Results 51 to 60 of about 257,150 (173)

Pseudo Pelger-Huet - 1

open access: yes, 2018
An image from a peripheral blood smear showing a hyposegmented neutrophil seen in a patient with Pseudo Pelger-Huet (100X oil immersion)
To, Michelle, Kwon, Gloria
core   +1 more source

Atypical chronic myeloid leukemia: From diagnosis to molecular features and therapeutic options

open access: yesHemaSphere, Volume 9, Issue 12, December 2025.
ABSTRACT Atypical chronic myeloid leukemia (aCML) is a rare form of myelodysplastic (MDS)/myeloproliferative neoplasm (MPN) overlap disorder characterized by neutrophilic leukocytosis with circulating immature myeloid cells (IMC), frequent hepatosplenomegaly, and poor prognosis with high rates of leukemic transformation.
Alessandra Iurlo   +3 more
wiley   +1 more source

Pseudo Pelger-Huet - 3

open access: yes, 2018
An image from a peripheral blood smear showing a hyposegmented neutrophil in a patient with Pseudo Pelger-Huet (100X oil immersion)
To, Michelle, Kwon, Gloria
core   +1 more source

Mutations in the gene encoding the lamin B receptor produce an altered nuclear morphology in granulocytes (Pelger-Huet anomaly).

open access: yes, 2002
Pelger-Huet anomaly (PHA; OMIM *169400) is an autosomal dominant disorder characterized by abnormal nuclear shape and chromatin organization in blood granulocytes.
Olins, A L   +16 more
core   +3 more sources

Pseudo Pelger-Huet - 2

open access: yes, 2018
An image from a peripheral blood smear showing a hyposegmented neutrophil in a patient with Pseudo Pelger-Huet (100X oil immersion)
To, Michelle, Kwon, Gloria
core   +1 more source

Anomalía de Pelger Hüet. A propósito. de un caso. Pelger-Hüet anomaly. Apropos of a case.

open access: yesRevista Médica Electrónica, 2009
La anomalía de Pelger Hüet fue descrita inicialmente en 1928 por el médico holandés Pelger y su origen genético fue descubierto más tarde por el pediatra Hüet.
Adys Gutiérrez Díaz   +5 more
doaj  

Clinical and Molecular Heterogeneity Underlying Monogenic Causes of Pediatric Diabetes Associated to Brain Developmental Disorders

open access: yesClinical Genetics, Volume 108, Issue 5, Page 495-510, November 2025.
A growing number of genetic variants linking non‐autoimmune diabetes to NDDs across different ages offer key insights about a common background of these phenotypes. These findings call for multidisciplinary approaches to care that integrate metabolic and neurological management in affected children.
Gabriele Di Pasquale   +6 more
wiley   +1 more source

Lamin B-receptor mutations in Pelger-Huët anomaly

open access: yes, 2002
Pelger-Huet anomaly is an inherited abnormality of neutrophils, characterized by reduced nuclear segementation and an apparently looser chromatin structure. Following linkage studies in two families, the lamin B-receptor (LBR) was sequenced and mutations
Garner, C   +14 more
core   +1 more source

Evaluation of Absolute Neutrophil Count in COVID-19 Patients in a Tertiary Care Hospital

open access: yesMedical Laboratory Journal, 2022
Background and objectives: Coronavirus disease 2019 (COVID-19) is a communicable disease caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2).
Harsha Jaykar   +2 more
doaj  

cTAGE5/MEA6 Regulates LBR Localization to Maintain Nuclear Envelope Integrity and Safeguard Against Aging

open access: yesAging Cell, Volume 24, Issue 10, October 2025.
cTAGE5 regulates LBR trafficking between the ER and the nucleus membrane to maintain the integrity of both the ER and the nuclear envelope. cTAGE5 KO results in LBR retention in the ER, reduced stability, and subsequent disruption of nuclear envelope integrity. ABSTRACT cTAGE5/MEA6 plays a pivotal role in COPII complex assembly, ER‐to‐Golgi trafficking,
Yaqing Wang   +9 more
wiley   +1 more source

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