Immunodeficiency disorders linked to cytoskeleton defects are rare and complex, often presenting with diverse clinical features. This case report highlights a patient with recurrent eosinophilia and a ...

The variants of ARPC1B described in the literature are displayed, with the red-highlighted variant indicating the one identified in our patient. (B) The variant identified in our patient is located in ...

A team of Indian researchers has identified a rare USP18 gene mutation linked to recurrent neurological decline in children. The rare USP18 gene mutation offers crucial insights into a neurological ...

The role of exosomal LINC00853 in gastric cancer progression. Predictive role of homologous recombination deficiency (HRD) for irinotecan in combination with venadaparib, a novel PARP1/2 inhibitor, as ...

(MENAFN- IANS) New Delhi, Nov 27 (IANS) A team of Indian researchers has identified a rare USP18 gene mutation linked to recurrent neurological decline in children. The rare USP18 gene mutation offers ...

A new study on the interleukin 1 (IL-1) pathway and its involvement in systemic inflammation and autoinflammatory diseases has described a mutation of the IL-1 receptor type 1 (IL-1R1) receptor ...

Karyopharm Therapeutics Inc (NASDAQ:KPTI) announced the presentation of updated exploratory subgroup analyses from the SIENDO study in patients with advanced or recurrent TP53 wild-type endometrial ...

Think of the bone marrow as the body’s factory for blood and immune cells. In myelodysplastic syndromes (MDS), that factory breaks down—producing too few cells, and the ones that do roll off the line ...

Guardant360® CDx is the first companion diagnostic to be approved in Japan to identify ESR1 mutations in patients with hormone receptor-positive, HER2-negative breast cancer for treatment with imlunes ...