规范要多
发表于 2025-3-23 13:14:55
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Monocle
发表于 2025-3-23 15:25:04
Denise Rotta Ruttkay Pereira,Claudia Schweiger,Carolina F. de Souza,Simone Fagondes,Denise Manica,Roy located but differ greatly in their mutation acceptance rates. Thus, each gene is an independent mutational entity. Synonymous mutations, and correlated mutations in regions that do not encode amino acids, may be important for changing the ‘pattern’ of a genome, so sparking the onset of branching
过时
发表于 2025-3-23 20:11:28
Helen Beard,Sofia Hassiotis,Amanda J. Luck,Tina Rozaklis,John J. Hopwood,Kim M. Hemsleythese purposes. Purine-loading pressure would have supported protein-pressure in provoking the splitting into introns of what might otherwise have been large exons. From this perspective we can understand why the genes of the malaria parasite are extraordinarily long, and we can identify the potenti
经典
发表于 2025-3-24 01:21:11
Ulrike Schueler,Christine Kaneski,Alan Remaley,Stephen Demosky,Nancy Dwyer,Joan Blanchette-Mackie,Joetween symbols (letters, bases). In DNA this finds expression as Chargaff’s second parity rule (PR2), namely Chargaff’s first parity rule for duplex DNA (PR1) also applies, to a close approximation, to single-stranded DNA. Selective forces generating the PR2 equivalences may have acted at higher oli
体贴
发表于 2025-3-24 05:02:36
Erratum to: LC-MS/MS Analysis of Cerebrospinal Fluid Metabolites in the Pterin Biosynthetic Pathway
linguistics
发表于 2025-3-24 09:56:52
Erratum to: Treatment with Mefolinate (5-Methyltetrahydrofolate), but Not Folic Acid or Folinic Aci
解脱
发表于 2025-3-24 11:06:34
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legacy
发表于 2025-3-24 16:38:35
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悬崖
发表于 2025-3-24 20:47:41
A Highly Diverse Portrait: Heterogeneity of Neuropsychological Profiles in cblC Defect,ment. This study underscores the importance of conducting in-depth neuropsychological assessments in individuals with cblC, the results of which may be particularly helpful for clinical management, guidance toward rehabilitation services, and educational/vocational planning.
Incommensurate
发表于 2025-3-25 01:42:31
Heterozygous Monocarboxylate Transporter 1 (MCT1, ,) Deficiency as a Cause of Recurrent Ketoacidosi8Ter) was detected in both boys. It was shared by their healthy mother and by the proband’s half-sister, but was absent in the proband’s father. MCT1 deficiency may be more prevalent than is apparent, as clinical manifestations can occur both in individuals with bi- and monoallelic mutations. It may