technical term; word or phrase that is part of genetics terminology
4 statements, 0 sitelinks - 13:07, 30 June 2023
medical specialty that involves the diagnosis and management of hereditary disorders
2 statements, 0 sitelinks - 13:33, 30 June 2023
language used in the field of genetics
4 statements, 0 sitelinks - 13:07, 30 June 2023
concept in genetics
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Wikimedia glossary list article
2 statements, 0 sitelinks - 13:06, 30 June 2023
science of genes, heredity, and variation in living organisms
6 statements, 0 sitelinks - 09:48, 29 June 2023
genetics term
4 statements, 0 sitelinks - 13:11, 30 June 2023
American multinational biopharmaceutical company
17 statements, 1 sitelink - 09:35, 16 August 2023
skin color of an individual as a result of genetics
4 statements, 0 sitelinks - 23:04, 10 December 2023
investigative technique used in pre-clinical and clinical research, epidemiology, chemistry, immunology, genetics and other areas
1 statement, 0 sitelinks - 10:22, 12 January 2024
==Molecular genetics==
...haliana|volume=40|issue=12|pages=1489–92|doi=10.1038/ng.253|journal=Nature Genetics|s2cid=13225884|url=http://www.repository.naturalis.nl/document/456722}}</re
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| former_names = Applied Molecular Genetics<br>(1980–1983)
*'''Amgen''' <small>(Founded 1983 as Applied Molecular Genetics)</small>
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...o a mutation in the sodium glucose cotransporter (SGLT2) | journal = Human Genetics | volume = 111 | issue = 6 | pages = 544–7 | date = Dec 2002 | pmid = 12436
...are responsible for autosomal recessive renal glucosuria | journal = Human Genetics | volume = 114 | issue = 3 | pages = 314–6 | date = Feb 2004 | pmid = 14614
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5 KB (466 words) - 08:59, 19 February 2024
...o a mutation in the sodium glucose cotransporter (SGLT2) | journal = Human Genetics | volume = 111 | issue = 6 | pages = 544–7 | date = Dec 2002 | pmid = 12436
...are responsible for autosomal recessive renal glucosuria | journal = Human Genetics | volume = 114 | issue = 3 | pages = 314–6 | date = Feb 2004 | pmid = 14614
...
5 KB (601 words) - 19:48, 18 February 2024
...o a mutation in the sodium glucose cotransporter (SGLT2) | journal = Human Genetics | volume = 111 | issue = 6 | pages = 544–7 | date = Dec 2002 | pmid = 12436
...are responsible for autosomal recessive renal glucosuria | journal = Human Genetics | volume = 114 | issue = 3 | pages = 314–6 | date = Feb 2004 | pmid = 14614
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5 KB (625 words) - 19:48, 18 February 2024
胞子形成の開始には、σHとSpo0Aという2つの[[Transcription (genetics)/ja|転写]]制御因子が重要な役割を果たす。主にSpo0A〜Pの蓄積濃度を制御することによって、さらにいくつかのタンパク質が関与している。Spo0A
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8 KB (377 words) - 21:43, 17 April 2024
| [[Medical genetics/ja]] || None
|[[Anatomy/ja|解剖学]]、[[Biochemistry/ja|生化学]]、[[Embryology/ja|発生学]]、[[Genetics/ja|遺伝学]]、[[Pharmacology/ja|薬理学]]、[[Toxicology/ja|毒物学]]
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医師や基礎研究者は脂質異常症を2つの方法で分類している。ひとつは体内での発現（増加する脂質の種類を含む）である。もう1つは、その病態の根本的な原因（[[genetics/ja|遺伝]]、または他の病態による二次的なもの）によるものである。ほとんどの疾患は遺伝と生活習慣の問題が交差しているため、この分類には問題がある。し
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19 KB (475 words) - 20:46, 13 April 2024
* [[Clinical genetics/ja]]
* [[Clinical Genetics/ja|臨床遺伝学]]
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35 KB (1,165 words) - 13:04, 20 February 2024
| [[Medical genetics]] || None
|[[Anatomy]], [[Biochemistry]], [[Embryology]], [[Genetics]], [[Pharmacology]], [[Toxicology]]
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36 KB (4,478 words) - 16:51, 19 February 2024