Lawrence M. Nelson
YOU?
Author Swipe
View article: Draft genome of <i>Corynebacterium glycinophilum</i> S209 isolated from healthy human skin
Draft genome of <i>Corynebacterium glycinophilum</i> S209 isolated from healthy human skin Open
Corynebacterium glycinophilum is an understudied species of this genus, although it has been identified in dairy products as well as the human skin microbiome. Recently, we isolated a strain from the skin of a healthy human female, and her…
View article: Draft genome sequences of <i>Staphylococcus</i> species isolated from urine samples from asymptomatic females
Draft genome sequences of <i>Staphylococcus</i> species isolated from urine samples from asymptomatic females Open
The female urinary tract is host to several different Staphylococcus species, both uropathogens and commensals. To further investigate these species, we sequenced the genomes of four isolates from voided urine samples collected from asympt…
View article: Draft genome sequences of <i>Staphylococcus hominis</i> strains O226 and O218 and <i>Micrococcus luteus</i> O220 isolated from the buccal swabs of healthy individuals
Draft genome sequences of <i>Staphylococcus hominis</i> strains O226 and O218 and <i>Micrococcus luteus</i> O220 isolated from the buccal swabs of healthy individuals Open
To investigate the genomic features of rare oral commensals in healthy individuals, we present the draft genome sequences of Staphylococcus hominis strains O226 and O218 and Micrococcus luteus strain O220. All three of these isolates were …
View article: Draft genome sequence of <i>Staphylococcus aureus</i> N208 isolated from a nasal swab of a healthy female
Draft genome sequence of <i>Staphylococcus aureus</i> N208 isolated from a nasal swab of a healthy female Open
Staphylococcus aureus , a common member of the healthy human microbiota, is an opportunistic pathogen. To investigate the genomic features of this species in healthy individuals, we present the draft genome sequence of S. aureus N208, isol…
View article: Women’s hormonal health research and care: the times, they are a-changin’
Women’s hormonal health research and care: the times, they are a-changin’ Open
View article: Editorial: Insights in developmental endocrinology: 2023
Editorial: Insights in developmental endocrinology: 2023 Open
Keywords: developmental endocrinology, wisdom of the body, homeostasis, integrative biology, maternal fetal interface, women's hormonal health, hormonal literacy, science advocacy
View article: A social movement: mind the gap in women’s healthcare and research
A social movement: mind the gap in women’s healthcare and research Open
View article: Primary Ovarian Insufficiency: A Case of the Cart before the Horse
Primary Ovarian Insufficiency: A Case of the Cart before the Horse Open
Overt Primary Ovarian Insufficiency (POI) is a rare disorder characterized by a constellation of other rare conditions, posing significant diagnostic and management challenges. This disorder necessitates a global mechanism for information …
View article: Editorial: Pathophysiology and management of amenorrhea and estradiol deficiency in girls and young women
Editorial: Pathophysiology and management of amenorrhea and estradiol deficiency in girls and young women Open
Editorial: Pathophysiology and management of amenorrhea and estradiol deficiency in girls and young women
View article: A call for a US National Institute of Women’s Health and Human Development
A call for a US National Institute of Women’s Health and Human Development Open
Keywords: women's health activism, women's health funding, women's health policy, women's health research, digital medical hub, community-based participatory research
View article: Primary Ovarian Insufficiency: A new paradigm for care and research
Primary Ovarian Insufficiency: A new paradigm for care and research Open
bone, heart, and brain health.There is a natural decrease in 17-Beta-Estradiol levels towards menopause, but 17-Beta-Estradiol deficiency is also seen in POI.Unfortunately, women's health is widely under-researched, and this becomes obviou…
View article: My 28 Days - a global digital women’s health initiative for evaluation and management of secondary amenorrhea: case report and literature review
My 28 Days - a global digital women’s health initiative for evaluation and management of secondary amenorrhea: case report and literature review Open
There is a need to close the gap between knowledge and action in health care. Effective care requires a convenient and reliable distribution process. As global internet and mobile communication increase capacity, innovative approaches to d…
View article: The truth about 17-beta estradiol: menopause beyond “old wives’ tales”
The truth about 17-beta estradiol: menopause beyond “old wives’ tales” Open
OPINION article Front. Endocrinol., 11 September 2023Sec. Developmental Endocrinology Volume 14 - 2023 | https://doi.org/10.3389/fendo.2023.1229804
View article: Editorial: A year in review: discussions in developmental endocrinology
Editorial: A year in review: discussions in developmental endocrinology Open
EDITORIAL article Front. Endocrinol., 25 May 2023Sec. Developmental Endocrinology Volume 14 - 2023 | https://doi.org/10.3389/fendo.2023.1213095
View article: Editorial: Insights in developmental endocrinology: 2021
Editorial: Insights in developmental endocrinology: 2021 Open
EDITORIAL article Front. Endocrinol., 02 February 2023Sec. Developmental Endocrinology Volume 14 - 2023 | https://doi.org/10.3389/fendo.2023.1129090
View article: Causal and Candidate Gene Variants in a Large Cohort of Women With Primary Ovarian Insufficiency
Causal and Candidate Gene Variants in a Large Cohort of Women With Primary Ovarian Insufficiency Open
Context A genetic etiology likely accounts for the majority of unexplained primary ovarian insufficiency (POI). Objective We hypothesized that heterozygous rare variants and variants in enhanced categories are associated with POI. Design T…
View article: Optimizing Fertility in Primary Ovarian Insufficiency: Case Report and Literature Review
Optimizing Fertility in Primary Ovarian Insufficiency: Case Report and Literature Review Open
Primary ovarian insufficiency (POI) is a clinical spectrum of ovarian dysfunction. Overt POI presents with oligo/amenorrhea and hypergonadotropic hypogonadism before age 40 years. Overt POI involves chronic health problems to include incre…
View article: OR31-06 Candidate Gene Variants in a Large Cohort of Women with Primary Ovarian Insufficiency
OR31-06 Candidate Gene Variants in a Large Cohort of Women with Primary Ovarian Insufficiency Open
Primary ovarian insufficiency (POI) is highly heritable. The majority of cases have no known cause. We hypothesized that mutations in previously identified genes or genes from the same pathways are the cause of POI in a recessive or domina…
View article: PMU87 REVIEW OF ORPHAN TREATMENTS ASSESSED BY NICE AND THE SMC IN THE UK.
PMU87 REVIEW OF ORPHAN TREATMENTS ASSESSED BY NICE AND THE SMC IN THE UK. Open
View article: Fragile X Associated Primary Ovarian Insufficiency (FXPOI): Case Report and Literature Review
Fragile X Associated Primary Ovarian Insufficiency (FXPOI): Case Report and Literature Review Open
Abnormalities in the X-linked FMR1 gene are associated with a constellation of disorders, which have broad and profound implications for the person first diagnosed, and extended family members of all ages. The rare and pleiotropic n…
View article: A randomized controlled study of a consent intervention for participating in an NIH genome sequencing study
A randomized controlled study of a consent intervention for participating in an NIH genome sequencing study Open
View article: The long Heavy Chain Determinant Region 3 (HCDR3) antibodies that neutralize virus bind the CD4 binding site (CD4 bs).
The long Heavy Chain Determinant Region 3 (HCDR3) antibodies that neutralize virus bind the CD4 binding site (CD4 bs). Open
Purified recombinant monoclonal antibodies (mAbs) were assayed by ELISA for (A) blocking the binding of soluble CD4 to AE.A244gp120, and (B) sensitivity to the CD4 binding site mutations Δ371I/P363N, D368R, N276A, and T278A in the AE.A244g…
View article: Hormone replacement therapy in young women with primary ovarian insufficiency and early menopause
Hormone replacement therapy in young women with primary ovarian insufficiency and early menopause Open
View article: Hormone replacement therapy in young women with surgical primary ovarian insufficiency
Hormone replacement therapy in young women with surgical primary ovarian insufficiency Open
View article: Functional characteristics of <i>C</i>. <i>albicans</i>- and CMV-specific CD4 T cells in healthy subjects.
Functional characteristics of <i>C</i>. <i>albicans</i>- and CMV-specific CD4 T cells in healthy subjects. Open
(A) Representative flow cytometric plots are shown for different cytokine expression in CFSE-low CD4+ T cells in PBMC after cognate antigen C. albicans (top) or CMV (bottom) stimulation. CFSE-labeled healthy donor PBMCs were …
View article: Characteristics of HIV-infected subjects from the RV21 cohort<sup>*</sup>.
Characteristics of HIV-infected subjects from the RV21 cohort<sup>*</sup>. Open
Characteristics of HIV-infected subjects from the RV21 cohort*.
View article: HIV infectivity in functional subsets of <i>C</i>. <i>albicans</i>-specific CD4 T cells.
HIV infectivity in functional subsets of <i>C</i>. <i>albicans</i>-specific CD4 T cells. Open
(A) Overall in vitro HIV susceptibility of C. albicans- and CMV-specific CD4 T cells in the same healthy donor PBMCs. CFSE-labeled PBMCs were stimulated with C. albicans (left) or CMV (right) for 3 days, and exp…
View article: Primer sequences of HIV DNA quantification.
Primer sequences of HIV DNA quantification. Open
View article: Primer sequences for quantification of gene expression.
Primer sequences for quantification of gene expression. Open
View article: Proteome-wide survey of the autoimmune target repertoire in autoimmune polyendocrine syndrome type 1
Proteome-wide survey of the autoimmune target repertoire in autoimmune polyendocrine syndrome type 1 Open
Autoimmune polyendocrine syndrome type 1 (APS1) is a monogenic disorder that features multiple autoimmune disease manifestations. It is caused by mutations in the Autoimmune regulator (AIRE) gene, which promote thymic display of thousands …