Results 121 to 130 of about 22,374,088 (435)
Incidence, outcomes, and risk factors of pleural effusion in patients receiving dasatinib therapy for Philadelphia chromosome-positive leukemia. [PDF]
Dasatinib, a second-generation BCR-ABL1 tyrosine kinase inhibitor, is approved for the treatment of chronic myeloid leukemia and Philadelphia chromosome-positive acute lymphoblastic leukemia, both as first-line therapy and after imatinib intolerance or ...
Abruzzese, Elisabetta+10 more
core +2 more sources
Worth the Effort: Lessons for Discovery and Care From an Unusual Case of Gorlin Syndrome
ABSTRACT Gorlin‐Goltz Syndrome (GGS) is a rare autosomal dominant genetic disorder encompassing a diverse range of clinical manifestations, including congenital anomalies and predisposition to cancer. Pathogenic variants in PTCH1 and SUFU account for up to 79% and 6% of cases, respectively. Currently, an estimated 15%–27% of individuals with a clinical
V. Taliercio+13 more
wiley +1 more source
Medical Implementation of Microarray Technology
Microarray technology represents a critical new advance in molecular cytogenetics. The de-velopment of this approach has provided fundamental insights into the molecular pathogenesis in clinical cytogenetics and has provided a clue to many unidentified ...
Ji Un Kang
doaj +1 more source
Amaç: İnsan sağlığına ilişkin bilimsel araştırmalarda memelilerin sınırlı kullanımı yeni araştırma stratejilerinin geliştirilmesine yol açmıştır. Bunlardan birisi memeli hücre kültürü tekniğidir.
M. Bertan YILMAZ+8 more
doaj +1 more source
The order Scorpiones is one of the most cytogenetically interesting groups within Arachnida by virtue of the combination of chromosome singularities found in the 59 species analyzed so far.
M. C. Schneider+4 more
semanticscholar +1 more source
BCR::ABL1‐Positive Acute Myeloid Leukemia
American Journal of Hematology, EarlyView.
Alban Canali+3 more
wiley +1 more source
ABSTRACT Rare diseases impact approximately 1 in 10 people worldwide, and yet, less than 5% of all rare diseases currently have an approved treatment option available. This is due to many challenges unique to rare diseases, including small, diverse patient populations, the cost of drug development that is not proportionate to the number of patients who
Caleb P. Bupp+7 more
wiley +1 more source
Most of the previous studies on the genetic variability in Spanish “Berrenda” breeds have been carried out using DNA microsatellites. The present work aimed to estimate the genetic diversity, population structure, and potential genetic differences among ...
Rafael González-Cano+6 more
doaj +1 more source
Molecular markers and cytogenetics of Eleven O’Clock Portulaca umbraticola: a non-conventional edible ornamental crop [PDF]
Portulaca umbraticola, commonly known as “Eleven o'clock”, is a popular ornamental plant in Brazil, but its potential as a non-conventional food source remains underexplored.
J. S. Souza+6 more
doaj +1 more source
The Karyotype Ontology: a computational representation for human cytogenetic patterns [PDF]
The karyotype ontology describes the human chromosome complement as determined cytogenetically, and is designed as an initial step toward the goal of replacing the current system which is based on semantically meaningful strings. This ontology uses a novel, semi-programmatic methodology based around the tawny library to construct many classes rapidly ...
arxiv