Results 71 to 80 of about 257,150 (173)
Pelger-Huet Changes in Mature Polymorphonuclear Leukocytes
Pelger-Huet changes in mature ...
Lawrence, Christine
core
Vimentin regulates nuclear segmentation in neutrophils
Granulocytes are indispensable for various immune responses. Unlike other cell types in the body, the nuclei of granulocytes, particularly neutrophils, are heavily segmented into multiple lobes.
Guo, Q. +6 more
core +1 more source
Dysplastic Changes in WBC with Pelger-Huet Changes
peripheral smear dysplastic changes in WBC with Pelger-Huet ...
Lawrence, Christine
core
Hypersegmented and Pelger-Huet Polymorphonuclear Leukocytes, Changes Secondary to Sepsis
peripheral smear with hypersegmented poly and Pelger-Huet poly, changes secondary to ...
Lawrence, Christine
core
Marked Pelger-Huet Mononuclear Mature Granulocytes in Acute Erythroleukemia
PS with marked Pelger-Huet mononuclear mature granulocytes stained with ...
Lawrence, Christine
core
Leukocyte Function in Pelger-Huët Anomaly of Dogs
Leukocyte function was evaluated in five dogs with Pelger-Huët (P-H) anomaly and in five control dogs. No significant differences were found between groups in neutrophil adherence, random movement, chemotaxis, phagocytosis, or bacterial killing of ...
John Brown +4 more
core +1 more source
The nature of the wild-type gene product at the mouse ichthyosis (ic) locus has been of great interest because mutations at this locus cause marked abnormalities in nuclear heterochromatin, similar to those observed in Pelger–Huët anomaly (PHA).
Olins, A L +26 more
core +1 more source
Mutations in the _SC4MOL_ gene encoding a novel methyl sterol oxidase cause autosomal recessive psoriasisiform dermatitis, microcephaly and developmental delay [PDF]
Disorders of cholesterol biosynthesis have clinical manifestations involving skeleton, eyes, neurologic development, and skin. We describe a patient with congenital cataracts, developmental delay, microcephaly, and low serum cholesterol who developed ...
Jushua Michel +8 more
core
We report two unrelated patients with a multisystem disease involving liver, eye, immune system, connective tissue, and bone, caused by biallelic mutations in the neuroblastoma amplified sequence (NBAS) gene.
Francis L. Munier +67 more
core +1 more source

