Publications by authors named "L Karnik"

Article Synopsis
  • Many cancers and ribosomopathies, like Diamond-Blackfan anemia (DBA), are linked to ribosome dysfunction due to mutations in ribosomal proteins.
  • Research using patient-derived bone marrow cells shows that different mutations can lead to distinct developmental pathways in red blood cell progenitors, resulting in varying clinical symptoms.
  • The study uncovers unique mechanisms of erythroid failure in DBA, which could aid in finding new treatment options for this condition.
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Background: Haploidentical bone marrow transplant (haplo-BMT) offers near universal donor availability as a curative modality for individuals with severe sickle cell disease (SCD). However, the required intense immunodepletion is associated with increased infectious complications. A paucity of data exists on immune reconstitution following haplo-BMT for SCD.

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Curative therapy for individuals with severe sickle cell disease (SCD) who lack an HLA-identical sibling donor has been frustratingly elusive. In with the goal of improving engraftment while minimizing transplantation-related morbidity, a multi-institutional learning collaborative was developed in the context of a Phase II clinical trial of nonmyeloablative, related HLA-haploidentical (haplo) bone marrow transplantation (BMT) with post-transplantation cyclophosphamide. All eligible participants had hemoglobin SS, and 89% (16 of 18) had an identifiable donor.

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Liver resection is the standard treatment for any liver lesion. Laparoscopic liver resection is associated with lower intra-operative blood loss and fewer complications than open resection. Access to the posterior part of the right liver lobe is very uncomfortable and difficult for surgeons due the anatomic position, especially when employing laparoscopic surgery.

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