Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Neha Sodhi"'
Autor:
Cleber A Trujillo, Jason W Adams, Priscilla D Negraes, Cassiano Carromeu, Leon Tejwani, Allan Acab, Ben Tsuda, Charles A Thomas, Neha Sodhi, Katherine M Fichter, Sarah Romero, Fabian Zanella, Terrence J Sejnowski, Henning Ulrich, Alysson R Muotri
Publikováno v:
EMBO Molecular Medicine, Vol 13, Iss 1, Pp 1-18 (2020)
Abstract Duplication or deficiency of the X‐linked MECP2 gene reliably produces profound neurodevelopmental impairment. MECP2 mutations are almost universally responsible for Rett syndrome (RTT), and particular mutations and cellular mosaicism of M
Externí odkaz:
https://doaj.org/article/62a5f92686b74314967f1f52b82ce189
Autor:
Ileana Slavin, Steven Dea, Priyanka Arunkumar, Neha Sodhi, Sandro Montefusco, Jair Siqueira-Neto, Janet Seelke, Mary Anne Lofstrom, Blake Anson, Fabian Zanella, Cassiano Carromeu
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 4, p 1908 (2021)
With increasing global health threats has come an urgent need to rapidly develop and deploy safe and effective therapies. A common practice to fast track clinical adoption of compounds for new indications is to repurpose already approved therapeutics
Externí odkaz:
https://doaj.org/article/e1ea4556e8d64a8390882339fe1a6956
Publikováno v:
Indian Dermatology Online Journal, Vol 7, Iss 2, Pp 93-95 (2016)
Acne fulminans (AF) is a very rare severe form of acne seen in young males, characterized by a sudden and explosive onset of hemorrhagic pustules and ulceration on the trunk, systemic features in the form of fever, polyarthropathy, malaise, erythema
Externí odkaz:
https://doaj.org/article/21d0c08bd5c64a6d92a20eceab263d3c
Publikováno v:
Indian Journal of Dermatology, Vol 61, Iss 4, Pp 467-467 (2016)
Hereditary porphyrias are a group of metabolic disorders of heme biosynthesis pathway that are characterized by acute neurovisceral symptoms, skin lesions, or both. Congenital erythropoietic porphyria (CEP) is an extremely rare disease with a mutatio
Externí odkaz:
https://doaj.org/article/bf643b97308f48a59933af34ff1e7d05
Autor:
Fabian Zanella, Mary Anne Lofstrom, Janet Seelke, Blake Anson, Sandro Montefusco, Steven Dea, Priyanka Arunkumar, Ileana Slavin, Neha Sodhi, Jair L. Siqueira-Neto, Cassiano Carromeu
Publikováno v:
International Journal of Molecular Sciences
Volume 22
Issue 4
International Journal of Molecular Sciences, Vol 22, Iss 1908, p 1908 (2021)
Volume 22
Issue 4
International Journal of Molecular Sciences, Vol 22, Iss 1908, p 1908 (2021)
With increasing global health threats has come an urgent need to rapidly develop and deploy safe and effective therapies. A common practice to fast track clinical adoption of compounds for new indications is to repurpose already approved therapeutics
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f09cbe3654adbcb3f1a76306763d4b9c
http://europepmc.org/articles/PMC7918576
http://europepmc.org/articles/PMC7918576
Autor:
Neha Sodhi, Oksana Sirenko, Oivin Guicherit, Grischa Chandy, Carole Crittenden, Sergio Mora-Castilla, Fabian Zanella, Steven Biesmans, Mamta Behl, Sarah Vargas-Hurlston, Frederick M. Parham, Ryan Gordon, Kristen Ryan, Steven Dea, Cassiano Carromeu
Publikováno v:
Toxicological Sciences. 167:58-76
Neurological disorders affect millions of people worldwide and appear to be on the rise. Whereas the reason for this increase remains unknown, environmental factors are a suspected contributor. Hence, there is an urgent need to develop more complex,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::186f610094385f613df7d83c4cf014f5
https://doi.org/10.1093/toxsci/kfy218
https://doi.org/10.1093/toxsci/kfy218
Publikováno v:
Medical Journal Armed Forces India. 74:300-303
A 60-year-old female presented with a 20-year history of progressive dark bluish discoloration of skin and passage of dark colored urine, painful arthritis and a recent history of invasive ductal carcinoma of right breast. Skin biopsy revealed hyalin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8af62fdfe80160af9f15abad73025d25
https://doi.org/10.1016/j.mjafi.2017.06.009
https://doi.org/10.1016/j.mjafi.2017.06.009
Autor:
Tony Harrington, Grace Woodruff, Cassiano Carromeu, Sergio Mora-Castilla, Fabian Zanella, Sarah Romero, Aurian Saleh, Steven Dea, Steven Biesmans, Neha Sodhi
Publikováno v:
Journal of Pharmacological and Toxicological Methods. 99:106595
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dddbd237f38d08f32662f8fea4026724
https://doi.org/10.1016/j.vascn.2019.05.190
https://doi.org/10.1016/j.vascn.2019.05.190
Publikováno v:
Indian Journal of Dermatology, Vol 61, Iss 4, Pp 467-467 (2016)
Indian Journal of Dermatology
Indian Journal of Dermatology
Hereditary porphyrias are a group of metabolic disorders of heme biosynthesis pathway that are characterized by acute neurovisceral symptoms, skin lesions, or both. Congenital erythropoietic porphyria (CEP) is an extremely rare disease with a mutatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ec11c256f76061bf291e1d5a2a70bd4
http://www.e-ijd.org/article.asp?issn=0019-5154
http://www.e-ijd.org/article.asp?issn=0019-5154