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Results 1 to 25 of 215

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Human monogenic disorders : a source of novel drug targetsBRINKMAN, Ryan R; DUBE, Marie-Pierre; ROULEAU, Guy A et al.Nature reviews. Genetics (Print). 2006, Vol 7, Num 4, pp 249-260, issn 1471-0056, 12 p.Article

The genetic and molecular bases of monogenic disorders affecting proteolytic systemsRICHARD, I.Journal of medical genetics. 2005, Vol 42, Num 7, pp 529-539, issn 0022-2593, 11 p.Article

Lessons from studying monogenic disease for common diseasePELTONEN, Leena; PEROLA, Markus; NAUKKARINEN, Jussi et al.Human molecular genetics (Print). 2006, Vol 15, issn 0964-6906, R67-R74, NSArticle

Monogenic Mendelian disorders in general neurological practiceLARNER, A. J.International journal of clinical practice (Esher). 2008, Vol 62, Num 5, pp 744-746, issn 1368-5031, 3 p.Article

Monogenic and other unusual causes of diabetes mellitusNAKHLA, Meranda; POLYCHRONAKOS, Constantin.The Pediatric clinics of North America. 2005, Vol 52, Num 6, issn 0031-3955, viii, 1637-150 [15 p.]Article

Identifying modifier genes of monogenic disease : strategies and difficultiesGENIN, Emmanuelle; FEINGOLD, Josué; CLERGET-DARPOUX, Francoise et al.Human genetics. 2008, Vol 124, Num 4, pp 357-368, issn 0340-6717, 12 p.Article

Investigating monogenic and complex diseases with pluripotent stem cellsHAO ZHU; MENSCH, M. William; CAHAN, Patrick et al.Nature reviews. Genetics (Print). 2011, Vol 12, Num 4, pp 266-275, issn 1471-0056, 10 p.Article

Le séquençage de l'exome au secours des maladies génétiques = Exome sequencing applied to monogenic disordersCRIQUI, Audrey; BAULANDE, Sylvain.MS. Médecine sciences. 2010, Vol 26, Num 5, pp 452-454, issn 0767-0974, 3 p.Article

WFS1 mutations are frequent monogenic causes of juvenile-onset diabetes mellitus in LebanonZALLOUA, Pierre A; AZAR, Sami T; JULIER, Cécile et al.Human molecular genetics (Print). 2008, Vol 17, Num 24, pp 4012-4021, issn 0964-6906, 10 p.Article

Monogenic dyslipidemias: Window on determinants of plasma lipoprotein metabolismHEGELE, Robert A.American journal of human genetics. 2001, Vol 69, Num 6, pp 1161-1177, issn 0002-9297Article

Monogenic mechanisms of blood pressure regulationPLOTH, David W.The American journal of the medical sciences. 2001, Vol 322, Num 6, issn 0002-9629, p. 301Conference Paper

DNA diagnosis in monogenic diseases : Genetic technologyALFORD, R. L; ROSSITER, B. J. F; CASKEY, C. T et al.International journal of technology assessment in health care. 1994, Vol 10, Num 4, pp 628-643, issn 0266-4623Article

Insights into the molecular correlates modulating functional compensation between monogenic and polygenic disease gene duplicates in humanPODDER, Soumita; TAPASH CHANDRA GHOSH.Genomics (San Diego, Calif.). 2011, Vol 97, Num 4, pp 200-204, issn 0888-7543, 5 p.Article

Vérification de l'hypothèse monogénique par pédigrés de structure arbitraire sélectionnés pour le sujet atteint. I. Caractère alternatifGINZBURG, EH. KH; AKSENOVICH, T. I.Genetika. 1986, Vol 22, Num 3, pp 413-422, issn 0016-6758Article

Thiamine transporter mutation : an example of monogenic diabetes mellitusALZAHRANI, Ali S; BAITEI, Essa; MINGING ZOU et al.European journal of endocrinology. 2006, Vol 155, Num 6, pp 787-792, issn 0804-4643, 6 p.Article

Population programs for the detection of couples at risk for severe monogenic genetic diseasesZLOTOGORA, Joël.Human genetics. 2009, Vol 126, Num 2, pp 247-253, issn 0340-6717, 7 p.Article

Disparity from monogenic phaseFELSBERG, Michael.Lecture notes in computer science. 2002, pp 248-256, issn 0302-9743, isbn 3-540-44209-X, 9 p.Conference Paper

Vérification de l'hypothèse monogénique par pédigrés de structure arbitraire sélectionnés pour le sujet atteint. II. Problèmes de prédictionAKSENOVICH, T. I; GINZBURG, EH. KH.Genetika. 1986, Vol 22, Num 3, pp 423-433, issn 0016-6758Article

ER-associated protein degradation is a common mechanism underpinning numerous monogenic diseases including Robinow syndromeYING CHEN; BELLAMY, William P; SEABRA, Miguel C et al.Human molecular genetics (Print). 2005, Vol 14, Num 17, pp 2559-2569, issn 0964-6906, 11 p.Article

Salivary glands as a potential gene transfer target for gene therapeutics of some monogenetic endocrine disordersVOUTETAKIS, Antonis; BOSSIS, Ioannis; KOK, Marc R et al.Journal of endocrinology. 2005, Vol 185, Num 3, pp 363-372, issn 0022-0795, 10 p.Article

Les diabètes monogéniques: les formes MODYSALET, R.Médecine & enfance. 2013, Vol 33, Num 3, pp 69-71, issn 0291-0233, 3 p.Article

Lessons from Extreme Human Obesity : Monogenic DisordersRANADIVE, Sayali A; VAISSE, Christian.Endocrinology and metabolism clinics of North America. 2008, Vol 37, Num 3, issn 0889-8529, x, 733-751 [20 p.]Article

Selection of dieldrin-resistant strains of Lucilia cuprina (Diptera: Calliphoridae) after ethyl methanesulfonate mutagenesis of a susceptible strainSMYTH, K.-A; PARKER, A. G; YEN, J. L et al.Journal of economic entomology. 1992, Vol 85, Num 2, pp 352-358, issn 0022-0493Article

Les diabètes monogéniques : une dimension à intégrer dans la pratique clinique des diabétologues = Monogenic diabetes: a useful dimension for diabetology practiceVALERO, R; BELIARD, S; PAQUIS-FLUCKINGER, V et al.Annales d'endocrinologie. 2005, Vol 66, Num 3, pp 279-283, issn 0003-4266, 5 p.Conference Paper

Genetic epidemiology of essential hypertensionGAVRAS, I; MANOLIS, A; GAVRAS, H et al.Journal of human hypertension. 1999, Vol 13, Num 4, pp 225-229, issn 0950-9240Article

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