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The US federal restriction (the Dickey-Wicker Amendment) only prohibits federally funded research that creates or destroys a human embryo. The US 14-day limit is not a federal policy or guideline, but was developed by a nongovernmental organization, the National Academies of Sciences, Engineering and Medicine.
Today, federal funding of human non-embryonic stem cell research outweighs funding for human embryonic stem cell research. Of that total, $213 million was allocated to human embryonic stem cell research. Non-embryonic human stem cell research, however, received $480 million more than twice as much.
On one end of the spectrum, eight states (California, Connecticut, Illinois, Iowa, Maryland, Massachusetts, New Jersey and New York) encourage embryonic stem cell research, while on the other end of the spectrum, South Dakota strictly forbids research on embryos.
Prop 71 amended the California Constitution to establish a right to conduct stem cell research which includes research involving adult stem cells, cord blood stem cells, pluripotent stem cells, and/or progenitor cells. The right to do stem cell research (including SCNT) and the prohibition on reproductive cloning
It stipulated that the clinical use of stem cells was not permitted, and any use in clinical context (with the exception of already standardized use in autologous bone marrow transplantation and epithelial therapies for corneal disorders) must be the part of a clinical study, after due approval from the Institutional

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NIH funding of the derivation of stem cells from human embryos is prohibited by the annual appropriations ban on funding of human embryo research (Section 509, Omnibus Appropriations Act, 2009, Pub. L. 111-8, 3/11/09), otherwise known as the Dickey Amendment.
The Executive Order states that the Secretary of Health and Human Services, through the Director of NIH, may support and conduct responsible, scientifically worthy human stem cell research, including human embryonic stem cell (hESC) research, to the extent permitted by law.
The GESCR Committee requires that all state and/or federal requirements are met before a human stem cell line can be approved by the Committee. The pre-approval considerations may include, but are not limited to, consent from the gamete and/or embryo donors and payment reimbursement of donors.

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