Portrait of a Man, probably a Member of the Van Beresteyn Family

Rembrandt van Rijn; 3 ft. 8 1/64 in.x 2 ft. 11 in.; oil on canvas

Portrait of a Woman, probably a Member of the Van Beresteyn Family

Rembrandt van Rijn; 3 ft. 8 1/64 in.x 2 ft. 11 in.; oil on canvas

The Van Cortlandt family papers /

Includes bibliographical references and index.

Genealogies and sketches of some old families who have taken prominent part in the development of Virginia and Kentucky especially, and later of many other states of this Union.

Lewis family.--Phillips family.--Moss family.--Van Meter family.--Cunningham family.--Harness family.--[J. H. McNeill and his company of rangers]

William Van Every fonds, 1784, 1804-1806, 1815-1816, 1828, 1832, n.d.

William Van Every, son of McGregory and Mary Wilcox (Jaycocks) Van Every, was born in New York state in 1765. During the Revolutionary War he joined Butler’s Rangers and served under Captain John McDonnell. He was granted three lots of land in the Township of Niagara, with additional lands granted at later dates. William married Elizabeth, daughter of George Young. Elizabeth was the widow of Col. Frederick Dochstader and mother of Catherine Dochstader, b. 1781. William Van Every died in 1832, his wife Elizabeth in 1851. Both are buried in the Warner Cemetery, in present day Niagara Falls. The children of William Van Every and Elizabeth Young were Mary, Elizabeth, Phoebe, John, Peter, William, Rebecca, Samuel and Joseph. Source: Mary Blackadar Piersol, The Records of the Van Every Family, Toronto : Best Printing, 1947. And, Patricia M. Orr, Historic Woodend, sponsored by Niagara Peninsula Conservation Authority, 1980?

Subgroup-specific structural variation across 1,000 medulloblastoma genomes

Medulloblastoma, the most common malignant paediatric brain tumour, is currently treated with nonspecific cytotoxic therapies including surgery, whole-brain radiation, and aggressive chemotherapy. As medulloblastoma exhibits marked intertumoural heterogeneity, with at least four distinct molecular variants, previous attempts to identify targets for therapy have been underpowered because of small samples sizes. Here we report somatic copy number aberrations (SCNAs) in 1,087 unique medulloblastomas. SCNAs are common in medulloblastoma, and are predominantly subgroup-enriched. The most common region of focal copy number gain is a tandem duplication of SNCAIP, a gene associated with Parkinson's disease, which is exquisitely restricted to Group 4 alpha. Recurrent translocations of PVT1, including PVT1-MYC and PVT1-NDRG1, that arise through chromothripsis are restricted to Group 3. Numerous targetable SCNAs, including recurrent events targeting TGF-beta signalling in Group 3, and NF-kappa B signalling in Group 4, suggest future avenues for rational, targeted therapy.

The Van Vechten genealogy /

Mode of access: Internet.

Effectiviteit van Preventieve Interventies op het Gezinsfunctioneren bij hoogangstige Kinderen

Het doel van dit onderzoek is inzicht geven in het effect van preventieve angstinterventies op verschillende stijlen (algeheel, functioneel, disfunctioneel) van het gezinsfunctioneren bij hoogangstige kinderen en hun ouders. De proefpersonen (N = 2494) werden gerekruteerd op basisscholen. Uiteindelijk bleven 150 respondenten over. Deze respondenten bestaan uit 70 (46.7%) jongens en 80 (53.3%) meisjes. De respondenten zijn kinderen van 8 tot 13 jaar. De gemiddelde leeftijd van de respondenten is 9.83 jaar (SD = 1.14), de jongste is 8 en de oudste is 13 jaar. De screeningsprocedure is uitgevoerd met de kindversie van de zelfrapportage vragenlijst Screen for Child Anxiety Related Emotional Disorders. Na screening werden de hoogangstige kinderen en hun ouders gerandomiseerd over de drie onderzoekscondities. Daarnaast werd aan de deelnemers gevraagd de Family Functioning Scale in te vullen. Maximaal 3 maanden na de screening vond de voormeting plaats bij kinderen en ouders, hierna vond na maximaal 6 weken de interventie plaats. Na de voormeting volgden de follow-up metingen na respectievelijk 1 en 2 jaar. Om de variabele angst te meten is gebruik gemaakt van de Screen for Child Anxiety Related Emotional Disorder (SCARED-71; Bodden, Bögels, & Muris, 2009). Om de variabele gezinsfunctioneren te meten is gebruik gemaakt van de Family Functioning Scale (FFS; Bloom, 1985). De resultaten lieten zien dat het gezinsfunctioneren bij hoogangstige kinderen en hun ouders niet verbetert na het volgen van een interventie of geen interventie. Daarnaast is geen verschil in effectiviteit gevonden tussen de kind- of oudergerichte interventie op de verschillende aspecten van het gezinsfunctioneren.

The Contemporary Group, February 14, 1973

Concert program for The Contemporary Group, February 14, 1973

Subgroup-specific structural variation across 1,000 medulloblastoma genomes.

Medulloblastoma, the most common malignant paediatric brain tumour, is currently treated with nonspecific cytotoxic therapies including surgery, whole-brain radiation, and aggressive chemotherapy. As medulloblastoma exhibits marked intertumoural heterogeneity, with at least four distinct molecular variants, previous attempts to identify targets for therapy have been underpowered because of small samples sizes. Here we report somatic copy number aberrations (SCNAs) in 1,087 unique medulloblastomas. SCNAs are common in medulloblastoma, and are predominantly subgroup-enriched. The most common region of focal copy number gain is a tandem duplication of SNCAIP, a gene associated with Parkinson's disease, which is exquisitely restricted to Group 4α. Recurrent translocations of PVT1, including PVT1-MYC and PVT1-NDRG1, that arise through chromothripsis are restricted to Group 3. Numerous targetable SCNAs, including recurrent events targeting TGF-β signalling in Group 3, and NF-κB signalling in Group 4, suggest future avenues for rational, targeted therapy.

Dianna Hostetter funeral invitation, 1861

The invitation is a request of Jacob Hostetter to his friends and acquaintances to attend the funeral of his wife, Dianna on Tuesday, October 29, 1861. Dianna, also known as Dinah, was the second daughter of Joseph and Mary Heslop Van Every. She was born in 1831 and married Jacob Hostetter of Grantham Township. Jacob died a year later, leaving two children, Joseph Blain Hostetter (1860-1896) and Laura Diana Hostetter (1861-1933). Jacob was the son of Capt. Herman Hostetter of Ten Mile Creek who had died from wounds received at the Battle of Queenston Heights. Jacob and Dianna Hostetter are buried in the Warner Cemetery, Niagara Falls, Ont.

Active2010 and the Ontario School System: A Top-Down Policy Implementation Analysis

In 2004, the Ontario Ministry of Health Promotion and Sport (MHPS) established Active2010: Ontario’s Sport and Physical Activity Strategy. Active2010 demonstrates a strong provincial government policy emphasis regarding sport participation and physical activity (PA), and identifies the school system as a primary vehicle for enhancing PA levels. This study examines the sport and PA initiatives MHPS is undertaking within the school system. Theoretical context regarding neo-liberalism in Canada and Canadian sport frames this study, while a revised version of Van Meter and Van Horn’s (1975) top-down model of policy implementation guides the research process. A case study of the school-based PA system is conducted which relies on the analysis of 11 semi-structured interviews and 47 official organizational documents. Four emergent categories of Jurisdictional Funding, Coercive Policy, Sector Silos, and Community Champions are identified. Additional insight is provided regarding neo-liberalism, provincial level government, interministerial collaboration, and government/non-profit sector partnership.

Eficacia del diagnóstico prenatal no invasivo por células fetales libres en sangre materna 1990-2014. Revisión sistemática

ANTECEDENTES: El aislamiento de células fetales libres o ADN fetal en sangre materna abre una ventana de posibilidades diagnósticas no invasivas para patologías monogénicas y cromosómicas, además de permitir la identificación del sexo y del RH fetal. Actualmente existen múltiples estudios que evalúan la eficacia de estos métodos, mostrando resultados costo-efectivos y de menor riesgo que el estándar de oro. Este trabajo describe la evidencia encontrada acerca del diagnóstico prenatal no invasivo luego de realizar una revisión sistemática de la literatura. OBJETIVOS: El objetivo de este estudio fue reunir la evidencia que cumpla con los criterios de búsqueda, en el tema del diagnóstico fetal no invasivo por células fetales libres en sangre materna para determinar su utilidad diagnóstica.  MÉTODOS: Se realizó una revisión sistemática de la literatura con el fin de determinar si el diagnóstico prenatal no invasivo por células fetales libres en sangre materna es efectivo como método de diagnóstico.  RESULTADOS: Se encontraron 5,893 artículos que cumplían con los criterios de búsqueda; 67 cumplieron los criterios de inclusión: 49.3% (33/67) correspondieron a estudios de corte transversal, 38,8% (26/67) a estudios de cohortes y el 11.9% (8/67) a estudios casos y controles. Se obtuvieron resultados de sensibilidad, especificidad y tipo de prueba. CONCLUSIÓN: En la presente revisión sistemática, se evidencia como el diagnóstico prenatal no invasivo es una técnica feasible, reproducible y sensible para el diagnóstico fetal, evitando el riesgo de un diagnóstico invasivo.