Results 231 to 240 of about 2,696,673 (357)
Using twin studies to label disease as genetic or environmental is inappropriate [PDF]
Alex J. MacGregor
openalex +1 more source
This study used longitudinal transcriptomics and gene‐pattern classification to uncover patient‐specific mechanisms of chemotherapy resistance in breast cancer. Findings reveal preexisting drug‐tolerant states in primary tumors and diverse gene rewiring patterns across patients, converging on a few dysregulated functional modules. Despite receiving the
Maya Dadiani+14 more
wiley +1 more source
Understanding Heritable Variation Among Hosts in Infectious Diseases Through the Lens of Twin Studies. [PDF]
Smatti MK+3 more
europepmc +1 more source
Genetics vs. environment in inflammatory bowel disease: Concordance rates in 130 twin pairs
NP Thompson+3 more
openalex +1 more source
The Genetics of Coronary Heart Disease: The Contribution of Twin Studies [PDF]
Alun Evans+15 more
openalex +1 more source
B‐cell chronic lymphocytic leukemia (B‐CLL) and monoclonal B‐cell lymphocytosis (MBL) show altered proteomes and phosphoproteomes, analyzed using mass spectrometry, protein microarrays, and western blotting. Identifying 2970 proteins and 316 phosphoproteins, including 55 novel phosphopeptides, we reveal BCR and NF‐kβ/STAT3 signaling in disease ...
Paula Díez+17 more
wiley +1 more source
A case of aortic root replacement for acute type A dissection in Marfan syndrome with twin pregnancy. [PDF]
Yang Y, Jia B, Li C, Zhu J.
europepmc +1 more source
Ubiquitination of transcription factors in cancer: unveiling therapeutic potential
In cancer, dysregulated ubiquitination of transcription factors contributes to the uncontrolled growth and survival characteristics of tumors. Tumor suppressors are degraded by aberrant ubiquitination, or oncogenic transcription factors gain stability through ubiquitination, thereby promoting tumorigenesis.
Dongha Kim, Hye Jin Nam, Sung Hee Baek
wiley +1 more source
Death after transplantation. An analysis of sixty cases [PDF]
Dahrling, BE+3 more
core +1 more source
Prenatal diagnosis and molecular cytogenetic analyses of a rare 15q21.3 and 16p11.2 microduplication family. [PDF]
Zhang F, Liao G, Wen X, Zhang C.
europepmc +1 more source