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Pelger-Huet Anomaly

Known as: Pelger Huët Nuclear Anomaly, Pelger Huet Anomaly, anomaly huet pelger 
Autosomal dominant anomaly characterized by abnormal ovoid shape GRANULOCYTE nuclei and their clumping chromatin. Mutations in the LAMIN B receptor… 
National Institutes of Health

Papers overview

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Highly Cited
2005
Highly Cited
2005
Abstract The fifth-generation Pennsylvania State University–National Center for Atmospheric Research (PSU–NCAR) Mesoscale Model… 
Highly Cited
1996
Highly Cited
1996
Autosomal dominant iridogoniodysgenesis anomaly (IGDA) is characterized by iris hypoplasia and goniodysgenesis with frequent… 
Highly Cited
1989
Highly Cited
1989
We studied the proliferative response of PBL to the mitogens PHA and PWM and Candida albicans Ag in 301 HIV seropositive… 
Highly Cited
1987
Highly Cited
1987
Peripheral lymphocytes stimulated with phytohemagglutinin (PHA-blasts) were examined for their responsiveness to exogenous… 
Highly Cited
1984
Highly Cited
1984
Because interleukin 2 (IL 2) production and IL 2 receptor (IL 2R) expression are essential steps in T cell proliferation, we… 
1980
1980
Polymorphonuclear leukocytes (PMNL) from two individuals with congenital Pelger-Huet anomaly (PHA) were examined to determine… 
Highly Cited
1977
Highly Cited
1977
Acid α‐naphthyl acetate esterase (ANAE) activity is charecteristic of resting human T lymphocytes. The expression of the ANAE… 
1972
1972
All five members of one generation in an Icelandic family were affected by acute myeloid leukaemia or preleukaemia. Two sibs died… 
Highly Cited
1959
Highly Cited
1959
THE abnormality of granulocytic leukocytes manifested by poor segmentation and condensation of nuclear chromatin was first…