نتایج جستجو برای: autozygosity mapping

تعداد نتایج: 198456  

Journal: :American journal of human genetics 2009
Mohammad R Abdollahi Ewan Morrison Tamara Sirey Zoltan Molnar Bruce E Hayward Ian M Carr Kelly Springell C Geoff Woods Mushtaq Ahmed Louise Hattingh Peter Corry Daniela T Pilz Neil Stoodley Yanick Crow Graham R Taylor David T Bonthron Eamonn Sheridan

The critical importance of cytoskeletal function for correct neuronal migration during development of the cerebral cortex has been underscored by the identities of germline mutations underlying a number of human neurodevelopmental disorders. The proteins affected include TUBA1A, a major alpha-tubulin isoform, and microtubule-associated components such as doublecortin, and LIS1. Mutations in the...

Journal: :Human molecular genetics 2009
Mehrnaz Narooie-Nejad Seyed Hassan Paylakhi Seyedmehdi Shojaee Zeinab Fazlali Mozhgan Rezaei Kanavi Naveed Nilforushan Shahin Yazdani Farbod Babrzadeh Fatemeh Suri Mostafa Ronaghi Elahe Elahi Coro Paisán-Ruiz

Glaucoma is a heterogeneous group of optic neuropathies that manifests by optic nerve head cupping or degeneration of the optic nerve, resulting in a specific pattern of visual field loss. Glaucoma leads to blindness if left untreated, and is considered the second leading cause of blindness worldwide. The subgroup primary congenital glaucoma (PCG) is characterized by an anatomical defect in the...

2015
F Seymen K-E Lee M Koruyucu K Gencay M Bayram EB Tuna ZH Lee J-W Kim

OBJECTIVE Hereditary defects in tooth enamel formation, amelogenesis imperfecta (AI), can be non-syndromic or syndromic phenotype. Integrins are signaling proteins that mediate cell-cell and cell-extracellular matrix communication, and their involvement in tooth development is well known. The purposes of this study were to identify genetic cause of an AI family and molecular pathogenesis underl...

2010
Neil V. Morgan Mark R. Morris Hakan Cangul Diane Gleeson Anna Straatman-Iwanowska Nicholas Davies Stephen Keenan Shanaz Pasha Fatimah Rahman Dean Gentle Maaike P. G. Vreeswijk Peter Devilee Margaret A. Knowles Serdar Ceylaner Richard C. Trembath Carlos Dalence Erol Kismet Vedat Köseoğlu Hans-Christoph Rossbach Paul Gissen David Tannahill Eamonn R. Maher

The histiocytoses are a heterogeneous group of disorders characterised by an excessive number of histiocytes. In most cases the pathophysiology is unclear and treatment is nonspecific. Faisalabad histiocytosis (FHC) (MIM 602782) has been classed as an autosomal recessively inherited form of histiocytosis with similarities to Rosai-Dorfman disease (RDD) (also known as sinus histiocytosis with ma...

2009
David A. Parry Carmel Toomes Lina Bida Michael Danciger Katherine V. Towns Martin McKibbin Samuel G. Jacobson Clare V. Logan Manir Ali Jacquelyn Bond Rebecca Chance Steven Swendeman Lauren L. Daniele Kelly Springell Matthew Adams Colin A. Johnson Adam P. Booth Hussain Jafri Yasmin Rashid Eyal Banin Tim M. Strom Debora B. Farber Dror Sharon Carl P. Blobel Edward N. Pugh Eric A. Pierce Chris F. Inglehearn

Cone-rod dystrophy (CRD) is an inherited progressive retinal dystrophy affecting the function of cone and rod photoreceptors. By autozygosity mapping, we identified null mutations in the ADAM metallopeptidase domain 9 (ADAM9) gene in four consanguineous families with recessively inherited early-onset CRD. We also found reduced photoreceptor responses in Adam9 knockout mice, previously reported ...

2009
Mehrnaz Narooie-Nejad Fereshteh Chitsazian Betsabeh Khoramian Tusi Faride Mousavi Massoud Houshmand Mohammad R. Rohani Azam S. Hosseinipour Akram Rismanchian Elahe Elahi

PURPOSE To assess whether loci other than GLC3A, GLC3B, and GLC3C are linked to primary congenital glaucoma (PCG). METHODS The gene CYP1B1 at GLC3A was screened in 19 Iranian PCG probands who had been recruited mostly from among individuals of Turkish ethnicity and individuals from central and eastern Iran. The gene MYOC was screened in patients from this cohort who lacked CYP1B1 mutations an...

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