Findings of Research Misconduct, 53303-53304 [2010-21579]
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Federal Register / Vol. 75, No. 168 / Tuesday, August 31, 2010 / Notices
conflict with a fundamental economic
purpose of ARRA, which is to create or
retain jobs.
The Municipal Assistance Unit (CMU)
has reviewed this waiver request and
has determined that the supporting
documentation provided by Sturbridge
establishes both a proper basis to
specify a particular manufactured good,
and that the domestic manufactured
goods that are currently available do not
meet the design specifications for the
proposed project. The information
provided is sufficient to meet the
following criteria listed under Section
1605(b) of the ARRA and in the April
28, 2009 Memorandum: Iron, steel, and
the manufactured goods are not
produced in the United States in
sufficient and reasonably available
quantities and of a satisfactory quality.
The March 31, 2009 Delegation of
Authority Memorandum provided
Regional Administrators with temporary
authority to issue exceptions to Section
1605 of the ARRA within the geographic
boundaries of their respective regions
and with respect to requests by
individual grant recipients.
Having established both a proper
basis to specify the particular good
required for this project and that this
manufactured good was not available
from a producer in the United States,
the Town of Sturbridge, Massachusetts
is hereby granted a waiver from the Buy
American requirements of Section
1605(a) of Public Law 111–5. This
waiver permits use of ARRA funds for
the purchase of a foreign manufactured
submersible mixer in Sturbridge’s
waiver request submittal dated May 25,
2010. This supplementary information
constitutes the detailed written
justification required by Section 1605(c)
for waivers based on a finding under
subsection (b).
Authority: Pub. L. 111–5, section 1605.
Dated: August 19, 2010.
Ira W. Leighton,
Acting Regional Administrator, EPA Region
1—New England.
Date and Time: The regular
meeting of the Board will be held at the
offices of the Farm Credit
Administration in McLean, Virginia, on
September 8, 2010, from 9 a.m. until
such time as the Board concludes its
business.
DATES:
FOR FURTHER INFORMATION CONTACT:
Roland E. Smith, Secretary to the Farm
Credit Administration Board, (703) 883–
4009, TTY (703) 883–4056.
ADDRESSES: Farm Credit
Administration, 1501 Farm Credit Drive,
McLean, Virginia 22102–5090.
SUPPLEMENTARY INFORMATION: Parts of
this meeting of the Board will be open
to the public (limited space available),
and parts will be closed to the public.
In order to increase the accessibility to
Board meetings, persons requiring
assistance should make arrangements in
advance. The matters to be considered
at the meeting are:
Open Session
A. Approval of Minutes
• August 12, 2010.
B. New Business
• Merger of the Louisiana Ag Credit
ACA, and Subsidiaries with Southern
AgCredit, ACA, and Subsidiaries.
• Fall 2010 Abstract of the Unified
Agenda of Federal Regulatory and
Deregulatory Actions and Fall 2010
Regulatory Performance Plan.
• Farm Credit Administration
Revised FY 2011 and Proposed FY 2012
Budget.
Closed Session*
• OSMO Quarterly Report.
*Session Closed—Exempt pursuant to
5 U.S.C. 552b(c)(8) and (9).
Dated: August 27, 2010.
Roland E. Smith,
Secretary, Farm Credit Administration Board.
[FR Doc. 2010–21859 Filed 8–27–10; 4:15 pm]
BILLING CODE 6705–01–P
FINANCIAL CRISIS INQUIRY
COMMISSION
Notice of Public Hearing
srobinson on DSKHWCL6B1PROD with NOTICES
FARM CREDIT ADMINISTRATION
Financial Crisis Inquiry
Commission.
ACTION: Notice.
AGENCY:
Farm Credit Administration Board;
Sunshine Act; Regular Meeting
AGENCY: Farm Credit Administration.
SUMMARY: Notice is hereby given,
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16:33 Aug 30, 2010
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The next public hearing of the
Financial Crisis Inquiry Commission
(FCIC) is titled ‘‘Too Big to Fail:
Expectations and Impact of
Extraordinary Government Intervention
and the role of Systemic Risk in the
SUMMARY:
pursuant to the Government in the
Sunshine Act (5 U.S.C. 552b(e)(3)), of
the regular meeting of the Farm Credit
Administration Board (Board).
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Financial Crisis.’’ The forum will also be
webcast live at https://www.FCIC.gov.
DATES: The hearing will be held on:
Wednesday, September 1, 2010, 9 a.m.
EDT; and Thursday, September 2, 2010,
9 a.m. EDT.
ADDRESSES: The hearing will be held at:
Dirksen Senate Office Building, Room
538, Washington, DC 20515.
FOR FURTHER INFORMATION CONTACT:
Gretchen Kinney Newsom, Financial
Crisis Inquiry Commission, 1717
Pennsylvania Avenue, Suite 800,
Washington, DC 20006. 202–292–2799;
202–632–1604 fax.
SUPPLEMENTARY INFORMATION: The
purpose of the Financial Crisis Inquiry
Commission is to examine the causes,
domestic and global, of the current
financial and economic crisis in the
United States, per the requirements of
the Fraud Enforcement and Recovery
Act of 2009 (‘‘FERA’’), Section 5, Public
Law 111–21–123 Stat. 1617 (2009).
Public Participation: The hearing is
open to the public. The Chairman of the
Commission will lead the hearing for
the orderly conduct of business.
Dated: August 25, 2010.
Gretchen Kinney Newsom,
Certifying Official and Special Assistant to
the Chairman, Financial Crisis Inquiry
Commission.
[FR Doc. 2010–21613 Filed 8–30–10; 8:45 am]
BILLING CODE 6820–RK–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Office of the Secretary
Reports
[FR Doc. 2010–21676 Filed 8–30–10; 8:45 am]
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Findings of Research Misconduct
Office of the Secretary, HHS.
Notice.
AGENCY:
ACTION:
Notice is hereby given that
the Office of Research Integrity (ORI)
and the Assistant Secretary for Health
have taken final action in the following
case:
Hung-Shu Chang, PhD, Washington
State University: Based on the report of
an investigation conducted by the
Washington State University (WSU) and
additional analysis by ORI in its
oversight review, the U.S. Public Health
Service (PHS) found that Hung-Shu
Chang, PhD, former postdoctoral fellow,
WSU, engaged in research misconduct
in research supported by National
Institute of Environmental Health
Sciences (NIEHS), National Institutes of
Health (NIH), grant R01 ES012974.
PHS found that the Respondent
engaged in scientific (42 CFR 50.102)
and research misconduct by fabricating
SUMMARY:
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Federal Register / Vol. 75, No. 168 / Tuesday, August 31, 2010 / Notices
and falsifying data in Figure 3 of a paper
published in Endocrinology.1
Specifically, PHS found that:
• Respondent, by not conducting any
of the claimed bisulfite sequencing,
fabricated the methylation status of CpG
sites in eight candidate genes identified
in both Figures 3 and 4 as No. 11, No.
12, No. 13, No. 14, 15, No. 22, No. 26,
No. 31, and No. 19, to support the
hypothesis that the environmental
compound, vinclozolin, induces a
permanent alteration in the epigenetic
reprogramming of the germline that
promotes transgenerational disease
states.
• Respondent, by conducting only a
small fraction of the claimed bisulfite
sequencing, and falsifying the results
obtained, falsified the methylation
status of CpG sites in eight additional
candidate genes, identified in Figures 3
and 4 as No. 2, 3, 24, No. 5, 6, 9, No.
8, No. 16, No. 17, 18, No. 27, 28, No. 29,
and No. 33.
Dr. Chang has entered into a Voluntary
Settlement Agreement in which he has
voluntarily agreed, for a period of three
(3) years, beginning on July 21, 2010:
(1) To exclude himself from serving in
any advisory capacity to PHS, including
but not limited to service on any PHS
advisory committee, board, and/or peer
review committee, or as a consultant;
(2) that any institution that submits an
application for PHS support for a
research project on which the
Respondent’s participation is proposed
or that uses him in any capacity on
PHS-support research, or that submits a
report of PHS-funded research in which
the Respondent is involved, must
concurrently submit a plan for
supervision of the Respondent’s duties
to the funding agency for approval. The
supervisory plan must be designed to
ensure the scientific integrity of the
Respondent’s research contribution
while applying for or conducting PHSsupported research. Respondent agrees
to ensure that a copy of the supervisory
plan is submitted to ORI by the
institution for ORI approval.
Respondent agrees not to participate in
any PHS-supported research until such
a supervisory plan is submitted to ORI.
srobinson on DSKHWCL6B1PROD with NOTICES
FOR FURTHER INFORMATION CONTACT:
Director, Division of Investigative
Oversight, Office of Research Integrity,
1 Chang, H.S., Anway, M.D., Rekow, S.S., &
Skinner, M.K. ‘‘Transgenerational epigenetic
imprinting of the male germline by endocrine
disruption exposure during gonadal sex
determination.’’ Endocrinology 147(12):5524–5541;
hereafter referred to as the ‘‘Endocrinology paper.’’
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16:33 Aug 30, 2010
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1101 Wootton Parkway, Suite 750,
Rockville, MD 20852, (240) 453–8800.
John Dahlberg,
Director, Division of Investigative Oversight,
Office of Research Integrity.
[FR Doc. 2010–21579 Filed 8–30–10; 8:45 am]
BILLING CODE 4150–31–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Office of the Secretary
Office of the Assistant Secretary for
Health; Statement of Organization,
Functions, and Delegations of
Authority
Part A, Office of the Secretary,
Statement of Organizations, Functions
and Delegations of Authority for the
Department of Health and Human
Services (HHS) is being amended at
Chapter AA, ‘‘Immediate Office of the
Secretary,’’ which was last amended at
75 FR 20364–65, dated April 19, 2010,
and at Chapter AC, ‘‘Office of Public
Health and Science (OPHS),’’ which was
last amended at 72 FR 58095–96, dated
October 12, 2007. This amendment will
accomplish two tasks: (1) In Chapter
AC, revise the title of the office headed
by the Assistant Secretary for Health
(ASH) from the ‘‘Office of Public Health
and Science’’ to the ‘‘Office of the
Assistant Secretary for Health,’’ and; (2)
add information about a new office
reporting to the Assistant Secretary for
Health (ASH), the ‘‘Office of Adolescent
Health,’’ established in section 1708 of
the Public Health Service (PHS) Act (42
U.S.C. 300u–7), and most recently
addressed in the December 8, 2009,
Conference Report (House Report 111–
366) accompanying the Consolidated
Appropriations Act, 2010 (Pub. L. 111–
117). The changes are as follows:
A. Under Part A, Chapter AA, Section
AA.10 Organization, replace the ‘‘Office
of Public Health and Science (AC)’’ with
the ‘‘Office of the Assistant Secretary for
Health (AC).’’
B. Under Part A generally and Part A,
Chapter AC, replace all references to the
‘‘Office of Public Health and Science’’
with the ‘‘Office of the Assistant
Secretary for Health’’ and all references
to ‘‘OPHS’’ with ‘‘OASH.’’
C. Under Part A, Chapter AC, Section
AC.10 Organization, insert ‘‘M. Office of
Adolescent Health (ACR)’’ immediately
after ‘‘L. Office of Commissioned Corps
Force Management (ACQ).’’
D. Under Part A, Chapter AC, Section
AC.20 Functions, insert the following
text immediately after item, ‘‘L. Office of
Commissioned Corps Force
Management (ACQ)’’:
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M. Office of Adolescent Health (ACR)
Section ACR.00 Mission. The Director
of the Office of Adolescent Health
(OAH) is the principal advisor to the
Assistant Secretary for Health (ASH) on
health-related policy and program
issues related to adolescents. These
issues cut across Health and Human
Services (HHS) components which
provide research, services, prevention,
promotion, treatment, training,
education, and information
dissemination related to adolescent
health. OAH is responsible for
implementing activities authorized by
section 1708 of the Public Health
Service (PHS) Act.
Section ACR.10 Organization. The
Office of Adolescent Health is headed
by a Director who reports to the
Assistant Secretary for Health and is
includes the following components:
A. Immediate Office of the Director
(ACR)
B. Division of Program Development
and Operations (ACR1)
C. Division of Policy, Planning, and
Communications (ACR2)
Section ACR.20
Functions
1. Immediate Office of the Director
(ACR). The Immediate Office of the
Director (IOD) plans and directs
financial management and policy
development, including budget
formulation and execution. The IOD
also oversees legislative activities
related to adolescent health, acts as a
liaison on personnel management to the
Office of the Assistant Secretary for
Health (OASH) and the Program
Support Center, and coordinates
correspondence control and executive
secretariat functions for OAH. The IOD
also manages the day-to-day operations
of OAH, plans, coordinates, monitors,
and evaluates OAH grants and contracts,
and ensures the appropriate exercise of
delegated authorities and
responsibilities.
2. Division of Program Development
and Operations (ACR1). The Division of
Program Development and Operations
(DPDO) advises the OAH Director on the
development of new programs and
policies, oversees the implementation
and administration of competitive
grants and cooperative agreements,
monitors grantee activities, evaluates
the focus and impact of ongoing
programs, prepares analytical reports on
program trends, provides training and
technical assistance for grant programs,
and assesses performance of grantee
operations. The Division manages the
development of funding announcements
and contract scopes of work and the
review and award of program grants,
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Agencies
[Federal Register Volume 75, Number 168 (Tuesday, August 31, 2010)]
[Notices]
[Pages 53303-53304]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-21579]
=======================================================================
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Office of the Secretary
Findings of Research Misconduct
AGENCY: Office of the Secretary, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: Notice is hereby given that the Office of Research Integrity
(ORI) and the Assistant Secretary for Health have taken final action in
the following case:
Hung-Shu Chang, PhD, Washington State University: Based on the
report of an investigation conducted by the Washington State University
(WSU) and additional analysis by ORI in its oversight review, the U.S.
Public Health Service (PHS) found that Hung-Shu Chang, PhD, former
postdoctoral fellow, WSU, engaged in research misconduct in research
supported by National Institute of Environmental Health Sciences
(NIEHS), National Institutes of Health (NIH), grant R01 ES012974.
PHS found that the Respondent engaged in scientific (42 CFR 50.102)
and research misconduct by fabricating
[[Page 53304]]
and falsifying data in Figure 3 of a paper published in
Endocrinology.\1\ Specifically, PHS found that:
---------------------------------------------------------------------------
\1\ Chang, H.S., Anway, M.D., Rekow, S.S., & Skinner, M.K.
``Transgenerational epigenetic imprinting of the male germline by
endocrine disruption exposure during gonadal sex determination.''
Endocrinology 147(12):5524-5541; hereafter referred to as the
``Endocrinology paper.''
---------------------------------------------------------------------------
Respondent, by not conducting any of the claimed bisulfite
sequencing, fabricated the methylation status of CpG sites in eight
candidate genes identified in both Figures 3 and 4 as No. 11, No. 12,
No. 13, No. 14, 15, No. 22, No. 26, No. 31, and No. 19, to support the
hypothesis that the environmental compound, vinclozolin, induces a
permanent alteration in the epigenetic reprogramming of the germline
that promotes transgenerational disease states.
Respondent, by conducting only a small fraction of the
claimed bisulfite sequencing, and falsifying the results obtained,
falsified the methylation status of CpG sites in eight additional
candidate genes, identified in Figures 3 and 4 as No. 2, 3, 24, No. 5,
6, 9, No. 8, No. 16, No. 17, 18, No. 27, 28, No. 29, and No. 33.
Dr. Chang has entered into a Voluntary Settlement Agreement in which he
has voluntarily agreed, for a period of three (3) years, beginning on
July 21, 2010:
(1) To exclude himself from serving in any advisory capacity to
PHS, including but not limited to service on any PHS advisory
committee, board, and/or peer review committee, or as a consultant;
(2) that any institution that submits an application for PHS
support for a research project on which the Respondent's participation
is proposed or that uses him in any capacity on PHS-support research,
or that submits a report of PHS-funded research in which the Respondent
is involved, must concurrently submit a plan for supervision of the
Respondent's duties to the funding agency for approval. The supervisory
plan must be designed to ensure the scientific integrity of the
Respondent's research contribution while applying for or conducting
PHS-supported research. Respondent agrees to ensure that a copy of the
supervisory plan is submitted to ORI by the institution for ORI
approval. Respondent agrees not to participate in any PHS-supported
research until such a supervisory plan is submitted to ORI.
FOR FURTHER INFORMATION CONTACT: Director, Division of Investigative
Oversight, Office of Research Integrity, 1101 Wootton Parkway, Suite
750, Rockville, MD 20852, (240) 453-8800.
John Dahlberg,
Director, Division of Investigative Oversight, Office of Research
Integrity.
[FR Doc. 2010-21579 Filed 8-30-10; 8:45 am]
BILLING CODE 4150-31-P