Sequential growth factor delivery from complexed microspheres for bone tissue engineering
Aim of the study was to design a 3D tissue-engineering scaffold capable of sequentially
delivering two bone morphogenetic proteins (BMP). The novel delivery system consisted of …
delivering two bone morphogenetic proteins (BMP). The novel delivery system consisted of …
[PDF][PDF] Mutations in POGLUT1, encoding protein O-glucosyltransferase 1, cause autosomal-dominant Dowling-Degos disease
FB Basmanav, AM Oprisoreanu, SM Pasternack… - The American Journal of …, 2014 - cell.com
Dowling-Degos disease (DDD) is an autosomal-dominant genodermatosis characterized by
progressive and disfiguring reticulate hyperpigmentation. We previously identified loss-of-…
progressive and disfiguring reticulate hyperpigmentation. We previously identified loss-of-…
Translational impact of omics studies in alopecia areata: recent advances and future perspectives
FB Basmanav, RC Betz - Expert Review of Clinical Immunology, 2022 - Taylor & Francis
Introduction Alopecia areata (AA) is a non-scarring, hair loss disorder and a common
autoimmune-mediated disease with an estimated lifetime risk of about 2%. To date, the treatment of …
autoimmune-mediated disease with an estimated lifetime risk of about 2%. To date, the treatment of …
Short anagen hair syndrome: association with mono- and biallelic variants in WNT10A and a genetic overlap with male pattern hair loss
…, S Heilmann-Heimbach, FB Basmanav… - British Journal of …, 2023 - academic.oup.com
Background Short anagen hair (SAH) is a rare paediatric hair disorder characterized by a
short anagen phase, an inability to grow long scalp hair and a negative psychological impact. …
short anagen phase, an inability to grow long scalp hair and a negative psychological impact. …
Genomewide analysis of copy number variants in alopecia areata in a Central European cohort reveals association with MCHR2
…, A Hofmann, S Redler, FB Basmanav… - Experimental …, 2017 - Wiley Online Library
Alopecia areata ( AA ) is a common hair loss disorder of autoimmune aetiology, which often
results in pronounced psychological distress. Understanding of the pathophysiology of AA is …
results in pronounced psychological distress. Understanding of the pathophysiology of AA is …
Pathogenicity of POFUT1 in Dowling-Degos disease: additional mutations and clinical overlap with reticulate acropigmentation of kitamura
FB Basmanav, G Fritz… - The Journal of …, 2015 - pubmed.ncbi.nlm.nih.gov
… F Buket Basmanav …
Investigation of the involvement of MIR185 and its target genes in the development of schizophrenia
AJ Forstner, FB Basmanav, M Mattheisen… - Journal of Psychiatry and …, 2014 - jpn.ca
Background: Schizophrenia is a complex neuropsychiatric disorder of unclear etiology. The
strongest known genetic risk factor is the 22q11.2 microdeletion. Research has yet to confirm …
strongest known genetic risk factor is the 22q11.2 microdeletion. Research has yet to confirm …
Assessment of the genetic spectrum of uncombable hair syndrome in a cohort of 107 individuals
FB Basmanav, N Cesarato, S Kumar… - JAMA …, 2022 - jamanetwork.com
Importance Uncombable hair syndrome (UHS) is a rare hair shaft anomaly that manifests
during infancy and is characterized by dry, frizzy, and wiry hair that cannot be combed flat. Only …
during infancy and is characterized by dry, frizzy, and wiry hair that cannot be combed flat. Only …
[HTML][HTML] Altered Notch signaling in Dowling-Degos disease: additional mutations in POGLUT1 and further insights into disease pathogenesis
…, H Takeuchi, G Fritz, FB Basmanav… - The Journal of …, 2019 - ncbi.nlm.nih.gov
… Following our identification of POGLUT1 mutations in DDD (Basmanav et al., 2014), we
studied additional DDD patients. Ethical approval was obtained from the ethics committee of …
studied additional DDD patients. Ethical approval was obtained from the ethics committee of …
[HTML][HTML] Recent advances in the genetics of alopecia areata
F Buket Basmanav, RC Betz - Medizinische Genetik, 2023 - degruyter.com
Alopecia areata (AA) is a common autoimmune-mediated hair loss disorder in humans with
an estimated lifetime risk of approximately 2 %. Episodes of hair loss usually begin with …
an estimated lifetime risk of approximately 2 %. Episodes of hair loss usually begin with …