about
Mutation analysis of the cathepsin C gene in Indian families with Papillon-Lefèvre syndromeLoss-of-function mutations in the cathepsin C gene result in periodontal disease and palmoplantar keratosisEvaluation of a new binary system of grading oral epithelial dysplasia for prediction of malignant transformation.Imaging mass spectrometry using chemical inkjet printing reveals differential protein expression in human oral squamous cell carcinoma.The presence of multiple regions of homozygous deletion at the CSMD1 locus in oral squamous cell carcinoma question the role of CSMD1 in head and neck carcinogenesis.Oculofaciocardiodental and Lenz microphthalmia syndromes result from distinct classes of mutations in BCOR.Non-penetrance and late appearance of polyps in families with familial adenomatous polyposis.An overview of the molecular pathology of head and neck cancer, and its clinical implications.Tumor expression of major vault protein is an adverse prognostic factor for radiotherapy outcome in oropharyngeal carcinoma.Spatial metabolic fingerprinting using FT-IR spectroscopy: investigating abiotic stresses on Micrasterias hardyi.Characterization of neutrophil function in Papillon-Lefèvre syndrome.Loss of epithelial markers is an early event in oral dysplasia and is observed within the safety margin of dysplastic and T1 OSCC biopsies.The role of cathepsin C in Papillon-Lefèvre syndrome, prepubertal periodontitis, and aggressive periodontitis.DLC1 is unlikely to be a primary target for deletions on chromosome arm 8p22 in head and neck squamous cell carcinoma.Loss of CSMD1 expression is associated with high tumour grade and poor survival in invasive ductal breast carcinoma.Dento-osseous changes as diagnostic markers in familial adenomatous polyposis families.Why oral histopathology suffers inter-observer variability on grading oral epithelial dysplasia: an attempt to understand the sources of variation.Frequent allelic loss and homozygous deletion in chromosome band 8p23 in oral cancer.Novel and recurrent mutations in the neurofibromatosis type 1 (NF1) geneDeletion mapping defines three discrete areas of allelic imbalance on chromosome arm 8p in oral and oropharyngeal squamous cell carcinomasDNA studies underestimate the major role of CDKN2A inactivation in oral and oropharyngeal squamous cell carcinomasFocal palmoplantar and gingival hyperkeratosis: a case reportTumours of the oral cavityAnalysis of head and neck carcinoma progression reveals novel and relevant stage-specific changes associated with immortalisation and malignancy
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description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Nalin Thakker
@ast
Nalin Thakker
@en
Nalin Thakker
@es
Nalin Thakker
@nl
Nalin Thakker
@sl
type
label
Nalin Thakker
@ast
Nalin Thakker
@en
Nalin Thakker
@es
Nalin Thakker
@nl
Nalin Thakker
@sl
prefLabel
Nalin Thakker
@ast
Nalin Thakker
@en
Nalin Thakker
@es
Nalin Thakker
@nl
Nalin Thakker
@sl
P106
P1153
7004666289
P31
P496
0000-0002-8664-1508