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View article: Bioinformatic and genomic analysis identifies C allele of APOE rs7412 as the most prominent variant limiting extreme human longevity
Bioinformatic and genomic analysis identifies C allele of APOE rs7412 as the most prominent variant limiting extreme human longevity Open
The genetic factors influencing human longevity have long been a subject of curiosity, linking ancient historical records with modern genomic research. This study seeks to identify key genetic contributors to lifespan by integrating genome…
View article: 3D organoid cultivation improves the maturation and functional differentiation of cholangiocytes from human pluripotent stem cells
3D organoid cultivation improves the maturation and functional differentiation of cholangiocytes from human pluripotent stem cells Open
Idiopathic cholangiopathies are diseases that affect cholangiocytes, and they have unknown etiologies. Currently, orthotopic liver transplantation is the only treatment available for end-stage liver disease. Limited access to the bile duct…
View article: Cell and Gene Therapy for Anemia: Hematopoietic Stem Cells and Gene Editing
Cell and Gene Therapy for Anemia: Hematopoietic Stem Cells and Gene Editing Open
Hereditary anemia has various manifestations, such as sickle cell disease (SCD), Fanconi anemia, glucose-6-phosphate dehydrogenase deficiency (G6PDD), and thalassemia. The available management strategies for these disorders are still unsat…
View article: Knowledge, Attitude, and Practice of Malaria Community Worker towards Prevention and Control of Malaria in Kokap, Kulon Progo: A Pilot Study
Knowledge, Attitude, and Practice of Malaria Community Worker towards Prevention and Control of Malaria in Kokap, Kulon Progo: A Pilot Study Open
Background: Malaria Community Worker (CMW) has a crucial role in malaria prevention and control in the community. However, a number of studies showed that there is a lack of competence from MCW in carrying out its duties. Knowledge, attitu…
View article: Aberrant Expressions and Variant Screening of SEMA3D in Indonesian Hirschsprung Patients
Aberrant Expressions and Variant Screening of SEMA3D in Indonesian Hirschsprung Patients Open
Background: The semaphorin 3D (SEMA3D) gene has been implicated in the pathogenesis of Hirschsprung disease (HSCR), a complex genetic disorder characterized by the loss of ganglion cells in varying lengths of gastrointestinal tract. We wis…
View article: The impact of down-regulated SK3 expressions on Hirschsprung disease
The impact of down-regulated SK3 expressions on Hirschsprung disease Open
Our study shows that the down-regulated SK3 expression in ganglionic intestines might contribute to the persistent bowel symptoms following a properly performed pull-through surgery in Indonesian HSCR patients. Furthermore, this study is t…
View article: Combined Puestow and choledocoduodenostomy for concomitant large pancreatic duct and primary choledochal stones: A case series
Combined Puestow and choledocoduodenostomy for concomitant large pancreatic duct and primary choledochal stones: A case series Open
The incidence of multiple pancreatic duct stones and large choledochal stones is infrequent. Surgical treatment with combined longitudinal pancreatojejunostomy Roux-en-Y and Choledoco-duodenostomy is safe and effective to resolve jaundice …
View article: AB053. NRG1 rare variant effects in Hirschsprung disease patients
AB053. NRG1 rare variant effects in Hirschsprung disease patients Open
Background: Hirschsprung disease (HSCR) is a heterogeneous genetic disorder characterized by absence of ganglion cells along intestines resulting in functional bowel obstruction. NRG1 gene has been implicated in the intestinal ganglionosis…