चैनल का पता:
श्रेणियाँ:
शिक्षा
भाषा: हिंदी
ग्राहकों:
8.69K
चैनल से विवरण
🌐The Best educational channel on Biochemistry that Provides Latest 2021 Biochemistry materials
(Notes,Book,Videos)✔️
💠Premium 2020
💐CME videos
💐USMLE Videos
💐NEET Materials
Join now and Invite your friends
Ratings & Reviews
Reviews can be left only by registered users. All reviews are moderated by admins.
5 stars
1
4 stars
1
3 stars
0
2 stars
0
1 stars
0
नवीनतम संदेश 12
2022-05-27 08:12:01
A healthy couple, who recently emigrated from Eastern Europe, bring their 3-year-old son to the office for evaluation of an eczematous rash. On examination, the child also shows signs of intellectual disability and gait abnormality and has a musty body odor.
300 views05:12
2022-05-26 20:12:01
Educational objective: The nucleolus is a dense intranuclear body visible by light and electron microscopy that functions as the primary site of ribosome synthesis and assembly. All ribosomal RNA except SS rRNA is transcribed in the nucleolus.
345 views17:12
2022-05-26 08:12:01
41 voters375 views05:12
2022-05-26 08:11:01
352 views05:11
2022-05-25 21:12:01
Educational objective: In prokaryotes, DNA polymerase I has 5' to 3' exonuclease activity in addition to 5' to 3' polymerase and 3' to 5' exonuclease activities. This 5' to 3' exonuclease activity functions to remove the RNA primer created by RNA primase and repair damaged DNA sequences.
397 views18:12
2022-05-25 08:11:01
18 voters170 views05:11
2022-05-25 08:10:25
A pharmaceutical researcher develops a novel antibacterial drug that works by inhibiting exonuclease activity during DNA replication. When actively dividing Escherichia coli is exposed to the drug, enzymemediated nucleotide removal in the 5' to 3' direction is impaired, leading to inhibition of bacterial growth.
172 views05:10
2022-05-24 21:10:30
Educational objective: Achondroplasia is an autosomal dominant (AD) disorder that results in a gain-of-function mutation in the FGFR3 gene. Most individuals affected by AD disorders are heterozygous and have a 50% chance of transmitting the mutation to their offspring.
226 views18:10
2022-05-24 08:10:18
28 voters259 views05:10
2022-05-24 08:09:01
A married couple comes to the physician for routine prenatal counseling. The husband is 120 cm (3 ft 11 in) tall with disproportionately short upper and lower extremities, a large head, and a prominent forehead. He is unable to provide a biological family history as he was adopted. His spouse is of average height with
normal constitutional features, and her family history is insignificant. They are concerned about their unborn child's height.
248 views05:09
U
