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Kindler syndrome, 12/2005
Kindler syndrome is a rare autosomal recessive disorder associated with skin fragility. It is characterized by blistering in infancy, photosensitivity and... 
Kindler syndrome, Poikiloderma, Kindler-Weary syndrome
Journal
Dermatology Online Journal, ISSN 1087-2108, 03/2018, Volume 24, Issue 3
Kindler syndrome is a rare, autosomal recessive genodermatosis, caused by mutations in the FERMT1 gene. It is thought to be primarily a skin disease, but other... 
Fermt1 gene | Phenotype | Colitis | Kindler syndrome | Cholangitis
Journal Article
Journal Article
Trials, ISSN 1745-6215, 12/2019, Volume 20, Issue 1, pp. 1 - 13
Abstract Background Epidermolysis bullosa (EB) is a group of rare, genetic diseases that affect the integrity of epithelial tissues, most notably the skin.... 
Birch bark | Betulin | Epidermolysis bullosa | Kindler syndrome | Oleogel | Trial design
Journal Article
Gulhane Medical Journal, ISSN 1302-0471, 2015, Volume 57, Issue 3, pp. 319 - 320
Journal Article
Annales de Pathologie, ISSN 0242-6498, 08/2011, Volume 31, Issue 4, pp. 246 - 250
Introduction: Kindler's syndrome is a rare type of genetic skin condition belonging to the class of bullous poikilodermia. We report three new sibling cases of... 
Kindler syndrome | Poikilodermia
Journal Article
Journal Article
Journal of Dental Materials and Techniques, ISSN 2322-4150, 06/2014, Volume 3, Issue 3, pp. 134 - 138
Kindler syndrome (KS) is a rare, autosomal recessive genodermatosis characterized by skin blistering and photosensitivity in infancy, progressive poikiloderma,... 
Case report | genodermatosis | Kindler Syndrome
Journal Article
Journal of Investigative Dermatology, ISSN 0022-202X, 02/2019, Volume 139, Issue 2, pp. 369 - 379
Kindler syndrome is an autosomal recessive genodermatosis that results from mutations in the gene encoding t kindlin-1. Kindlin-1 localizes to focal adhesion... 
KINDLER-SYNDROME | LOCALIZATION | DOMAIN | FOCAL ADHESION | PROTEIN | GENE | MIGFILIN | INTEGRIN | MUTATIONS | CELL | DERMATOLOGY | MST, microscale thermophoresis | FRET, fluorescence resonance energy transfer | KS, Kindler syndrome | PBS, phosphate buffered saline | WT, wild type | EGFR, epidermal growth factor receptor | IP, immunoprecipitation
Journal Article
International Journal of Biomedical and Advance Research, ISSN 2229-3809, 02/2014, Volume 5, Issue 2, p. 131
Journal Article
Journal Article
Journal of Pathology, ISSN 0022-3417, 12/2007, Volume 213, Issue 4, pp. 462 - 470
Kindlin-1 is an epithelium-specific phosphoprotein and focal adhesion adaptor component. Mutations in the corresponding gene (KIND1) cause Kindler syndrome... 
Skin blistering | Diarrhoea | Colitis | Poikiloderma | Kindler syndrome | KIND1 | CONTACTS | colitis | PROTEIN | ACTIN | kindler syndrome | poikiloderma | PATHOLOGY | diarrhoea | skin blistering | INFLAMMATORY-BOWEL-DISEASE | ONCOLOGY | MUTATIONS
Journal Article
European Annals of Otorhinolaryngology, Head and Neck Diseases, ISSN 1879-7296, 2017, Volume 135, Issue 1, pp. 59 - 61
Abstract Introduction Kindler syndrome is a very rare, autosomal recessive genodermatosis characterized by skin fragility and photosensitivity in infancy with... 
Otolaryngology | Hard palate | Photosensitivity | Poikiloderma | Invasive squamous cell carcinoma | Kindler syndrome | OTORHINOLARYNGOLOGY
Journal Article
The British journal of dermatology, ISSN 0007-0963, 01/2016, Volume 174, Issue 1, pp. 56 - 67
Journal Article
JOURNAL OF MOLECULAR BIOLOGY, ISSN 0022-2836, 12/2009, Volume 394, Issue 5, pp. 944 - 956
The integrin family of heterodimeric cell adhesion molecules exists in both low- and high-affinity states, and integrin activation requires binding of the... 
focal adhesion | BETA TAILS | BIOCHEMISTRY & MOLECULAR BIOLOGY | CHEMICAL-SHIFT | CELL-MATRIX ADHESION | structure | FILAMIN BINDING | KINDLER-SYNDROME | PROTEIN STRUCTURES | talin | kindlin | CYTOPLASMIC TAILS | BINDING-LIKE DOMAIN | LEUKOCYTE ADHESION | integrin
Journal Article
ORPHANET JOURNAL OF RARE DISEASES, ISSN 1750-1172, 07/2019, Volume 14, Issue 1, pp. 183 - 15
BackgroundKindler Syndrome (KS) is a rare genodermatosis characterized by skin fragility, skin atrophy, premature aging and poikiloderma. It is caused by... 
MEDICINE, RESEARCH & EXPERIMENTAL | DIAGNOSIS | KINDLIN-1 | Prevalence | PROTEIN | Kindler syndrome | PHENOTYPE | EPIDERMOLYSIS-BULLOSA | Skin cancer | DELETION | SCC | Bullous disease | GENETICS & HEREDITY | SQUAMOUS-CELL CARCINOMA | FERMT1 GENE | MUTATIONS | SPECTRUM |