錯義突變 (Chinese Wikipedia)

Analysis of information sources in references of the Wikipedia article "錯義突變" in Chinese language version.

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Minde, David P; Anvarian, Zeinab; Rüdiger, Stefan GD; Maurice, Madelon M. Messing up disorder: how do missense mutations in the tumor suppressor protein APC lead to cancer?. Molecular Cancer. 1 January 2011, 10 (1): 101. PMC 3170638 . PMID 21859464. doi:10.1186/1476-4598-10-101.
Boillée, S; Vande Velde, C; Cleveland, D. W. ALS: A disease of motor neurons and their nonneuronal neighbors. Neuron. 2006, 52 (1): 39–59. PMID 17015226. doi:10.1016/j.neuron.2006.09.018 .
Al-Haggar M, Madej-Pilarczyk A, Kozlowski L, Bujnicki JM, Yahia S, Abdel-Hadi D, Shams A, Ahmad N, Hamed S, Puzianowska-Kuznicka M. A novel homozygous p.Arg527Leu LMNA mutation in two unrelated Egyptian families causes overlapping mandibuloacral dysplasia and progeria syndrome.. Eur J Hum Genet. 2012, 20 (11): 1134–40. PMC 3476705 . PMID 22549407. doi:10.1038/ejhg.2012.77.
Bullock, AN; Henckel, J; DeDecker, BS; Johnson, CM; Nikolova, PV; Proctor, MR; Lane, DP; Fersht, AR. Thermodynamic stability of wild-type and mutant p53 core domain. Proc. Natl. Acad. Sci. U.S.A. 23 December 1997, 94 (26): 14338–42. Bibcode:1997PNAS...9414338B. PMC 24967 . PMID 9405613. doi:10.1073/pnas.94.26.14338 .
Minde, DP; Maurice, MM; Rüdiger, SG. Determining biophysical protein stability in lysates by a fast proteolysis assay, FASTpp. PLOS ONE. 2012, 7 (10): e46147. Bibcode:2012PLoSO...746147M. PMC 3463568 . PMID 23056252. doi:10.1371/journal.pone.0046147 .

Definition of Missense mutation. MedTerms medical dictionary. MedicineNet. 2012-03-19 [2022-12-28]. （原始内容存档于2013-12-02）.

Henderson, Mark. A Monumental Breakthrough?. The News-Star. May 1, 2020: A1, A7 [21 November 2022]. （原始内容存档于2022-11-21）（英语）.

Minde, David P; Anvarian, Zeinab; Rüdiger, Stefan GD; Maurice, Madelon M. Messing up disorder: how do missense mutations in the tumor suppressor protein APC lead to cancer?. Molecular Cancer. 1 January 2011, 10 (1): 101. PMC 3170638 . PMID 21859464. doi:10.1186/1476-4598-10-101.
Boillée, S; Vande Velde, C; Cleveland, D. W. ALS: A disease of motor neurons and their nonneuronal neighbors. Neuron. 2006, 52 (1): 39–59. PMID 17015226. doi:10.1016/j.neuron.2006.09.018 .
Al-Haggar M, Madej-Pilarczyk A, Kozlowski L, Bujnicki JM, Yahia S, Abdel-Hadi D, Shams A, Ahmad N, Hamed S, Puzianowska-Kuznicka M. A novel homozygous p.Arg527Leu LMNA mutation in two unrelated Egyptian families causes overlapping mandibuloacral dysplasia and progeria syndrome.. Eur J Hum Genet. 2012, 20 (11): 1134–40. PMC 3476705 . PMID 22549407. doi:10.1038/ejhg.2012.77.
Bullock, AN; Henckel, J; DeDecker, BS; Johnson, CM; Nikolova, PV; Proctor, MR; Lane, DP; Fersht, AR. Thermodynamic stability of wild-type and mutant p53 core domain. Proc. Natl. Acad. Sci. U.S.A. 23 December 1997, 94 (26): 14338–42. Bibcode:1997PNAS...9414338B. PMC 24967 . PMID 9405613. doi:10.1073/pnas.94.26.14338 .
Minde, DP; Maurice, MM; Rüdiger, SG. Determining biophysical protein stability in lysates by a fast proteolysis assay, FASTpp. PLOS ONE. 2012, 7 (10): e46147. Bibcode:2012PLoSO...746147M. PMC 3463568 . PMID 23056252. doi:10.1371/journal.pone.0046147 .

Definition of Missense mutation. MedTerms medical dictionary. MedicineNet. 2012-03-19 [2022-12-28]. （原始内容存档于2013-12-02）.
Henderson, Mark. A Monumental Breakthrough?. The News-Star. May 1, 2020: A1, A7 [21 November 2022]. （原始内容存档于2022-11-21）（英语）.
141900 Hemoglobin—Beta Locus; HBB: .0243 Hemoglobin S. Sickle Cell Anemia, included. Malaria, Resistance to, included. HBB, GLU6VAL — 141900.0243. Online 'Mendelian Inheritance in Man' (OMIM). [2022-12-28]. （原始内容存档于2023-09-13）.