Results 71 to 80 of about 257,150 (173)

Pelger-Huet Changes in Mature Polymorphonuclear Leukocytes

open access: yes, 2002
Pelger-Huet changes in mature ...
Lawrence, Christine
core  

Vimentin regulates nuclear segmentation in neutrophils

open access: yes, 2023
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

open access: yes, 2002
peripheral smear dysplastic changes in WBC with Pelger-Huet ...
Lawrence, Christine
core  

Hypersegmented and Pelger-Huet Polymorphonuclear Leukocytes, Changes Secondary to Sepsis

open access: yes, 2002
peripheral smear with hypersegmented poly and Pelger-Huet poly, changes secondary to ...
Lawrence, Christine
core  

Marked Pelger-Huet Mononuclear Mature Granulocytes in Acute Erythroleukemia

open access: yes, 2002
PS with marked Pelger-Huet mononuclear mature granulocytes stained with ...
Lawrence, Christine
core  

Leukocyte Function in Pelger-Huët Anomaly of Dogs

open access: yes, 1989
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

Mutations at the mouse ichthyosis locus are within the lamin B receptor gene: a single gene model for human Pelger-Huet anomaly.

open access: yes, 2002
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

Publication Only

open access: yes
HemaSphere, Volume 9, Issue S1, June 2025.
wiley   +1 more source

Mutations in the _SC4MOL_ gene encoding a novel methyl sterol oxidase cause autosomal recessive psoriasisiform dermatitis, microcephaly and developmental delay [PDF]

open access: yes, 2008
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  

NBAS Mutations Cause a Multisystem Disorder Involving Bone, Connective Tissue, Liver, Immune System, and Retina

open access: yes, 2015
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

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