Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1965 1
1967 2
1968 5
1969 2
1970 3
1971 5
1972 4
1973 8
1974 6
1975 5
1976 1
1978 3
1979 2
1980 1
1981 1
1982 1
1983 2
1986 2
1988 1
1993 1
1997 1
1998 1
1999 2
2000 1
2001 1
2005 1
2006 2
2008 1
2009 1
2010 3
2011 1
2013 3
2020 1
2021 1
2023 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

77 results

Results by year

Filters applied: . Clear all
Page 1
ACE2 and gut amino acid transport.
Camargo SMR, Vuille-Dit-Bille RN, Meier CF, Verrey F. Camargo SMR, et al. Clin Sci (Lond). 2020 Nov 13;134(21):2823-2833. doi: 10.1042/CS20200477. Clin Sci (Lond). 2020. PMID: 33140827 Review.
The heterodimerization of the carboxypeptidase ACE2 with B0AT1 is suggested to favor the direct supply of substrate amino acids to the transporter, but whether this association impacts the ability of ACE2 to mediate viral infection is not known. B0AT1 mutations cause Hartnup
The heterodimerization of the carboxypeptidase ACE2 with B0AT1 is suggested to favor the direct supply of substrate amino acids to the trans …
Episodic Ataxias: Primary and Secondary Etiologies, Treatment, and Classification Approaches.
Hassan A. Hassan A. Tremor Other Hyperkinet Mov (N Y). 2023 Mar 28;13:9. doi: 10.5334/tohm.747. eCollection 2023. Tremor Other Hyperkinet Mov (N Y). 2023. PMID: 37008993 Free PMC article. Review.
EA may also be caused by gene mutations associated with chronic ataxias (SCA-14, SCA-27, SCA-42, AOA2, CAPOS), epilepsy syndromes (KCNA2, SCN2A, PRRT2), GLUT-1, mitochondrial disorders (PDHA1, PDHX, ACO2), metabolic disorders (Maple syrup urine disease, Hartnup d
EA may also be caused by gene mutations associated with chronic ataxias (SCA-14, SCA-27, SCA-42, AOA2, CAPOS), epilepsy syndromes (KCNA2, SC …
Ataxia.
Winchester S, Singh PK, Mikati MA. Winchester S, et al. Handb Clin Neurol. 2013;112:1213-7. doi: 10.1016/B978-0-444-52910-7.00043-X. Handb Clin Neurol. 2013. PMID: 23622331 Review.
., antiepileptics, lead, alcohol), postinfectious cerebellitis, hemorrhage, ischemic stroke, tumor (posterior fossa or cerebellum), brainstem encephalitis, occult neuroblastoma, Miller Fisher syndrome, conversion reaction, multiple sclerosis, epileptic pseudoataxia, vasculitis (e …
., antiepileptics, lead, alcohol), postinfectious cerebellitis, hemorrhage, ischemic stroke, tumor (posterior fossa or cerebellum), brainste …
Collectrin and ACE2 in renal and intestinal amino acid transport.
Singer D, Camargo SM. Singer D, et al. Channels (Austin). 2011 Sep-Oct;5(5):410-23. doi: 10.4161/chan.5.5.16470. Epub 2011 Sep 1. Channels (Austin). 2011. PMID: 21814048 Free article. Review.
We will conclude with some remarks concerning the relevance of this association to Hartnup disorder, where some mutations have been shown to differentially interact with the partner proteins....
We will conclude with some remarks concerning the relevance of this association to Hartnup disorder, where some mutations have been s …
Neutral amino acid transport in epithelial cells and its malfunction in Hartnup disorder.
Bröer S, Cavanaugh JA, Rasko JE. Bröer S, et al. Biochem Soc Trans. 2005 Feb;33(Pt 1):233-6. doi: 10.1042/BST0330233. Biochem Soc Trans. 2005. PMID: 15667315 Review.
Hartnup disorder is an autosomal recessive abnormality of renal and gastrointestinal neutral amino acid transport. ...These mutations lead to altered neutral amino acid transport function compared to the wild-type allele in vitro. One of the mutations occurs in members of
Hartnup disorder is an autosomal recessive abnormality of renal and gastrointestinal neutral amino acid transport. ...These mutations
Apical transporters for neutral amino acids: physiology and pathophysiology.
Bröer S. Bröer S. Physiology (Bethesda). 2008 Apr;23:95-103. doi: 10.1152/physiol.00045.2007. Physiology (Bethesda). 2008. PMID: 18400692 Free article. Review.
This is illustrated by inherited disorders of amino acid absorption, such as Hartnup disorder, cystinuria, iminoglycinuria, dicarboxylic aminoaciduria, and lysinuric protein intolerance, affecting separate groups of amino acids. Recent advances in the molecular identificat …
This is illustrated by inherited disorders of amino acid absorption, such as Hartnup disorder, cystinuria, iminoglycinuria, dicarboxy …
The role of the neutral amino acid transporter B0AT1 (SLC6A19) in Hartnup disorder and protein nutrition.
Bröer S. Bröer S. IUBMB Life. 2009 Jun;61(6):591-9. doi: 10.1002/iub.210. IUBMB Life. 2009. PMID: 19472175 Free PMC article. Review.
Hartnup disorder (OMIM 234500) is an autosomal recessive disorder, which was first described in 1956 as an aminoaciduria of neutral amino acids accompanied by a variety of symptoms, such as a photo-sensitive skin-rash and cerebellar ataxia. ...
Hartnup disorder (OMIM 234500) is an autosomal recessive disorder, which was first described in 1956 as an aminoaciduria of neutral a
Angiotensin-converting enzyme 2 (ACE2) in disease pathogenesis.
Imai Y, Kuba K, Ohto-Nakanishi T, Penninger JM. Imai Y, et al. Circ J. 2010 Mar;74(3):405-10. doi: 10.1253/circj.cj-10-0045. Epub 2010 Feb 4. Circ J. 2010. PMID: 20134095 Free article. Review.
For instance, in the acute respiratory distress syndrome (ARDS), ACE, AngII, and AT1R promote the disease pathogenesis, whereas ACE2 and the AT2R protect from ARDS. ...Furthermore, the recent explosion of research into the ACE2 homolog, collectrin, has revealed a new physi …
For instance, in the acute respiratory distress syndrome (ARDS), ACE, AngII, and AT1R promote the disease pathogenesis, whereas ACE2 …
Multiple functions of angiotensin-converting enzyme 2 and its relevance in cardiovascular diseases.
Kuba K, Imai Y, Penninger JM. Kuba K, et al. Circ J. 2013;77(2):301-8. doi: 10.1253/circj.cj-12-1544. Epub 2013 Jan 18. Circ J. 2013. PMID: 23328447 Free article. Review.
In addition, ACE2 is structurally a chimeric protein that has emerged from the duplication of 2 genes: homology with ACE at the carboxypeptidase domain and homology with Collectrin in the transmembrane C-terminal domain. ACE2 has been implicated in the pathology of Hartnup
In addition, ACE2 is structurally a chimeric protein that has emerged from the duplication of 2 genes: homology with ACE at the carboxypepti …
77 results