Acromegaly research, articles, guidelines & medical evidence database search.
Access the latest scientific research and medical evidence related to Acromegaly treatment, diagnosis and symptoms, quickly and easily with doctorAsyou.
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All Pubmed data courtesy of the U.S. National Library of Medicine. Library last updated 18 December 2020.
Clinical trials databases last updated 1 December 2020 (clinicaltrials.gov) and 1 December 2020 (ictrp)
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Research
Glia-to-Neuron Conversion by CRISPR-CasRx Alleviates Symptoms of Neurological Disease in Mice.
Zhou Haibo, Su Jinlin, Hu Xinde, Zhou Changyang, Li He ...
Cell Vol 181(3)
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Date 30 Apr 2020
Research
Stress-Induced Metabolic Disorder in Peripheral CD4+ T Cells Leads to Anxiety-like Behavior.
Fan Ke-Qi, Li Yi-Yuan, Wang Hao-Li, Mao Xin-Tao, Guo Jin-Xin ...
Cell Vol 179(4)
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Date 31 Oct 2019
Research
Human CLP1 mutations alter tRNA biogenesis, affecting both peripheral and central nervous system function.
Karaca Ender, Weitzer Stefan, Pehlivan Davut, Shiraishi Hiroshi, Gogakos Tasos ...
Cell Vol 157(3)
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Date 24 Apr 2014
Research
Biosynthesis of the major zona pellucida glycoprotein secreted by oocytes during mammalian oogenesis.
Greve J M, Salzmann G S, Roller R J, Wassarman P M
Cell Vol 31(3 Pt 2)
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Date 01 Dec 1982
Research
Impaired intracellular transport of class I MHC antigens as a possible means for adenoviruses to evade immune surveillance.
Andersson M, Pääbo S, Nilsson T, Peterson P A
Cell Vol 43(1)
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Date 01 Nov 1985
Research
Biosynthesis of the IgA antibody receptor: a model for the transepithelial sorting of a membrane glycoprotein.
Solari R, Kraehenbuhl J P
Cell Vol 36(1)
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Date 01 Jan 1984
Research
Retinal ligatin recognizes glycoproteins bearing oligosaccharides terminating in phosphodiester-linked glucose.
Marchase R B, Koro L A, Kelly C M, McClay D R
Cell Vol 28(4)
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Date 01 Apr 1982
Research
A Drosophila model for xeroderma pigmentosum and Cockayne's syndrome: haywire encodes the fly homolog of ERCC3, a human excision repair gene.
Mounkes L C, Jones R S, Liang B C, Gelbart W, Fuller M T
Cell Vol 71(6)
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Date 11 Dec 1992
Research
Deficiency of the GPI anchor caused by a somatic mutation of the PIG-A gene in paroxysmal nocturnal hemoglobinuria.
Takeda J, Miyata T, Kawagoe K, Iida Y, Endo Y ...
Cell Vol 73(4)
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Date 21 May 1993
Research
Conformation-independent binding of monoglucosylated ribonuclease B to calnexin.
Zapun A, Petrescu S M, Rudd P M, Dwek R A, Thomas D Y ...
Cell Vol 88(1)
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Date 10 Jan 1997
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