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Advances in the genetics of sarcoidosis
Clinical Genetics, 2008Sarcoidosis is an uncommon disease of granulomatous inflammation. Genetic predisposition to sarcoidosis is indicated by observations of familial clustering, increased concordance in monozygotic twins over other siblings, and variations in susceptibility and disease presentation among different ethnic groups.
G, Smith +3 more
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Recent advances in the genetics of sarcoidosis
Journal of Medical Genetics, 2013Sarcoidosis is a heterogeneous inflammatory disorder of unknown origin that may affect virtually any organ, although intrathoracic engagement is almost universal. Sarcoidosis may present rather dramatically as an acute disease, which usually resolves either spontaneously or with treatment, while other patients have an insidious onset and a chronic ...
SPAGNOLO, Paolo, Grunewald J.
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2015
Glaucoma is presumed to be a complex progressive neurodegenerative disorder caused by genetic and environmental factors, and it is also one of the leading causes of irreversible blindness worldwide. Glaucoma is divided into two major forms: primary open-angle glaucoma (POAG) and primary angle-closure glaucoma (PACG).
Yoichi, Sakurada, Fumihiko, Mabuchi
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Glaucoma is presumed to be a complex progressive neurodegenerative disorder caused by genetic and environmental factors, and it is also one of the leading causes of irreversible blindness worldwide. Glaucoma is divided into two major forms: primary open-angle glaucoma (POAG) and primary angle-closure glaucoma (PACG).
Yoichi, Sakurada, Fumihiko, Mabuchi
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2015
The major histocompatibility complex (MHC) is a genetic system of over 70 known genes that occupies the midportion of the short arm of the sixth chromosome (C6p) and spans about 4 million base pairs of DNA. The high-resolution typing of class I and class II MHC genes and the identification of genes between and near them has increased the definition of ...
D, Corzo +3 more
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The major histocompatibility complex (MHC) is a genetic system of over 70 known genes that occupies the midportion of the short arm of the sixth chromosome (C6p) and spans about 4 million base pairs of DNA. The high-resolution typing of class I and class II MHC genes and the identification of genes between and near them has increased the definition of ...
D, Corzo +3 more
openaire +2 more sources
Current Opinion in Pediatrics, 1993
For many years, the mainstay of pediatric genetic testing was chromosomal analysis. Based on a technology developed in the 1950s and refined in the 1960s, this approach permitted the detection of abnormalities of chromosome number and some structural rearrangements.
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For many years, the mainstay of pediatric genetic testing was chromosomal analysis. Based on a technology developed in the 1950s and refined in the 1960s, this approach permitted the detection of abnormalities of chromosome number and some structural rearrangements.
openaire +2 more sources
Recent advances in epilepsy genetics
Neuroscience Letters, 2018In last few years there has been rapid increase in the knowledge of epilepsy genetics. Nowadays, it is estimated that genetic epilepsies include over than 30% of all epilepsy syndromes. Several genetic tests are now available for diagnostic purposes in clinical practice.
Orsini A., Zara F., Striano P.
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Genetic testing in prostate cancer management: Considerations informing primary care
Ca-A Cancer Journal for Clinicians, 2022Mary-Ellen Taplin +2 more
exaly
Heritability and Genetic Advance Estimates of Key Shea Fruit Traits
Agronomy, 2023Silas Wintuma Avicor +2 more
exaly
Genetic variation and genetic advance in cowpea based on yield and yield-related traits
Acta Agriculturae Scandinavica - Section B Soil and Plant Science, 2020Jacob Mashilo, Hussein Shimelis
exaly

