نتایج جستجو برای: nevoid basal cell carcinoma syndrome

تعداد نتایج: 2469788  

Journal: :Developmental cell 2008
Shinsuke Ohba Hiroshi Kawaguchi Fumitaka Kugimiya Toru Ogasawara Naohiro Kawamura Taku Saito Toshiyuki Ikeda Katsunori Fujii Tsuyoshi Miyajima Akira Kuramochi Toshiyuki Miyashita Hiromi Oda Kozo Nakamura Tsuyoshi Takato Ung-Il Chung

Hedgehog (Hh)-Patched1 (Ptch1) signaling plays essential roles in various developmental processes, but little is known about its role in postnatal homeostasis. Here, we demonstrate regulation of postnatal bone homeostasis by Hh-Ptch1 signaling. Ptch1-deficient (Ptch1+/-) mice and patients with nevoid basal cell carcinoma syndrome showed high bone mass in adults. In culture, Ptch1+/- cells showe...

Journal: :Cancer research 1997
I Vorechovský A B Undén B Sandstedt R Toftgård M Ståhle-Bäckdahl

The nevoid basal cell carcinoma (Gorlin) syndrome (NBCCS) is an autosomal dominant disorder characterized by multiple developmental defects and cancer susceptibility. NBCCS is caused by mutations in the human homologue (PTCH) of the Drosophila patched gene, a developmental regulator implicated in signaling of hedgehog and smoothened. The PTCH gene was found to contain somatic mutations also in ...

Journal: :Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas 2003
F Granja P L Santarosa J L A A P Leite L S Ward

There is strong evidence that the patched (PTCH) gene is a gene for susceptibility to the nevoid basal cell carcinoma syndrome. PTCH has also been shown to mutate in both familial and sporadic basal cell carcinomas. However, mutations of the gene seem to be rare in squamous cell carcinomas. In order to characterize the role of the gene in the broader spectrum of sporadic skin malignant and pre-...

Journal: :world journal of plastic surgery 0
maria alessandra bocchiotti turin, italy denis codazzi bergamo, italy enrico robotti bergamo, italy

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Journal: :Human molecular genetics 2005
Kazuaki Nagao Naoyuki Togawa Katsunori Fujii Hideki Uchikawa Yoichi Kohno Masao Yamada Toshiyuki Miyashita

Mutations in the human ortholog of Drosophila patched (PTCH) have been identified in patients with autosomal dominant nevoid basal cell carcinoma syndrome (NBCCS), characterized by minor developmental anomalies and an increased incidence of cancers such as medulloblastoma and basal cell carcinoma. We identified many isoforms of PTCH mRNA involving exons 1-5, exon 10 and a novel exon, 12b, gener...

2006
Corey Raffel Robert B. Jenkins Lori Frederick Deanne Hebrink Benjamin Alderete Daniel W. Fults David James

Nevoid basal cell carcinoma syndrome (NBCCS), or Gorlin's syn drome, is an autosomal dominant disorder that predisposes to develop mental defects and various forms of cancer. PTCH was recently proposed as a candidate gene for NBCCS due to its frequent mutation in basal cell carcinomas, the cancer most often associated with this syndrome. Another NBCCS-associated cancer is medulloblastoma, a com...

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