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Ladinin-1 is a protein that in humans is encoded by the LAD1 gene. The protein encoded by this gene may be an anchoring filament that is a component of...
Click to read more »of leukocyte adhesion deficiency include LAD1, LAD2, and LAD3. LAD1 is the most common. Patients with LAD1 have an inherited molecular defect that causes...
Click to read more »Leukocyte adhesion deficiency-1 (LAD1) is a rare and often fatal genetic disorder in humans. The main sign of the disease is life-threatening, recurrent...
Click to read more »functioning neutrophils. LAD1, a subtype of LAD, is caused by a lack of integrins that contain the beta subunit, including LFA-1. LAD1 is characterized by...
Click to read more »patients with LAD1, including pneumonia, periodontitis, otitis media, and localized cellulitis. Similar to that in patients with LAD1, their infections...
Click to read more »Racimo F, Dannemann M, et al. (May 2015). "Long-Term Balancing Selection in LAD1 Maintains a Missense Trans-Species Polymorphism in Humans, Chimpanzees, and...
Click to read more »P83111 8521 LACTB2 HGNC:18512; Q53H82 8522 LACTBL1 HGNC:35445; A8MY62 8523 LAD1 HGNC:6472; O00515 8524 LAG3 HGNC:6476; P18627 8525 LAGE3 HGNC:26058; Q14657...
Click to read more »pemphigoid Laminin 5 (Epiligrin, Laminin 332) Linear IgA bullous dermatosis LAD1 portion of BPAG2 Collagen type VII 97 290/145 Protein 105 pemphigoid Protein...
Click to read more »phagocytosis Chemotaxis and degranulation Leukocyte adhesion deficiency LAD1 LAD2 Chédiak–Higashi syndrome Neutrophil-specific granule deficiency Respiratory...
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