AUTH:"Bakhshoodeh B" - Search results

Search results

1-6 of 6 results

Sort by:

Relevance ^{Relevance: This is determined based on a ranking of criteria including term frequency, rarity of term, recency of article, whether there is a Title or Author field match, etc.}

Times cited

Date

Loss of symmetric cell division of apical neural progenitors drives DENND5A-related developmental and epileptic encephalopathy.
Banks E, Francis V, Lin SJ, Kharfallah F, Fonov V, Lévesque M, Han C, Kulasekaran G, Tuznik M, Bayati A, Al-Khater R, Alkuraya FS, Argyriou L, Babaei M, Bahlo M, Bakhshoodeh B, Barr E, Bartik L, Bassiony M, [...] McPherson PS
Nat Commun, 15(1):7239, 22 Aug 2024
Cited by: 0 articles | PMID: 39174524 | PMCID: PMC11341845
Add to export list
This article is in the Europe PMC Open access subset. Refer to the copyright information in the article for licensing details.
Free full text in Europe PMC
Human TRMT1 and TRMT1L paralogs ensure the proper modification state, stability, and function of tRNAs
Zhang K, Manning AC, Lentini JM, Howard J, Dalwigk F, Maroofian R, Efthymiou S, Chan P, Eliseev SI, Yang Z, Chang H, Karimiani EG, Bakhshoodeh B, Houlden H, Kaiser SM, Lowe TM, Fu D
bioRxiv, 21 May 2024
Cited by: 0 articles | PPR: PPR855506
Add to export list Preprint
This article is in the Europe PMC Open access subset. Refer to the copyright information in the article for licensing details.
Free full text in Europe PMC
Bi-allelic truncating variants in CASP2 underlie a neurodevelopmental disorder with lissencephaly.
Uctepe E, Vona B, Esen FN, Sonmez FM, Smol T, Tümer S, Mancılar H, Geylan Durgun DE, Boute O, Moghbeli M, Ghayoor Karimiani E, Hashemi N, Bakhshoodeh B, Kim HG, Maroofian R, Yesilyurt A
Eur J Hum Genet, 32(1):52-60, 26 Oct 2023
Cited by: 3 articles | PMID: 37880421 | PMCID: PMC10772072
Add to export list
This article is in the Europe PMC Open access subset. Refer to the copyright information in the article for licensing details.
Free full text in Europe PMC
Loss of symmetric cell division of apical neural progenitors drivesDENND5A-related developmental and epileptic encephalopathy
Banks E, Francis V, Lin S, Kharfallah F, Fonov V, Levesque M, Han C, Kulasekaran G, Tuznik M, Bayati A, Al-Khater R, Alkuraya FS, Argyriou L, Babaei M, Bahlo M, Bakhshoodeh B, Barr E, Bartik L, Bassiony M, [...] McPherson PS
medRxiv, 26 Aug 2022
Cited by: 0 articles | PPR: PPR536501
Add to export list Preprint
Adult Onset of Xanthelasmoid Mastocytosis: Report of a Rare Entity.
Nabavi NS, Nejad MH, Feli S, Bakhshoodeh B, Layegh P
Indian J Dermatol, 61(4):468, 01 Jul 2016
Cited by: 0 articles | PMID: 27512209 | PMCID: PMC4966424
Add to export list
This article is in the Europe PMC Open access subset. Refer to the copyright information in the article for licensing details.
Free full text in Europe PMC
Qulaity of life in cystic fibrosis children.
Kianifar HR, Bakhshoodeh B, Hebrani P, Behdani F
Iran J Pediatr, 23(2):149-153, 01 Apr 2013
Cited by: 9 articles | PMID: 23724174 | PMCID: PMC3663304
Add to export list
This article is in the Europe PMC Open access subset. Refer to the copyright information in the article for licensing details.
Free full text in Europe PMC

1-6 of 6 results

Search life-sciences literature (45,104,145 articles, preprints and more)

Search results

Loss of symmetric cell division of apical neural progenitors drives DENND5A-related developmental and epileptic encephalopathy.

Human TRMT1 and TRMT1L paralogs ensure the proper modification state, stability, and function of tRNAs

Bi-allelic truncating variants in CASP2 underlie a neurodevelopmental disorder with lissencephaly.

Loss of symmetric cell division of apical neural progenitors drivesDENND5A-related developmental and epileptic encephalopathy

Adult Onset of Xanthelasmoid Mastocytosis: Report of a Rare Entity.

Qulaity of life in cystic fibrosis children.

Partnerships & funding