Results 231 to 240 of about 1,025,592 (331)

Correction: Genome-wide identification of the phosphofructokinase gene family in maize (Zea Mays L.) and their expression levels under abiotic stress and phytohormones. [PDF]

BMC Plant Biol
Fu W, Fan D, Liu S, Bu Y.
europepmc   +1 more source

The Synaptinemal Complex in Homologous and Nonhomologous Pairing of Chromosomes

Cold Spring Harbor Symposia on Quantitative Biology, 1974
C. B. Gillies, Søren W. Rasmussen, D. von Wettstein   +2 more
openaire   +3 more sources

Clinical validation of a DNA methylation biomarker associated with overall survival of relapsed ovarian cancer patients

International Journal of Cancer, EarlyView.
What's New? Most patients with ovarian cancer (OC) relapse after first‐line chemotherapy, and prognosis with second‐line treatment depends largely on the platinum‐free interval. However, reliable biomarkers to predict response to second‐line therapy remain lacking.
Muhammad Habiburrahman, Nahal Masrour, Naina Patel, Anna M. Piskorz, Robert Brown, James D. Brenton, Iain A. McNeish, James M. Flanagan   +7 more
wiley   +1 more source

Gene order and recombination rate in homologous chromosome regions of the chicken and a passerine bird.

Molecular biology and evolution, 2007
D. Dawson, Mikael Åkesson, T. Burke, J. Pemberton, J. Slate, B. Hansson   +5 more
semanticscholar   +1 more source

A Case of Metastatic Castration‐Resistant Prostate Cancer With RAD54L Mutation Responding to Niraparib

IJU Case Reports, EarlyView.
ABSTRACT Introduction A certain proportion of prostate cancers have alterations in homologous recombination repair (HRR)‐ related genes. poly ADP‐ribose polymerase (PARP) inhibitors have been approved for metastatic castration‐resistant prostate cancer (mCRPC) with mutations in the BRCA1/2 gene.
Yusuke Sato, Yoichi Fujii, Masaki Nakamura, Chiharu Tanai, Yuta Yamada, Kousuke Watanabe, Hidenori Kage, Kuniko Sunami, Katsutoshi Oda, Haruki Kume   +9 more
wiley   +1 more source

Isodicentric Y chromosome with SRY duplication in a female with complete gonadal dysgenesis. [PDF]

Mol Cytogenet
Salmaninejad A, Yaghoubi Z, Haghzad T, Latifi M, Bayat R, Esnaashari S, Dalili S.   +6 more
europepmc   +1 more source

DNA replication meets genetic exchange: Chromosomal damage and its repair by homologous recombination

, 2001
Andrei Kuzminov
openalex   +1 more source

New insights into applications of base editor in hereditary disorders

Interdisciplinary Medicine, EarlyView.
Abstract Hereditary disorders are a group of diseases caused by genetic mutations or chromosomal variations. Although the incidence of each genetic disorder is relatively low, patients affected by the disease generally experience a range of severe symptoms, including blindness, disability, and even premature death. In addition, the available treatments
Maoping Cai, Linhui Zhang, Liqing Li, Yue Liu, Canbin Lv, Yan Shi, Jianyuan Zhao, Dingwei Ye, Yuanyuan Qu   +8 more
wiley   +1 more source

Chromosome-level genome assembly for Sichuan taimen (Hucho bleekeri) reveals the extraordinary tandem repeat proportions and its persistent population shrinkage. [PDF]

BMC Genomics
Zhang X, Xiong D, Jian S, Jiang Y, Wang L.   +4 more
europepmc   +1 more source

Four Pharmacogenomic Variants Strongly Linked to Corticosteroid‐Induced Avascular Necrosis in Children with Cancer

The Journal of Clinical Pharmacology, EarlyView.
Abstract Corticosteroids are effective anti‐cancer agents for treating hematologic malignancies in children. However, avascular necrosis (AVN) is a common and debilitating adverse effect, leading to bone death and impacting long‐term quality of life. This study aimed to uncover the genetic factors contributing to corticosteroid‐induced AVN in a well ...
Miguel Cordova‐Delgado, Erika N. Scott, Shahrad R. Rassekh, Catrina M. Loucks, Wan‐Chun Chang, Edward J. Raack, Jessica N. Trueman, Colin J. D. Ross, Bruce C. Carleton, the Canadian Pharmacogenomics Network for Drug Safety Consortium   +9 more
wiley   +1 more source