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Tegesé saka "enzyme deficiency" ing bausastra Basa Inggris

Bausastra
BAUSASTRA
section

PANGOCAP SAKA ENZYME DEFICIENCY ING BASA INGGRIS

enzyme deficiency  [ˈenzaɪm dɪˈfɪʃənsɪ] play
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GOLONGAN PARAMASASTRA SAKA ENZYME DEFICIENCY

tembung aran
tembung sipat
tembung kriya
tembung katrangan
tembung ganti
preposition
panyambung
panemtu
seru

APA TEGESÉ ENZYME DEFICIENCY ING BASA INGGRIS?

Klik kanggo deleng deifinisi asli saka «enzyme deficiency» ing bausastra Basa Inggris.
Klik kanggo deleng pertalan otomatis saka definisi ing Basa Jawa.

Kesalahan metabolisme inborn

Inborn error of metabolism

Kasus metabolisme inborn mbentuk kelas penyakit genetik sing gedhe sing nglibatake kelainan metabolisme. Mayoritas amarga cacat saka gén tunggal sing kode kanggo enzim sing nggampangake konversi warna zat menyang liyane. Ing akèh gangguan, masalah muncul amarga akumulasi zat-zat sing beracun utawa ngganggu fungsi normal, utawa kanggo efek ngurangi kemampuan kanggo nyintesis senyawa penting. Kesalahan metabolisme inborn saiki asring diarani minangka penyakit metabolis kongenital utawa penyakit metabolik sing diwarisake. Kasalahan metabolisme ing kasunyatan dicipta dening dokter Inggris, Archibald Garrod, ing awal abad kaping 20. Dheweke dikenal amarga karya sing ngowahi hipotesis "siji gene-siji", adhedhasar studi marang sifat lan warisan alkaptonuria. Tèks mani, Inborn Errors of Metabolism diterbitaké taun 1923. Inborn errors of metabolism form a large class of genetic diseases involving disorders of metabolism. The majority are due to defects of single genes that code for enzymes that facilitate conversion of various substances into others. In most of the disorders, problems arise due to accumulation of substances which are toxic or interfere with normal function, or to the effects of reduced ability to synthesize essential compounds. Inborn errors of metabolism are now often referred to as congenital metabolic diseases or inherited metabolic diseases. The term inborn error of metabolism was coined by a British physician, Archibald Garrod, in the early 20th century. He is known for work that prefigured the "one gene-one enzyme" hypothesis, based on his studies on the nature and inheritance of alkaptonuria. His seminal text, Inborn Errors of Metabolism was published in 1923.

Definisi saka enzyme deficiency ing bausastra Basa Inggris

Defisiensi enzim sing ana ing kamus kasebut yaiku kegagalan awak kanggo ngasilake enzim tartamtu.

The definition of enzyme deficiency in the dictionary is failure of the body to produce a specific enzy.

Klik kanggo deleng deifinisi asli saka «enzyme deficiency» ing bausastra Basa Inggris.
Klik kanggo deleng pertalan otomatis saka definisi ing Basa Jawa.

TEMBUNG BASA INGGRIS KANG KALARAS PADHA KARO ENZYME DEFICIENCY


agency
ˈeɪdʒənsɪ
cecutiency
sɪˈkjuːʃənsɪ
currency
ˈkʌrənsɪ
deficiency
dɪˈfɪʃənsɪ
dissentiency
dɪˈsɛnʃənsɪ
efficiency
ɪˈfɪʃənsɪ
emergency
ɪˈmɜːdʒənsɪ
frequency
ˈfriːkwənsɪ
immunodeficiency
ˌimjʊnəʊdɪˈfɪʃənsɪ
inefficiency
ˌɪnɪˈfɪʃənsɪ
insufficiency
ˌɪnsəˈfɪʃənsɪ
physiciancy
fɪˈzɪʃənsɪ
potency
ˈpəʊtənsɪ
pregnancy
ˈprɛɡnənsɪ
proficiency
prəˈfɪʃənsɪ
self-sufficiency
ˌsɛlfsəˈfɪʃənsɪ
sentiency
ˈsenʃənsɪ
sufficiency
səˈfɪʃənsɪ
superefficiency
ˌsuːpərɪˈfɪʃənsɪ
trenchancy
ˈtrɛntʃənsɪ

TEMBUNG BASA INGGRIS KANG AWIT KAYA ENZYME DEFICIENCY

enwrapping
enwrappings
enwreath
Enzed
Enzedder
enzian
enzone
enzootic
enzootically
enzymatic
enzymatically
enzyme
enzyme-linked immunosorbent assay
enzymic
enzymically
enzymological
enzymologist
enzymology
enzymolysis
enzymolytic

TEMBUNG BASA INGGRIS KANG WUSANANÉ KAYA ENZYME DEFICIENCY

adrenal insufficiency
conveniency
current efficiency
energy efficiency
expediency
fuel efficiency
heat efficiency
immune deficiency
leniency
luminous efficiency
mental deficiency
parturiency
protein deficiency
quantum efficiency
resiliency
saliency
tendency
thermal efficiency
transiency
vitamin deficiency
volumetric efficiency

Dasanama lan kosok bali saka enzyme deficiency ing bausastra dasanama Basa Inggris

DASANAMA

Pertalan saka «enzyme deficiency» menyang 25 basa

PAMERTAL
online translator

PERTALAN SAKA ENZYME DEFICIENCY

Weruhi pertalan saka enzyme deficiency menyang 25 basa nganggo Basa Inggris pamertal multi basa kita.
pertalan saka enzyme deficiency saka Basa Inggris menyang basa liyané kang kasuguhaké ing perangan iki kajupuk saka pertalan statistik otomatis; ing ngendhi inti unit pertalan yaiku tembung «enzyme deficiency» ing Basa Inggris.

Pamertal Basa Inggris - Basa Cina

酶缺乏症
1,325 yuta pamicara

Pamertal Basa Inggris - Basa Spanyol

deficiencia de la enzima
570 yuta pamicara

Basa Inggris

enzyme deficiency
510 yuta pamicara

Pamertal Basa Inggris - Basa India

एंजाइम की कमी
380 yuta pamicara
ar

Pamertal Basa Inggris - Basa Arab

نقص انزيم
280 yuta pamicara

Pamertal Basa Inggris - Basa Rusia

фермент дефицит
278 yuta pamicara

Pamertal Basa Inggris - Basa Portugis

deficiência da enzima
270 yuta pamicara

Pamertal Basa Inggris - Basa Bengali

এনজাইমের অভাব
260 yuta pamicara

Pamertal Basa Inggris - Basa Prancis

déficit enzymatique
220 yuta pamicara

Pamertal Basa Inggris - Basa Malaysia

Kekurangan enzim
190 yuta pamicara

Pamertal Basa Inggris - Basa Jerman

Enzymmangel
180 yuta pamicara

Pamertal Basa Inggris - Basa Jepang

酵素欠損
130 yuta pamicara

Pamertal Basa Inggris - Basa Korea

효소 결핍
85 yuta pamicara

Pamertal Basa Inggris - Basa Jawa

Kekurangan enzim
85 yuta pamicara
vi

Pamertal Basa Inggris - Basa Vietnam

thiếu hụt enzyme
80 yuta pamicara

Pamertal Basa Inggris - Basa Tamil

நொதி குறைபாடு
75 yuta pamicara

Pamertal Basa Inggris - Basa Marathi

सजीवांच्या शरीरात निर्मार्ण होणारे समरूपता कमी
75 yuta pamicara

Pamertal Basa Inggris - Basa Turki

Enzim eksikliği
70 yuta pamicara

Pamertal Basa Inggris - Basa Italia

deficit enzimatico
65 yuta pamicara

Pamertal Basa Inggris - Basa Polandia

niedobór enzymu
50 yuta pamicara

Pamertal Basa Inggris - Basa Ukrania

фермент дефіцит
40 yuta pamicara

Pamertal Basa Inggris - Basa Romawi

deficit enzimatic
30 yuta pamicara
el

Pamertal Basa Inggris - Basa Yunani

ανεπάρκεια του ενζύμου
15 yuta pamicara
af

Pamertal Basa Inggris - Basa Afrikaans

ensiemtekort
14 yuta pamicara
sv

Pamertal Basa Inggris - Basa Swedia

enzymbrist
10 yuta pamicara
no

Pamertal Basa Inggris - Basa Norwegia

enzym mangel
5 yuta pamicara

Trèn migunakaké enzyme deficiency

TRÈN

KEKAREPAN PANGGUNAN ARAN «ENZYME DEFICIENCY»

0
100%
ARANG KEREPÉ
Umum digunakaké
70
/100
Kart kang kapituduh ing dhuwur nuduhaké arang kerepé kagunané aran «enzyme deficiency» ing negara kang béda-béda.
Dhasar kekarepan panggolékan lan kagunaan kang umum saka enzyme deficiency
Daptar dhasar panggolékan kang dilakoni dening pangguna kanggo migunakaké Basa Inggris bausastra online kita lan gupita kang asring digunakaké nganggo tembung «enzyme deficiency».

ARANG KEREPÉ PANGGUNANÉ ARAN «ENZYME DEFICIENCY» SALAWASÉ IKI

Gambar awujudaké arang kerepé evolusi taunan panggunané saka tembung «enzyme deficiency» sasuwiné 500 taun. Panggunané andedhasar panalitén sapira asringé aran «enzyme deficiency» metu ing sumber kang kacé digital ing Basa Inggris antaraning taun 1500-an lan wektu iki.

Tuladha kang kagunakaké ing sastra Basa Inggris, pethikan lan warta babaganenzyme deficiency

TULADHA

BUKU BASA INGGRIS KAKAIT KARO «ENZYME DEFICIENCY»

Temukaké kagunané saka enzyme deficiency ing pilihan bibliografi iki. Buku kang kakait dening enzyme deficiency lan pethikan cekak kang padha kanggo nyediyakaké panggunané ing sastra Basa Inggris.
1
Walker's Pediatric Gastrointestinal Disease
... excess with OTC deficiency. CPS I deficiency is a rare condition resulting from an autosomal recessive mutation. This mutation gives rise to a wide clinical heterogenicity in patients affected depending on the degree of enzyme deficiency .
Ronald (Professor of Paediatrics Kleinman, 2008
2
Modern Hematology: Biology and Clinical Management
Class I variants: severe enzyme deficiency (rare, chronic active hemolysis) • Class II variants: severe enzyme deficiency (only intermittent severe hemolysis, frequent in Mediterranean patients) • Class III variants: moderate enzyme deficiency ...
Reinhold Munker, Erhard Hiller, Jonathan Glass, 2007
3
NORD Guide to Rare Disorders
The pathogenesis of these forms of hemolytic anemia is related to enzyme deficiency related to defects in the gly- colytic pathway, the pentose phosphate pathway, nucleo- tide, or glutathione metabolism. It is the most common disorder of red ...
National Organization for Rare Disorders, 2003
4
Genetic Disorders and the Fetus: Diagnosis, Prevention and ...
Partial enzyme deficiency has been observed in obligate carriers by measurement of enzyme activity in leukocytes, erythrocytes or skin fibroblasts. 114'1 15 Prenatal diagnosis is available for the infantile fatal forms of GSD IV, by measuring ...
Aubrey Milunsky, Jeff Milunsky, 2011
5
Mayo Clinic Internal Medicine Review
G6PD deficiency: the most common RBC enzyme deficiency; it is inherited on the X chromosome. • G6PD deficiency provides some protection against falciparum malaria. • Half-life: normal enzyme, 62 days; reticulocytes, 124 days; and aged ...
Thomas M. Habermann, 2006
6
Clinical Reproductive Medicine and Surgery
The classic forms of neonatal virilization result from a severe enzyme deficiency. Nonclassic forms, due to a less severe enzyme deficiency, may result in delayed signs of androgen excess. In this chapter, the three enzyme deficiencies that ...
Tommaso Falcone, William W. Hurd, 2007
7
Lysosomal Storage Disorders
As for many other genetic diseases the most frequent cause of enzyme deficiency in metachromatic leukodystrophy is the misfolding of the enzyme, its retention in the endoplasmic reticulum, and subsequent degradation (e.g., Kafert et al., ...
John A. Barranger, Mario Cabrera-Salazar, 2007
8
Clinical Gynecologic Endocrinology and Infertility
Finally, heterozygotes for either the mild or severe deficiency exhibit the mildest enzyme deficiency and are clinically asymptomatic. However, the severity of clinical presentation (phenotype) cannot accurately predict the genotype; this ...
Leon Speroff, Marc A. Fritz, 2005
9
Disorders of Voluntary Muscle
... enzyme deficiency are necessary. However, in the work-up of patients with exercise intolerance and myoglobinuria, analysis of aldolase activity in skeletal muscle specimens needs to be included. Myoadenylate deaminase deficiency ...
George Karpati, David Hilton-Jones, Robert C. Griggs, 2001
10
Clinical Laboratory Medicine
The enzyme deficiency can be demonstrated in liver or fibroblasts. GSD Type V ( McArdle Disease) GSD type V is caused by complete deficiency of muscle glycogen phosphorylase enzyme. Characteristically, patients present in their third or ...
Kenneth D. McClatchey, 2002

BABAGAN WARTA KANG NGLEBOKAKÉ ARAN «ENZYME DEFICIENCY»

Weruhi yèn pawarta nasional lan internasional wis ngomongaké lan kepriyé aran enzyme deficiency digunakaké ing babagan warta iki.
1
Coprophagia, anyone?
Some medical issues that can bring on this habit in your dog are pancreatic insufficiency or enzyme deficiency. Intestinal malabsorption and ... «The Suburban Newspaper, Jul 15»
2
Research Analysts' Weekly Ratings Updates for Celladon Corp …
Its therapeutic portfolio for diseases characterized by SERCA enzyme deficiency includes both gene therapies and small molecule compounds. «sleekmoney, Jul 15»
3
Celladon Corp Rating Reiterated by BMO Capital Markets (CLDN)
Its therapeutic portfolio for diseases characterized by SERCA enzyme deficiency includes both gene therapies and small molecule compounds. «The Legacy, Jul 15»
4
Natural Health from A to Z
If ENZYMES keep you from getting indigestion, then your indigestion was an enzyme deficiency. Levels of enzymes available to digest food ... «Mason County News, Jul 15»
5
Celladon Corp's Market Perform Rating Reiterated at BMO Capital …
Its therapeutic portfolio for diseases characterized by SERCA enzyme deficiency includes both gene therapies and small molecule compounds. «WKRB News, Jul 15»
6
Celladon Corp Rating Reiterated by HC Wainright (CLDN)
Its therapeutic portfolio for diseases characterized by SERCA enzyme deficiency includes both gene therapies and small molecule compounds. «sleekmoney, Jun 15»
7
Hot Stocks: Intuit Inc. (NASDAQ:INTU), FireEye Inc. (NASDAQ:FEYE …
... portfolio includes both gene therapies and small molecule compounds targeting diseases characterized by SERCA enzyme deficiency. «Citizen Dispatch, Jun 15»
8
Analysts' Downgrades for June, 27th (ACHI, AWAY, BLDR, BNCL …
... genetic enzyme replacement therapy to correct the Sarco/endoplasmic reticulum Ca2+-ATPase 2a enzyme deficiency in heart failure patients ... «Mideast Time, Jun 15»
9
Celladon Corporation Short Interest Update
Its therapeutic portfolio for diseases characterized by SERCA enzyme deficiency includes both gene therapies and small molecule compounds. «OTC Outlook, Jun 15»
10
MP: I'll battle for Harvey in parliament
The inherited illness is caused by an enzyme deficiency, which means Harvey's skeleton will not develop properly. His organs will continue to ... «Southwark News, Jun 15»

KAITAN
« EDUCALINGO. Enzyme deficiency [online]. Kasedya <https://educalingo.com/jv/dic-en/enzyme-deficiency>. Mei 2024 ».
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