نتایج جستجو برای: part families

تعداد نتایج: 759361  

1982
Jerry L. Cromwell David K. Baugh Rachel A. Schurman Allen Dobson

Because person-level data are not currently available at the Federal level, many questions regarding the use and expenditures of Medicaid services remain unanswered. This article demonstrates the capability of State Medicaid Management Information Systems (MMIS) to provide data that can address a variety of Medicaid program issues at both the State and Federal levels. Using data from the Tennes...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2017
Guido Uguzzoni Shalini John Lovis Francesco Oteri Alexander Schug Hendrik Szurmant Martin Weigt

Proteins have evolved to perform diverse cellular functions, from serving as reaction catalysts to coordinating cellular propagation and development. Frequently, proteins do not exert their full potential as monomers but rather undergo concerted interactions as either homo-oligomers or with other proteins as hetero-oligomers. The experimental study of such protein complexes and interactions has...

Journal: :Journal of molecular biology 2005
Diana Ekman Asa K Björklund Johannes Frey-Skött Arne Elofsson

Comparative studies of the proteomes from different organisms have provided valuable information about protein domain distribution in the kingdoms of life. Earlier studies have been limited by the fact that only about 50% of the proteomes could be matched to a domain. Here, we have extended these studies by including less well-defined domain definitions, Pfam-B and clustered domains, MAS, in ad...

Journal: :British Journal of Psychiatry 2004

Journal: :Archives of neurology 2003
E E Kors J Haan N J Giffin L Pazdera C Schnittger G G Lennox G M Terwindt F L M J Vermeulen A M J M Van den Maagdenberg R R Frants M D Ferrari

BACKGROUND Familial hemiplegic migraine (FHM) is a rare autosomal dominant subtype of migraine with aura. Missense mutations in the chromosome 19 CACNA1A calcium channel gene have been found in approximately half of the families. The T666M mutation, replacing a threonine by a methionine at residue number 666, is the most frequent mutation, reported in 14 independent FHM families; other mutation...

Today, with the increase in the elderly population and life expectancy, the need to use care services for this significant part of the population is increasing. Beliefs, cultures, and social norms among different ethnicities and races are vital in the extent and nature of care. Two types of care exist, informal and formal. According to statistics by the Secretariat of the National Council on Ag...

Journal: :The British journal of ophthalmology 1973
A Tomlinson D A Leighton

It has long been recognized that heredity plays a part in the aetiology of glaucoma. Fran §ois and Heintz-de Bree (I966) postulated a dominant heredity in open-angle glaucoma. They noted a 98 per cent. penetrance for a dominant gene in some families, but admitted that in other families the penetrance for a dominant gene was very low. Armaly (i 967a), on the other hand, suggested a polygenic inh...

2011
Nesrine Akkari Henrik Enghoff

Surface structures have rarely been the subject of a comprehensive study in Polydesmida despite their tremendous variety within this order. A number of these peripheral structures are here studied in most families of the suborders Polydesmidea and Dalodesmidea (sensu Hoffman 1980), using scanning electron microscopy. An illustrated description of the surface sculpture of the prozonite, the limb...

Journal: :Journal of applied genetics 2004
Janusz Menkiszak Marek Brzosko Bohdan Górski Jacek Fliciński Anna Jakubowska Dariusz Zebiełowicz Jacek Gronwald Tomasz Huzarski Tomasz Byrski Leszek Teresiński Maria Chosia Izabella Rzepka-Górska Jan Lubiński

The study aimed to determine whether hereditary ovarian cancers that are not caused by BRCA1/BRCA2 constitutional mutations are associated with a predisposition to cystadenoma. The study consisted of two parts. Part one concerned the incidence of ovarian cystadenoma in females from families with hereditary ovarian cancer unassociated with BRCA1 mutations. The study group included 62 female pati...

2009
Victoria Hosegood

HIV is no longer a new or emerging disease in southern Africa. In the era of HIV and AIDS, families and households have continued to form, build, migrate and dissolve. Children born in the 1980s with the risk of mother-to-child HIV transmission have already gone on to start the next generation of families and households. Isolating the impact of HIV and AIDS on families and households is complex...

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