Landscapes, Myths and Artifacts by Mariella Zoppi

“…The synergy between people’s labour and the earth has generated the magnificence of the landscapes which we have inherited from previous generations. Today, their safeguard has to be linked to the capacity to plan their transformations. …”
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Stability analysis of linear multistep methods for delay differential equations by V. L. Bakke, Z. Jackiewicz

“…It is known that the solution of this equation is bounded if and only if |a|<−b and we examine whether this property is inherited by multistep methods with Lagrange interpolation and by parametrized Adams methods.…”
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Genetic history of the Koryaks and Evens of the Magadan region based on Y chromosome polymorphism data by B. A. Malyarchuk, M. V. Derenko

“…The shared components of the gene pools of the Koryaks and Evens are haplogroups R-M17 and I-P37.2 inherited as a result of admixture with Eastern Europeans (mainly Russians). …”
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A Case of Familial Mediterranean Fever with Extensive Lymphadenopathy and Complex Heterozygous Genotype Presenting in the Fourth Decade by Jawad Al-Khafaji, Fran Ganz-Lord, Venkata Rajesh Konjeti, Aaron D. Viny

“…Familial Mediterranean fever (FMF) is an inherited disease caused by loss of function mutations in the MEFV gene encoding pyrin, a negative regulator of interleukin-1. …”
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Anti-inflammatory and immunomodulating effects of clarithromycin in patients with cystic fibrosis lung disease by Alexander L. Pukhalsky, Galina V. Shmarina, Nikolai I. Kapranov, Svetlana N. Kokarovtseva, Daria Pukhalskaya, Natalia J. Kashirskaja

“…BACKGROUND and aim: Macrolide antibiotics are widely used in the treatment of suppurative lung diseases including cystic fibrosis (CF), the most common inherited fatal disease in the Caucasian population. …”
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Interplay between Epigenetics and Genetics in Cancer by Jae Duk Choi, Jong-Soo Lee

“…Genomic instability, which occurs through both genetic mechanisms (underlying inheritable phenotypic variations caused by DNA sequence-dependent alterations, such as mutation, deletion, insertion, inversion, translocation, and chromosomal aneuploidy) and epigenomic aberrations (underlying inheritable phenotypic variations caused by DNA sequence-independent alterations caused by a change of chromatin structure, such as DNA methylation and histone modifications), is known to promote tumorigenesis and tumor progression. …”
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Cornelia de Lange Syndrome: A Newborn with Imperforate Anus and a NIPBL Mutation by Rose H. Mende, David P. Drake, Raimos M. Olomi, Ben C. J. Hamel

“…Cornelia de Lange syndrome is a dominantly inherited, genetically heterogeneous and clinically variable syndrome with multiple congenital anomalies and developmental delay. …”
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A Case Report on VT from TV: DVT and PE from Prolonged Television Watching by Alan Lucerna, James Espinosa, Lindsey Ackley, Philip Carhart, Douglas Stranges, Risha Hertz

“…Well known risk factors for thromboembolic events include immobility, malignancy, pregnancy, surgery, and acquired or inherited thrombophilias, obesity, cigarette smoking, and hypertension. …”
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Psudoxanthoma elasticum: An Unusual Case of Gastrointestinal Bleeding by Deborah J. Cook, Samih S. Salama, Robert J. Tuttle

“…Pseudoxanchoma elasticum (PXE) is an inherited disorder of connective tissue, characterized by calcification and degeneration of elastin. …”
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Arthrogryposis Multiplex Congenita: Case Report by Ayla Aktulay, Saliha Sağnıç, Özlem Moraloğlu Tekin, Yaprak Engin Üstün, Elif Gül Yapar Eyi, Leyla Mollamahmutoğlu

“…Although it is autosomal recessively inherited, sporadic cases have also been reported. …”
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L’émergence par la créativité au Cap by Thomas Radovcic

“…Nonetheless, whereas social, spatial and racial inequalities inherited from the apartheid era are still persisting, this strategy aims to strengthen Cape Town’s assets to internationally compete with other cities. …”
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Idiopathic Generalized Epilepsy and Hypokalemic Periodic Paralysis in a Family of South Indian Descent by Muthiah Subramanian, N. Senthil, S. Sujatha

“…Inherited channelopathies are a heterogeneous group of disorders resulting from dysfunction of ion channels in cellular membranes. …”
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Coexistence of Factor VII Deficiency and Hereditary Spastic Paraplegia in Two Siblings by Hortensia De la Corte-Rodriguez, E. Carlos Rodriguez-Merchan, M. Teresa Alvarez-Roman, Ana L. Hernandez-Moreno

“…We present the case of two patients aged 12 years and 7 years who were referred to our hospital for factor VII deficiency inherited in an autosomal recessive pattern, who had suffered from previous multiple joint haemarthroses. …”
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Mitochondrial trifunctional protein deficiency caused by a deep intronic deletion leading to aberrant splicing by Thomas Cassini, Sarah Silverstein, Molly Behan, Cynthia J. Tifft, May Christine Malicdan, David R. Adams, Undiagnosed Diseases Network, Sun‐Young Ahn, Debra S. Regier

“…Initial sequencing of the TFP‐associated genes HADHA and HADHB showed only a paternally inherited variant in HADHB, NM_000183.3:c.1059del (p.Gly354AspfsTer10). …”
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Myoclonus by R. Rimšienė, S. Andruškevičius, R. Mameniškienė

“…They can be physiological and pathological, inherited or acquired due to various structural brain damage or systemic diseases. …”
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A Semi-Analytical Solution of Inverse Laplace Transform by Shuang Luo, Fu-yao Zhao

“…Bearing their credits, this method inherits all the merits such as analytical expression, avoiding free parameters, simple calculation with high accuracy, and the availability of error estimation. …”
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Shanzhai et culture du faire en Chine by Julia Nawrocki

“…It shows how Shenzhen’s maker movement has developed in an inherited manufacturing region, echoing local shanzhai culture. …”
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Chronic Psychosis in a Patient with Usher Syndrome by Abhay Keshava Bhat, Sheetal Reshram Meshram, Maithili S. Umate, Prakhar D. Jain

“…Usher syndrome refers to a group of inherited disorders characterized by visual and auditory impairment. …”
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The APOA1 p.Leu202Arg variant potentially causes autosomal recessive cardiac amyloidosis by Shusuke Yagi, Ryosuke Miyamoto, Masayoshi Tasaki, Hiroyuki Morino, Ryuji Otani, Muneyuki Kadota, Takayuki Ise, Hiroki Yamazaki, Kenya Kusunose, Koji Yamaguchi, Hirotsugu Yamada, Takeshi Soeki, Tetsuzo Wakatsuki, Daiju Fukuda, Mitsuharu Ueda, Masataka Sata

“…ApoA-I amyloidosis is caused by amyloidogenic variants of APOA1 that are inherited in an autosomal dominant manner. Here, we report a 69-year-old man with sporadic cardiac amyloidosis who was born to consanguineous parents and carried a homozygous variant of p.Leu202Arg in APOA1.…”
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Details of Walker 256 carcinosarcoma growth in Brattleboro and ISIAH lines of rats by I. I. Khegay

“…ISIAH rats are carriers of inherited stress-induced arterial hypertension. Vascular rigidity is accompanied by additional pleiotropic effects. …”
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