent Stem Cell-Derived Teratoma presents an embryonic neoplastic niche for in vivo studies of Neuroectodermal Childhood Tumors [PDF]

, 2012
Therapy-resistance and relapse remain problematic in many cancer patients, despite the advancement in anti-cancer therapies. There is a constant need of developing new anti-cancer drugs to combat tumors keeping in mind also the increasing incidence
Jamil, Seema
core   +1 more source

The Homeobox Genes: Classification, Regulation, Biological Functions, and Diseases

MedComm, Volume 7, Issue 4, April 2026.
Overview of the homeobox gene superfamily and its pathophysiological roles. The homeobox superfamily comprises several major classes, including ANTP, PRD, TALE, LIM, POU, and others. Among these, the HOX clusters (A–D) play critical roles in embryonic development specifically in conferring cellular identity, regulating morphogenesis, and guiding axial ...
Maedeh Dadzadi, Shahin Ramazi, Mona Darvazi, Sepideh Yoosefi, Melika Abbasi, Shirin Farsad   +5 more
wiley   +1 more source

Primitive Neuroectodermal Tumor of the Kidney in a 22-Year-Old Male: A Rare Entity

Middle East Journal of Cancer, 2014
Primitive neuroectodermal tumors of the kidney are rare tumors representing about 1% of all sarcomas. Extraskeletal primitive neuroectodermal tumors may be found in the genitourinary tract, the testes, ovaries, uterus, or pancreas.
Veena Gupta , Rajeev Sen , Ashima Batra , Promil Jain   +3 more
doaj  

A Case of Long-term Survival in a Patient with Primary Primitive Neuroectodermal Tumor of the Lung [PDF]

Kosin Medical Journal, 2018
Primitive neuroectodermal tumor (PNET) arising primarily in the lung is an extremely rare and aggressive malignancy with poor chances of patient survival.
Lae Hyung Kang, Hyeong Jin Kim, Jin Ho Jang, Jun Hyun Kim, Kyoung Un Choi, Doosoo Jeon   +5 more
doaj   +1 more source

Diffuse intrinsic pontine glioma biopsy: A single institution experience [PDF]

, 2014
Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/109626/1/pbc25224 ...
Altinok, Deniz, Bhambhani, Kanta, Miller, Kathy, Poulik, Janet, Rao, Latha, Sood, Sandeep, Wang, Zhihong J.   +6 more
core   +1 more source

Primary Malignant Pulmonary Glomus Tumor: A Case Report and Literature Review

The Clinical Respiratory Journal, Volume 20, Issue 3, March 2026.
We report a case of primary malignant pulmonary glomus tumor. A mass in the upper lobe of the right lung, with multiple speckled calcifications. The enhanced scan showed uneven enhancement in the arterial phase and progressive enhancement in the venous phase. ABSTRACT Malignant glomus tumors originating from the lungs are relatively rare.
Shishi Luo, Xiaoyan Lei, Tianxu Fu, Fujin Liu, Zhenping Wang   +4 more
wiley   +1 more source