Disease: Congenital aplastic anemia
- A Fanca knockout mouse model reveals novel Fancd2 function
- A murine model to evaluate immunotherapy effectiveness for human Fanconi anemia-mutated acute myeloid leukemia
- A rare case of Fanconi anemia with Mitomycin C sensitivity: A pediatrics case report
- A Review of the Repair of DNA Double Strand Breaks in the Development of Oral Cancer
- Aberrant R-loop-mediated immune evasion, cellular communication, and metabolic reprogramming affect cancer progression: a single-cell analysis
- Alloengraftment without significant toxicity or GVHD in CD45 antibody-drug conjugate conditioned Fanconi anemia mice
- Author Correction: Hypomorphic Brca2 and Rad51c double mutant mice display Fanconi anemia, cancer and polygenic replication stress
- BRCA2 Mutation Profile in a Proband with Hereditary Breast and Ovarian Cancer-Two Germline Pathogenic Variants Aligned in the Cis Position
- Case report: The evolving phenotype of <em>ESCO2</em> spectrum disorder in a 15-year-old Malaysian child
- Concepts of multi-level dynamical modelling: understanding mechanisms of squamous cell carcinoma development in Fanconi anemia
- Counselling Framework for Germline <em>BRCA1/2</em> and <em>PALB2</em> Carriers Considering Risk-Reducing Mastectomy
- CRISPRmap: Sequencing-free optical pooled screens mapping multi-omic phenotypes in cells and tissue
- Cytogenetics in the management of bone marrow failure syndromes: Guidelines from the Groupe Francophone de Cytogénétique Hématologique (GFCH)
- Deregulated protein homeostasis constrains fetal hematopoietic stem cell pool expansion in Fanconi anemia
- Development of specific growth charts for children with Fanconi anemia
- DNA Damage Response and Mismatch Repair Gene Defects in Advanced and Metastatic Prostate Cancer
- Donor-type bone marrow aplasia following hematopoietic stem cell transplantation in a child with a novel <em>SAMD9L</em> variant
- drexml: A command line tool and Python package for drug repurposing
- Dynamic Tracking of Native Polyclonal Hematopoiesis in Adult Mice
- Editorial: NK cell defects: diagnosis and treatment
- Establishing a novel Fanconi anemia signaling pathway-associated prognostic model and tumor clustering for pediatric acute myeloid leukemia patients
- Exploring DNA repair deficient CHO cell response to low dose rate radiation
- Exploring the hub genes and potential drugs involved in Fanconi anemia using microarray datasets and bioinformatics analysis
- Exploring the Impact of Blood Disorders on Dental Caries
- Expression levels and clinical significance of ferroptosis-related genes in patients with myocardial infarction
- External Evaluation of a Mammography-based Deep Learning Model for Predicting Breast Cancer in an Ethnically Diverse Population
- FANCA c.3624C>T (p.Ser1208=) is a hypomorphic splice variant associated with delayed onset of Fanconi anemia
- FANCD2 deficiency sensitizes SHH medulloblastoma to radiotherapy via ferroptosis
- FANCD2-dependent mitotic DNA synthesis relies on PCNA K164 ubiquitination
- FANCI serve as a prognostic biomarker correlated with immune infiltrates in skin cutaneous melanoma
- FANCJ DNA helicase is recruited to the replisome by AND-1 to ensure genome stability
- Fanconi Anemia Complementary Group A (FANCA) Facilitates the Occurrence and Progression of Liver Hepatocellular Carcinoma
- Fanconi anemia complementation group D2 promotes sensitivity of endometrial cancer cells to chemotherapeutic agents by inhibiting the ferroptosis pathway
- Fanconi Anemia Neuroinflammatory Syndrome (FANS): Brain Lesions and Neurologic Injury in Fanconi Anemia
- Fanconi anemia pathway regulation by FANCI in prostate cancer
- Further Evidence for <em>RFWD3</em> Gene Causing Fanconi Anemia Complementation Group W: Detailed Clinical Report of the Second Case in the Literature
- Genetic analysis of PALB2 gene WD40 domain in canine mammary tumour patients
- Genomic profiling of relapsed small cell lung cancer reveals potential pathways of therapeutic targets
- Hematopoiesis post anti-CD117 monoclonal antibody treatment in wild-type and Fanconi anemia settings
- Histological and molecular difference in albumen quality between post-adolescent hens and aged hens
- HLA-haploidentical stem cell transplantation in children with inherited bone marrow failure syndromes: A retrospective analysis on behalf of EBMT severe aplastic Anemia and pediatric diseases working parties
- HLA-haploidentical T-cell receptor αβT/B-cell-depleted stem cell transplantation for Fanconi anemia
- Homologous Recombination Deficiency Landscape of Breast Cancers and Real-World Effectiveness of Poly ADP-Ribose Polymerase Inhibitors in Patients With Somatic <em>BRCA1</em>/<em>2</em>, Germline <em>PALB2</em>, or Homol
- Identification and characterization of inhibitors covalently modifying catalytic cysteine of UBE2T and blocking ubiquitin transfer
- Identification and prognostic analysis of ferroptosis‑related gene HSPA5 to predict the progression of lung squamous cell carcinoma
- Identification of Multiple Bowen's Disease Skin Lesions by Careful Physical Examination in a Patient With Fanconi Anemia
- Identifying an AML Prognostic Model Using 10 Marker Genes from Single-Cell Transcriptome and Bulk Transcriptome Analysis
- Inherited bone marrow failure syndromes: phenotype as a tool for early diagnostic suspicion at a major reference center in Mexico
- Liver abnormalities are frequent and persistent in patients with Fanconi anemia
- Loss of CD5-positive T-cells following anti-thymocyte globulin treatment
- Male with an apparently normal phenotype carrying a BRCA1 exon 20 duplication in trans to a BRCA1 frameshift variant
- Management of Fanconi anemia beyond childhood
- Minimal intensity conditioning strategies for bone marrow failure: is it time for "preventative" transplants?
- Most Fanconi anemia heterozygotes are not at increased cancer risk: a genome-first DiscovEHR cohort population study
- Moyamoya Disease in a Child With Fanconi Anemia: An Anomaly or a Complication
- MutSβ-MutLβ-FANCJ axis mediates the restart of DNA replication after fork stalling at cotranscriptional G4/R-loops
- NEIL3: A unique DNA glycosylase involved in interstrand DNA crosslink repair
- Neovaginal cancer after sigmoid vaginoplasty: Implications for postoperative cancer surveillance
- New insights into the all-testis differentiation in zebrafish with compromised endogenous androgen and estrogen synthesis
- Novel compound heterozygous variants in FANCI cause premature ovarian insufficiency
- Optimization of radiotherapy in Fanconi anemia-related medulloblastoma
- Oral cancer and oral potentially malignant disorders in patients with Fanconi anemia - A systematic review
- Outcome of allogeneic stem cell transplant for Fanconi anemia in India
- PALB2-mutated human mammary cells display a broad spectrum of morphological and functional abnormalities induced by increased TGFβ signaling
- Pan-cancer analysis of the tumorigenic role of Fanconi anemia complementation group D2 (FANCD2) in human tumors
- Pancancer analysis of the prognostic and immunological role of FANCD2: a potential target for carcinogenesis and survival
- Pediatric acute promyelocytic leukemia and Fanconi anemia: Case report and literature review
- Pleomorphic/solid lobular carcinoma of male breast with PALB2 germline mutation: case report and literature review
- Posttransplant complications in patients with marrow failure syndromes: are we improving long-term outcomes?
- Prevalence of BRCA1, BRCA2, and PALB2 genomic alterations among 924 Taiwanese breast cancer assays with tumor-only targeted sequencing: extended data analysis from the VGH-TAYLOR study
- Profiling of the genetic features of patients with breast, ovarian, colorectal and extracolonic cancers: Association to CHEK2 and PALB2 germline mutations
- Purification and biochemical characterization of the G4 resolvase and DNA helicase FANCJ
- Recruitment and Retention of Hematopoietic Cell Transplantation and Cellular Therapy Physicians: A Report from the ASTCT Talent Acquisition Task Force
- Renal transplantation for infantile and juvenile cystinosis: Two case report and review of the literature
- Research on the resistance of isoviolanthin to hydrogen peroxide-triggered injury of skin keratinocytes based on Transcriptome sequencing and molecular docking
- REV7-p53 interaction inhibits ATM-mediated DNA damage signaling
- RNF4 sustains Myc-driven tumorigenesis by facilitating DNA replication
- SMARCAL1 ubiquitylation controls its association with RPA-coated ssDNA and promotes replication fork stability
- Spatial organization and functions of Chk1 activation by TopBP1 biomolecular condensates
- Squamous Carcinoma of the Oral Cavity in Patient with Fanconi Anemia: A Challenging Reconstruction with Double-barrel Free Fibula Flap Case Report
- Suspicion of constitutional abnormality at diagnosis of childhood leukemia: Update of the leukemia committee of the French Society of Childhood Cancers
- Targeting BRCA and PALB2 in Pancreatic Cancer
- The DNA Damage Response (DDR) landscape of endometrial cancer defines discrete disease subtypes and reveals therapeutic opportunities
- The DNA Damage Response (DDR) landscape of endometrial cancer defines discrete disease subtypes and reveals therapeutic opportunities
- The enrichment of Fanconi anemia/homologous recombination pathway aberrations in ATM/ATR-mutated NSCLC was accompanied by unique molecular features and poor prognosis
- The FANCI/FANCD2 complex links DNA damage response to R-loop regulation through SRSF1-mediated mRNA export
- The Fanconi anemia pathway repairs colibactin-induced DNA interstrand cross-links
- The onset and progression of oral potentially malignant disorders in Fanconi anemia patients: Highlighting early detection of oral cancer
- The state of the art in the treatment of severe aplastic anemia: immunotherapy and hematopoietic cell transplantation in children and adults
- Tissue-specific toxic effects of nano-copper on zebrafish
- To determine the frequency of aldehyde dehydrogenase type 2 (aldh2) deficiency in aplastic anaemia: A single center experience from pakistan
- Treatment of Fanconi anemia patient with synchronous esophageal and tongue cancer in COVID-19 era: a case report
- Two cases of cytopenia associated with multiple malformations
- Two siblings with Fanconi anemia (FANCQ, ERCC4/XPF) presenting with tumor-mimicking lesions in the brain and acute neurological deterioration
- Type 2 cytokine signaling in macrophages protects from cellular senescence and organismal aging
- Umbilical Cord Blood Transplantation for Fanconi Anemia With a Special Focus on Late Complications: a Study on Behalf of Eurocord and SAAWP-EBMT
- Uncovering the Challenges of Rare Diseases: Insights From a Retrospective Cross-Sectional Study in Albania (2005-2022)
- What are the DNA lesions underlying formaldehyde toxicity?
- When to consider inherited marrow failure syndromes in adults
- Whole-exome sequencing reveals genetic variants that may play a role in neurocytomas