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searching for I-mutation 32 found (76 total)

alternate case: i-mutation

Yellowface I budgerigar mutation (930 words) [view diff] no match in snippet view article find links to article

markings. The appearance of birds with other combinations of the Yellowface I mutation is discussed under Genetics below. In the UK, a yellowfaced bird was first

Variably protease-sensitive prionopathy (910 words) [view diff] no match in snippet view article find links to article

patients with a genetic CJD linked to PrP Valine (V) to isoleucine (I) mutation at residue 180 (PrPV180I); moreover, they found that the pathological

E caudata (849 words) [view diff] exact match in snippet view article find links to article

In a few texts in Old Norse, it represents short /æ/, the result of i-mutation of Proto-Germanic */a/, and contrasts with e, which represents Proto-Germanic

West Germanic gemination (641 words) [view diff] exact match in snippet view article find links to article

but not before any /j/ that it may have developed from had triggered i-mutation. It also triggered palatalization of velar consonants in Old English and

Italo-Celtic (1,431 words) [view diff] exact match in snippet view article find links to article

phenomenon is probably related to the feminine long ī stems and the Luwian i-mutation. the formation of superlatives with reflexes of the PIE suffix *-ism̥mo-

Ø (1,739 words) [view diff] exact match in snippet view article find links to article

∅ The letter arose to represent an /ø/ sound resulting primarily from i-mutation of /o/. There are at least two theories about the origin of the letter

Faroese orthography (537 words) [view diff] exact match in snippet view article find links to article

historical form of the word; ⟨ø⟩ was used when the vowel resulted from I-mutation of /o/ while ⟨ö⟩ was used when the vowel resulted from U-mutation of /a/

Hrethel (568 words) [view diff] exact match in snippet view article find links to article

root vowel using the early graphs ⟨œ⟩ (for the vowel resulting from the i-mutation of Common Germanic /o:/) and ⟨d⟩ (for the phoneme /θ/, pronounced [ð])

Old English phonology (3,167 words) [view diff] exact match in snippet view article find links to article

(distinguished as ie and īe in modern editions), which developed from i-mutation or umlaut of eo or ea, ēo or ēa. Scholars do not agree on how they were

Oisc of Kent (919 words) [view diff] exact match in snippet view article find links to article

=> *[oːs-ika-] (by the Ingvaeonic nasal spirant law) => [øːs-ika-] (by i-mutation) => [øːsk] (by high vowel loss and apocope). This form was represented

Blue budgerigar mutation (1,020 words) [view diff] no match in snippet view article find links to article

is situated on one of the autosomal chromosomes. The Yellowface Blue I mutation, the Yellowface II mutation form an autosomal co-dominant series of alleles

Foot (3,445 words) [view diff] exact match in snippet view article find links to article

"foot"), from PIE root *ped- "foot". The plural form feet is an instance of i-mutation. The human foot is a strong and complex mechanical structure containing

Anglo-Frisian languages (1,613 words) [view diff] exact match in snippet view article find links to article

Frisian ā/a OE breaking; in West Saxon palatal diphthongization follows i-mutation followed by syncope; Old Frisian breaking follows Phonemicization of palatals

Inch (3,154 words) [view diff] exact match in snippet view article find links to article

Phonological history of Old English § Palatalization and Germanic umlaut § I-mutation in Old English for more information. "Inch" is cognate with "ounce" (Old

Lamivudine (1,566 words) [view diff] no match in snippet view article find links to article

tolerated. In HIV, high level resistance is associated with the M184V/I mutation in the reverse transcriptase gene as reported by Raymond Schinazi's group

Complement factor I (2,243 words) [view diff] no match in snippet view article find links to article

"Recurrent atypical hemolytic uremic syndrome associated with factor I mutation in a living related renal transplant recipient". American Journal of Kidney

Middle English phonology (4,046 words) [view diff] exact match in snippet view article find links to article

⟨y⟩ is a development of earlier (West Saxon) ⟨ie⟩ from i-mutation of ⟨ea⟩, as the normal i-mutation of ⟨ea⟩ in Anglian is ⟨e⟩; for example, stern < styrne

Yiddish grammar (4,726 words) [view diff] exact match in snippet view article find links to article

order to form any diminutive, there sometimes needs to be a vowel shift (i-mutation/ i-umlaut). There are certain instances where only the plural can get

Andalusi Arabic (2,881 words) [view diff] exact match in snippet view article find links to article

particularly with short vowels, [ɪ] in certain circumstances, particularly when i-mutation was possible. Contact with native Romance speakers led to the introduction

RGS16 (1,521 words) [view diff] no match in snippet view article find links to article

"Palmitoylation regulates regulators of G-protein signaling (RGS) 16 function. I. Mutation of amino-terminal cysteine residues on RGS16 prevents its targeting to

Apolipoprotein AI (2,555 words) [view diff] no match in snippet view article find links to article

L, Dufour R, et al. (March 2006). "A novel nonsense apolipoprotein A-I mutation (apoA-I(E136X)) causes low HDL cholesterol in French Canadians". Atherosclerosis

History of English (6,054 words) [view diff] exact match in snippet view article find links to article

the Early Middle English period. The most important umlaut process was *i-mutation (c. 500 CE), which led to pervasive alternations of all sorts, many of

Middle Dutch (4,671 words) [view diff] exact match in snippet view article find links to article

singular present indicative forms, instead of e. This is a remnant of older i-mutation in these forms. Umlaut is also sometimes found in the past subjunctive

Lydian language (3,539 words) [view diff] exact match in snippet view article find links to article

Histories, I, 86. Sasseville, David (2017). "The Lydian nominal paradigm of i-mutation". Indo-European Linguistics. 5 (1): 130–146. doi:10.1163/22125892-00501002

NDUFA2 (1,125 words) [view diff] no match in snippet view article find links to article

Willems PH, Smeitink JA, van den Heuvel LP (Jun 2008). "NDUFA2 complex I mutation leads to Leigh disease". American Journal of Human Genetics. 82 (6): 1306–1315

Cytochrome b5 reductase (3,249 words) [view diff] no match in snippet view article find links to article

I MHb deficiency. Mechanisms and reactions are also similar to a type I mutation, but variants of this mutation can subsequently develop into chronic cyanosis

NDUFS8 (1,401 words) [view diff] no match in snippet view article find links to article

van den Heuvel L (December 1998). "The first nuclear-encoded complex I mutation in a patient with Leigh syndrome". American Journal of Human Genetics

English plurals (7,737 words) [view diff] exact match in snippet view article find links to article

belong to the Old English consonant declension, see Germanic umlaut § I-mutation in Old English. There are many compounds of man and woman that form their

Old High German lullaby (1,238 words) [view diff] exact match in snippet view article find links to article

According to Howard, scholars at the time regarded the /e/-sound from i-mutation as open, and a forger would therefore have chosen the Hebrew Segol instead

Elmer H. Antonsen (341 words) [view diff] case mismatch in snippet view article find links to article

University of Illinois Urbana-Champaign (Ph.D.) Thesis The Investigation of I-Mutation in the Germanic Languages Doctoral advisor Ernst Alfred Philippson Academic

Solid white (chicken plumage) (3,966 words) [view diff] no match in snippet view article

few breeds such as White Leghorn and Hamburg have a "dominant white" I mutation for plumage color. This mutation selectively inhibits black color and

CUX1 (4,649 words) [view diff] no match in snippet view article find links to article

Patrikis M, Bryan E, Thomas N, Rice G, Quinn M, Baker M, and Campbell I. "Mutation analysis of CDP, TP53, and KRAS in uterine leiomyomas". Molecular Carcinogenesis