Value of adaptive water resources management in Northern California under climatic variability and change: Reservoir management

Autor: Georgakakos, A.P., Yao, H., Kistenmacher, M., Georgakakos, K.P., Graham, N.E., Cheng, F.-Y., Spencer, C., Shamir, E.

Publikováno v: In Journal of Hydrology 2012 412:34-46

Insights from a Comprehensive Capacity Expansion Planning Modeling on the Operation and Value of Hydropower Plants under High Renewable Penetrations.

Autor: Chatzistylianos, Evangelos S.¹ (AUTHOR) gpsarros@mail.ntua.gr, Psarros, Georgios N.¹ (AUTHOR), Papathanassiou, Stavros A.¹ (AUTHOR) vxatzistylianos@mail.ntua.gr

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Bet-hedging against larval herbivory and seed bank mortality in the evolution of heterocarpy.

Autor: Kistenmacher M; University of Oklahoma, Department of Microbiology and Plant Biology 770 Van Vleet Oval, Norman, Oklahoma 73019 USA., Gibson JP; University of Oklahoma, Department of Biology, 730 Van Vleet Oval, Norman, Oklahoma 73019 USA jpgibson@ou.edu.

Publikováno v: American journal of botany [Am J Bot] 2016 Aug; Vol. 103 (8), pp. 1383-95. Date of Electronic Publication: 2016 Aug 09.

An Xp22 microdeletion associated with ocular albinism and ichthyosis: approximation of breakpoints and estimation of deletion size by using cloned DNA probes and flow cytometry

Autor: Schnur, R E, Trask, B J, van den Engh, G, Punnett, H H, Kistenmacher, M, Tomeo, M A, Naids, R E, Nussbaum, R L

Ocular albinism of the Nettleship-Falls type (OA1) and X-linked ichthyosis (XI) due to steroid sulfatase (STS) deficiency are cosegregating in three cytogenetically normal half-brothers. The mother has patchy fundal hypopigmentation consistent with r

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::268706e7f238c396c3e3f8c007067477
https://europepmc.org/articles/PMC1683435/

OA1 mutations and deletions in X-linked ocular albinism.

Autor: Schnur RE; Division of Genetics, Children's Regional Hospital, Camden, NJ 08103, USA. schnurre@umdnj.edu, Gao M, Wick PA, Keller M, Benke PJ, Edwards MJ, Grix AW, Hockey A, Jung JH, Kidd KK, Kistenmacher M, Levin AV, Lewis RA, Musarella MA, Nowakowski RW, Orlow SJ, Pagon RS, Pillers DA, Punnett HH, Quinn GE, Tezcan K, Wagstaff J, Weleber RG

Publikováno v: American journal of human genetics [Am J Hum Genet] 1998 Apr; Vol. 62 (4), pp. 800-9.