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2008, 1. Aufl., The Frank J. Fabozzi series, ISBN 0470117648, xxii, 986
Filled with a comprehensive collection of information from experts in the commodity investment industry, this detailed guide shows readers how to successfully... 
Commodity futures | Investments & Securities | General | BUSINESS & ECONOMICS | Personal Investing | Finance & Economics
Book
PLoS Genetics, ISSN 1553-7390, 12/2017, Volume 13, Issue 12, pp. e1007137 - e1007137
Cohesin is crucial for genome stability, cell division, transcription and chromatin organization. Its functions critically depend on NIPBL, the cohesin-loader... 
SISTER-CHROMATID COHESION | NIPPED-B | HUMAN GENOME | CORNELIA | LONG NONCODING RNAS | GENE | TRANSCRIPTION | GENETICS & HEREDITY | DE-LANGE-SYNDROME | MUTATIONS | ANTISENSE OLIGONUCLEOTIDES | Physiological aspects | Cell division | Genetic transcription | RNA | Health aspects | Index Medicus | Life Sciences | Biochemistry, Molecular Biology | Genomics
Journal Article
Human Mutation, ISSN 1059-7794, 12/2018, Volume 39, Issue 12, pp. 2097 - 2109
In humans, mutations of Desert Hedgehog gene ( DHH ) have been described in patients with 46,XY gonadal dysgenesis (GD), associated or not with polyneuropathy.... 
Desert hedgehog | 46,XY DSD | gonadal dysgenesis | auto‐processing | polyneuropathy | auto-processing | LEYDIG-CELLS | VARIANTS | SONIC HEDGEHOG | SEX | DESERT-HEDGEHOG DHH | PREDICTION | NEUROPATHY | GENE | GENETICS & HEREDITY | HYPOSPADIAS | MAMLD1 | Literature reviews | Gonadal dysgenesis | Insects | Hedgehog protein | Proteolysis | Paracrine signalling | Autocrine signalling | Mutation | Polyneuropathy
Journal Article
Human Mutation, ISSN 1059-7794, 09/2014, Volume 35, Issue 9, pp. 1114 - 1122
Journal Article
Human Mutation, ISSN 1059-7794, 12/2018, Volume 39, Issue 12, p. 2097
Journal Article
The Cerebellum, ISSN 1473-4222, 8/2018, Volume 17, Issue 4, pp. 504 - 506
To access, purchase, authenticate, or subscribe to the full-text of this article, please visit this link: http://dx.doi.org/10.1007/s12311-018-0931-8 
Neurology | Neurosciences | Biomedicine | Neurobiology | NEUROSCIENCES | FAMILY | Frameshift mutation | Ataxia
Journal Article
Parkinsonism & related disorders, ISSN 1353-8020, 05/2019
Journal Article
by Karp, Daniel S and Chaplin-Kramer, Rebecca and Meehan, Timothy D and Martin, Emily A and DeClerck, Fabrice and Grab, Heather and Gratton, Claudio and Hunt, Lauren and Larsen, Ashley E and Martínez-Salinas, Alejandra and O’Rourke, Megan E and Rusch, Adrien and Poveda, Katja and Jonsson, Mattias and Rosenheim, Jay A and Schellhorn, Nancy A and Tscharntke, Teja and Wratten, Stephen D and Zhang, Wei and Iverson, Aaron L and Adler, Lynn S and Albrecht, Matthias and Alignier, Audrey and Angelella, Gina M and Anjum, Muhammad Zubair and Avelino, Jacques and Batáry, Péter and Baveco, Johannes M and Bianchi, Felix J. J. A and Birkhofer, Klaus and Bohnenblust, Eric W and Bommarco, Riccardo and Brewer, Michael J and Caballero-López, Berta and Carrière, Yves and Carvalheiro, Luísa G and Cayuela, Luis and Centrella, Mary and Ćetković, Aleksandar and Henri, Dominic Charles and Chabert, Ariane and Costamagna, Alejandro C and De la Mora, Aldo and de Kraker, Joop and Desneux, Nicolas and Diehl, Eva and Diekötter, Tim and Dormann, Carsten F and Eckberg, James O and Entling, Martin H and Fiedler, Daniela and Franck, Pierre and van Veen, F. J. Frank and Frank, Thomas and Gagic, Vesna and Garratt, Michael P. D and Getachew, Awraris and Gonthier, David J and Goodell, Peter B and Graziosi, Ignazio and Groves, Russell L and Gurr, Geoff M and Hajian-Forooshani, Zachary and Heimpel, George E and Herrmann, John D and Huseth, Anders S and Inclán, Diego J and Ingrao, Adam J and Iv, Phirun and Jacot, Katja and Johnson, Gregg A and Jones, Laura and Kaiser, Marina and Kaser, Joe M and Keasar, Tamar and Kim, Tania N and Kishinevsky, Miriam and Landis, Douglas A and Lavandero, Blas and Lavigne, Claire and Le Ralec, Anne and Lemessa, Debissa and Letourneau, Deborah K and Liere, Heidi and Lu, Yanhui and Lubin, Yael and Luttermoser, Tim and Maas, Bea and Mace, Kevi and Madeira, Filipe and Mader, Viktoria and Cortesero, Anne Marie and Marini, Lorenzo and Martinez, Eliana and Martinson, Holly M and Menozzi, Philippe and Mitchell, Matthew G. E and Miyashita, Tadashi and Molina, Gonzalo A. R and Molina-Montenegro, Marco A and ...
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 08/2018, Volume 115, Issue 33, pp. E7863 - E7870
Journal Article
Journal Article
PLoS Genetics, ISSN 1553-7390, 03/2014, Volume 10, Issue 3
  Genome-wide association studies (GWAS) have identified chromosomal loci that affect risk of coronary heart disease (CHD) independent of classical risk... 
Studies | Heart | Transcription factors | Mortality | Atherosclerosis | Cardiovascular disease | Smooth muscle | Genomes | Muscular system | Gene expression | Binding sites
Journal Article
JAMA Neurology, ISSN 2168-6149, 09/2014, Volume 71, Issue 9, pp. 1177 - 1177
  Despite recessive inheritance, X-linked dystonia-parkinsonism (Lubag disease) has also been described in women presenting with a late-onset isolated... 
Neurology | Womens health | Parkinsons disease | Epigenetics | Mutation | Epidemiology | Chromosomes
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 06/2012, Volume 90, Issue 6, pp. 1014 - 1027
Journal Article