Results 141 to 150 of about 1,792 (176)

Clinical management of bullous pemphigoid-The importance of cytology in diagnosis. [PDF]

J Oral Maxillofac Pathol
Ramesh P, Divyambika CV, Warrier AS, Joseph LD.   +3 more
europepmc   +1 more source

Bullous pemphigoid and mucous membrane pemphigoid humoral responses differ in reactivity towards BP180 midportion and BP230. [PDF]

Front Immunol
Mariotti F, Pira A, De Luca N, Giampetruzzi AR, Russo F, Cerri A, Gasparini G, Cozzani E, Marzano AV, Antiga E, Caproni M, Quaglino P, Carrozzo M, Didona B, Di Zenzo G.   +14 more
europepmc   +1 more source

Sensory-motor circuit is a therapeutic target for <i>dystonia musculorum</i> mice, a model of hereditary sensory and autonomic neuropathy 6. [PDF]

Sci Adv
Yoshioka N, Kurose M, Sano H, Tran DM, Chiken S, Tainaka K, Yamamura K, Kobayashi K, Nambu A, Takebayashi H.   +9 more
europepmc   +1 more source

Occurrence of Bullous Pemphigoid in a Longstanding Case of Rheumatoid Arthritis in an Indian Patient: A Rare Association. [PDF]

Cureus
Deo KS, Chaurasia P, Sharma Y, Gupta A, Malik N.   +4 more
europepmc   +1 more source

Microtubule stability, Golgi organization, and transport flux require dystonin-a2–MAP1B interaction [PDF]

Journal of Cell Biology, 2012
Loss of function of dystonin cytoskeletal linker proteins causes neurodegeneration in dystonia musculorum (dt) mutant mice. Although much investigation has focused on understanding dt pathology, the diverse cellular functions of dystonin isoforms remain poorly characterized.
Scott D Ryan, Yves De Repentigny, Alexandre Blais   +2 more
exaly   +5 more sources

Dystonin/Bpag1—A link to what? [PDF]

Cytoskeleton, 2007
AbstractThe dystonin/Bpag1 cytoskeletal interacting proteins play important roles in maintaining cytoarchitecture integrity in skin and in the neuromuscular system. The most profound phenotype observed in the dystonin mutant dystonia musculorum (dt) mice is a severe movement disorder, attributed in large part to sensory neuron degeneration.
Rashmi Kothary
exaly   +4 more sources

Cloning and Characterization of the Neural Isoforms of Human Dystonin

Genomics, 1995
Dystonia musculorum (dt) is a hereditary neurodegenerative disease in mice that leads to a sensory ataxia. We have identified and cloned a gene encoded at the dt locus. The product of the dt gene, dystonin, is a neural isoform of a hemidesmosomal protein bullous pemphigoid antigen 1 (bpag1).
Arthur Brown, Gratien Dalpé, Rashmi Kothary   +2 more
exaly   +4 more sources

The Intermediate Filament Protein Peripherin Is the Specific Interaction Partner of Mouse BPAG1-n (Dystonin) in Neurons [PDF]

Journal of Cell Biology, 1999
The dystonia musculorum (dt) mouse suffers from severe degeneration of primary sensory neurons. The mutated gene product is named dystonin and is identical to the neuronal isoform of bullous pemphigoid antigen 1 (BPAG1-n). BPAG1-n contains an actin-binding domain at its NH2 terminus and a putative intermediate filament-binding domain at its COOH ...
Conrad L. Leung, Dongming Sun, Ronald K.H. Liem   +2 more
exaly   +4 more sources

Roles of dystonin isoforms in the maintenance of neural, muscle, and cutaneous tissues

Anatomical Science International, 2023
Dystonin (DST), also known as bullous pemphigoid antigen 1 (BPAG1), encodes cytoskeletal linker proteins belonging to the plakin family. The DST gene produces several isoforms, including DST-a, DST-b, and DST-e, which are expressed in neural, muscle, and cutaneous tissues, respectively.
Nozomu Yoshioka
openalex   +3 more sources

MAP1B and Clathrin Are Novel Interacting Partners of the Giant Cyto-linker Dystonin

Journal of Proteome Research, 2011
Dystonin is a large multidomain cytoskeletal-associated protein that plays an essential role in the nervous system. Loss of dystonin results in neuromuscular dysfunction and early death in a mouse mutant called dystonia musculorum. Conserved among related proteins, the plakin domain is a defining feature of all major dystonin isoforms, yet its ...
Rashmi Kothary
exaly   +4 more sources